ZnO@NiO core-shell heterojunction photoanode modified with NiOOH co-catalyst for high-performance self-powered photoelectrochemical-type UV photodetector

被引:2
|
作者
Tan, Guiying [1 ]
Tang, Qixin [1 ]
Zhang, Hong [1 ]
Li, Honglin [1 ]
Pang, Di [1 ]
Tang, Yan [1 ]
Ye, Lijuan [1 ]
Fang, Liang [2 ]
Kong, Chunyang [1 ]
Li, Wanjun [1 ]
机构
[1] Chongqing Normal Univ, Coll Phys & Elect Engn, Chongqing 401331, Peoples R China
[2] Chongqing Univ, Coll Phys, Chongqing 401331, Peoples R China
关键词
ZnO@NiO core-shell nanowires; Reconstruction; Self-power; Photoelectrochemical photodetectors;
D O I
10.1016/j.apsusc.2024.161579
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
ZnO, a promising photoanode material, faces significant challenges in achieving high-efficient photoelectrochemical (PEC) type UV photodetectors due to inadequate charge separation and sluggish surface reaction kinetics. Constructing heterojunction nanostructures by coupling of p-NiO to n-ZnO nanowire arrays with wellaligned energy band positions presents a feasible strategy for enhancing PEC-type photodetector performance. Herein, we demonstrate that the designed ZnO@NiO core-shell nanowire arrays form a spatial charge transfer channel, facilitating efficient generation and extraction of charge carriers. The exceptional catalytic properties of NiOOH, derived from the transformation of NiO in an aqueous alkaline environment, serve as a potent cocatalyst, effectively accelerating the kinetics of the surface oxygen evolution reaction. Benefiting from the synergistic effect of the heterojunction and cocatalyst, the optimized photoanode achieves a high responsivity of 438.36 mA/W, a large detectivity of 4.85 x 1012 Jones, and rapid response time of 150.05/150.26 ms, while simultaneously exhibiting long-time PEC stability. This work highlights the critical role of nanostructure design in developing high-performance self-powered UV photodetectors.
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页数:10
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