回流
非金属
等离子体子
催化作用
异戊二烯
材料科学
化学
光化学
光电子学
有机化学
金属
工程类
复合材料
机械工程
共聚物
入口
聚合物
作者
Peiyu Hu,Jianjun Zhang,Guijie Liang,Jiaguo Yu,Feiyan Xu
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2024-09-27
卷期号:14 (20): 15025-15035
被引量:33
标识
DOI:10.1021/acscatal.4c04644
摘要
Constructing traditional heterojunctions involving noble metal cocatalysts is a well-established strategy for boosting photocatalytic efficiency by separating electron/hole pairs and improving light absorption through localized surface plasmon resonance (LSPR) effects. However, the high cost and limited availability of noble metals constrain their application, while the impact of plasmon effects on charge carrier dynamics and lifetimes, crucial for regulating photocatalytic performance, has been overlooked. Here, we propose integrating graphitic carbon dots (CDs) as proficient nonmetal cocatalysts into SnO 2 nanofibers to facilitate high-efficiency photoreactions. Under light irradiation, photoelectrons within the SnO 2 migrate to the CDs driven by the bent bands and the internal electric field, alongside inherent free electrons, stimulating into high-energy excited electrons due to LSPR effects. These energized electrons subsequently backflow to the SnO 2 for stabilization, initiating a cyclic process that effectively prolongs carrier lifetimes within the SnO 2 /CDs nanohybrids, as confirmed by femtosecond transient absorption spectroscopy. Synergizing with enhanced optical absorption and CO 2 chemisorption facilitated by the CDs, the resulting SnO 2 /CDs nanofibers demonstrate improved CO 2 photoreduction performance.
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