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溴氧化铋向钨酸铋的拓扑化学转变:用于增强光催化 CO 还原的单晶{001}面纳米片的带隙调制

Topotactic Transformation of Bismuth Oxybromide into Bismuth Tungstate: Bandgap Modulation of Single-Crystalline {001}-Faceted Nanosheets for Enhanced Photocatalytic CO Reduction.

作者信息

Kong Xin Ying, Tong Tong, Ng Boon-Junn, Low Jingxiang, Zeng Tingying Helen, Mohamed Abdul Rahman, Yu Jiaguo, Chai Siang-Piao

机构信息

Multidisciplinary Platform of Advanced Engineering, Chemical Engineering Discipline, School of Engineering, Monash University, Jalan Lagoon Selatan, Bandar Sunway, 47500 Selangor, Malaysia.

State Key Laboratory of Advanced Technology for Material Synthesis and Processing, Wuhan University of Technology, Luoshi Road 122, Wuhan 430070, P. R. China.

出版信息

ACS Appl Mater Interfaces. 2020 Jun 17;12(24):26991-27000. doi: 10.1021/acsami.9b15950. Epub 2020 Jun 5.

Abstract

The photocatalytic conversion of CO to energy-rich CH solar fuel is an ideal strategy for future energy generation as it can resolve global warming and the imminent energy crisis concurrently. However, the efficiency of this technology is unavoidably hampered by the ineffective generation and utilization of photoinduced charge carriers. In this contribution, we report a facile topotactic transformation approach where {001}-faceted BiOBr nanosheets (BOB-NS) were employed as the starting material for the formation of single-crystalline ultrathin BiWO nanosheets (BWO-NS). The as-obtained BWO-NS not only preserved the advantageous properties of the 2D nanostructure and predominantly exposed {001} facets but also possessed enlarged specific surface areas as a result of sample thickness reduction. As opposed to the commonly observed bandgap broadening when the particle sizes decrease to an ultrathin nanoscale owing to the quantum size effect, the developed BWO-NS exhibited a fascinating bandgap narrowing compared to those of pristine BiWO nanoplates (BWO-P) synthesized from a conventional one-step hydrothermal approach. Moreover, the electronic band positions of BWO-NS were modulated as a result of ion exchange for the reconstruction of the energy bands, where BWO-NS demonstrated significant upshifting of CB and VB levels; these are beneficial for photocatalytic reduction applications. This propitious design of BWO-NS through integrating the merits of BOB-NS caused BWO-NS to exhibit substantial 2.6 and 9.3-fold enhancements of CH production over BOB-NS and BWO-P, respectively.

摘要

将一氧化碳光催化转化为富含能量的甲烷太阳能燃料是未来能源生产的理想策略,因为它可以同时解决全球变暖和迫在眉睫的能源危机。然而,这项技术的效率不可避免地受到光生电荷载流子产生和利用效率低下的阻碍。在本论文中,我们报道了一种简便的拓扑转变方法,其中以{001}面的溴氧化铋纳米片(BOB-NS)作为起始材料来制备单晶超薄钨酸铋纳米片(BWO-NS)。所制备的BWO-NS不仅保留了二维纳米结构的优势特性且主要暴露{001}面,而且由于样品厚度减小而具有更大的比表面积。与由于量子尺寸效应导致粒径减小到超薄纳米尺度时通常观察到的带隙变宽相反,与通过传统一步水热法合成的原始钨酸铋纳米板(BWO-P)相比,所制备的BWO-NS表现出令人着迷的带隙变窄。此外,通过离子交换重建能带,BWO-NS的电子能带位置得到调制,其中BWO-NS的导带(CB)和价带(VB)水平显著上移;这些有利于光催化还原应用。通过整合BOB-NS的优点对BWO-NS进行的这种有利设计,使得BWO-NS的甲烷产量分别比BOB-NS和BWO-P提高了2.6倍和9.3倍。

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