材料科学
兴奋剂
吸收(声学)
可见光谱
超快激光光谱学
碳纤维
X射线光电子能谱
光化学
光催化
纳米颗粒
载流子
光诱导电荷分离
光电子学
纳米技术
光谱学
化学工程
人工光合作用
有机化学
催化作用
复合数
工程类
复合材料
物理
化学
量子力学
作者
G. Murali,Jeevan Kumar Reddy Modigunta,Seongmin Park,Seongeun Lee,Hwi-Young Lee,Jiwon Yeon,Hye-Jin Kim,Young Ho Park,Sung Young Park,James R. Durrant,Hyojung Cha,Tae Kyu An,Insik In
标识
DOI:10.1021/acsami.1c01879
摘要
Limited light absorption beyond the UV region and rapid photocarrier recombination are critical impediments for the improved photocatalytic performance of carbon quantum dots (CQDs) under visible-light irradiation. Herein, we demonstrate single-step microwave-assisted syntheses of O-CQDs (typical CQDs terminated by carboxylic and hydroxyl functional groups) from a sucrose precursor and Cl-doped CQDs (Cl-CQDs) from a sucralose precursor in short reaction times and without using obligatory strong acids for Cl doping. The doping of Cl into the CQDs is observed to widen the absorption range and facilitate an enhanced separation of photoexcited charge carriers, which is confirmed by the results of optical absorption, photothermal response, and pump-probe ultrafast transient absorption spectroscopy measurements of the O-CQDs and Cl-CQDs. The photoexcited charge carriers with their longer lifetimes in Cl-CQDs enabled the quick degradation of methylene blue dye, rapid conversion of Ag+ ions to metallic Ag nanoparticles on the CQD surfaces, and reduction of GO to a well-dispersed rGO through the photoelectron transfer reactions under visible-light irradiation. The facile Cl doping strategy, hybridization of Ag nanoparticles or rGO to CQDs, and the elevated charge separation mechanism would open up new avenues in designing CQD-based materials for futuristic applications.
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