United States

The storage of excess electrical generation enabled through the electrolytic production of hydrogen from water would allow “load-shifting” of power generation. This paves the way for hydrogen as an energy carrier to be further used as a zero‑carbon fuel for land air and sea transportation. However challenges in hydrogen storage and transportation ultimately pose restrictions on its wider adaption along horizontal and vertical vectors. This paper investigates chemical energy carriers ranging from small molecules such as ammonia and methane to formic acid as well as other more complex hydrocarbons in response to this timely engineering problem. The hydrogenation and dehydrogenation of such carrier molecules require energy lowering the effective net heating value of hydrogen up to 32 %. Different carrier approaches are discussed in the light of availability energetics water requirements and suitability for applications in power generation shipping trucking and aviation supplemented by a comprehensive safety review making this study unique in its field. It is found that hydrogen delivered without a carrier is ideal for power generation applications due to the large quantities required. Aviation would benefit from either ammonia or hydrogen and is generally a field challenging to decarbonize. Ammonia appears also to be a good medium for shipping hydrogen between continents and to power container ships due to its high energy density and lower liquid temperature compared with hydrogen. At the same time ammonia can also be used to power the ship's engine. Long-haul trucking would benefit the most from cryogenic or compressed hydrogen due to the lower quantities required and purity requirements of the fuel cells.

Because of their high surface areas crystallinity and tunable propertiesmetal−organic frameworks (MOFs) have attracted intense interest as next-generationmaterials for gas capture and storage. While much effort has been devoted to thediscovery of new MOFs a vast catalog of existing MOFs resides within the CambridgeStructural Database (CSD) many of whose gas uptake properties have not beenassessed. Here we employ data mining and automated structure analysis to identify“cleanup” and rapidly predict the hydrogen storage properties of these compounds.Approximately 20 000 candidate compounds were generated from the CSD using analgorithm that removes solvent/guest molecules. These compounds were thencharacterized with respect to their surface area and porosity. Employing the empiricalrelationship between excess H2 uptake and surface area we predict the theoretical total hydrogen storage capacity for the subsetof ∼4000 compounds exhibiting nontrivial internal porosity. Our screening identifies several overlooked compounds having hightheoretical capacities; these compounds are suggested as targets of opportunity for additional experimental characterization.More importantly screening reveals that the relationship between gravimetric and volumetric H2 density is concave downwardwith maximal volumetric performance occurring for surface areas of 3100−4800 m2 /g. We conclude that H2 storage in MOFswill not benefit from further improvements in surface area alone. Rather discovery efforts should aim to achieve moderate massdensities and surface areas simultaneously while ensuring framework stability upon solvent removal.

This perspective article delves into the critical role of hydrogen as a sustainable energy carrier in the context of the ongoing global energy transition. Hydrogen with its potential to decarbonize various sectors has emerged as a key player in achieving decarbonization and energy sustainability goals. This article provides an overview of the current state of hydrogen technology its production methods and its applications across diverse industries. By exploring the challenges and opportunities associated with hydrogen integration we aim to shed light on the pathways toward achieving a sustainable hydrogen economy. Additionally the article underscores the need for collaborative efforts among policymakers industries and researchers to overcome existing hurdles and unlock the full potential of hydrogen in the transition to a low-carbon future. Through a balanced analysis of the present landscape and future prospects this perspective article aims to contribute valuable insights to the discourse surrounding hydrogen’s role in the global energy transition.

Long-duration energy storage is the key challenge facing renewable energy transition in the future of well over 50% and up to 75% of primary energy supply with intermittent solar and wind electricity while up to 25% would come from biomass which requires traditional type storage. To this end chemical energy storage at grid scale in the form of fuel appears to be the ideal option for wind and solar power. Renewable hydrogen is a much-considered fuel along with ammonia. However these fuels are not only difficult to transport over long distances but they would also require totally new and prohibitively expensive infrastructure. On the other hand the existing natural gas pipeline infrastructure in developed economies can not only transmit a mixture of methane with up to 20% hydrogen without modification but it also has more than adequate long-duration storage capacity. This is confirmed by analyzing the energy economies of the USA and Germany both possessing well-developed natural gas transmission and storage systems. It is envisioned that renewable methane will be produced via well-established biological and/or chemical processes reacting green hydrogen with carbon dioxide the latter to be separated ideally from biogas generated via the biological conversion of biomass to biomethane. At the point of utilization of the methane to generate power and a variety of chemicals the released carbon dioxide would be also sequestered. An essentially net zero carbon energy system would be then become operational. The current conversion efficiency of power to hydrogen/methane to power on the order of 40% would limit the penetration of wind and solar power. Conversion efficiencies of over 75% can be attained with the on-going commercialization of solid oxide electrolysis and fuel cells for up to 75% penetration of intermittent renewable power. The proposed hydrogen/methane system would then be widely adopted because it is practical affordable and sustainable.

Electrolysis of water to generate hydrogen fuel is an attractiverenewable energy storage technology. However grid-scale fresh-water electrolysis would put a heavy strain on vital water re-sources. Developing cheap electrocatalysts and electrodes that cansustain seawater splitting without chloride corrosion could ad-dress the water scarcity issue. Here we present a multilayer anodeconsisting of a nickel–iron hydroxide (NiFe) electrocatalyst layeruniformly coated on a nickel sulfide (NiSx) layer formed on porousNi foam (NiFe/NiSx-Ni) affording superior catalytic activity andcorrosion resistance in solar-driven alkaline seawater electrolysisoperating at industrially required current densities (0.4 to 1 A/cm2)over 1000 h. A continuous highly oxygen evolution reaction-active NiFe electrocatalyst layer drawing anodic currents towardwater oxidation and an in situ-generated polyatomic sulfate andcarbonate-rich passivating layers formed in the anode are respon-sible for chloride repelling and superior corrosion resistance of thesalty-water-splitting anode.