Wu Yishang, Cai Jinyan, Xie Yufang, Niu Shuwen, Zang Yipeng, Wu Shaoyang, Liu Yun, Lu Zheng, Fang Yanyan, Guan Yong, Zheng Xusheng, Zhu Junfa, Liu Xiaojing, Wang Gongming, Qian Yitai
Hefei National Laboratory for Physical Science at the Microscale, Department of Chemistry, University of Science and Technology of China, Hefei, Anhui, 230026, P. R. China.
National Synchrotron Radiation Laboratory, University of Science & Technology of China, Hefei, Anhui, 230029, P. R. China.
Adv Mater. 2020 Jul;32(26):e1904346. doi: 10.1002/adma.201904346. Epub 2020 May 25.
The capability of manipulating the interfacial electronic coupling is the key to achieving on-demand functionalities of catalysts. Herein, it is demonstrated that the electronic coupling of Fe N can be effectively regulated for hydrogen evolution reaction (HER) catalysis by vacancy-mediated orbital steering. Ex situ refined structural analysis reveals that the electronic and coordination states of Fe N can be well manipulated by nitrogen vacancies, which impressively exhibit strong correlation with the catalytic activities. Theoretical studies further indicate that the nitrogen vacancy can uniquely steer the orbital orientation of the active sites to tailor the electronic coupling and thus benefit the surface adsorption capability. This work sheds light on the understanding of the catalytic mechanism in real systems and could contribute to revolutionizing the current catalyst design for HER and beyond.
操纵界面电子耦合的能力是实现催化剂按需功能的关键。在此,证明了通过空位介导的轨道调控,可以有效调节Fe N的电子耦合用于析氢反应(HER)催化。非原位精细结构分析表明,Fe N的电子和配位状态可以通过氮空位得到很好的调控,这与催化活性呈现出显著的相关性。理论研究进一步表明,氮空位可以独特地引导活性位点的轨道取向,以调整电子耦合,从而有利于表面吸附能力。这项工作有助于理解实际系统中的催化机制,并可能推动当前用于HER及其他领域的催化剂设计发生变革。