TY - JOUR
T1 - Sea urchin-like CoTe-CoP heterostructure catalyst for efficient hydrogen evolution in all-pH range
AU - Zhu, Shaoke
AU - Xing, Minghui
AU - Lu, Zhankuan
AU - Qiao, Zelong
AU - Wang, Shitao
AU - Zhao, Qinglan
AU - Shao, Minhua
AU - Yun, Jimmy
AU - Cao, Dapeng
N1 - Publisher Copyright:
© Science China Press 2024.
PY - 2024/6
Y1 - 2024/6
N2 - The development of robust and pH-adaptable hydrogen evolution reaction (HER) catalysts is of great significance to achieve a mass-scale hydrogen production. The interface engineering is one of the most effective strategies due to its unique properties. Herein, the sea urchin-like heterostructure catalyst CoTe-CoP/NF is constructed successfully. The synergy of CoTe and CoP not only optimizes the electronic structure and exposes more active sites, but also effectively improves the hydrophilicity and aerophobicity of the catalyst. Meanwhile, density functional theory calculations further unveil that the interaction between CoTe and CoP efficiently reduces the dissociation energy barrier of water, and simultaneously enhances H* adsorption. All these results endow CoTe-CoP/NF excellent HER performance and catalytic stability at full pH range. The CoTe-CoP/NF electrode only needs 51, 53, and 75 mV overpotentials at 10 mA cm−2 for HER in acidic, alkaline, and neutral media, respectively. In short, this work provides an interface engineering strategy to construct high-performance HER catalysts in all-pH range. (Figure presented.)
AB - The development of robust and pH-adaptable hydrogen evolution reaction (HER) catalysts is of great significance to achieve a mass-scale hydrogen production. The interface engineering is one of the most effective strategies due to its unique properties. Herein, the sea urchin-like heterostructure catalyst CoTe-CoP/NF is constructed successfully. The synergy of CoTe and CoP not only optimizes the electronic structure and exposes more active sites, but also effectively improves the hydrophilicity and aerophobicity of the catalyst. Meanwhile, density functional theory calculations further unveil that the interaction between CoTe and CoP efficiently reduces the dissociation energy barrier of water, and simultaneously enhances H* adsorption. All these results endow CoTe-CoP/NF excellent HER performance and catalytic stability at full pH range. The CoTe-CoP/NF electrode only needs 51, 53, and 75 mV overpotentials at 10 mA cm−2 for HER in acidic, alkaline, and neutral media, respectively. In short, this work provides an interface engineering strategy to construct high-performance HER catalysts in all-pH range. (Figure presented.)
KW - all-pH range
KW - heterostructure
KW - hydrogen evolution reactions
KW - interface engineering
KW - synergy effect
UR - https://www.webofscience.com/wos/woscc/full-record/WOS:001220863900001
UR - https://openalex.org/W4396834143
UR - https://www.scopus.com/pages/publications/85192849207
U2 - 10.1007/s40843-024-2820-0
DO - 10.1007/s40843-024-2820-0
M3 - Journal Article
SN - 2095-8226
VL - 67
SP - 1891
EP - 1899
JO - Science China Materials
JF - Science China Materials
IS - 6
ER -