Plasmonic silver nanoparticles matched with vertically aligned nitrogen-doped titanium dioxide nanotube arrays for enhanced photoelectrochemical activity

被引:22
作者
Jiao, Jiqing [1 ,2 ]
Tang, Jianguo [1 ,2 ]
Gao, Wei [3 ]
Kuang, Daibin [4 ]
Tong, Yexiang [4 ]
Chen, Liuping [4 ]
机构
[1] Qingdao Univ, Inst Hybrid Mat, Natl Base Int S&T Cooperat Hybrid Mat, Qingdao 266071, Peoples R China
[2] Qingdao Univ, Growing Base State Key Lab, Qingdao 266071, Peoples R China
[3] Guangdong Pharmaceut Univ, Coll Pharm, Guangzhou 510006, Guangdong, Peoples R China
[4] Sun Yat Sen Univ, Sch Chem & Chem Engn, KLGHEI Environm & Energy Chem, Guangzhou 510275, Peoples R China
关键词
Plasmonic; Silver nanoparticles; Titanium dioxide; Nanotube arrays; Photoelectrochemistry; PHOTOCATALYTIC ACTIVITY; TIO2; STABILITY; DEGRADATION; IRRADIATION; EFFICIENCY; REDUCTION; COMPOSITE;
D O I
10.1016/j.jpowsour.2014.10.074
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 plasmonic Ag nanoparticles match with vertically aligned N-doped TiO2 nanotube arrays, which display improving photoelectrochemical performance. N-doped anatase nanotube arrays are fabricated firstly, and then cubic Ag nanoparticles of diameter 5 nm are deposited on TiO2 nanotubes without organic additives at room temperature. X-ray photoelectron spectroscopy shows that the oxygen vacancies and N impurity are revealed in N-doped TiO2. The electrical properties of samples are investigated by systematic photoelectrochemical measurement. The charge transfer ability of TiO2, N-doped TiO2 and Ag/N-doped TiO2 is presented directly by Electrochemical impedance spectroscopy and Mott-Schottky measurement, respectively. The carrier density of Ag/N-doped TiO2 is higher 2 orders of magnitude enhancement of TiO2. Furthermore, its photocurrent responds rapidly with illumination owing to fast photoelectron transport. And photocurrent density is 0.14 mA cm(-2) at 123 V-RHE, which is the highest among samples. Finally, the mechanism of improving photoelectrochemical cell. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:464 / 470
页数:7
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