光催化
材料科学
三乙醇胺
可见光谱
氮化碳
X射线光电子能谱
纳米颗粒
光电流
氮化硼
化学工程
光化学
催化作用
纳米技术
化学
光电子学
分析化学(期刊)
工程类
生物化学
色谱法
作者
Min Zhou,Sibo Wang,Pengju Yang,Caijin Huang,Xinchen Wang
标识
DOI:10.1021/acscatal.8b00104
摘要
Ternary boron carbon nitride (BCN) semiconductors have been developed as emerging metal-free photocatalysts for visible-light reduction of CO2, but the achieved efficiency is still not satisfying. Herein, we report that the CO2 photoreduction performance of a bulk BCN semiconductor can be substantially improved by surface engineering with CdS nanoparticles. The CdS/BCN photocatalysts are characterized completely by diverse tests (e.g., XRD, FTIR, XPS, DRS, SEM, TEM, N2 sorption, PL, and transient photocurrent spectroscopy). Performance of the CdS/BCN heterostructures is evaluated by reductive CO2 conversion reactions with visible light under benign reaction conditions. Compared with bare BCN material, the optimized CdS/BCN photocatalyst exhibits a 10-fold-enhanced CO2 reduction activity and high stability, delivering a considerable CO production rate of 12.5 μmol h–1 (250 μmol h–1 g–1) with triethanolamine (TEOA) as the reducing agent. The reinforced photocatalytic CO2 reduction activity is mainly assigned to the obviously improved visible-light harvesting and the greatly accelerated separation/transport kinetics of light-triggered electron–hole pairs. Furthermore, a possible visible-light-induced CO2 reduction mechanism is proposed on the basis of photocatalytic and photo(electro)chemical results.
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