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

Authors
Park, KeeminChoi, SeunggunKwon, JiseokKim, JaeikJo, SeonghanLee, KangchunPark, Ho BumHan, HyukSuPaik, UngyuSong, Taeseup
Issue Date
Mar-2023
Publisher
American Chemical Society
Keywords
oxygen evolution reaction; heterostructure; electrocatalyst; metal-metalloid; layered double hydroxide
Citation
ACS Applied Energy Materials, v.6, no.6, pp.3432 - 3441
Indexed
SCIE
SCOPUS
Journal Title
ACS Applied Energy Materials
Volume
6
Number
6
Start Page
3432
End Page
3441
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/191593
DOI
10.1021/acsaem.2c04146
ISSN
2574-0962
Abstract
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.
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