Visible-light photocatalytic activity of TiOxNy thin films obtained by reactive multi-pulse High Power Impulse Magnetron Sputtering

被引:22
作者
Demeter, Alexandra [1 ]
Samoila, Florentina [1 ]
Tiron, Vasile [1 ]
Stanescu, Dana [2 ]
Magnan, Helene [2 ]
Straticiuc, Mihai [3 ]
Burducea, Ion [3 ]
Sirghi, Lucel [1 ]
机构
[1] Alexandru Ioan Cuza Univ, IPARC, Fac Phys, Iasi 700506, Romania
[2] Univ Paris Saclay, CEA Saclay, CNRS, SPEC,CEA, F-91191 Gif Sur Yvette, France
[3] Horia Hulubei Natl Inst Phys & Nucl Engn, Magurele 077125, Romania
关键词
Titanium oxynitride; m-HiPIMS deposition; Visible-light photocatalyst; Water splitting; TIO2; PHOTOCATALYSIS; SURFACE; WATER;
D O I
10.1016/j.surfcoat.2016.10.011
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Reactive High Power Impulse Magnetron Sputtering operated in multi-pulse mode (m-HiPIMS) of a pure Ti target in Ar/N-2/O-2 gas mixture (mass flow rates of 50, 2 and 0.16 sccm, respectively) has been used for the deposition of titanium oxynitride (TiOxNy) thin films with variable content of nitrogen (from 0.6 at.% to 24.2 at.%). Increase of the nitrogen content in the deposited TiOxNy thin films determined a decrease of the optical bandgap energy and a corresponding increase of visible light adsorption. The photocatalytic activity for water molecule splitting of the films deposited on metallic substrate, which were used as the photo-anode in an electrochemical cell, has been investigated by measurements of photoelectrochemical current intensity versus biasing voltage during on/off cycles of visible light irradiation (sun light simulated by a xenon lamp). The as-deposited films have a short range order corresponding to rutile and anatase structures and showed very weak photocatalytic activity and chemical instability in the electrolyte of the photoelectrochemical cell. However, a post-deposition annealing treatment of the film with low content of nitrogen (0.6 at.%) improved considerably the visible-light photocatalytic activity, the film crystalline order and chemical stability. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:614 / 619
页数:6
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