Zhao Yufei, Wu Jinhu, Cao Xianjun, Li Dongfang, Huang Peng, Gao Hong, Gu Qinfen, Zhang Jinqiang, Wang Guoxiu, Liu Hao
School of Mathematical and Physical Sciences, Faculty of Science, University of Technology Sydney, Broadway, Sydney, NSW, 2007, Australia.
Joint International Laboratory on Environmental and Energy Frontier Materials, School of Environmental and Chemical Engineering, Shanghai University, Shanghai, 200444, China.
Adv Mater. 2025 Sep;37(36):e2506117. doi: 10.1002/adma.202506117. Epub 2025 Jun 16.
Green hydrogen production via water electrolysis is pivotal for achieving energy sustainability. However, the inherently sluggish kinetics of the hydrogen evolution reaction and oxygen evolution reaction impede the progress of water-splitting technology. Recently, high-entropy materials (HEMs) composed of at least five elements have garnered significant attention as promising electrocatalysts for water splitting, owing to their compositional versatility, structural robustness, and synergistic interactions among elements. This review comprehensively explores the development of HEMs, tracing their emergence and structural evolution via atomic nanoengineering strategies (i.e., from bulk to nanostructuring, from random distributions to relatively ordered architectures, from bare HEMs to reconstructed HEMs, from intact HEMs to defective structures, from pristine HEMs to functionalized variants) and revealing how these evolutionary steps contribute to the properties and enhance catalytic performance in water splitting. The fundamental roles of individual elements (e.g., active sites, promoters, stabilizers) in shaping the structure, stability, and catalytic activity of HEMs are examined, laying a foundation for the rational design of efficient HEM-based electrocatalysts. The review also highlights recent advances in HEM-based catalysts for water splitting, emphasizing desirable properties and elemental contributions. Finally, the remaining challenges and perspectives on the future directions of HEM-based materials in energy conversion technologies are discussed.
通过水电解生产绿色氢气对于实现能源可持续性至关重要。然而,析氢反应和析氧反应固有的缓慢动力学阻碍了水分解技术的发展。最近,由至少五种元素组成的高熵材料(HEMs)作为有前景的水分解电催化剂受到了广泛关注,这归因于它们的成分多样性、结构稳健性以及元素之间的协同相互作用。本综述全面探讨了高熵材料的发展,通过原子纳米工程策略追溯它们的出现和结构演变(即从块体到纳米结构,从随机分布到相对有序的结构,从裸高熵材料到重构高熵材料,从完整高熵材料到缺陷结构,从原始高熵材料到功能化变体),并揭示这些演变步骤如何影响性能并增强水分解中的催化性能。研究了单个元素(如活性位点、促进剂、稳定剂)在塑造高熵材料的结构、稳定性和催化活性方面的基本作用,为合理设计高效的基于高熵材料的电催化剂奠定了基础。该综述还强调了基于高熵材料的水分解催化剂的最新进展,重点介绍了理想的性能和元素贡献。最后,讨论了基于高熵材料的材料在能量转换技术中面临的剩余挑战以及未来方向的展望。