Hydrogen battery relieves the pressure for clean energy storage

Source: © Sergey Klopotov/Shutterstock

Hydrogen is currently far harder to store than electrochemical energy, meaning that it is still difficult to turn renewable energy into an energy source that can be called upon when the sun isn’t shining or the wind isn’t blowing. However, a Japanese team thinks that they’ve now made progress towards this goal

Hydrogen offers many advantages for clean energy storage, but storing it generally requires either a lot of pressure, a lot of heat or both. To avoid the enormous pressures needed to store pure hydrogen in manageable volumes, researchers have looked at hydrogen compounds. However, so far these approaches have suffered a catalogue of issues from high operating temperatures impeding the energy efficiency and stability of devices to low hydrogen storage capacity. Now researchers led by Naoki Matsui and Ryoji Kanno at the Institute of Science Tokyo in Japan have developed an electrolyte that allows high performance hydrogen storage.

There are currently two main approaches to solid state hydrogen storage. The more thoroughly researched is ‘thermodynamic’, whereby certain alloys absorb hydrogen and form hydrogen compounds that then break down and release hydrogen at higher temperatures. However, while some light-element metal hydrides, such as MgH₂ and LiH have a high hydrogen storage capacity, temperatures of around 300°C are required to release the hydrogen. An alternative approach dates back to the work of Stanford University’s Robert Huggins, who in 1985 proposed that hydride ions could be electrochemically inserted into a metal using a liquid electrolyte and an applied voltage. However, once again the approach was complicated by high temperatures. Recent advances in solid state electrolytes may offer a way around this if adequate ionic conductivity and stability at lower temperatures can be achieved.

‘As we had been developing solid-state ionic conductors capable of transporting hydride ions, we recognised the potential for applying these materials to hydride driven electrochemical hydrogen storage,’ Matsui and Kanno told Chemistry World in an email. They had noted reports of superionic conductivity by combining ions of different sizes, and in pursuing a similar approach landed upon a compound combining barium, calcium and sodium ions: BaH₂–CaH₂–NaH.

Initial experiments used the electrolyte in a test system sandwiched between molybdenum current collectors and an acetylene black conduction additive, and TiH₂ and titanium reference electrodes. This setup allowed them to determine the stable potential window of the solid electrolyte and Matsui and Kanno say that it is the best ever reported.

Source: © Institute of Science Tokyo

Solid Electrolyte for Low-Temperature Hydrogen Storage

Key points:

• Magnesium (Mg) is a promising hydrogen (H₂) storage material due to its high storage capacity (~7.6 wt.%).

• However, its practical use has been limited by the need for very high operating temperatures (>300°C).

New Solution: Mg–H₂ Cells with a Hydride-Ion (H⁻)-Conducting Solid Electrolyte

Electrolyte formula: Ba₀.₅Ca₀.₃₅Na₀.₁₅H₁.₈₅

• Working principle:

  • Discharge (H₂ absorption): Mg reacts with H₂ to form MgH₂.

  • Charge (H₂ release): MgH₂ decomposes to release H₂, regenerating Mg.

• Crystal structure: Anti-α-AgI type with 3D tetrahedral–octahedral pathways, enabling efficient H⁻ ion movement.

Key Achievements

• Achieved full Mg/MgH₂ hydrogen storage capacity (7.6 wt.% ~ 23,030 mAh g⁻¹).

• Reversible hydrogen storage at 90°C (much lower than 300°C).

• High ionic conductivity (2.1 × 10⁻³ S cm⁻¹ at room temperature).

• High electrochemical stability (0.13 – 0.53 V vs. Ti/TiH₂).

• Efficient ion transport pathways within the 3D crystal structure.

Conclusion

Mg–H₂ cells with the H⁻-conducting solid electrolyte Ba₀.₅Ca₀.₃₅Na₀.₁₅H₁.₈₅ provide a safe and efficient solution for low-temperature hydrogen storage.

Source: Hirose et al. (2025) | Science – Institute of Science Tokyo

They also reported an unusually high hydride ion conductivity, which they attribute to the body-centred cubic crystal (bcc) structure of the solid-state electrolyte. ‘The energy barrier for ionic conduction is primarily determined by interactions with the surrounding framework,’ they explain. The bcc structure has a lower packing density compared with other common structures, ‘providing an open pathway for ion transport’. They also point out that the highly polarisable cations in the framework contribute to the high ion conductivity, as this reduces the repulsion between the cations and the hydride ions moving through.

To test the hydrogen storage capabilities directly they produced a cell with a magnesium hydride anode and a LaH_x cathode. With this setup operating at 90°C and an applied potential of 0.12V, they were able to demonstrate the theoretical capacity of MgH₂ over five cycles.

‘This paper, which demonstrates the new possibility of “hydrogen storage via electrochemical reactions”, represents an important milestone,’ says Genki Kobayashi, an inorganic chemist at RIKEN in Japan, who was not directly involved in the work. ‘I believe this work marks a turning point, and I look forward to further advances in the creation of new devices that utilise hydrides.’

Next, Matsui and Kanno plan to focus future work on developing solid electrolytes and electrode materials with higher ionic conductivity, alongside device designs with lower operating temperatures and improved energy efficiency.

References

T Hirose et al, Science, 2025, 389, 1252 (DOI: 10.1126/science.adw1996)