Tang Cheng, Jiao Yan, Shi Bingyang, Liu Jia-Ning, Xie Zhenhua, Chen Xiao, Zhang Qiang, Qiao Shi-Zhang
Centre for Materials in Energy and Catalysis, School of Chemical Engineering and Advanced Materials, The University of Adelaide, Adelaide, SA, 5005, Australia.
School of Life Sciences, Henan University, Kaifeng, Henan, 475004, China.
Angew Chem Int Ed Engl. 2020 Jun 2;59(23):9171-9176. doi: 10.1002/anie.202003842. Epub 2020 Apr 7.
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 H O 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.
单原子催化剂(SACs)在电催化领域具有巨大潜力。通过定制金属原子、相邻的配位掺杂剂和金属负载量,可以合理优化它们的性能。然而,由于合成方法有限以及对结构-性能关系的理解不足,这样做仍然是一个巨大的挑战。在此,我们报道了一种新型的Mo SAC,它具有独特的O、S配位以及超过10 wt%的高金属负载量。通过高角度环形暗场扫描透射电子显微镜和扩展X射线吸收精细结构确定了其孤立状态和局部环境。该SACs在0.10 m KOH中通过2e途径催化氧还原反应(ORR),H₂O选择性超过95%。电化学测试和理论计算均揭示了Mo单原子和配位结构的关键作用。