Sequential doping strategy in rutile TiO2 nanorod for high performance photoanode

被引:1
|
作者
Lee, Sang Yeon [1 ,2 ,7 ,8 ]
Lee, Young Jae [1 ,2 ]
Yoo, Il-Han [1 ,2 ]
Kim, Hyeon Woo [3 ,4 ]
Song, Hyejeong [3 ]
Heo, Soo Won [5 ]
Kalanur, Shankara S. [6 ]
Mohapatra, Gourab [1 ,2 ]
Rohma
Ko, Hyunseok [3 ]
Seo, Hyungtak [1 ,2 ]
机构
[1] Ajou Univ, Dept Energy Syst Res, Suwon 16499, South Korea
[2] Ajou Univ, Dept Mat Sci & Engn, Suwon 16499, South Korea
[3] Korea Inst Ceram Engn & Technol KICET, Div Carbon Neutral & Digitalizat, Jinju 52851, South Korea
[4] Hanyang Univ, Divison Mat Sci & Engn, Seoul 04763, South Korea
[5] Korea Inst Ceram Engn & Technol KICET, Nano Convergence Mat Ctr, Jinju 52851, South Korea
[6] Univ Quebec Trois Rivieres, Hydrogen Res Inst, Trois Rivieres, PQ G9A 5H7, Canada
[7] Katholieke Univ Leuven, Sensors & Actuators Team SAT, IMEC, B-3001 Leuven, Belgium
[8] Katholieke Univ Leuven, Elect Engn ESAT, B-3001 Leuven, Belgium
基金
新加坡国家研究基金会;
关键词
Sequential doping; Plasma treatment; Fluorine; TiO2; Water splitting; Photoanode; HYDROGEN; LAYER; ARRAY;
D O I
10.1016/j.apsusc.2023.159213
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
Clean hydrogen production technologies are in high demand as an alternative to fossil fuels in order to achieve a carbon-neutral society. One promising approach is photoelectrochemical water splitting, which uses sunlight as an energy source to produce hydrogen. In this study, we propose a strategy for achieving highly efficient photoelectrochemical performance in TiO2 2 nanorods without the need for additional heterojunction or catalyst reactions. We introduce the plasma-assisted sequential doping process using H and F species to demonstrate highly efficient photoanode for water splitting. In the first stage, hydrogenated TiO2 2 generated oxygen vacancies and interstitial H in the TiO2 2 lattice structure, and in the second stage, fluorinated TiO2 2 exhibited a sequentially cured reaction of oxygen vacancy resulting in enhanced photoelectrochemical performance. Furthermore, theoretical simulations revealed that the sequential doping process induced a stabilized reaction in F compared to direct doping without H plasma doping. This sequential doping strategy can be applied to a wide range of materials and applications, not just to enhance photoelectrochemical devices.
引用
收藏
页数:8
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