Deactivation-Tolerance of Heterojunction Anatase and Bronze TiO2 in the Photocatalytic Mineralization of Toluene

被引:2
作者
Kim, Dong Jin [1 ]
Park, Jiyeon [1 ]
Ham, Gayoung [2 ]
Cha, Hyojung [2 ,3 ]
Han, Dong Suk [4 ]
Kim, Minho [5 ]
Park, Hyunwoong [1 ]
机构
[1] Kyungpook Natl Univ, Sch Energy Engn, Daegu 41566, South Korea
[2] Kyungpook Natl Univ, Dept Energy Convergence & Climate Change, Daegu 41566, South Korea
[3] Kyungpook Natl Univ, Dept Hydrogen & Renewable Energy, Daegu 41566, South Korea
[4] Qatar Univ, Ctr Adv Mat, Doha 2713, Qatar
[5] Kyung Hee Univ, Dept Appl Chem, Yongin 17104, Gyeonggi, South Korea
来源
ACS ES&T ENGINEERING | 2024年 / 4卷 / 10期
基金
新加坡国家研究基金会;
关键词
heterojunction; bronze; toluene; mineralization; oxygen vacancy; MOLECULAR-DYNAMICS; DEGRADATION; SURFACE; OXIDATION; MECHANISM; HYDROGEN; NANOPARTICLES; SPECTROSCOPY; NANOFIBERS; ELECTRONS;
D O I
10.1021/acsestengg.4c00281
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Heterojunctioning anatase (A) and rutile (R) TiO2 is considered a benchmark strategy for high photocatalytic activity. In this study, we synthesized heterojunctions of anatase (A) and bronze (B) TiO2 via hydrothermal and annealing processes using low-cost commercial A-TiO2. The as-synthesized AB-TiO2 shows remarkable activity for toluene mineralization and a strong tolerance to deactivation. The activity and durability of AB-TiO2 far exceed those of A-, R-, B-, and AR-TiO2, which are bare and even Pt-deposited (a total of 10 TiO2 samples). AB-TiO2 exhibits highly active {001} facets for the generation of hydroxyl radicals and oxygen vacancies beneficial for O-2 adsorption. Transient absorption and time-resolved photoluminescence spectroscopies reveal the characteristic lifetimes of electrons and holes. Density functional theory calculations demonstrate facile charge separation and identify the catalytically active surface for oxidation as the anatase surface in AB-TiO2. The observed high activity and durability are analyzed in terms of photochemical and catalytic factors.
引用
收藏
页码:2474 / 2484
页数:11
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