Lai Wei-Hong, Wang Heng, Zheng Lirong, Jiang Quan, Yan Zi-Chao, Wang Lei, Yoshikawa Hirofumi, Matsumura Daiju, Sun Qiao, Wang Yun-Xiao, Gu Qinfen, Wang Jia-Zhao, Liu Hua-Kun, Chou Shu-Lei, Dou Shi-Xue
College of Materials Science and Engineering, Shenzhen University, Shenzhen, 518060, China.
College of Physics and Optoelectronic Engineering, Shenzhen University, Shenzhen, 518060, China.
Angew Chem Int Ed Engl. 2020 Dec 1;59(49):22171-22178. doi: 10.1002/anie.202009400. Epub 2020 Sep 23.
Herein, we report a comprehensive strategy to synthesize a full range of single-atom metals on carbon matrix, including V, Mn, Fe, Co, Ni, Cu, Ge, Mo, Ru, Rh, Pd, Ag, In, Sn, W, Ir, Pt, Pb, and Bi. The extensive applications of various SACs are manifested via their ability to electro-catalyze typical hydrogen evolution reactions (HER) and conversion reactions in novel room-temperature sodium sulfur batteries (RT-Na-S). The enhanced performances for these electrochemical reactions arisen from the ability of different single active atoms on local structures to tune their electronic configuration. Significantly, the electrocatalytic behaviors of diverse SACs, assisted by density functional theory calculations, are systematically revealed by in situ synchrotron X-ray diffraction and in situ transmission electronic microscopy, providing a strategic library for the general synthesis and extensive applications of SACs in energy conversion and storage.
在此,我们报告了一种在碳基质上合成全系列单原子金属的综合策略,这些金属包括V、Mn、Fe、Co、Ni、Cu、Ge、Mo、Ru、Rh、Pd、Ag、In、Sn、W、Ir、Pt、Pb和Bi。各种单原子催化剂(SACs)的广泛应用通过它们在新型室温钠硫电池(RT-Na-S)中电催化典型析氢反应(HER)和转化反应的能力得以体现。这些电化学反应性能的增强源于局部结构上不同单活性原子调整其电子构型的能力。值得注意的是,借助密度泛函理论计算,通过原位同步辐射X射线衍射和原位透射电子显微镜系统地揭示了各种SACs的电催化行为,为SACs在能量转换和存储中的通用合成及广泛应用提供了一个策略库。