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首页> 外文期刊>Angewandte Chemie >Coordination Tunes Selectivity: Two-Electron Oxygen Reduction on High-Loading Molybdenum Single-Atom Catalysts
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Coordination Tunes Selectivity: Two-Electron Oxygen Reduction on High-Loading Molybdenum Single-Atom Catalysts

机译:协调曲调选择性:高负荷钼单原子催化剂的双电子氧还原

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摘要

Single-atom catalysts (SACs) have great potential in electrocatalysis. Their performance can be rationally optimized by tailoring the metal atoms, adjacent coordinative dopants, and metal loading. However, doing so is still a great challenge because of the limited synthesis approach and insufficient understanding of the structure-property relationships. Herein, we report a new kind of Mo SAC with a unique O,S coordination and a high metal loading over 10 wt %. The isolation and local environment was identified by high-angle annular dark-field scanning transmission electron microscopy and extended X-ray absorption fine structure. The SACs catalyze the oxygen reduction reaction (ORR) via a 2 e(-) pathway with a high H2O2 selectivity of over 95 % in 0.10 m KOH. The critical role of the Mo single atoms and the coordination structure was revealed by both electrochemical tests and theoretical calculations.
机译:单原子催化剂(SACS)具有巨大的电殖分析。 它们的性能可以通过定制金属原子,相邻的协调掺杂剂和金属载荷来合理优化。 然而,由于有限的合成方法和对结构性质关系的理解不足,这样做仍然是一个巨大的挑战。 在此,我们报告了一种具有独特O,S的协调和高金属负荷超过10wt%的新种类囊。 通过大角度环形暗场扫描透射电子显微镜和延伸的X射线吸收细结构来识别隔离和局部环境。 SACS通过2 e( - )途径催化氧还原反应(ORR),高H2O2选择性为0.10m KOH的95%以上。 电化学试验和理论计算揭示了Mo单个原子和协调结构的关键作用。

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