化学
催化作用
分解水
析氧
纳米结构
兴奋剂
纳米技术
吸附
能量转换
电化学能量转换
电催化剂
制作
化学工程
电化学
过电位
材料科学
物理化学
电极
有机化学
光电子学
物理
光催化
工程类
热力学
病理
医学
替代医学
作者
Cheng Wang,Hui Xu,Yuan Wang,Hongyuan Shang,Liujun Jin,Fangfang Ren,Tongxin Song,Jun Guo,Yukou Du
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2020-07-31
卷期号:59 (16): 11814-11822
被引量:51
标识
DOI:10.1021/acs.inorgchem.0c01832
摘要
Hollow nanostructures with intricate interior and catalytic effects have been the focus of researchers in energy conversion and storage. Although tremendous efforts have been made, the fabrication of well-defined hollow nanostructures has been rarely reported due to the limitations of the synthetic methods. Herein, we have proposed a general synthetic strategy for the construction of V-doped CoMx (M = P, S, O) nanoboxes (NBs), where the doped V effectively modifies the electronic structure of CoMx to provide a favorable surface electrochemical environment for the adsorption of reaction intermediates (*O, *OH, and *OOH), leading to a significant enhancement in electrocatalytic performance. More importantly, the hollow nanostructures can expose abundant surface active areas and promote the chemical adsorption of reactants and intermediates, greatly contributing to the promotion of electrocatalytic performance. Impressively, the optimal V-doped CoS2 NBs show excellent electrocatalytic oxygen evolution reaction (OER) performance with an overpotential of only 290 mV at 10 mA cm–2, along with outstanding overall water-splitting performance. This work supplies pivotal insights for constructing high-performance OER catalysts on the basis of electronic and geometric engineering.
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