Promoting Surface Reconstruction of NiFe Layered Double Hydroxide for Enhanced Oxygen Evolution

被引:239
|
作者
Lei, Hang [1 ,2 ]
Ma, Liang [3 ]
Wan, Qixiang [1 ]
Tan, Shaozao [1 ]
Yang, Bo [2 ,4 ]
Wang, Zilong [3 ]
Mai, Wenjie [3 ]
Fan, Hong Jin [2 ]
机构
[1] Jinan Univ, Coll Chem & Mat Sci, Dept Chem, Guangdong Engn & Technol Res Ctr Graphene Mat & P, Guangzhou 510632, Peoples R China
[2] Nanyang Technol Univ, Sch Phys & Math Sci, Singapore 637371, Singapore
[3] Jinan Univ, Guangdong Prov Engn Technol Res Ctr Vacuum Coatin, Siyuan Lab, Dept Phys, Guangzhou 510632, Peoples R China
[4] Jilin Univ, Coll Phys, Key Lab Phys & Technol Adv Batteries, Minist Educ, Changchun 130012, Peoples R China
基金
中国国家自然科学基金;
关键词
layered double hydroxides; operando Raman; oxygen evolution reaction; surface reconstruction; water splitting; METAL-ORGANIC FRAMEWORKS; ELECTROCATALYSTS; EFFICIENT; COORDINATION; PERFORMANCE; ARRAYS; SITES; PLANE;
D O I
10.1002/aenm.202202522
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A dynamic surface reconstruction of oxide electrocatalysts in alkaline media is widely observed especially for layered double hydroxide (LDH), but little is known about how to promote the reconstruction toward desired surfaces for improved oxygen evolution reaction (OER). Here, surface reconstruction of NiFe LDH nanosheets is successfully induced to a higher degree via in situ sulfur doping than that by natural electrochemical activation. Theoretical calculations, operando Raman, and various ex situ characterizations reveal the S anion-induced effect can lower the energy barrier and facilitate the phase transformation into highly active S-doped oxyhydroxides. The generated S-NixFeyOOH can optimize the intermediate adsorption and facilitate the OER kinetics. The reconstructed S-oxyhydroxides catalyst presents superior OER activity and long-term durability compared to undoped ones. This work provides a structure-composition-activity relationship during the in situ surface restructuring of NiFe LDH pre-catalysts.
引用
收藏
页数:9
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