石墨烯
乙二胺
光催化
材料科学
硫化镉
胺气处理
氧化物
无机化学
光电流
吸附
光化学
可见光谱
表面改性
化学工程
化学
催化作用
纳米技术
有机化学
物理化学
冶金
工程类
光电子学
作者
Kyeong Min Cho,Kyung Hwan Kim,Kangho Park,Chansol Kim,Sungtak Kim,Ahmed AlSaggaf,Issam Gereige,Hee‐Tae Jung
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2017-09-06
卷期号:7 (10): 7064-7069
被引量:230
标识
DOI:10.1021/acscatal.7b01908
摘要
This study provides a significant enhancement in CO2 photoconversion efficiency by the functionalization of a reduced graphene oxide/cadmium sulfide composite (rGO/CdS) with amine. The amine-functionalized graphene/CdS composite (AG/CdS) was obtained in two steps. First, graphene oxide (GO) was selectively deposited via electrostatic interaction with CdS nanoparticles modified with 3-aminopropyltriethoxysilane. Subsequently, ethylenediamine (NH2C2H4NH2) was grafted by an N,N′-dicyclohexylcarbodiimide coupling reaction between the amine group of ethylenediamine and the carboxylic group of GO. As a result, a few layers of amine-functionalized graphene wrapped CdS uniformly, forming a large interfacial area. Under visible light, the photocurrent through the AG/CdS significantly increased because of enhanced charge separation in CdS. The CO2 adsorption capacity on AG/CdS was 4 times greater than that on rGO/CdS at 1 bar. These effects resulted in a methane formation rate of 2.84 μmol/(g h) under visible light and CO2 at 1 bar, corresponding to 3.5 times that observed for rGO/CdS. Interestingly, a high methane formation rate (1.62 μmol/(g h)) was observed for AG/CdS under CO2 at low pressure (0.1 bar), corresponding to a value 20 times greater than that observed for the rGO/CdS. Thus, the enhanced performance for photocatalytic reduction of CO2 on the AG/CdS is due to the improved CO2 adsorption related to the amine groups on amine-functionalized graphene, which sustains the strong absorption of visible light and superior charge-transfer properties in comparison with those of graphene.
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