China, People’s Republic

In this paper the accidental release of hydrogen from cryogenic liquid storage tank and the subsequent consequences are studied including hydrogen cold cloud fire ball jet fire flash fire and vapor cloud explosion. The cold effect thermal effects and explosion overpressures from the above consequences are evaluated using IGC and TNO harm criteria. Results show that for instantaneous releases of liquid hydrogen the sequence of harm effect distances is that vapor cloud explosion>flash fire>cold cloud> fireball. For continuous releases of liquid hydrogen the sequence of harm effect distances is that vapor cloud explosion>jet fire>flash fire>cold cloud. The vapor cloud explosion is the leading consequence of both instantaneous and continuous releases and may be used for the determination of safety distances of a liquid hydrogen tank. Besides the harm effect distances of liquid hydrogen tank are compared with those of compressed hydrogen storages with equivalent mass. Results show that the liquid hydrogen storage may be safer than 70MPa gaseous storage in case of leak scenario but may be more dangerous than 70MPa storage in case of catastrophic rupture. It is difficult to tell which storage is safer from a consequence perspective. Further investigation need to be made from a standpoint of risk which combined both consequences and the likelihood of scenarios.

Blending hydrogen into existing natural gas pipelines has been proposed as a means of increasing the output of renewable energy systems such as large wind farms. X80 pipeline steel is commonly used for transporting natural gas and such steel is subjected to concurrent hydrogen invasion with mechanical loading while being exposed to hydrogen containing environments directly resulting in hydrogen embrittlement (HE). In accordance with American Society for Testing and Materials (ASTM) standards the mechanical properties of X80 pipeline steel have been tested in natural gas/hydrogen mixtures with 0 5.0 10.0 20.0 and 50.0vol% hydrogen at the pressure of 12 MPa. Results indicate that X80 pipeline steel is susceptible to hydrogen-induced embrittlement in natural gas/hydrogen mixtures and the HE susceptibility increases with the hydrogen partial pressure. Additionally the HE susceptibility depends on the textured microstructure caused by hot rolling especially for the notch specimen. The design calculation by the measured fatigue data reveals that the fatigue life of the X80 steel pipeline is dramatically degraded by the added hydrogen.

Laminar burning velocities (SL) of hydrogen/ammonia mixtures in air at atmospheric pressure were studied experimentally and numerically. The blending of hydrogen with ammonia two fuels that have been proposed as promising carriers for renewable energy causes the laminar flame speed of the mixture SL to decrease significantly. However details of this have not previously available. Systematic measurements were therefore performed for a series of hydrogen/ammonia mixtures with wide ranges of mole fractions of blended ammonia (XNH3) and equivalence ratio using a heat flux method based on heat flux of a flat flame transferred to the burner surface. It was found that the mixture of XNH3 = 40% has a value of SL close to that of methane which is the dominant component of natural gas. Using three chemical kinetic mechanisms available in the literature i.e. the well-known GRI-Mech 3.0 mechanism and two mechanisms recently released SL were also modelled for the cases studied. However the discrepancies between the experimental and numerical results can exceed 50% with the GRI-Mech 3.0 mechanism. Discrepancies were also found between the numerical results obtained with different mechanisms. These results can contribute to an increase in both the safety and efficiency of the coutilization of these two types of emerging renewable fuel and to guiding the development of better kinetic models.

In this work a mixed-cation borohydride (K2Mn(BH4)4) with P21/n structure was successfully synthesized by mechanochemical milling of the 2KBH4–MnCl2 sample under argon. The structural and thermal decomposition properties of the borohydride compounds were investigated using XRD Raman spectroscopy FTIR TGA-MS and DSC. Apart from K2Mn(BH4)4 the KMnCl3 and unreacted KBH4 compounds were present in the milled 2KBH4–MnCl2. The two mass loss regions were observed for the milled sample: one was from 100 to 160 °C with a 1.6 ± 0.1 wt% loss (a release of majority hydrogen and trace diborane) which was associated with the decomposition of K2Mn(BH4)4 to form KBH4 boron and finely dispersed manganese; the other was from 165 to 260 °C with a 1.9 ± 0.1 wt% loss (only hydrogen release) which was due to the reaction of KBH4 with KMnCl3 to give KCl boron finely dispersed manganese. Simultaneously the formed KCl could dissolve in KBH4 to yield a K(BH4)xCl1−x solid solution and also react with KMnCl3 to form a new compound K4MnCl6.

Today in order to reduce the increase of the carbon dioxide emissions a large number of renewable energy resources (RES) are already implemented. Considering both the intermittency and uncertainty of the RES the energy storage system (ESS) is still needed for balancing and stabilizing the power system. Among different existing categories of ESS the hydrogen storage systems (HSS) have the highest energy density and are crucial for the RES integration. In addition RES are located in faraway regions and are often transmitted to the terminal consumption center through HVDC (high voltage direct current) due to its lower power loss. In this paper we present a power supply system that achieves low-carbon emissions through combined HSS and HVDC technology. First the combined HSS and the HVDC model are established. Secondly the rule-based strategy for operating the HSS microgrid is presented. Then an operating strategy for a typical network i.e. the pure RES generation station-HVDC transmission-microgrids is demonstrated. Finally the best sizing capacities for all components are found by the genetic algorithm. The results prove the efficiency of the presented sizing approach for a pure RES electric system.

Hydrogen storage is a key link in hydrogen economy where solid-state hydrogen storage is considered as the most promising approach because it can meet the requirement of high density and safety. Thereinto magnesium-based materials (MgH2) are currently deemed as an attractive candidate due to the potentially high hydrogen storage density (7.6 wt%) however the stable thermodynamics and slow kinetics limit the practical application. In this study we design a ternary transition metal sulfide FeNi2S4 with a hollow balloon structure as a catalyst of MgH2 to address the above issues by constructing a MgH2/Mg2NiH4−MgS/Fe system. Notably the dehydrogenation/hydrogenation of MgH2 has been significantly improved due to the synergistic catalysis of active species of Mg2Ni/Mg2NiH4 MgS and Fe originated from the MgH2-FeNi2S4 composite. The hydrogen absorption capacity of the MgH2-FeNi2S4 composite reaches to 4.02 wt% at 373 K for 1 h a sharp contrast to the milled-MgH2 (0.67 wt%). In terms of dehydrogenation process the initial dehydrogenation temperature of the composite is 80 K lower than that of the milled-MgH2 and the dehydrogenation activation energy decreases by 95.7 kJ mol–1 compared with the milled-MgH2 (161.2 kJ mol–1). This method provides a new strategy for improving the dehydrogenation/hydrogenation performance of the MgH2 material.

The fatigue crack growth rate of warm-rolled AISI 316 austenitic stainless steel was investigated by controlling rolling strain and temperature in argon and hydrogen gas atmospheres. The fatigue crack growth rates of warm-rolled 316 specimens tested in hydrogen decreased with increasing rolling temperature especially 400 °C. By controlling the deformation temperature and strain the influences of microstructure (including dislocation structure deformation twins and α′ martensite) and its evolution on hydrogen-induced degradation of mechanical properties were separately discussed. Deformation twins deceased and dislocations became more uniform with the increase in rolling temperature inhibiting the formation of dynamic α′ martensite during the crack propagation. In the cold-rolled 316 specimens deformation twins accelerated hydrogen-induced crack growth due to the α′ martensitic transformation at the crack tip. In the warm-rolled specimens the formation of α′ martensite around the crack tip was completely inhibited which greatly reduced the fatigue crack growth rate in hydrogen atmosphere.

Deflagration-to-Detonation Transition Ratio (DDTR) is an important parameter in measuring the hazard of hydrogen detonation at given thermodynamic conditions. It’s among the major tasks to evaluate DDTR in the study of hydrogen safety in a nuclear containment. With CFD tools detailed distribution of thermodynamic parameters at each instant can be simulated with considerable reliability. Then DDTR can be estimated using related CFD output. Forstochastic or epistemic reasons uncertainty always exists in input parameters during computations. This lack of accuracy can finally be reflected in the uncertainty of computation results e.g. DDTR in our consideration. The analysis of the influence of the input uncertainty is therefore a key step to understand the model’s response on the output and possibly to improve the accuracy. The increase of computational power makes it possible to perform statistics-based sensitivity and uncertainty (SU) analysis on CFD simulations. This paper aims at presenting some ideas on the procedure in safety analysis on hydrogen in nuclear containment. A hydrogen recombiner case is constructed and simulated with CFD method. DDTR at each instant is computed using a semi-empirical method. RBD-FAST based SU analysis is performed on the result.

Hydrogen embrittlement is one of the largest obstacles against the commercialisation of ultra-high strength quenching and partitioning (Q&P) steels with ultimate tensile strength over 1500 MPa including the hot stamped steel parts that have undergone a Q&P treatment. In this work the influence of partitioning temperature on hydrogen embrittlement of ultra-high strength Q&P steels is studied by pre-charged tensile tests with both dog-bone and notched samples. It is found that hydrogen embrittlement resistance is enhanced by the higher partitioning temperature. Then the hydrogen embrittlement mechanism is analysed in terms of hydrogen retained austenite and martensite matrix. Thermal desorption analysis (TDA) shows that the hydrogen trapping properties are similar in the Q&P steels which cannot explain the enhancement of hydrogen embrittlement resistance. On the contrary it is found that the relatively low retained austenite stability after the higher temperature partitioning ensures more sufficient TRIP effect before hydrogen-induced fracture. Additionally dislocation recovery and solute carbon depletion at the higher partitioning temperature can reduce the flow stress of the martensite matrix improving its intrinsic toughness and reducing its hydrogen sensitivity both of which result in the higher hydrogen embrittlement resistance.

Hydrogen is considered a secondary source of energy commonly referred to as an energy carrier. It has the highest energy content when compared to other common fuels by weight having great potential for further development. Hydrogen can be produced from various domestic resources but based on the fossil resource conditions in China coal-based hydrogen energy is considered to be the most valuable because it is not only an effective way to develop clean energy but also a proactive exploration of the clean usage of traditional coal resources. In this article the sorption-enhanced water–gas shift technology in the coal-to-hydrogen section and the hydrogen-storage and transport technology with liquid aromatics are introduced and basic mechanisms technical advantages latest progress and future R&D focuses of hydrogen-production and storage processes are listed and discussed. As a conclusion after considering the development frame and the business characteristics of CHN Energy Group a conceptual architecture for developing coal-based hydrogen energy and the corresponding supply chain is proposed.

A possible consequence of pressurized hydrogen release is an under-expanded jet fire. Knowledge of the flame length radiative heat flux and fraction as well as the effects of variations in ground reflectance is important for safety assessment. The present study applies an open source CFD code FireFOAM to study the radiation characteristics of hydrogen and hydrogen/methane jet fires. For combustion the eddy dissipation concept for multi-component fuels recently developed by the authors in the large eddy simulation (LES) framework is used. The radiative heat is computed with the finite volume discrete ordinates model in conjunction with the weighted-sum-of-gray-gases model for the absorption/emission coefficient. The pseudo-diameter approach is used in which the corresponding parameters are calculated using the correlations of Birch et al. [22]. The predicted flame length and radiant fraction are in good agreement with the measurements of Schefer et al. [2] Studer et al. [3] and Ekoto et al. [6]. In order to account for the effects of variation in ground surface reflectance the emissivity of hydrogen flames was modified following Ekoto et al. [6]. Four cases with different ground reflectance are computed. The predictions show that the ground surface reflectance only has minor effect on the surface emissive power of the hydrogen jet fire. The radiant fractions fluctuate from 0.168 to 0.176 close to the suggested value of 0.16 by Ekoto et al.[6] based on the analysis of their measurements.

Significant challenges still remain in the development of suitable materials for storing hydrogen for practical applications. Clathrate hydrates as a special inclusion compounds could be tailored by changing the storage pressure and temperature to adapt ambient conditions. In this work the hydrates were adopted to encage hydrogen in tetrahydrofuran (THF) aqueous solution with concentration of 3.0 mol%. The formation and dissociation behaviours were investigated by a high pressure micro-differential scanning calorimeter at the operating pressure of 18 MPa 25 MPa and 34 MPa. Experimental results show that the memory water only affects the hydrate formation behaviour instead of the hydrate dissociation behaviour. The dissociation temperature of the THF-H2 hydrate increases with the increase of the operating pressure and its dissociation equilibrium data can be obtained. The dissociation temperatures of the THF-H2 hydrate are 9.26 ℃ 10.94 ℃ and 12.67 ℃ at the operating pressure of 18 MPa 25 MPa and 34 MPa respectively. It is fundamental for performing the kinetics and microscopic experiments.

An experimental study of hydrogen/air premixed flame propagation in a closed rectangular channel with the inhibitions (N2 or CO2) was conducted to investigate the inhibiting effect of N2 and CO2 on the flame properties during its propagation. Both Schlieren system and the pressure sensor were used to capture the evolution of flame shape and pressure changes in the channel. It was found that both N2 and CO2 have considerable inhibiting effect on hydrogen/air premixed flames. Compared with N2 CO2 has more prominent inhibition which has been interpreted from thermal and kinetic standpoints. In all the flames the classic tulip shape was observed. With different inhibitor concentration the flame demonstrated three types of deformation after the classic tulip inversion. A simple theoretical analysis has also been conducted to indicate that the pressure wave generated upon the first flame-wall contact can affect the flame deformation depending on its meeting moment with the flame front. Most importantly the meeting moment is always behind the start of tulip inversion which suggests the non-dominant role of pressure wave on this featured phenomenon.

This manuscript presents the results of a multi-lateral international activity intended to understand how to execute a cycle stress test as specified in a chosen standard (GTR SAE ISO EIHP …). The purpose of this work was to establish a harmonized test method protocol to ensure that the same results would be achieved regardless of the testing facility. It was found that accurate temperature measurement of the working fluid is necessary to ensure the test conditions remain within the tolerances specified. Continuous operation is possible with adequate cooling of the working fluid but this becomes more demanding if the cycle frequency increases. Recommendations for future test system design and operation are presented.

As the depletion of traditional fossil fuels and environmental pollution become a serious problem of human society researchers are actively finding renewable green energy sources. Considered as a clean efficient and renewable alternative Hydrogen energy is considered the most promising energy source. However the safe and efficient storage of hydrogen has become the major problem that hinders its application. To solve this gap this paper proposes to utilize surfactant modified graphene for hydrogen storage. With Hummers method and ultrasonic stripping method this study prepared graphene from graphene oxide with NaBH4. Surfactant sodium dodecylbenzene sulfonate (SDBS) was used as a dispersant during the reduction process to produce the dispersion-stabilized graphene suspensions. The characteristics of the graphene suspensions then were examined by XRD SEM TEM FT-IR Raman XPS TG and N2 adsorption-desorption tests. The hydrogen adsorption properties of the samples were investigated with Langmuir and Freundlich fitting. The results show that the adsorption behavior is consistent with the Freundlich adsorption model and the process is a physical adsorption.

Spontaneous ignition of compressed hydrogen release through a length of tube with different internal geometries is numerically investigated using our previously developed model. Four types of internal geometries are considered: local contraction local enlargement abrupt contraction and abrupt enlargement. The presence of internal geometries was found to significantly increase the propensity to spontaneous ignition. Shock reflections from the surfaces of the internal geometries and the subsequent shock interactions further increase the temperature of the combustible mixture at the contact region. The presence of the internal geometry stimulates turbulence enhanced mixing between the shock-heated air and the escaping hydrogen resulting in the formation of more flammable mixture. It was also found that forward-facing vertical planes are more likely to cause spontaneous ignition by producing the highest heating to the flammable mixture than backward-facing vertical planes.

Hydrogen transportation systems require very high pressure hydrogen storage containers to enable sufficient vehicle range for practical use. Current proposed designs have pressures up to 70 MPa with leakage due to damage or deterioration at such high pressures a great safety concern. Accurate models are needed to predict the flammability envelopes around such leaks which rapidly vary with time. This paper compares CFD predictions of jet flows for low pressure jets with predictions using the integral turbulent buoyant jet model. The results show that the CFD model predicts less entrainment and that the turbulent Schmidt number should be smaller with 0.55 giving better results. Then CFD predictions for very high pressure flows are compared with analytical models for choked flows that generate underexpanded jets into the ambient to evaluate the effects of the model assumptions and the effects of real exit geometries. Real gas effects are shown to accelerate the blowdown process and that real flow effects in the CFD model slow the flow rate and increase the exit temperature.

Hydrogen energy is a clean zero-carbon long-term storage flexible and efficient secondary energy. Accelerating the development of the hydrogen energy industry is a strategic choice to cope with global climate change achieve the goal of carbon neutrality and realize high-quality economic and social development. This study aimed to analyze the economic impact of introducing valueadded services to the hydrogen energy market on hydrogen energy suppliers. Considering the network effect of value-added services this study used a two-stage game model to quantitatively analyze the revenue of hydrogen energy suppliers under different scenarios and provided the optimal decision. The results revealed that (1) the revenue of a hydrogen energy supplier increases only if the intrinsic value of value-added services exceeds a certain threshold; (2) the revenue of hydrogen energy suppliers is influenced by a combination of four key factors: the intrinsic value of value-added services network effects user scale and the sales strategies of rivals; (3) the model developed in this paper can provide optimal decisions for hydrogen energy suppliers to improve their economic efficiency and bring more economic investment to hydrogen energy market in the future.

The effects of sponge blockage ratio on flame structure evolution and flame acceleration were experimentally investigated in an obstructed cross-section tube filled with stoichiometric hydrogen-air mixture. Experimental results show that the mechanisms responsible for flame acceleration can be in terms of the positive feedback of the unburned gas field generated ahead of the flame the area change of the gap between the sponge and the tube and the interaction between the flame and the shear layer appearing at the sponge left top corner. Especially the last one dominates the flame acceleration and causes its speed to be sonic. Then both the second and third contribute to the violent flame acceleration. In addition the unburned gas pockets can be found in both upstream and downstream regions of the sponge. With increasing blockage ratio the unburned gas pockets disappear easier and the flame acceleration is more pronounced. Moreover the sponge tilts more evidently and resultantly the maximum tilt angle increases.

As hydrogen fuel cell vehicles become more widely adopted by consumers the demand for refuelling stations increases. Most vehicles require high-pressure (either 350 or 700 bar) hydrogen and therefore the refuelling infrastructure must support these pressures. Fast running reduced order physical models of releases from high-pressure sources are needed so that quantitative risk assessment can guide the safety certification of these stations. A release from a high pressure source is choked at the release point forming the complex shock structures of an under-expanded jet before achieving a characteristic Gaussian pro le for velocity density mass fraction etc. downstream. Rather than using significant computational resources to resolve the shock structure an equivalent source model can be used to quickly and accurately describe the ow in terms of velocity diameter and thermodynamic state after the shock structure. In this work we present correlations for the equivalent boundary conditions of a subsonic jet as a high-pressure jet downstream of the shock structure. Schlieren images of under-expanded jets are used to show that the geometrical structure of under-expanded jets scale with the square root of the static to ambient pressure ratio. Correlations for an equivalent source model are given and these parameters are also found to scale with square root of the pressure ratio. We present our model as well as planar laser Rayleigh scattering validation data for static pressures up to 60 bar.

"This paper is aimed at revealing the inhibiting effects of He Ar N2 and CO2 on confined hydrogen explosion. The flame characteristics under thermo diffusive instability and hydrodynamic instability are analyzed using Lewis number and ratio of density ratio to flame thickness. The inhibiting effects of inert gas on confined hydrogen explosion are evaluated using maximum explosion pressure and maximum pressure rise rate. The inhibiting mechanism is obtained by revealing thermal diffusivity maximum mole fraction and net reaction rate of active radicals. The results demonstrated that the strongest destabilization effect of hydrodynamic instability and thermodiffusive instability occurs when the inert gas is Ar and CO2 respectively. Taking maximum explosion pressure and maximum rate of pressure rise as an indicator the effects of confined hydrogen explosion inhibition from strong to weak are CO2 N2 Ar and He. Laminar burning velocity thermal diffusivity maximum mole fraction and net reaction rate of active radicals continues to decrease in the order of He Ar N2 and CO2. The elementary reactions of generating and consuming active radicals at the highest net reaction rate are mainly consisted of R1 (H+O2=OH+O) R2 (H2+O=OH+H) R3 (H2+OH=H2O+H) and R10 (HO2+H=2OH).

(Mg-10wt.%Ni)-10wt.%Ce (Mg10Ni10Ce) was ball-milled with SnO2 nanotubes and Mg10Ni10Ce-xSnO2 (x=0 5 10 and 15wt.%) composites have been prepared. The phase compositions microstructures morphologies and hydrolysis H2 generation performance in different aqueous systems (distilled water tap water and simulated seawater) have been investigated and the corresponding hydrolysis mechanism of Mg10Ni10Ce and Mg10Ni10Ce-SnO2 has been proposed. Adding a small amount of SnO2 nanotubes can significantly enhance the hydrolysis reaction of Mg10Ni10Ce especially the initial hydrolysis kinetics and the final H2 generation yield. Unfortunately the Mg10Ni10Ce-xSnO2 hardly react with distilled water at room temperature. The hydrolysis reaction rate of Mg10Ni10Ce-5SnO2 composite in tap water is still very slow with only 17.3% generation yield after 1 hour at 303 K. Fortunately in simulated seawater (3.5wt.% NaCl solution) the hydrolytic H2 generation behavior of the Mg10Ni10Ce-5SnO2 composite has been greatly improved which can release as high as 468.6 mL/g H2 with about 60.9% generation yield within 30 s at 303 K. The Cl- destroys the passivation layer on Mg-Ni-Ce alloy surface and the added SnO2 nanotubes accelerate the hydrolysis reaction rate and enhance the H2 generation yield. The Mg10Ni10Ce-5SnO2 composite can rapidly generate a large amount of H2 in simulate seawater in a short time which is expected to be applied on portable H2 generators in the future.

Developing low-cost high-performance catalysts is of fundamental significance for electrochemical energy conversion and storage. In recent years metal@carbon core@shell nanocomposites have emerged as a unique class of functional nanomaterials that show apparent electrocatalytic activity towards a range of reactions such as hydrogen evolution reaction oxygen evolution reaction oxygen reduction reaction and CO2 reduction reaction that are important in water splitting fuel cells and metal-air batteries. The activity is primarily attributed to interfacial charge transfer from the metal core to the carbon shell that manipulate the electronic interactions between the catalyst surface and reaction intermediates and varies with the structures and morphologies of the metal core (elemental composition core size etc.) and carbon shell (doping layer thickness etc.). Further manipulation can be achieved by the incorporation of a third structural component. A perspective is also included highlighting the current gap between theoretical modeling and experimental results and technical challenges for future research.

Hydrogen mixed natural gas for combustion can improve combustion characteristics and reduce carbon emission which has important engineering application value. A casing swirl burner model is adopted to numerically simulate and research the natural gas hydrogen mixing technology for combustion in gas boilers in this paper. Under the condition of conventional air atmosphere and constant air excess coefficient the six working conditions for hydrogen mixing proportion into natural gas are designed to explore the combustion characteristics and the laws of pollution emissions. The temperature distributions composition and emission of combustion flue gas under various working conditions are analyzed and compared. Further investigation is also conducted for the variation laws of NOx and soot generation. The results show that when the boiler heating power is constant hydrogen mixing will increase the combustion temperature accelerate the combustion rate reduce flue gas and CO2 emission increase the generation of water vapor and inhibit the generation of NOx and soot. Under the premise of meeting the fuel interchangeability it is concluded that the optimal hydrogen mixing volume fraction of gas boilers is 24.7%.

In this paper the deflagration region and characteristics of the hydrogen flow which was generated by high-pressure hydrogen discharge from storage vessels were studied. A 3-D analytic model is established based on the species transfer model and the SST k −ω turbulence model. The established model is applied to the research of the flow characteristics of the hydrogen under-expanded jet under different filling pressures of 30 MPa 35 MPa and 40 MPa respectively. The evolution process of hydrogen combustible cloud is analyzed under the filling pressure of 30 MPa. It is revealed that a supersonic jet is formed after the high-pressure hydrogen discharge outlet In the vicinity of the Mach disk the hydrogen jet velocity and temperature reach the maximum values and the variation of filling pressure has little effect on the peak values of the hydrogen jet flow velocity and temperature during the considered pressure range. In the rear of the Mach disk the variation rates of the hydrogen flow velocity and temperature are in inversely proportional to the hydrogen filling pressure. At the preliminary stage the discharged hydrogen is apple-shaped which expands along the radial and then the axial growth rate of the hydrogen cloud increases with the passage of time.

Hydrogen generation by the reaction of pure Al powder in water with the addition of Al(OH)3 γ- Al2O3 α-Al2O3 or TiO2 at mild temperatures was investigated. It was found that the reaction of Al with water is promoted and the reaction induction time decreases greatly by the above hydroxide and oxides. X-ray diffraction analyses revealed that the hydroxide and oxide phases have no any change during the Al-water reaction indicating that they are just as catalysts to assist the reaction of Al with water. A possible mechanism was proposed which shows that hydroxide and oxides could dissociate water molecules and promote the hydration of the passive oxide film on Al particle surfaces.

The absorption of CO2 is of importance in carbon capture utilization and storage technology for greenhouse gas control. In the present work we clarified the mechanism of how metal-based ionic liquids (MBILs) Bmim[XCln]m (X is the metal atom) enhance the CO2 absorption capacity of ILs via performing molecular dynamics simulations. The sparse hydrogen bond interaction network constructed by CO2 and MBILs was identified through the radial distribution function and interaction energy of CO2-ion pairs which increase the absorption capacity of CO2 in MBILs. Then the dynamical properties including residence time and self-diffusion coefficient confirmed that MBILs could also promote the diffusion process of CO2 in ILs. That's to say the MBILs can enhance the CO2 absorption capacity and the diffusive ability simultaneously. Based on the analysis of structural energetic and dynamical properties the CO2 absorption capacity of MBILs increases in the order Cl− → [ZnCl4]2-→ [CuCl4]2-→ [CrCl4]- → [FeCl4]- revealing the fact that the short metal–Cl bond length and small anion volume could facilitate the performance of CO2 absorbing process. These findings show that the metal–Cl bond length and effective volume of the anion can be the effective factors to regulate the CO2 absorption process which can also shed light on the rational molecular design of MBILs for CO2 capture and other key chemical engineering processes such as IL-based gas sensors nano-electrical devices and so on.

Hydrogen production by steam reforming of ethylene glycol (EG) at 300 °C was investigated over SiO2 and CeO2 supported Pt–Ni bimetallic catalysts prepared by incipient wetness impregnation methods. It was observed that impregnation sequence of Pt and Ni can affect the performance of catalysts apparently. Catalyst with Pt first and then Ni addition showed higher EG conversion and H2 yield owing to the Ni enrichment on the surface and the proper interaction between Pt and Ni. It was observed that although SiO2 supported catalysts exhibited better activity and H2 selectivity CeO2 supported ones had better stability. This is attributed to the less coke formation on CeO2. Increasing Pt/Ni ratio enhanced the reaction activity and Pt3–Ni7 catalysts with 3 wt% Pt and 7 wt% Ni showed the highest activity and stability. Ni surficial enrichment facilitated the C—C bond rupture and water gas shift reactions; and Pt addition inhibited methanation reaction. Electron transfer and hydrogen spillover from Pt to Ni suppressed carbon deposition. These combined effects lead to the excellent performance of Pt3–Ni7 supported catalysts.

The design of ventilation system has implications for the safety of life and property and the development of regulations and standards in the space with the hydrogen storage equipment. The impact of both the position and the area of a single vent on the dispersion of hydrogen in a cuboid space (with dimensions L x W x H ¼ 2.90 0.74 1.22 m) is investigated with Computational Fluid Dynamics (CFD) in this study. Nine positions of the vent were compared for the leakage taking place at the floor to understand the gas dispersion. It was shown a cloud of 1% mole fraction has been formed near the ceiling of the space in less than 40 s for different positions of the vent which can activate hydrogen sensors. The models show that the hydrogen is removed more effectively when the vent is closer to the leakage position in the horizontal direction. The study demonstrates that the vent height of 1.00 m is safer for the particular scenario considered. The area of the vent has little effect on the hydrogen concentration for all vent positions when the area of the vent is less than 0.045 m2 and the height of the vent is less than 0.61 m.

Hydrogen is one of the promising energy sources in the future because it has the advantages of clean combustion products high efficiency and renewable energy. However hydrogen has the characteristics of low ignition energy wide flammable range (4% -75%) and fast burning flame speed which can cause explosion hazards. Typically the accidental release of hydrogen into confined or semi confined enclosures can often lead to a flammable hydrogen-air mixture with concentration gradients and possible flame acceleration and deflagration-to-detonation transition (DDT). The present study aims to test the capability of our in-house density-based solver ExplosionEngFoam for flame acceleration (FA) and deflagration-to-detonation transition (DDT) in homogenous/inhomogeneous hydrogen-air mixtures. The solver is based on the open source computational fluid dynamics (CFD) platform OpenFOAM and uses the modified Weller et al.’s combustion model taking into account LD and RT instabilities turbulence and non-unity Lewis number etc. Numerical simulations were conducted for both homogeneous and inhomogeneous mixtures in a long enclosed channel with 5.4 m in length and 0.06 m in height. The predictions demonstrate good quantitative agreement with the experimental measurements in flame tip position speed and pressure profiles by Boeck et al. The flow characteristics such as flame fine structure wave evolution etc. were also discussed.

Recent studies of J.H. Song et al. and S.Y. Yang et al. have been concentrated on mitigation measures against hydrogen risk. The authors have proposed installation of quenching meshes between compartments or around the essential equipment in order to contain hydrogen flames. Preliminary tests were conducted which demonstrated the possibility of flame extinction using metallic meshes of specific size.<br/>Considerable amount of numerical and theoretical work on flame quenching phenomenon has been performed in the second half of the last century and several techniques and models have been proposed to predict the quenching phenomenon of the laminar flame system. Most of these models appreciated the importance of heat loss to the surroundings as a primary cause of extinguishment in particular the heat transfer by conduction to the containing wall. The supporting simulations predict flame-quenching structure either between parallel plates (quenching distance) or inside a tube of a certain diameter (quenching diameter).<br/>In the present study the flame quenching is investigated assuming the laminar hydrogen flame propagating towards a quenching mesh using two-dimensional configuration and the earlier developed models. It is shown that due to a heat loss to a metallic grid the flame can be quenched numerically.

Energy–structure–function (ESF) maps can aid the targeted discovery of porous molecular crystals by predicting the stable crystalline arrangements along with their functions of interest. Here we compute ESF maps for a series of rigid molecules that comprise either a triptycene or a spiro-biphenyl core functionalized with six different hydrogen-bonding moieties. We show that the positioning of the hydrogen-bonding sites as well as their number has a profound influence on the shape of the resulting ESF maps revealing promising structure–function spaces for future experiments. We also demonstrate a simple and general approach to representing and inspecting the high-dimensional data of an ESF map enabling an efficient navigation of the ESF data to identify ‘landmark’ structures that are energetically favourable or functionally interesting. This is a step toward the automated analysis of ESF maps an important goal for closed-loop autonomous searches for molecular crystals with useful functions.

The cost reduction of hydrogen refueling stations (HRSs) is very important for the popularization of hydrogen vehicles. This paper proposes an optimized operation algorithm based on hydrogen energy demand estimation for on-site hydrogen refueling stations. Firstly the user’s hydrogen demand was estimated based on the simulation of their hydrogenation behavior. Secondly mixed integer linear programming method was used to optimize the operation of the hydrogen refueling station to minimize the unit hydrogen energy cost by using the peak–valley difference of the electricity price. We then used three typical scenario cases to evaluate the optimized operation method. The results show that the optimized operation method proposed in this paper can effectively reduce the rated configuration of electrolyzer and storage tank for HRS and can significantly reduce the unit hydrogen energy cost considering the construction cost compared with the traditional method. Therefore the optimization operation method of a local hydrogen production and hydrogen refueling station proposed in this paper can reduce the cost of a hydrogen refueling station and accelerate the popularization of hydrogen energy vehicles. Finally the scope of application of the proposed optimization method and the influence of the variation of the electricity price curve and the unit cost of the electrolyzer are discussed.

The use of so-called “green” hydrogen for decarbonisation of the energy and propulsion sectors has attracted considerable attention over the last couple of decades. Although advancements are achieved hydrogen still presents some constraints when used directly in power systems such as gas turbines. Therefore another vector such as ammonia can serve as a chemical to transport and distribute green hydrogen whilst its use in gas turbines can limit combustion reactivity compared to hydrogen for better operability. However pure ammonia on its own shows slow complex reaction kinetics which requires its doping by more reactive molecules thus ensuring greater flame stability. It is expected that in forthcoming years ammonia will replace natural gas (with ~ 90% methane in volume) in power and heat production units thus making the co-firing of ammonia/methane a clear path towards replacement of CH4 as fossil fuel. Hydrogen can be obtained from the precracking of ammonia thus denoting a clear path towards decarbonisation by the use of ammonia/hydrogen blends. Therefore ammonia/methane/hydrogen might be co-fired at some stage in current combustion units hence requiring a more intrinsic analysis of the stability emissions and flame features that these ternary blends produce. In return this will ensure that transition from natural gas to renewable energy generated e-fuels such as so-called “green” hydrogen and ammonia is accomplished with minor detrimentals towards equipment and processes. For this reason this work presents the analysis of combustion properties of ammonia/methane/hydrogen blends at different concentrations. A generic tangential swirl burner was employed at constant power and various equivalence ratios. Emissions OH*/NH*/NH2*/CH* chemiluminescence operability maps and spectral signatures were obtained and are discussed. The extinction behaviour has also been investigated for strained laminar premixed flames. Overall the change from fossils to e-fuels is led by the shift in reactivity of radicals such as OH CH CN and NH2 with an increase of emissions under low and high ammonia content. Simultaneously hydrogen addition improves operability when injected up to 30% (vol) an amount at which the hydrogen starts governing the reactivity of the blends. Extinction strain rates confirm phenomena found in the experiments with high ammonia blends showing large discrepancies between values at different hydrogen contents. Finally a 20/55/25% (vol) methane/ammonia/hydrogen blend seems to be the most promising at high equivalence ratios (1.2) with no apparent flashback low emissions and moderate formation of NH2/OH radicals for good operability.

Microgrid with hydrogen storage is an effective way to integrate renewable energy and reduce carbon emissions. This paper proposes an optimal operation method for a microgrid with hydrogen storage. The electrolyzer efficiency characteristic model is established based on the linear interpolation method. The optimal operation model of microgrid is incorporated with the electrolyzer efficiency characteristic model. The sequential decision-making problem of the optimal operation of microgrid is solved by a deep deterministic policy gradient algorithm. Simulation results show that the proposed method can reduce about 5% of the operation cost of the microgrid compared with traditional algorithms and has a certain generalization capability.

Hydrogen induced failure under uniaxial tension is simulated in a duplex stainless steel considering microstructural feature of the material. There are three key ingredients in the modelling approach: image processing and finite element representation of the experimentally observed microstructure stress driven hydrogen diffusion and diffusion coupled cohesive zone modelling of fracture considering mixed failure mode. The microstructure used as basis for the modelling work is obtained from specimens cut in the transverse and longitudinal directions. It is found that the microstructure significantly influences hydrogen diffusion and fracture. The austenite phase is polygonal and randomly distributed in the transverse direction where a larger effective hydrogen diffusion coefficient and a lower hydrogen fracture resistance is found compared to the specimen in the longitudinal direction where the austenite phase is slender and laminated. This indicates that the proper design and control of the austenite phase help improve hydrogen resistance of duplex stainless steel. The strength of the interface in the shear direction is found to dominate the fracture mode and initiation site which reveals the importance of considering mixed failure mode and calibrating the hydrogen induced strength reduction in shear.

In this work first-principles methods were performed to simulate interactions between hydrogen and common alloying elements of high strength low alloy (HSLA) steel. The world has been convinced that hydrogen could be one of the future clean energy sources. HSLA steel with a balance of strength toughness and hydrogen embrittlement susceptibility is expected for application in large-scale hydrogen storage and transportation. To evaluate the property deterioration under a hydrogen atmosphere hydrogen embrittlement (HE) of HSLA steel attracts attention. However due to the small size of hydrogen atoms the mechanism of HE is challenging to observe directly by current experimental methods. To understand the HE mechanism at an atomic level DFT methods were applied to simulate the effects of alloying elements doping in bcc-Fe bulk structure and grain boundary structure. Furthermore the potential application of DFT to provide theoretical advice for HSLA steel design is discussed.

Carbon dioxide capture and utilization (CCU) technology is a significant means by which China can achieve its ambitious carbon neutrality goal. It is necessary to explore the behavioral strategies of relevant companies in adopting CCU technology. In this paper an evolutionary game model is established in order to analyze the interaction process and evolution direction of local governments and coal-fired power plants. We develop a replicator dynamic system and analyze the stability of the system under different conditions. Based on numerical simulation we analyze the impact of key parameters on the strategies of stakeholders. The simulation results show that the unit prices of hydrogen and carbon dioxide derivatives have the most significant impact: when the unit price of hydrogen decreases to 15.9 RMB/kg or the unit price of carbon dioxide derivatives increases to 3.4 RMB/kg the evolutionary stabilization strategy of the system changes and power plants shift to adopt CCU technology. The results of this paper suggest that local governments should provide relevant support policies and incentives for CCU technology deployment as well as focusing on the synergistic development of CCU technology and renewable energy hydrogen production technology

In this age of human civilization there is a need for more efficient cleaner and renewable energy as opposed to that provided by nonrenewable sources such as coal and oil. In this sense hydrogen energy has been proven to be a better choice. In this paper a portable graphite crucible metal smelting furnace was used to prepare ten multi-element aluminum alloy ingots with different components. The microstructure and phase composition of the ingots and reaction products were analyzed by X-ray diffraction (XRD) scanning electron microscopy (SEM) and differential scanning calorimetry (DSC). The reaction was carried out in a constant temperature water bath furnace at 60°C and the hydrogen production performance of the multi-element aluminum alloys in different proportions was compared by the drainage gas collection method. The experimental results show that the as-cast microstructure of Al–Ga–In–Sn aluminum alloy is composed of a solid solution of Al and part of Ga and a second phase of In3Sn. After the hydrolysis reaction the products were dried at 150°C and then analyzed by XRD. The products were mainly composed of AlOOH and In3Sn. Alloys with different compositions react at the same hydrolysis temperature and the hydrogen production performance is related to the ratio of low-melting-point metal elements. By comparing two different ratios of Ga–In–Sn (GIS) the hydrogen production capacity and production rate when the ratio is 6:3:1 are generally higher than those when the ratio is 7:2:1. The second phase content affects the hydrogen production performance.

As a promising hydrogen storage medium methanol has many advantages such as a high hydrogen content (12.5 wt%) and low-cost. However conventional methanol–water reforming methods usually require a high temperature (>200 °C). In this research we successfully designed an effective strategy to fully convert methanol to hydrogen for at least 1900 min (∼32 h) at near-room temperature. The strategy involves two main procedures which are CH₃OH →HCOOH → H₂ and CH₃OH → NADH → H₂. HCOOH and the reduced form of nicotinamide adenine dinucleotide (NADH) are simultaneously produced through the dehydrogenation of methanol by the cooperation of alcohol dehydrogenase (ADH) and aldehyde dehydrogenase (ALDH). Subsequently HCOOH is converted to H₂ by a new iridium polymer complex catalyst and an enzyme mimic is used to convert NADH to H₂ and nicotinamide adenine dinucleotide (NAD+). NAD+ can then be reconverted to NADH by repeating the dehydrogenation of methanol. This strategy and the catalysts invented in this research can also be applied to hydrogen production from other small organic molecules (e.g. ethanol) or biomass (e.g. glucose) and thus will have a high impact on hydrogen storage and applications.

Magnesium hydride and its compounds have a high hydrogen storage capacity and are inexpensive and thus have been considered as one of the most promising hydrogen storage materials for on-board applications. Nevertheless Mg/MgH₂ systems suffer from great drawbacks in terms of kinetics and thermodynamics for hydrogen uptake/release. Over the past decades although significant progress has been achieved with respect to hydrogen sorption kinetics in Mg/MgH₂ systems their high thermal stability remains the main drawback which hinders their practical applications. Accordingly herein we present a brief summary of the synthetic routes and a comprehensive overview of the advantages and disadvantages of the promising strategies to effectively tune the thermodynamics of Mg-based materials such as alloying nanostructuring metastable phase formation changing reaction pathway and nano Mg-based composites. Among them nanostructuring and metastable phase formation which have the superiority of changing the thermodynamics without affecting the hydrogen capacity have attracted increasing interest in this field. To further optimize the hydrogen storage performance we specially emphasize novel nanostructured materials which have the advantage of combining alloy engineering nanostructuring and the synergistic effect to change the thermodynamics of Mg/MgH2 to some extent. Furthermore the remaining challenges and the directions of further research on MgH₂ including the fundamental mechanism of the Mg–H bond instability advanced synthetic routes stabilizing nanostructures and predicting novel composite materials are proposed.

Compressed hydrogen storage is currently widely used in fuel cell vehicles due to its simplicity in tank structure and refuelling process. For safety reason the final gas temperature in the hydrogen tank during vehicle refuelling must be maintained under a certain limit e.g. 85 °C. Many experiments have been performed to find the relations between the final gas temperature in the hydrogen tank and refueling conditions. The analytical solution of the hydrogen temperature in the tank can be obtained from the simplified thermodynamic model of a compressed hydrogen storage tank and it serves as function formula to fit experimental temperatures. From the analytical solution the final hydrogen temperature can be expressed as a weighted average form of initial temperature inflow temperature and ambient temperature inspired by the rule of mixtures. The weighted factors are related to other refuelling parameters such as initial mass initial pressure refuelling time refuelling mass rate average pressure ramp rate (APRR) final mass final pressure etc. The function formula coming from the analytical solution of the thermodynamic model is more meaningful physically and more efficient mathematically in fitting experimental temperatures. The simple uniform formula inspired by the concept of the rule of mixture and its weighted factors obtained from the analytical solution of lumped parameter thermodynamics model is representatively used to fit the experimental and simulated results in publication. Estimation of final hydrogen temperature from refuelling parameters based on the rule of mixtures is simple and practical for controlling the maximum temperature and for ensuring hydrogen safety during fast filling process.

Hydrogen evolution reaction (HER) plays a key role in generating clean and renewable energy. As the most effective HER electrocatalysts Pt group catalysts suffer from severe problems such as high price and scarcity. It is highly desirable to design and synthesize sustainable HER electrocatalysts to replace the Pt group catalysts. Due to their low cost high abundance and high activities cobalt-incorporated N-doped nanocarbon hybrids are promising candidate electrocatalysts for HER. In this report we demonstrated a robust and eco-friendly host-guest approach to fabricate metallic cobalt nanoparticles embedded in N-doped carbon fibers derived from natural silk fibers. Benefiting from the one-dimensional nanostructure the well-dispersed metallic cobalt nanoparticles and the N-doped thin graphitized carbon layer coating the best Co-based electrocatalyst manifests low overpotential (61 mV@10 mA/cm2) HER activity that is comparable with commercial 20% Pt/C and good stability in acid. Our findings provide a novel and unique route to explore high-performance noble-metal-free HER electrocatalysts.

Today as a result of the advancement of technology and increasing environmental problems the need for clean energy has considerably increased. In this regard hydrogen which is a clean and sustainable energy carrier with high energy density is among the well-regarded and effective means to deliver and store energy and can also be used for environmental remediation purposes. Renewable hydrogen energy carriers can successfully substitute fossil fuels and decrease carbon dioxide (CO2 ) emissions and reduce the rate of global warming. Hydrogen generation from sustainable solar energy and water sources is an environmentally friendly resolution for growing global energy demands. Among various solar hydrogen production routes semiconductor-based photocatalysis seems a promising scheme that is mainly performed using two kinds of homogeneous and heterogeneous methods of which the latter is more advantageous. During semiconductor-based heterogeneous photocatalysis a solid material is stimulated by exposure to light and generates an electron–hole pair that subsequently takes part in redox reactions leading to hydrogen production. This review paper tries to thoroughly introduce and discuss various semiconductor-based photocatalysis processes for environmental remediation with a specific focus on heterojunction semiconductors with the hope that it will pave the way for new designs with higher performance to protect the environment.

Imbalance costs caused by forecasting errors are considerable for grid-connected wind farms. In order to reduce such costs two onsite storage technologies i.e. power-to-hydrogen-to-power and lithium battery are investigated considering 14 uncertain technological and economic parameters. Probability density distributions of wind forecasting errors and power level are first considered to quantify the imbalance and excess wind power. Then robust optimal sizing of the onsite storage is performed under uncertainty to maximize wind-farm profit (the net present value). Global sensitivity analysis is further carried out for parameters prioritization to highlight the key influential parameters. The results show that the profit of power-to-hydrogen-to-power case is sensitive to the hydrogen price wind forecasting accuracy and hydrogen storage price. When hydrogen price ranges in (2 6) €/kg installing only electrolyzer can earn profits over 100 k€/MWWP in 9% scenarios with capacity below 250 kW/MWWP under high hydrogen price (over 4 €/kg); while installing only fuel cell can achieve such high profits only in 1.3% scenarios with capacity below 180 kW/MWWP. Installing both electrolyzer and fuel cell (only suggested in 22% scenarios) results in profits below 160 k€/MWWP and particularly 20% scenarios allow for a profit below 50 k€/MWWP due to the contradictory effects of wind forecasting error hydrogen and electricity price. For lithium battery investment cost is the single highly influential factor which should be reduced to 760 €/kWh. The battery capacity is limited to 88 kW h/MWWP. For profits over 100 k€/MWWP (in 3% scenarios) the battery should be with an investment cost below 510 €/kWh and a depth of discharge over 63%. The power-to-hydrogen-to-power case is more advantageous in terms of profitability reliability and utilization factor (full-load operating hours) while lithium battery is more helpful to reduce the lost wind and has less environmental impact considering current hydrogen market.

Hydrolysis of Mg-based materials is considered as a potential means of safe and convenient real-time control of H₂ release enabling efficient loading discharge and utilization of hydrogen in portable electronic devices. At present work the hydrogen generation properties of MgLi-graphite composites were evaluated for the first time. The MgLi-graphite composites with different doping amounts of expanded graphite (abbreviated as EG hereinafter) were synthesized through ball milling and the hydrogen behaviors of the composites were investigated in chloride solutions. Among the above doping systems the 10 wt% EG-doped MgLi exhibited the best hydrogen performance in MgCl₂ solutions. In particular the 22 h-milled MgLi-10 wt% EG composites possessed both desirable hydrogen conversion and rapid reaction kinetics delivering a hydrogen yield of 966 mL H₂ g⁻¹ within merely 2 min and a maximum hydrogen generation rate of 1147 mL H₂ min⁻¹ g⁻¹ as opposed to the sluggish kinetics in the EG-free composites. Moreover the EG-doped MgLi showed superior air-stable ability even under a 75 RH% ambient atmosphere. For example the 22 h-milled MgLi-10 wt% EG composites held a fuel conversion of 89% after air exposure for 72 h rendering it an advantage for Mg-based materials to safely store and transfer in practical applications. The similar favorable hydrogen performance of MgLi-EG composites in (simulate) seawater may shed light on future development of hydrogen generation technologies.

Synthetic natural gas (SNG) is one of the promising energy carriers for the excessive electricity generated from variable renewable energy sources. SNG production from renewable H₂ and CO₂  via catalytic CO₂ methanation has gained much attention since CO₂ emissions could be simultaneously reduced. In this study Ni–Fe/(MgAl)O_x alloy catalysts for CO₂ methanation were prepared via hydrotalcite precursors using a rapid coprecipitation method. The effect of total metal concentration on the physicochemical properties and catalytic behavior was investigated. Upon calcination the catalysts showed high specific surface area of above 230 m² g⁻¹. Small particle sizes of about 5 nm were obtained for all catalysts even though the produced catalyst amount was increased by 10 times. The catalysts exhibited excellent space-time yield under very high gas space velocity (34000 h⁻¹) irrespective of the metal concentration. The CO₂ conversions reached 73–79% at 300 °C and CH₄ selectivities were at 93–95%. Therefore we demonstrated the potential of large-scale production of earth-abundant Ni–Fe based catalysts for CO₂ methanation and the Power-to-Gas technology.

The hot electron transition of noble materials to catalysis accelerated by localized surface plasmon resonances (LSPRs) was detected by in situ irradiated X-ray photoelectron spectroscopy (ISI-XPS) in this article. This paper synthesized an Ag Nanowire (AgNW) @ WS₂ core-shell structure with an ultra-thin shell of WS₂(3 ∼ 7 nm) and characterized its photocatalytic properties. The AgNW@WS₂ core-shell structure exhibited different surface-enhanced Raman spectroscopy (SERS) effects by changing shell thickness indicating that the effect of AgNW could be controlled by WS₂ shell. Furthermore the hydrogen production of AgNW@WS₂ could reach to 356% of that of pure WS₂. The hot electrons arising from the LSPRs effect broke through the Schottky barrier between WS2 and AgNW and transferred to the WS₂ shell whose photocatalytic effect was thus enhanced. In addition when the LSPRs effect was intensified by reducing the shell thickness the hot electron transition of noble materials to catalysis was accelerated.

Titanium dioxide (TiO₂ ) has been widely investigated for photocatalytic H₂ evolution and photoelectrochemical (PEC) water splitting since 1972. However its wide bandgap (3.0–3.2 eV) limits the optical absorption of TiO₂ for sufficient utilization of solar energy. Blackening TiO₂ has been proposed as an effective strategy to enhance its solar absorption and thus the photocatalytic and PEC activities and aroused widespread research interest. In this article we reviewed the recent progress of black TiO₂ for photocatalytic H₂ evolution and PEC water splitting along with detailed introduction to its unique structural features optical property charge carrier transfer property and related theoretical calculations. As summarized in this review article black TiO₂ could be a promising candidate for photoelectrocatalytic hydrogen generation via water splitting and continuous efforts are deserved for improving its solar hydrogen efficiency.