Yuan Liu, Xixi Ren, Jiajun Wang, Haozhi Wang, Zexiang Yin, Yang Wang, Wenjie Huang, Xiaolin Hu, Zhichuan J. Xu, Yida Deng
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引用次数: 0
Abstract
Spin state of active sites is one of the most influencing factors for the catalytic performance of electrocatalysts. To date, most modulations are conducted on non-tetrahedrally coordinated metal sites, while tetrahedron-coordinated single-atom catalysts (TCSACs) have not been investigated yet. This article presents a correlation between the spin state of TCSACs and their activities toward CO2 electroreduction. TCSACs are made using ZnO as the substrate. The spin states of metal sites of TCSACs modulate the interactions between the catalyst and adsorbed intermediates. A volcano relationship is found between the transition metal (TM) magnetic moments and the limiting potential (UL) of the CO2 reduction reaction. Spin-state analysis indicates that the intermediate spin state of TMs is more favorable for the adsorption and conversion of CO2. Optimal interaction between the TM-t2 orbitals of the intermediate spin and the adsorbed molecule-pz orbitals significantly improves the catalytic activity of the TCSACs. As a result, Fe-TCSAC achieves a high FECO of 91.6% at −0.9 V vs RHE. These results provide a theoretical basis and guidelines for the spin-state effects of tetrahedron-coordinated single-atom catalysts.
活性位点的自旋状态是影响电催化剂催化性能的主要因素之一。迄今为止,大多数调制都是在非四面体配位的金属位点上进行的,而四面体配位的单原子催化剂(TCSACs)尚未得到研究。本文介绍了TCSACs自旋态与其CO2电还原活性之间的关系。TCSACs是用ZnO作为衬底制成的。TCSACs金属位的自旋态调节了催化剂与吸附中间体之间的相互作用。发现过渡金属(TM)磁矩与CO2还原反应的极限电位(UL)之间存在火山关系。自旋态分析表明,TMs的中间自旋态更有利于CO2的吸附和转化。中间自旋的TM-t2轨道与吸附的分子-pz轨道之间的最佳相互作用显著提高了TCSACs的催化活性。结果表明,Fe-TCSAC在−0.9 V vs RHE下获得了91.6%的高FECO。这些结果为研究四面体配位单原子催化剂的自旋态效应提供了理论依据和指导。
期刊介绍:
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