Hot electron assisted photoelectrochemical water splitting from Au-decorated ZnO@TiO2 nanorods array

被引:25
作者
Li, Hongdong [1 ,2 ,3 ]
Liu, Hongyan [4 ]
Wang, Fei [1 ]
Li, Guodong [1 ,2 ]
Wang, Xiaoli [1 ,2 ]
Tang, Zhiyong [1 ,2 ]
机构
[1] Natl Ctr Nanosci & Technol, CAS Ctr Excellence Nanosci, CAS Key Lab Nanosyst & Hierarch Fabricat, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Ctr Mat Sci & Optoelect Engn, Beijing 100049, Peoples R China
[3] Qingdao Univ Sci & Technol, Coll Chem & Mol Engn, Key Lab Ecochem Engn, Qingdao 266042, Peoples R China
[4] Beijing Inst Aeronaut Mat, Beijing 100095, Peoples R China
基金
中国国家自然科学基金;
关键词
surface plasmon resonance; energy transfer; transient absorption; hot electron; water splitting; CORE-SHELL NANOWIRES; EFFICIENT; TIO2; GOLD; NANOPARTICLES; DYNAMICS;
D O I
10.1007/s12274-022-4203-z
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
Engineering of semiconductor nanomaterials is critical to enhance the photoelectrochemical (PEC) performance for water splitting. However, semiconductors often show the low light absorption, slow charge transfer, and easy recombination of carriers, thus leading to the low catalytic efficiency. In this work, we show facile synthesis of ZnO@TiO2 core-shell nanorods (NRs) arrays modified with Au nanoparticles (NPs) as the photoelectrode for PEC water splitting. Impressively, the obtained ZnO@TiO2 (15 nm)/Au(8 nm) array shows the maximum photocurrent density of 3.14 mA/cm(2) at 1.2 V vs. reversible hydrogen electrode (RHE), 2.6 times and 1.7 times higher than those obtained from ZnO NRs and ZnO@TiO2 (15 nm) arrays. The electric-field simulation and transient absorption spectroscopy show that the Au-decorated core-shell nanostructures have an enhanced hot electron generation and prolonged decay time, indicating effective charge transfer and recombination inhibition of carriers. This work provides an efficient preparation strategy for photoelectrodes as well as great potential for the large-scale development of this technology.
引用
收藏
页码:5824 / 5830
页数:7
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