Nitrogen doping on the core-shell structured Au@TiO2 nanoparticles and its enhanced photocatalytic hydrogen evolution under visible light irradiation

被引:34
作者
Naik, Gautam Kumar [1 ,2 ]
Majhi, Sanjit Manohar [1 ,2 ,6 ]
Jeong, Kwang-Un [3 ,4 ]
Lee, In-Hwan [5 ]
Yu, Yeon Tae [1 ,2 ]
机构
[1] Chonbuk Natl Univ, Div Adv Mat Engn, Coll Engn, Jeonju 54899, South Korea
[2] Chonbuk Natl Univ, Res Ctr Adv Mat Dev, Coll Engn, Jeonju 54899, South Korea
[3] Chonbuk Natl Univ, Polymer Mat Fus Res Ctr, Jeonju 54896, South Korea
[4] Chonbuk Natl Univ, Dept Polymer Nano Sci & Technol, Jeonju 54896, South Korea
[5] Korea Univ, Dept Mat Sci & Engn, Seoul 02841, South Korea
[6] King Abdullah Univ Sci & Technol, Comp Elect & Math Sci & Engn Div, Ctr Adv Membranes Porous Mat AMPM, Thuwal 239556900, Saudi Arabia
基金
新加坡国家研究基金会;
关键词
TiO2; Core-shell; Nitrogen doped; Hydrogen evolution; Water splitting; TITANIUM-DIOXIDE; WATER; TIO2; DEGRADATION; AU/TIO2; AU; FILMS; ACID;
D O I
10.1016/j.jallcom.2018.08.277
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 current study concerns about the large band gap of TiO2 for its use as photocatalysts. The photocatalytic activity of core-shell structured Au@TiO2 nanoparticles were enhanced by the doping of nitrogen. The nitrogen doping has been done by simple hydrothermal method taking ethylenediamine as the precursor for nitrogen. The crystals structure of TiO2 shell remained unaltered even with the introduction of nitrogen. The photocatalytic activity of the prepared samples were evaluated towards the hydrogen evolution from photocatalytic water splitting under solar light irradiation. It was found that nitrogen doped core-shell structured Au@TiO2 nanoparticles (Au@N-TiO2) showed higher photocatalytic activity with an average H-2 evolution rate of 4880 mu mol h(-1) g(-1), which is 3.79 times more than that of bare TiO2 in 4 h under xenon light irradiation. The relationship among the other samples was in order of Au@N-TiO2 > Au@TiO2 > N-TiO2 > TiO2. This enhanced photocatalytic activity of Au@N-TiO2 can be responsible for the formation of an plasmonic photocatalyst and the formation of an impurity band between the conduction band (CB) and the valence band (VB) of TiO2. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:505 / 512
页数:8
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