催化作用
配体(生物化学)
氧气
锆
化学
吸附
氢
氧还原反应
电池(电)
材料科学
无机化学
电极
物理化学
电化学
有机化学
物理
受体
功率(物理)
量子力学
生物化学
作者
Xia Wang,Yun An,Lifeng Liu,Lingzhe Fang,Yannan Liu,Jiaxu Zhang,Haoyuan Qi,Thomas Heine,Tao Li,Agnieszka Kuc,Minghao Yu,Xinliang Feng
标识
DOI:10.1002/ange.202209746
摘要
Abstract Single‐atom catalysts (SACs), as promising alternatives to Pt‐based catalysts, suffer from the limited choice of center metals and low single‐atom loading. Here, we report a pentacoordinated Zr‐based SAC with nontrivial axial O ligands (denoted O−Zr−N−C) for oxygen reduction reaction (ORR). The O ligand downshifts the d‐band center of Zr and confers Zr sites with stable local structure and proper adsorption capability for intermediates. Consequently, the ORR performance of O−Zr−N−C prominently surpasses that of commercial Pt/C, achieving a half‐wave potential of 0.91 V vs. reversible hydrogen electrode and outstanding durability (92 % current retention after 130‐hour operation). Moreover, the Zr site shows good resistance towards aggregation, enabling the synthesis of Zr‐based SAC with high loading (9.1 wt%). With the high‐loading catalyst, the zinc‐air battery (ZAB) delivers a record‐high power density of 324 mW cm −2 among those of SAC‐based ZABs.
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