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Sodium borohydride (NaBH4) solution is a promising liquid “fuel” for continuous hydrogen supply through catalytic hydrolysis, offering a safer alternative to compressed hydrogen to fuel cells. However, the harsh thermal and chemical environments of concentrated NaBH4 hydrolysis cause rapid catalyst deactivation. Herein, we synthesized a high-entropy layered hydroxide (HELH, FeCoNiCuZn@ZIF-67 (ZIF-67 = zeolitic imidazolate framework-67)) nanocatalyst via an in-situ etching-growth strategy with ZIF-67. The mechanical structure of residual ZIF-67 inside ensures the robustness of active centers and particles. The efficiency of hydrogen generation is guaranteed by the synergy of different metals in high-entropy structures, which involves borohydride adsorption and H2 release. Benefiting from this cooperative architecture, the HELH catalyst achieves a high hydrogen generation rate of 8 L·min−1·g−1 in a 25 wt.% NaBH4 solution. Density functional theory and electrochemical analyses reveal that abundant oxygen vacancies and multi-metal synergy optimize water activation and lower the reaction barrier. This work provides an effective strategy for designing robust high-entropy catalysts for extreme conditions.

This is an open access article under the terms of the Creative Commons Attribution 4.0 International License (CC BY 4.0, https://creativecommons.org/licenses/by/4.0/).
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