Unveiling the Promotion of Surface-Adsorbed Chalcogenate on the Electrocatalytic Oxygen Evolution Reaction

被引:401
作者
Shi, Yanmei [1 ]
Du, Wei [1 ]
Zhou, Wei [1 ]
Wang, Changhong [1 ]
Lu, Shanshan [1 ]
Lu, Siyu [3 ]
Zhang, Bin [1 ,2 ]
机构
[1] Tianjin Univ, Sch Sci, Inst Mol Plus, Dept Chem, Tianjin 300072, Peoples R China
[2] Tianjin Univ, Frontiers Sci Ctr Synthet Biol, Tianjin Key Lab Mol Optoelect Sci, Minist Educ, Tianjin 300072, Peoples R China
[3] Zhengzhou Univ, Coll Chem, Green Catalysis Ctr, Zhengzhou 450000, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
active species; anion adsorption; electrochemical oxygen evolution reaction; in situ Raman spectroscopy; transition metal chalcogenides; SITU ELECTROCHEMICAL OXIDATION; EFFICIENT ELECTROCATALYST; IRON SULFIDE; NICKEL FOAM; CATALYSTS; NANOSHEETS; COBALT; NANOWIRES; ELECTRODE; OXIDES;
D O I
10.1002/anie.202011097
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Transition metal chalcogenides (TMCs) are efficient oxygen evolution reaction (OER) pre-electrocatalysts, and will in situ transform into metal (oxy)hydroxides under OER condition. However, the role of chalcogen is not fully elucidated after oxidation and severe leaching. Here we present the vital promotion of surface-adsorbed chalcogenates on the OER activity. Taking NiSe(2)as an example, in situ Raman spectroscopy revealed the oxidation of Se-Se to selenites (SeO32-) then to selenates (SeO42-). Combining the severe Se leaching and the strong signal of selenates, it is assumed that the selenates are rich on the surface and play significant roles. As expected, adding selenites to the electrolyte of Ni(OH)(2)dramatically enhance its OER activity. And sulfates also exhibit the similar effect, suggesting the promotion of surface-adsorbed chalcogenates on OER is universal. Our findings offer unique insight into the transformation mechanism of materials during electrolysis.
引用
收藏
页码:22470 / 22474
页数:5
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