Hefei National Laboratory for Physical Science at the Microscale, CAS Center for Excellence in Nanoscience, University of Science and Technology of China, Hefei, 230026, P. R. China.
College of Chemistry and Chemical Engineering, Xinjiang Normal University, Urumqi, Xinjiang, 830054, P. R. China.
Adv Mater. 2017 Aug;29(30). doi: 10.1002/adma.201701687. Epub 2017 Jun 8.
The electrocatalytic activity of transition-metal-based compounds is strongly related to the spin states of metal atoms. However, the ways for regulation of spin states of catalysts are still limited, and the underlying relationship between the spin states and catalytic activities remains unclear. Herein, for the first time, by taking Ni -based compounds without high or low spin states for example, it is shown that their spin states can be delocalized after introducing structural distortion to the atomic layers. The delocalized spin states for Ni atoms can provide not only high electrical conductivity but also low adsorption energy between the active sites and reaction intermediates for the system. As expected, the ultrathin nanosheets of nickel-chalcogenides with structural distortions show dramatically enhanced activity in electrocatalytic oxygen evolution compared to their corresponding bulk samples. This work establishes new way for the design of advanced electrocatalysts in transition-metal-based compounds via regulation of spin states.
过渡金属基化合物的电催化活性与其金属原子的自旋态密切相关。然而,调节催化剂自旋态的方法仍然有限,自旋态与催化活性之间的关系尚不清楚。在此,首次以没有高低自旋态的 Ni 基化合物为例,表明通过引入原子层的结构变形可以使它们的自旋态离域。Ni 原子的离域自旋态不仅提供了高导电性,而且降低了活性位与反应中间体之间的吸附能。不出所料,具有结构变形的镍-硫属化合物的超薄纳米片在电催化析氧反应中表现出比其相应体相样品显著增强的活性。这项工作为通过调节自旋态设计先进的过渡金属基化合物电催化剂开辟了新途径。