Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/122050
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Type: Journal article
Title: Synthesis of nitrogen and sulfur co-doped reduced graphene oxide as efficient metal-free cocatalyst for the photo-activity enhancement of CdS
Author: Han, W.
Chen, L.
Song, W.
Wang, S.
Fan, X.
Li, Y.
Zhang, F.
Zhang, G.
Peng, W.
Citation: Applied Catalysis B: Environmental, 2018; 236:212-221
Publisher: Elsevier
Issue Date: 2018
ISSN: 0926-3373
1873-3883
Statement of
Responsibility: 
Weiwei Han, Lulu Chen, Weiyu Song, Shaobin Wang, Xiaobin Fan, Yang Li, Fengbao Zhang, Guoliang Zhang, Wenchao Peng
Abstract: Nitrogen and sulfur co-doped reduced graphene oxide (NS-rGO) was synthesized using a facile low temperature calcination method, which was then used as support and cocatalyst for the anchor of CdS. The obtained CdS/NS-rGO nanocomposites exhibit ultra-high photocatalytic activity for hydrogen evolution and 4-nitrophenol (4-NP) reduction under visible light (λ ≥ 420 nm). Their activity could also be adjusted by changing the doping amount of S and N, or by changing the ratios between CdS and NS-rGO. The optimum percentage of NS-rGO is 5 wt%, at which CdS/NS-rGO photocatalyst could achieve the highest H2 evolution rate of 1701 μmol h–1 g–1. Moreover, the reduction from 4-NP to 4-aminophenol (4-AP) could be completed within only 6 min over this optimized composite. NS-rGO here could provide more active sites as well as tune the band gap structure to increase the photo-activity. The density functional theory (DFT) calculations reveal that NS-rGO has a small Gibbs free energy for H* adsorption (ΔGH), which could increase the utilization efficency of photo-generated electrons for H2 generation. NS-rGO is therefore an idea alternate cocatalyst of noble metals for new photocatalysts development.
Keywords: Nitrogen and sulfur co-doped rGO; photocatalysis; hydrogen generation; 4-nitrophenol reduction; DFT calculations
Rights: © 2018 Elsevier B.V. All rights reserved.
DOI: 10.1016/j.apcatb.2018.05.021
Published version: http://dx.doi.org/10.1016/j.apcatb.2018.05.021
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