Two-Dimensional Hierarchical CoTe/NiFe Layered Double Hydroxide Heterostructure for High-Performance Electrocatalytic Water Oxidation

被引:3
作者
Park, Keemin [2 ]
Choi, Seunggun [2 ]
Kwon, Jiseok [2 ]
Kim, Jaeik [2 ]
Jo, Seonghan [2 ]
Lee, Kangchun [2 ]
Park, Ho Bum [2 ]
Han, HyukSu [1 ]
Paik, Ungyu [2 ]
Song, Taeseup [2 ]
机构
[1] Konkuk Univ, Dept Energy Engn, Seoul 05029, South Korea
[2] Hanyang Univ, Dept Energy Engn, Seoul 04763, South Korea
来源
ACS APPLIED ENERGY MATERIALS | 2023年 / 6卷 / 06期
基金
新加坡国家研究基金会;
关键词
oxygen evolution reaction; heterostructure; electrocatalyst; metal-metalloid; layered double hydroxide; CATALYTIC-ACTIVITY; OXYGEN VACANCIES; CARBON CLOTH; TELLURIDE; NANORODS; ENERGY; CO3O4;
D O I
10.1021/acsaem.2c04146
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
The development of high-performance electrocatalysts with low cost is essential for electrocatalytic water oxidation. Here, we report a strategy for boosting oxygen evolution reaction (OER) catalytic activity of the NiFe layered double hydroxide (LDH) by implementing metal-metalloid compounds of CoTe nanosheets (NSs). The hybridized material (CoTe NS/NiFe LDH) shows an intriguing hierarchical 2D-2D heterostructure, where the intact interface between the CoTe NS and NiFe LDH is formed. Self-supported growth of the CoTe NS on the NiFe LDH improves charge transfer and reaction kinetics during the OER due to the enhanced metal-oxygen covalency caused by shifting metal d-orbitals and oxygen p-orbitals from the Fermi level. Moreover, the hierarchical heterostructure of the nanometer-scale CoTe NS on the micrometer-scale NiFe LDH could maximize the number of active sites for the OER. Therefore, CoTe NS/NiFe LDH exhibits low overpotentials of 235 and 252 mV at 30 and 80 mA cm-2 in an alkaline condition (1 M aqueous KOH solution), respectively, with excellent stability over 120 h, outperforming the benchmark RuO2 catalyst.
引用
收藏
页码:3432 / 3441
页数:10
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