Rapid cationic defect and anion dual-regulated layered double hydroxides for efficient water oxidation

被引:84
作者
Huang, Liangliang [1 ]
Chen, Ru [1 ]
Xie, Chao [1 ]
Chen, Chen [1 ]
Wang, Yanyong [1 ]
Zeng, Yifan [1 ]
Chen, Dawei [1 ,2 ]
Wang, Shuangyin [1 ,3 ,4 ]
机构
[1] Hunan Univ, Coll Chem & Chem Engn, Prov HunanKey Lab Graphene Mat & Devices, State Key Lab Chem Biosensing & Chemometr, Changsha 410082, Hunan, Peoples R China
[2] Qingdao Univ Sci & Technol, Coll Mat Sci & Engn, 53 Zhengzhou Rd, Qingdao 266042, Shandong, Peoples R China
[3] Shenzhen Univ, Minist Educ & Guangdong Prov, Key Lab Optoelect Devices & Syst, Shenzhen 518060, Peoples R China
[4] Hunan Univ, Shenzhen Res Inst, Shenzhen 518057, Peoples R China
基金
中国国家自然科学基金;
关键词
OXYGEN EVOLUTION REACTION; HIGHLY EFFICIENT; METAL-COMPOUNDS; ELECTROCATALYSTS; NANOSHEETS; RICH; PHOSPHORUS; MODULATION; VACANCIES;
D O I
10.1039/c8nr04402c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Defect engineering and anionic regulation are effective approaches to improve the intrinsic activity of oxygen evolution reaction (OER) catalysts, particularly for highly efficient and low-cost cobalt-based electrocatalysts. Layered double hydroxides (LDHs) are considered as promising electrocatalysts toward OER. However, their electronic properties and active sites need to be optimized for their large-scale application. Herein, rapidly cationic defect and anion dual-regulated CoAl LDHs (PS-CoAl LDHs) were in situ synthesized in a few minutes via a modified water DBD plasma treatment. Abundant Al3+ vacancies and a relatively rough surface for S2- regulation were formed by the etching effect of the plasma. Consequently, the as-obtained PS-LDHs possess improved intrinsic conductivity and an optimal electronic structure. Simultaneously, the synergistic effect of the Al3+ vacancies and S2- regulation promote the exposure of active Co sites, resulting in an amorphous and porous surface for improving the OER performance.
引用
收藏
页码:13638 / 13644
页数:7
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