Photothermal synergistic catalytic reactions: g-C3N4 assisted CeO2 for efficient selective aromatic alcohol oxidation

被引:6
|
作者
Wang, Ya [1 ]
Gui, Shu [1 ]
Chen, Gaoli [1 ]
Zhang, Sujuan [1 ]
Li, Jing [1 ]
Wang, Zhongliao [1 ]
Zheng, Xiuzhen [1 ]
Meng, Sugang [1 ]
Ruan, Chaohui [1 ]
Chen, Shifu [1 ]
机构
[1] Huaibei Normal Univ, Coll Chem & Mat Sci, Key Lab Green & Precise Synthet Chem & Applicat, Anhui Prov Key Lab Pollutant Sensit Mat & Environm, Huaibei 235000, Peoples R China
基金
中国国家自然科学基金;
关键词
Photothermal catalysis; Synergistic effect; Investigation of mechanism; Aromatic alcohol oxidation; ENHANCED PHOTOCATALYTIC ACTIVITY; VISIBLE-LIGHT; METAL-FREE; ORGANIC-COMPOUNDS; ULTRATHIN G-C3N4; MANGANESE OXIDES; LATTICE OXYGEN; QUANTUM DOTS; REDUCTION; WATER;
D O I
10.1016/j.apsusc.2023.158262
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
This paper investigates the enhanced effect of photothermal synergistic catalytic reactions and demonstrates this effect using CeO2 as an example. The experimental results demonstrate that CeO2 exhibits remarkable ability to efficiently harness both light and thermal energy for catalytic reactions, which can achieve the enhanced effect of photothermal synergistic catalytic reaction. The effect of photothermal co-catalysis is significantly greater than the simple algebraic sum of photocatalysis and thermal catalysis. Furthermore, by incorporating other materials such as g-C3N4, the photothermal catalytic performance of CeO2 can be further enhanced. Specifically, under visible light irradiation and a stable temperature of 363.15 K, the yield and selectivity of 50% CeO2/g-C3N4 (50% COCN) catalyst for the oxidation of benzyl alcohol to benzaldehyde reached 56.9% and 99%, respectively. Based on characterization and theoretical calculations, a possible mechanism of photothermal co-catalysis was pro-posed. This study provides a new idea for the implementation of photothermal synergistic catalytic reaction and provides a reference for the design and synthesis of related materials.
引用
收藏
页数:10
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