Harnessing Vis–NIR broad spectrum for photocatalytic CO2 reduction over carbon quantum dots-decorated ultrathin Bi2WO6 nanosheets

被引:4
|
作者
Xin Ying Kong
Wen Liang Tan
Boon-Junn Ng
Siang-Piao Chai
Abdul Rahman Mohamed
机构
[1] Monash University,Multidisciplinary Platform of Advanced Engineering, Chemical Engineering Discipline, School of Engineering
[2] Jalan Lagoon Selatan,Low Carbon Economy (LCE) Group, School of Chemical Engineering, Engineering Campus
[3] Universiti Sains Malaysia,undefined
[4] Seri Ampangan,undefined
来源
Nano Research | 2017年 / 10卷
关键词
photocatalysis; CO; reduction; near-infrared (NIR) light; carbon quantum dots; bismuth tungstate; ultrathin nanosheets;
D O I
暂无
中图分类号
学科分类号
摘要
The photocatalytic reduction of CO2 to energy-rich hydrocarbon fuels is a promising and sustainable method of addressing global warming and the imminent energy crisis concomitantly. However, a vast majority of the existing photocatalysts are only capable of harnessing ultraviolet (UV) or/and visible light (Vis), whereas the near-infrared (NIR) region still remains unexplored. In this study, carbon quantum dots (CQDs)-decorated ultrathin Bi2WO6 nanosheets (UBW) were demonstrated to be an efficient photocatalyst for CO2 photoreduction over the Vis–NIR broad spectrum. It is noteworthy that the synthesis procedure of the CQDs/UBW hybrid nanocomposites was highly facile, involving a one-pot hexadecyltrimethylammonium bromide (CTAB)-assisted hydrothermal process. Under visible light irradiation, the optimized 1CQDs/UBW (1 wt.% CQD content) exhibited a remarkable 9.5-fold and 3.1-fold enhancement of CH4 production over pristine Bi2WO6 nanoplatelets (PBW) and bare UBW, respectively. More importantly, the photocatalytic responsiveness of CQDs/UBW was successfully extended to the NIR region, which was achieved without involving any rare earth or noble metals. The realization of NIR-driven CO2 reduction could be attributed to the synergistic effects of (i) the ultrathin nanostructures and highly exposed {001} active facets of UBW, (ii) the excellent spectral coupling of UBW and CQDs, where UBW could be excited by the up-converted photoluminescence of CQDs, and (iii) the electron-withdrawing nature of the CQDs to trap the photogenerated electrons and retard the recombination of charge carriers.
引用
收藏
页码:1720 / 1731
页数:11
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