Efficient photocatalytic reduction of CO2 by a rhenium-doped TiO2-x/SnO2 inverse opal S-scheme heterostructure assisted by the slow-phonon effect

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作者
Ye, Jin [1 ]
Xu, Jiating [1 ]
Tian, Di [2 ]
Zhao, Xiaohan [3 ]
Wang, Qiang [1 ]
Wang, Jun [1 ]
Li, Yudong [4 ]
Zhao, Chunjian [1 ]
Liu, Zhiguo [1 ]
Fu, Yujie [1 ]
机构
[1] Key Laboratory of Forest Plant Ecology, Ministry of Education, College of Chemistry, Chemical Engineering and Resource Utilization, Northeast Forestry University, Harbin,150040, China
[2] Key Laboratory of Jiangxi Province for Persistent Pollutants Control and Resources Recycle, Nanchang Hangkong University, Nanchang,Jiangxi,330063, China
[3] Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology, School of Petrochemical Engineering, Changzhou University, Changzhou,213164, China
[4] Key Laboratory of Bio-Based Material Science and Technology of Ministry of Education, Northeast Forestry University, Harbin,150040, China
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摘要
Light harvesting and carrier separation play significant roles in determining the efficiency of photocatalytic reduction reactions. In this work, rhenium was doped into inverse opal TiO2-x/SnO2 to construct heterojunction catalysts in which Ti3+ is combined with oxygen vacancies (OVs). The slow-photon-effect of the inverse opal (IO) structure and the oxygen deficiency enable the catalysts to have high light-harvesting efficiency. SnO2 was selected to construct the heterojunction, and its excellent electron migration rate was highly beneficial for boosting the separation efficacy of the photogenerated carriers. As a result, the yield of CO in photocatalytic reduction of CO2 using the final obtained catalyst was 16.59 μmol·g−1·h−1, which is approximately 1.21, 2.14 and 7.44 times of the yields obtained using IO-TiO2-x/SnO2, IO-TiO2-x and SnO2, respectively. This strategy, which integrates the slow-photon-effect, oxygen vacancies, and element doping, affords a new avenue for preparing highly active heterojunction photocatalysts and improving photocatalytic performance. © 2021 Elsevier B.V.
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