催化作用
锆
氧还原反应
氧气
氢
材料科学
吸附
配体(生物化学)
锌
化学
电池(电)
氧还原
无机化学
物理化学
有机化学
电极
电化学
物理
生物化学
受体
量子力学
功率(物理)
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/anie.202209746
摘要
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
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