2026-05-15 中国科学院(CAS)
<関連情報>
- https://english.cas.cn/newsroom/cas-in-media/202605/t20260515_1159461.shtml
- https://www.cell.com/joule/abstract/S2542-4351(26)00159-5
気体固体水素化物イオン電池と水素・電気共貯蔵システム A gas-solid hydride ion battery and a hydrogen-electricity co-storage system
Shangshang Wang ∙ Weijin Zhang ∙ Liping Yang ∙ … ∙ Wanjun Li ∙ Rui Cai ∙ Ping Chen
Joule Published:May 13, 2026
DOI:https://doi.org/10.1016/j.joule.2026.102475
Graphical abstract

Context & scale
The hydride ion (H−), with the highest electron density and the largest polarizability per unit mass in nature, enables the construction of electrochemical processes distinctly different from existing cation-mediated systems, holding great promise for triggering major technological advances in the fields of energy storage and chemical conversion. Among these, rechargeable all-solid-state H− batteries (HIBs) have attracted considerable attention because of their unique characteristics, including being metal-dendrite-free, possessing high theoretical capacity, offering great potential for wide temperature operation, utilizing abundant hydrogen resources, and being environmentally friendly. Using H2 as the active material of an electrode, namely, the gas-solid HIB (g-HIB), can significantly improve capacity and energy density. More importantly, it provides a brand-new electrochemical pathway for high-capacity chemical hydrogen storage at room temperature and ambient pressure. This goal has remained elusive for over 60 years and is the present bottleneck for the large-scale utilization of hydrogen energy. This work demonstrates the first g-HIB Mg|3CeH3@BaH2|H2, which achieves a high capacity of 1,526 mAh/g, good cycling performance, and a wide operating temperature range (−20°C to 90°C). A novel hydrogen-electricity co-storage system is proposed by coupling this g-HIB with a secondary battery. Compared with other hydrogen storage technologies, this co-storage system delivers high hydrogen energy efficiency and may find great uses in mobile or stationary hydrogen utilization scenarios.
Highlights
- The first gas-solid hydride ion battery based on the Mg-H2 system was constructed
- It exhibits an initial capacity of 1,526 mAh/g and maintains >70% after 60 cycles
- A hydrogen-electricity co-storage system is proposed
- This co-storage system achieves a high hydrogen energy efficiency of 93.9%
Summary
Significant progress has been made in materials development for hydride ion (H−) conduction and H−-mediated electrochemical devices. However, a gas-solid H− battery (g-HIB) that utilizes H2 and metals as the active materials of the electrodes and offers the potential for high capacity and energy density has yet to be developed. Here, a typical metal-hydrogen system, Mg-H2, is employed to build such a g-HIB. Experimental results validate that hydrogenation and dehydrogenation of the anode lead to electric energy output and input, respectively, in the Mg|3CeH3@BaH2|H2 developed. This g-HIB exhibits an initial capacity of 1,526 mAh/g and maintains a capacity retention of over 70% after 60 cycles. It operates effectively across a wide temperature range of −20°C to 90°C. The integration of this g-HIB with a secondary ion battery could create a novel hydrogen-electricity co-storage system that can be applied to hydrogen-electricity powertrains of fuel cell vehicles or drones to deliver a high hydrogen energy efficiency of 93.9%.


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