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Enhancing visible-light driven photocatalytic performance of BiOBr by self-doping and in-situ deposition strategy: A synergistic effect between Bi5+ and metallic Bi

机译:通过自掺杂和原位沉积策略提高BioBR的可见光光催化性能:BI5 +和金属BI之间的协同效应

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摘要

A novel composite photocatalyst of Bi/BiOBr-Bi5+ was successfully developed via a facile two-step procedure. The co-existence of self-doped Bi5+ and in-situ deposited Bi(M) was evidenced by X-ray diffraction, field emission transmission electron microscope and X-ray photoelectron spectra. Its photocatalytic performance on the Rhodamine B (RhB) degradation under visible light irradiation displayed a significant improvement compared with that of Bi/BiOBr or BiOBr-Bi5+, which was mainly attributed to the synergistic effect between Bi(M) and Bi5+. For Bi(M), enhancement of visible-light absorption capacity was beneficial from surface plasmon resonance (SPR) effect while the promoted separation of photoinduced charge carriers was attributed to the formation of oxygen vacancies (OVs) and Schottky-barrier. Besides, Bi(M) induced a predominant exposure of (010) facet, further enhancing photocatalytic performance. Differently, Bi5+ brought a narrowed bandgap of BiOBr in increasing the carrier density. A plausible mechanism towards RhB degradation was proposed based on analysis of electron transfer pathway and determination of dominant active species. The work offers new routes to enhance the photocatalytic performance of Bi-based materials without introducing any impurities.
机译:通过容易的两步程序成功开发了Bi / BioBR-Bi5 +的新型复合光催化剂。通过X射线衍射,场发射透射电子显微镜和X射线光电子电流和X射线光电子光谱,证明了自掺杂Bi5 +和原位沉积Bi(M)的共存。其在可见光照射下的罗丹明B(RHB)降解的光催化性能显示出与BI / BIOBR或BIOBR-BI5 +相比的显着改善,这主要归因于BI(M)和BI5 +之间的协同效应。对于Bi(M),可见光吸收能力的增强是有益的,而光抑制电荷载体的促进分离归因于氧空位(OVS)和肖特基屏障的形成。此外,Bi(M)诱导了(010)刻面的主要暴露,进一步增强了光催化性能。不同,Bi5 +在增加载体密度时带来了BioBR的狭窄带隙。提出了一种基于电子转移途径的分析和显性活性物质的测定,提出了一种卓越的RHB降解机制。该工作提供了新的路线,以增强BI基材料的光催化性能而不引入任何杂质。

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