金属间化合物
正交晶系
材料科学
铱
杂原子
催化作用
晶体结构
溶解
结晶学
化学工程
冶金
化学
合金
有机化学
戒指(化学)
工程类
生物化学
作者
Caihong He,Chaoqun Ma,Jing Xia,Huaifang Zhang,Sumei Han,Yahui Tian,An‐Liang Wang,Xiang‐Min Meng,Wenbin Cao,Qipeng Lu
标识
DOI:10.1002/adfm.202311683
摘要
Abstract Iridium (Ir) is an efficient catalyst for overall water splitting, yet its widespread utilization is hampered by the substantial cost and limited stability. Alloying Ir with heteroatoms can optimize the electronic structure of the catalyst and reduce the required amount of Ir. Compared to solid solution alloys, Ir‐based intermetallic compounds (IMCs) with ordered and stronger Ir‐heteroatom bonds exhibit superior catalytic activity and durability. Hence, adjusting the crystal structure of Ir‐based IMCs is expected to further optimize the configurations of catalytic active sites with minimal usage of Ir. Here, IrIn 2 IMCs with unconventional face‐centered orthorhombic structure are synthesized by a high‐temperature annealing reduction method, in which the atomic percentage of Ir is only 33%. The calculation results show that the d‐band center of IrIn 2 is shifted upward compared to metallic Ir, resulting in enhanced adsorption with intermediates. Meanwhile, the formation of ordered Ir─In bonds improves the charge transfer effectively and makes the IrIn 2 IMCs resistant to atom migration and dissolution during the electrochemical reactions. For overall water splitting, the cell voltage required to achieve 10 mA cm −2 is as low as 1.51 V under acidic condition. And IrIn 2 IMCs exhibit excellent durability, with no degradation in performance >55 h.
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