Department of Chemistry, Indiana University, 800 East Kirkwood Avenue, Bloomington, Indiana 47401, United States.
Department of Chemistry, The University of Chicago, Chicago, Illinois 60637, United States.
J Am Chem Soc. 2021 May 12;143(18):7203-7208. doi: 10.1021/jacs.1c03427. Epub 2021 May 3.
This work reports on the generation of a graphite-conjugated diimine macrocyclic Co catalyst (GCC-CoDIM) that is assembled at -quinone edge defects on graphitic carbon electrodes. X-ray photoelectron spectroscopy and X-ray absorption spectroscopy confirm the existence of a new Co surface species with a coordination environment that is the same as that of the molecular analogue, [Co(DIM)Br]. GCC-CoDIM selectively reduces nitrite to ammonium with quantitative Faradaic efficiency and at a rate that approaches enzymatic catalysis. Preliminary mechanistic investigations suggest that the increased rate is accompanied by a change in mechanism from the molecular analogue. These results provide a template for creating macrocycle-based electrocatalysts based on first-row transition metals conjugated to an extreme redox-active ligand.
这项工作报道了一种石墨共轭二亚胺大环 Co 催化剂(GCC-CoDIM)的生成,该催化剂在石墨碳电极的醌边缘缺陷处组装。X 射线光电子能谱和 X 射线吸收光谱证实了一种新的 Co 表面物种的存在,其配位环境与分子类似物 [Co(DIM)Br] 相同。GCC-CoDIM 选择性地将亚硝酸盐还原为铵,法拉第效率定量,且反应速率接近酶催化。初步的机理研究表明,增加的速率伴随着从分子类似物的机理变化。这些结果为创建基于第一过渡金属与极端氧化还原活性配体共轭的大环电催化剂提供了模板。