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Carbon nanotube exfoliated porous reduced graphene oxide/CdS- diethylenetriamine heterojunction for efficient photocatalytic H_2 production

机译:碳纳米管剥落的多孔还原氧化石墨烯/ CdS-二亚乙基三胺异质结,用于高效光催化生产H_2

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Cadmium sulfide (CdS), as a promising candidate for photocatalytic hydrogen evolution (PHE), has been widely studied in recent years. However, the PHE performance of CdS is largely limited by the severe photocorrosion and low quantum efficiency. Herein, we reported multi-walled carbon nanotubes (MWCNTs) exfoliated porous reduced graphene oxide (PRGO)-supported inorganic-organic CdS-diethylenetriamine (DETA) hybrid, and the system is designed and prepared to adjust electronic structure and control photocorrosion property. Irradiated by visible light (lambda > 400 nm), this novel PRGO/CdS-DETA system exhibits advanced PHE performance of 10.5 mmol g(-1) h(-1) and apparent quantum efficiency is 29.5% with enhanced photostability. This result is 13.1, 3.9, 1.5 and 1.3 times higher than CdS nanoparticles, CdS-DETA hybrids, MWCNT/CdS-DETA and RGO/CdS-DETA composites. More importantly, the special connection between PRGO and CdS-DETA facilitates the charge carriers separation and large BET specific surface area (S-BET) boost the PHE of CdS-DETA. Density functional theory (DFT) calculation further confirms the high mobility for charge transport route from CdS-DETA to PRGO. The PRGO/CdS-DETA system photocatalyst with high PHE performance may provide a new insight into photocatalytic material design.
机译:近年来,硫化镉(CdS)作为光催化氢释放(PHE)的有希望的候选者,已经得到了广泛的研究。但是,CdS的PHE性能在很大程度上受到严重的光腐蚀和低量子效率的限制。在本文中,我们报道了多壁碳纳米管(MWCNTs)剥落的多孔还原氧化石墨烯(PRGO)负载的无机-有机CdS-二亚乙基三胺(DETA)杂化物,并设计并制备了该系统以调节电子结构和控制光腐蚀性能。这种新型PRGO / CdS-DETA系统受到可见光(λ> 400 nm)照射,具有10.5 mmol g(-1)h(-1)的先进PHE性能,表观量子效率为29.5%,并具有增强的光稳定性。该结果比CdS纳米颗粒,CdS-DETA杂化材料,MWCNT / CdS-DETA和RGO / CdS-DETA复合材料高13.1倍,3.9倍,1.5倍和1.3倍。更重要的是,PRGO和CdS-DETA之间的特殊连接促进了电荷载流子的分离,大的BET比表面积(S-BET)增强了CdS-DETA的PHE。密度泛函理论(DFT)的计算进一步证实了从CdS-DETA到PRGO的电荷传输路径的高迁移率。具有高PHE性能的PRGO / CdS-DETA系统光催化剂可能为光催化材料设计提供新的见解。

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