Transmission, Distribution & Storage

Hydrogen is often described as the fuel of the future especially for application in hydrogen powered fuel-cell vehicles (HFCV’s). However its widespread implementation in this role has been thwarted by the lack of a lightweight safe on-board hydrogen storage material. Here we show that benign readily available hydrocarbon wax is capable of rapidly releasing large amounts of hydrogen through microwave-assisted catalytic decomposition. This discovery offers a new material and system for safe and efficient hydrogen storage and could facilitate its application in a HFCV. Importantly hydrogen storage materials made of wax can be manufactured through completely sustainable processes utilizing biomass or other renewable feedstocks.

Liquid organic hydrogen carriers (LOHC) store hydrogen by reversible hydrogenation of a carrier material. Water can enter the system via wet hydrogen coming from electrolysis as well as via moisture on the catalyst. Removing this water is important for reliable operation of the LOHC system. Different approaches for doing this have been evaluated on three stages of the process. Drying of the hydrogen before entering the LOHC system itself is preferable. A membrane drying process turns out to be the most efficient way. If the water content in the LOHC system is still so high that liquid–liquid demixing occurs it is crucial for water removal to enhance the slow settling. Introduction of an appropriate packing can help to separate the two phases as long as the volume flow is not too high. Further drying below the rather low solubility limit is challenging. Introduction of zeolites into the system is a possible option. Water adsorbs on the surface of the zeolite and moisture content is therefore decreased.

This research activity aims at investigating the hydrogen embrittlement of Maraging steels in connection to real sudden failures of some of the suspension blades of the Virgo Project experimental apparatus. Some of them failed after 15 years of service in working conditions. Typically in the Virgo detector blades are loaded up to 50-60% of the material yield strength. For a deeper understanding of the failure the relationship between hydrogen concentration and mechanical properties of the material have been investigated with specimens prepared in order to simulate blade working conditions. A mechanical characterization of the material has been carried out by standard tensile testing in order to establish the effect of hydrogen content on the material strength. Further experimental activity was executed in order to characterize the fracture surface and to measure the hydrogen content. Finally some of the failed blades have been analyzed in DICI-UNIPI laboratory. The experimental results show that the blades failure can be related with the hydrogen embrittlement phenomenon.

Hydrogen storage in solid-state materials is believed to be a most promising hydrogen-storage technology for high efficiency low risk and low cost. Mg(BH4)2 is regarded as one of most potential materials in hydrogen storage areas in view of its high hydrogen capacities (14.9 wt% and 145–147 kg cm3 ). However the drawbacks of Mg(BH4)2 including high desorption temperatures (about 250 C–580 C) sluggish kinetics and poor reversibility make it difficult to be used for onboard hydrogen storage of fuel cell vehicles. A lot of researches on improving the dehydrogenation reaction thermodynamics and kinetics have been done mainly including: additives or catalysts doping nanoconfining Mg(BH4)2 in nanoporous hosts forming reactive hydrides systems multi-cation/anion composites or other derivatives of Mg(BH4)2. Some favorable results have been obtained. This review provides an overview of current research progress in magnesium borohydride including: synthesis methods crystal structures decomposition behaviors as well as emphasized performance improvements for hydrogen storage.

The exploration and evaluation of new composites possessing both processability and enhanced hydrogen storage capacity are of signifcant interest for onboard hydrogen storage systems and fuel cell based electric vehicle development. Here we demonstrate the fabrication of composite membranes with sufcient mechanical properties for enhanced hydrogen storage that are based on a polymer of intrinsic microporosity (PIM-1) matrix containing nano-sized fllers: activated carbon (AX21) or metal–organic framework (MIL-101). This is one of the frst comparative studies of diferent composite systems for hydrogen storage and in addition the frst detailed evaluation of the difusion kinetics of hydrogen in polymer-based nanoporous composites. The composite flms were characterised by surface area and porosity analysis hydrogen adsorption measurements mechanical testing and gas adsorption modelling. The PIM-1/AX21 composite with 60 wt% AX21 provides enhanced hydrogen adsorption kinetics and a total hydrogen storage capacity of up to 9.35 wt% at 77 K; this is superior to the US Department of Energy hydrogen storage target. Tensile testing indicates that the ultimate stress and strain of PIM-1/ AX21 are higher than those of the MIL-101 or PAF-1 containing composites and are sufcient for use in hydrogen storage tanks. The data presented provides new insights into both the design and characterisation methods of polymer-based composite membranes. Our nanoporous polymer-based composites ofer advantages over powders in terms of safety handling and practical manufacturing with potential for hydrogen storage applications either as means of increasing storage or decreasing operating pressures in high-pressure hydrogen storage tanks.

A stable energy supply will require balancing the fluctuations of renewable energy generation due to the transition to renewable energy sources. Intraday and seasonal storage systems are often limited to local geographical or infrastructural circumstances. This study experimentally verifies the application of inexpensive and abundant natural iron ores for energy storage with combined hydrogen and heat release. The incorporated iron oxides are reduced with hydrogen from electrolysis to store energy in chemically bonded form. The on–demand reoxidation releases either pure hydrogen or high-temperature heat as valuable products. Natural iron ores as storage material are beneficial as the specific costs are lower by an order of magnitude compared to synthetic iron oxide-based materials. Suitable iron ores were tested in TG analysis and in a 1 kW fixed-bed reactor. Siderite a carbonate iron ore was verified as promising candidate as it shows significantly lower reaction temperatures and twice the storage capacity over other commercial iron ores such as ilmenite. The specific storage costs are as low as 80–150 $ per MWh hydrogen stored based on the experimental in-situ tests. The experimentally determined volumetric energy storage capacity for the bulk material was 1.7 and 1.8 MWh m− 3 for hydrogen and heat release respectively. The raw siderite ore was stable for over 50 consecutive cycles at operating temperatures of 500–600 ◦C in in-situ lifetime tests. The combination of high abundance low price and reasonable capacity can thus result in very low specific energy storage costs. The study proofs that suitable natural iron ores are an interesting economic solution for large-scale and seasonal energy storage systems.

This paper is a critical review of selected real-world energy storage systems based on hydrogen ranging from lab-scale systems to full-scale systems in continuous operation. 15 projects are presented with a critical overview of their concept and performance. A review of research related to power electronics control systems and energy management strategies has been added to integrate the findings with outlooks usually described in separate literature. Results show that while hydrogen energy storage systems are technically feasible they still require large cost reductions to become commercially attractive. A challenge that affects the cost per unit of energy is the low energy efficiency of some of the system components in real-world operating conditions. Due to losses in the conversion and storage processes hydrogen energy storage systems lose anywhere between 60 and 85% of the incoming electricity with current technology. However there are currently very few alternatives for long-term storage of electricity in power systems so the interest in hydrogen for this application remains high from both industry and academia. Additionally it is expected that the share of intermittent renewable energy in power systems will increase in the coming decades. This could lead to technology development and cost reductions within hydrogen technology if this technology is needed to store excess renewable energy. Results from the reviewed projects indicate that the best solution from a technical viewpoint consists in hybrid systems where hydrogen is combined with short-term energy storage technologies like batteries and supercapacitors. In these hybrid systems the advantages with each storage technology can be fully exploited to maximize efficiency if the system is specifically tailored to the given situation. The disadvantage is that this will obviously increase the complexity and total cost of the energy system.<br/>Therefore control systems and energy management strategies are important factors to achieve optimal results both in terms of efficiency and cost. By considering the reviewed projects and evaluating operation modes and control systems new hybrid energy systems could be tailored to fit each situation and to reduce energy losses.

Global energy sources are being transformed from hydrocarbon-based energy sources to renewable and carbon-free energy sources such as wind solar and hydrogen. The biggest challenge with hydrogen as a renewable energy carrier is the storage and delivery system’s complexity. Therefore other media such as ammonia for indirect storage are now being considered. Research has shown that at reasonable pressures ammonia is easily contained as a liquid. In this form energy density is approximately half of that of gasoline and ten times more than batteries. Ammonia can provide effective storage of renewable energy through its existing storage and distribution network. In this article we aimed to analyse the previous studies and the current research on the preparation of ammonia as a next-generation renewable energy carrier. The study focuses on technical advances emerging in ammonia synthesis technologies such as photocatalysis electrocatalysis and plasmacatalysis. Ammonia is now also strongly regarded as fuel in the transport industrial and power sectors and is relatively more versatile in reducing CO₂ emissions. Therefore the utilisation of ammonia as a renewable energy carrier plays a significant role in reducing GHG emissions. Finally the simplicity of ammonia processing transport and use makes it an appealing choice for the link between the development of renewable energy and demand.

An opportunity to decarbonise the offshore oil and gas sector lies in the integration of renewable energy sources with energy storage in a hybrid energy system (HES). Such concept enables maximising the exploitation of carbon-free renewable power while minimising the emissions associated with conventional power generation systems such as gas turbines. Offshore plants in addition to electrical and mechanical power also require process heat for their operation. Solutions that provide low-emission heat in parallel to power are necessary to reach a very high degree of decarbonisation. This paper investigates different options to supply process heat in offshore HES while the electric power is mostly covered by a wind turbine. All HES configurations include energy storage in the form of hydrogen tied to proton exchange membrane (PEM) electrolysers and fuel cells stacks. As a basis for comparison a standard configuration relying solely on a gas turbine and a waste heat recovery unit is considered. A HES combined with a waste heat recovery unit to supply heat proved efficient when low renewable power capacity is integrated but unable to deliver a total CO2 emission reduction higher than around 40%. Alternative configurations such as the utilization of gas-fired or electric heaters become more competitive at large installed renewable capacity approaching CO2 emission reductions of up to 80%.

Through the integration of multiple energy carriers with related technologies multi-energy systems (MES) can exploit the synergies coming from their interplay for several benefits towards decarbonization. In such a context inclusion of Power-to-X technologies in periods of excess renewable electricity supply removes the need for curtailment of renewable electricity generation. In order to achieve the environmental benefits of MES without neglecting their economic feasibility the optimal design problem is as crucial as challenging and requires the adoption of a multi-objective approach. This paper extends the results of a previous work by investigating hydrogen-based non-conventional storage for PV power in the eco-energetic optimization of an MES. The system under study consists of a reversible fuel cell (r-SOC) photovoltaic (PV) electric heat pump absorption chiller and thermal storage and allows satisfying the multi-energy needs of a residential end-user. A multi-objective linear problem is established to find the optimal MES configuration including the sizes of the involved technologies with the goal of reducing the total annual cost and the fossil primary energy input. Simulation results are compared with those obtained in previous work with a conventional nanogrid where a combined heat and power (CHP) system with gas-fired internal combustion engine and a battery were present instead of an r-SOC. The optimized configuration of the non-conventional nanogrid allows achieving a maximum primary energy reduction amounting to 66.3% compared to the conventional nanogrid. In the face of the environmental benefits the non-conventional nanogrid leads to an increase in total annual costs which compared to the conventional nanogrid is in the range of 41–65%.

Deep eutectic solvents (DES) are compounds of a hydrogen bond donor (HBD) and a hydrogen bond acceptor (HBA) that contain a depressed melting point compared to their individual constituents. DES have been studied for their use as carbon capture media and biogas upgrading. However contaminants’ presence in biogas might affect the carbon capture by DES. In this study conductor-like screening model for real solvents (COSMO-RS) was used to determine the effect of temperature pressure and selective contaminants on five DES’ namely choline chloride-urea choline chloride-ethylene glycol tetra butyl ammonium chloride-ethylene glycol tetra butyl ammonium bromide-decanoic acid and tetra octyl ammonium chloride-decanoic acid. Impurities studied in this paper are hydrogen sulfide ammonia water nitrogen octamethyltrisiloxane and decamethylcyclopentasiloxane. At infinite dilution CO₂ solubility dependence upon temperature in each DES was examined by means of Henry’s Law constants. Next the systems were modeled from infinite dilution to equilibrium using the modified Raoults’ Law where CO₂ solubility dependence upon pressure was examined. Finally solubility of CO₂ and CH₄ in the various DES were explored with the presence of varying mole percent of selective contaminants. Among the parameters studied it was found that the HBD of the solvent is the most determinant factor for the effectiveness of CO₂ solubility. Other factors affecting the solubility are alkyl chain length of the HBA the associated halogen and the resulting polarity of the DES. It was also found that choline chloride-urea is the most selective to CO₂  but has the lowest CO₂ solubility and is the most polar among other solvents. On the other hand tetraoctylammonium chloride-decanoic acid is the least selective has the highest maximum CO₂ solubility is the least polar and is the least affected by its environment.

The presented work is dedicated to evaluation of strain and fatigue behaviour of the ferrite-pearlite low-alloyed pipeline steels under known hydrogen concentration in a bulk of metal. Tensile test results have shown on the existence of some characteristic value of the hydrogen concentration CH at which the mechanism of hydrogen influence changes namely: below this value the enhanced plasticity (decreasing of the yield stress value) takes place and above – the hydrogen embrittlement occurs. The ambiguous relationship between fatigue crack growth rate and hydrogen concentration CH in the bulk of steels under their cyclic loading in hydrogen-contained environments has been found. There is a certain CH value at which the crack growth resistance of steel increases and the diagram of fatigue crack growth rate shifts to higher values of stress intensity factor. The generalised diagram of hydrogen concentration effect on strength behaviour of low-alloyed ferrite-pearlite pipeline steels is presented and discussed with the aim of evaluation of different mechanisms of hydrogen effect conditions of their realization and possible co-existence.

The hydrogen permeation coefficient (ϕ) is generally used as a measure to show hydrogen permeation ability through dense metallic membranes which is the product of the Fick’s diffusion coefficient (D) and the Sieverts’ solubility constant (K). However the hydrogen permeability of metal membranes cannot be analyzed consistently with this conventional description. In this paper various methods for consistent analysis of hydrogen permeability are reviewed. The derivations of the descriptions are explained in detail and four applications of the consistent descriptions of hydrogen permeability are introduced: (1) prediction of hydrogen flux under given conditions (2) comparability of hydrogen permeability (3) understanding of the anomalous temperature dependence of hydrogen permeability of Pd-Ag alloy membrane and (4) design of alloy composition of non-Pd-based alloy membranes to satisfy both high hydrogen permeability together with strong resistance to hydrogen embrittlement.

Ductile cast iron (DCI) is one of prospective materials used for the hydrogen equipment because of low-cost good workability and formability. The wide range of mechanical properties of DCI is obtained by controlling microstructural factors such as graphite size volume fraction of graphite matrix structure and so on. Therefore it is important to find out an optimal microstructural condition that is less susceptible to hydrogen embrittlement. In this study the effects of graphite size on the hydrogen absorption capability and the hydrogen-induced ductility loss of ferritic DCI were investigated.<br/>Several kinds of ferritic DCIs with a different graphite diameter of about 10 µm - 30 µm were used for the tensile test and the hydrogen content measurement. Hydrogen charging was performed prior to the tensile test by exposing a specimen to high-pressure hydrogen gas. Then the tensile test was performed in air at room temperature. The hydrogen content of a specimen was measured by a thermal desorption analyzer.<br/>It was found that the amount of hydrogen stored in DCI was dependent on the graphite size. As the graphite diameter increased the hydrogen content sharply increased at a certain graphite diameter and then it became nearly constant irrespective of increase in graphite diameter. In other words there was the critical graphite diameter that significantly changed the hydrogen absorption capability. The ductility was decreased by hydrogen and the hydrogen-induced ductility loss was dependent on the hydrogen content. Therefore the hydrogen embrittlement of DCI became remarkable when the graphite size was larger than the critical value.

Precipitation hardenable (PH) nickel (Ni) alloys are often the most reliable engineering materials for demanding oilfield upstream and subsea applications especially in deep sour wells. Despite their superior corrosion resistance and mechanical properties over a broad range of temperatures the applicability of PH Ni alloys has been questioned due to their susceptibility to hydrogen embrittlement (HE) as confirmed in documented failures of components in upstream applications. While extensive work has been done in recent years to develop testing methodologies for benchmarking PH Ni alloys in terms of their HE susceptibility limited scientific research has been conducted to achieve improved foundational knowledge about the role of microstructural particularities in these alloys on their mechanical behaviour in environments promoting hydrogen uptake. Precipitates such as the γ′ γ′′ and δ-phase are well known for defining the mechanical and chemical properties of these alloys. To elucidate the effect of precipitates in the microstructure of the oil-patch PH Ni alloy 718 on its HE susceptibility slow strain rate tests under continuous hydrogen charging were conducted on material after several different age-hardening treatments. By correlating the obtained results with those from the microstructural and fractographic characterization it was concluded that HE susceptibility of oil-patch alloy 718 is strongly influenced by the amount and size of precipitates such as the γ′ and γ′′ as well as the δ-phase rather than by the strength level only. In addition several HE mechanisms including hydrogen-enhanced decohesion and hydrogen-enhanced local plasticity were observed taking place on oil-patch alloy 718 depending upon the characteristics of these phases when present in the microstructure.

Link to document download on Royal Society Website

CO₂ capture utilization and storage (CCUS) is recognized as a uniquely important option in global efforts to control anthropogenic greenhouse-gas (GHG) emissions. Despite significant progress globally in advancing the maturity of the various component technologies and their assembly into full-chain demonstrations a gap remains on the path to widespread deployment in many countries. In this paper we focus on the importance of business models adapted to the unique technical features and sociopolitical drivers in different regions as a necessary component of commercial scale-up and how lessons might be shared across borders. We identify three archetypes for CCUS development—resource recovery green growth and low-carbon grids—each with different near-term issues that if addressed will enhance the prospect of successful commercial deployment. These archetypes provide a framing mechanism that can help to translate experience in one region or context to other locations by clarifying the most important technical issues and policy requirements. Going forward the archetype framework also provides guidance on how different regions can converge on the most effective use of CCUS as part of global deep-decarbonization efforts over the long term.

The Pr and Sm co-doped ceria (with up to 20 mol.% of dopants) compounds were examined as catalytic layers on the surface of SOFC anode directly fed by biogas to increase a lifetime and the efficiency of commercially available DIR-SOFC without the usage of an external reformer.

The XRD SEM and EDX methods were used to investigate the structural properties and the composition of fabricated materials. Furthermore the electrical properties of SOFCs with catalytic layers deposited on the Ni-YSZ anode were examined by a current density-time and current density-voltage dependence measurements in hydrogen (24 h) and biogas (90 h). Composition of the outlet gasses was in situ analysed by the FTIR-based unit.

It has been found out that Ce_0.9Sm_0.1O_2-δ and Ce_0.8Pr_0.05Sm_0.15O_2-δ catalytic layers show the highest stability over time and thus are the most attractive candidates as catalytic materials in comparison with other investigated lanthanide-doped ceria enhancing direct internal reforming of biogas in SOFCs.

Marked degradation of tensile properties induced by plastic deformation after dynamic interactions between strain-induced martensite transformation and hydrogen has been investigated for type 316L stainless steel by hydrogen thermal desorption analysis. Upon modified hydrogen charging reported previously the amount of hydrogen desorbed in the low temperature range increases; the degradation of tensile properties induced by interactions between plastic deformation and hydrogen at 25 °C or induced by interactions between martensite transformation and hydrogen at −196 °C occurs even for the stainless steel with high resistance to hydrogen embrittlement. The hydrogen thermal desorption behavior is changed by each interaction suggesting changes in hydrogen states. For specimen fractured at 25 °C the facet-like morphology and transgranular fracture are observed on the outer part of the fracture surface. At −196 °C a quasi-cleave fracture is observed at the initiation area. Modified hydrogen charging significantly interacts both plastic deformation and martensite transformation eventually enhancing the degradation of tensile properties. Upon plastic deformation at 25° C after the interactions between martensite transformation and hydrogen by straining to 0.2 at −196 °C cracks nucleate in association with martensite formed by the interactions at −196 °C and marked degradation of tensile properties occurs. It is likely that the interactions between martensite transformation and hydrogen induce damage directly related to the degradation thereby affecting subsequent deformation. Upon dehydrogenation after the interactions between the martensite transformation and hydrogen no degradation of tensile properties is observed. The damage induced by the interactions between martensite transformation and hydrogen probably changes to harmless defects during dehydrogenation.

Smart energy hubs (Smart Hubs) equipped with Vehicle-to-Grid (V2G) charging photovoltaic (PV) energy generation and hydrogen storage capabilities are an emerging technology with potential to alleviate the impact of electric vehicles (EV) on the electricity grid. Their operation however is characterised by intermittent PV energy generation as well as uncertainties in EV traffic and driver preference. These uncertainties when combined with the need to maximise their financial return while guaranteeing driver satisfaction yields a challenging decision-making problem. This paper presents a novel Monte-Carlo-based modelling and computational framework for simulating the operation of Smart Hubs — providing a means for a holistic assessment of their technical and financial viability. The framework utilises a compact and representative mathematical model accounting for power losses PV module degradation variability in EV uptake price inflation driver preference and diversity in charge points and EVs. It provides a comprehensive approach for dealing with uncertainties and dependencies in EV data while being built on an energy management algorithm that maximises revenue generation ensures driver satisfaction and preserves battery life. The energy management problem is formulated as a mixed-integer linear programming problem constituting a business case that includes an adequate V2G reward model for drivers. To demonstrate its applicability the framework was used to assess the financial viability of a fleet management site for various caps on vehicle stay at the site. From the assessment controlled charging was found to be more financially rewarding in all cases yielding between 1.7% and 3.1% more revenue than uncontrolled charging. The self-consumption of the site was found to be nearly 100% due mainly to local load shifting and dispatchable hydrogen generation. V2G injection was however negligible — suggesting its unattractiveness for sites that do not participate in the demand side response market. Overall the numerical results obtained validate the applicability of the proposed framework as a decision-support tool in the sustainable design and operation of Smart Hubs for EV charging.

Among several candidates of hydrogen storage liquid hydrogen methylcyclohexane (MCH) and ammonia are considered as potential hydrogen carriers in terms of their characteristics application feasibility and economic performance. In addition as a main motor in the hydrogen introduction Japan has focused and summarized the storage methods for hydrogen into these three methods. Each of them has advantages and disadvantages compared to each other. This study focuses on the effort to analyze and clarify the potential of these three hydrogen storages especially in terms of physical characteristics energy efficiency and economic cost. Liquid hydrogen faces challenges in huge energy consumption during liquefaction and boil-off during storage. MCH has main obstacles in largely required energy in dehydrogenation. Lastly ammonia encounters high energy demand in both synthesis and decomposition (if required). In terms of energy efficiency ammonia is predicted to have the highest total energy efficiency (34–37%) followed by liquid hydrogen (30–33%) and MCH (about 25%). In addition from cost calculation ammonia with direct utilization (without decomposition) is considered to have the highest feasibility for being massively adopted as it shows the lowest cost (20–22 JPY/Nm3-H2 in 2050). However in case that highly pure hydrogen (such as for fuel cell) is demanded liquid hydrogen looks to be promising (24–25 JPY/Nm3-H2 in 2050) compared to MCH and ammonia with decomposition and purification.

Renewable energy is free abundant clean and could contribute towards a significant reduction of the global warming emissions. It is massively introduced as a source of electricity production across the globe and is expected to become the primary source of energy within the following decades. However despite the naturally replenished energy the supply is not always available. For this reason it is necessary at times of excess energy any surplus quantity to be sufficiently captured stored and later used when a deficit occurs. In this paper an overview of a backup power system operating with a hydrogen-biodiesel dual-fuel internal combustion engine is provided. The system is utilizing the organic chemical hydride method for safe hydrogen storage and transportation. The high energy content of hydrogen stored in the form of an organic hydride under ambient conditions makes it an ideal energy backup medium for large-scale and long-term applications. The research work focusses on the operation and emissions output of the dual-fuel internal combustion engine running on fully renewable fuels and the results are compared with the conventional petroleum-derived diesel engine. Biodiesel-hydrogen operation shows significant benefits in the reduction of carbon and soot emissions but deteriorates the NOx formation compared to the conventional diesel-powered engines. The operation of the engine at high loads can provide high exhaust thermal energy while alternative combustion strategies are necessary to be implemented at low load conditions for the optimum operation of the backup power system.

The increasing penetration of renewable and distributed resources signals a global boom in energy transition but traditional grid utilities have yet to share in much of the triumph at the current stage. Higher grid management costs lower electricity prices fewer customers and other challenges have emerged along the path toward renewable energy but many more opportunities await to be seized. Most importantly there are insufficient studies on how grid utilities can thrive within the hydrogen economy. Through a case study on the State Grid Corporation of China we identify the strengths weaknesses opportunities and threats (SWOT) of grid utilities within the hydrogen economy. Based on these factors we recommend that grids integrate hydrogen into the energy-as-a-service model and deliver it to industrial customers who are under decarbonization pressure. We also recommend that grid utilities fund a joint venture with pipeline companies to optimize electricity and hydrogen transmissions simultaneously.

With the imminent threat of the energy crises innovation in energy technologies is happening world-wide. The aim is to reduce our reliance on fossil fuels. Electric vehicles with fuel-cells that use hydrogen as an energy carrier are touted to be one of the most important potential replacements of the gasoline vehicle in both future transportation scenarios and emerging smart energy grids. However hydrogen storage is a major technical barrier that lies between where we are now and the mass application of hydrogen energy. Further exploration of onboard hydrogen storage systems (OHSS) is urgently needed and in this regard a comprehensive technology opportunity analysis will help. Hence with this research we drew on scientific papers and patents related to OHSS and developed a novel methodology for investigating the past present and future development trends in OHSS. Specifically we constructed a heterogeneous knowledge network using a unique multi-component structure with three core components: hydrogen carriers hydrogen storage materials and fuel cells. From this network we extracted both the developed and underdeveloped technological solutions in the field and applied a well-designed evaluation system and prediction model to score the future development potential of these technological solutions. What emerged was the most promising directions of research in the short medium and long term. The results show that our methodology can effectively identify technology opportunities in OHSS along with providing valuable decision support to researchers and enterprise managers associated with the development and application of OHSS.

Implementation of the hydrogen economy for emission reduction will require storage facilitiesand underground hydrogen storage (UHS) in porous media offers a readily available large-scale option. Lack ofstudies on multiphase hydrogen flow in porous media is one of the several barriers for accurate predictions ofUHS. This paper reports for the first time measurements of hysteresis in hydrogen-water relative permeabilityin a sandstone core under shallow storage conditions. We use the steady state technique to measure primarydrainage imbibition and secondary drainage relative permeabilities and extend laboratory measurements withnumerical history matching and capillary pressure measurements to cover the whole mobile saturation range.We observe that gas and water relative permeabilities show strong hysteresis and nitrogen as substitute forhydrogen in laboratory assessments should be used with care. Our results serve as calibrated input to field scalenumerical modeling of hydrogen injection and withdrawal processes during porous media UHS.

Green hydrogen is identified as one of the prime clean energy carriers due to its high energy density and a zero emission of CO2. A possible solution for the transport of H2 in a safe and low-cost way is in the form of liquid organic hydrogen carriers (LOHCs). As an alternative to loading LOHC with H2 via a two-step procedure involving preliminary electrolytic production of H2 and subsequent chemical hydrogenation of the LOHC we explore here the possibility of electrochemical hydrogen storage (EHS) via conversion of proton of a proton donor into a hydrogen atom involved in covalent bonds with the LOHC (R) via a proton-coupled electron transfer (PCET) reaction: . 2 + +2 ― + ox↔ 0 2red We chose 9-fluorenone/fluorenol (Fnone/Fnol) conversion as such a model PCET reaction. The electrochemical activation of Fnone via two sequential electron transfers was monitored with in-situ and operando spectroscopies in absence and in presence of different alcohols as proton donors of different reactivity which enabled us to both quantify and get the mechanistic insight on PCET. The possibility of hydrogen extraction from the loaded carrier molecule was illustrated by chemical activation.