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制备 In-S 共掺杂二维 BiOCl 耦合表面羟化以同时提高光催化水修复中的电荷分离和氧化还原能力。

Fabrication of In-S-co-doped two-dimensional BiOCl coupling with surface hydroxylation toward simultaneously efficient charge separation and redox capability for photocatalytic water remediation.

机构信息

Engineering Research Center of Conducting Materials and Composite Technology, Ministry of Education; Shaanxi Engineering Research Center of Metal-Based Heterogeneous Materials and Advanced Manufacturing Technology; Shaanxi Province Key Laboratory for Electrical Materials and Infiltration Technology; School of Materials Science and Engineering, Xi'an University of Technology, Xi'an, 710048, Shaanxi, People's Republic of China.

Engineering Research Center of Conducting Materials and Composite Technology, Ministry of Education; Shaanxi Engineering Research Center of Metal-Based Heterogeneous Materials and Advanced Manufacturing Technology; Shaanxi Province Key Laboratory for Electrical Materials and Infiltration Technology; School of Materials Science and Engineering, Xi'an University of Technology, Xi'an, 710048, Shaanxi, People's Republic of China.

出版信息

Chemosphere. 2023 Feb;315:137742. doi: 10.1016/j.chemosphere.2023.137742. Epub 2023 Jan 3.

Abstract

Tailoring energy band structure of bismuth oxychloride (BiOCl)-based photocatalysts by virtue of the metal and/or non-metal elements is one of the promising strategy to address environmental issues, especially plays a crucial role in water remediation. However, it still remains a great challenge to balance the light-harvesting and charge carriers separation. Herein, a feasible strategy was proposed for the simultaneous integration of energy-band modulation and surface hydroxylation to alleviate the as-mentioned contradiction and long-standing issues. By using a simple one-pot hydrothermal method, In-S-co-doped BiOCl photocatalyst coupling with surface hydroxylation (denoted as In/BOC-S-OH) was prepared by the simultaneous co-precipitation and ripening process and exhibited a good photocatalytic activity for removing tetracycline (TC) under visible light-irradiation than the counterparts of In-doped BiOCl (In/BOC), S-doped BiOCl (In/BOC-S) or surface -OH modification BiOCl (In/BOC-OH). Such satisfied photocatalytic efficiency benefits from the synergistic effect on the visible light capture, charge migration and separation associated with the introduction of intermediate energy levels and surface defect, respectively. Accompanying with the introduction of In and S hetero-atoms intercalation, both the potentials of valence and conduction bands were adjusted and the reduction of the bandgap could promote the capture of photons. Meanwhile, the powerful polarization effect associated with the non-uniform charge distribution could promote the special separation of carriers. More importantly, the surface defects induced by hydroxylation could act as traps for photogenerated electrons to stimulate the rapid separation of carriers, thereby causing the cleavage of antibiotics on the catalytic surface. This research offers a reliable strategy and promising scheme via effective solar energy conversion and charge carrier separation to advance photocatalytic wastewater remediation.

摘要

通过金属和/或非金属元素来调整 BiOCl 基光催化剂的能带结构是解决环境问题的一种很有前途的策略,在水修复方面尤其具有重要意义。然而,平衡光捕获和载流子分离仍然是一个巨大的挑战。在此,提出了一种可行的策略,同时进行能带调制和表面羟化,以缓解上述矛盾和长期存在的问题。通过使用简单的一步水热法,通过共沉淀和陈化过程同时将能带调节和表面羟化引入到 In-S 共掺杂 BiOCl 光催化剂中(表示为 In/BOC-S-OH),并在可见光照射下表现出良好的四环素(TC)去除光催化活性,优于单掺 In 的 BiOCl(In/BOC)、单掺 S 的 BiOCl(In/BOC-S)或表面 -OH 修饰的 BiOCl(In/BOC-OH)。这种令人满意的光催化效率得益于可见光捕获、电荷迁移和分离的协同效应,分别与引入中间能级和表面缺陷有关。伴随 In 和 S 杂原子插层的引入,价带和导带的电位都得到了调整,带隙的降低可以促进光子的捕获。同时,非均匀电荷分布引起的强极化效应可以促进载流子的特殊分离。更重要的是,羟化诱导的表面缺陷可以作为光生电子的陷阱,从而促进载流子的快速分离,从而导致在催化表面上抗生素的断裂。这项研究通过有效的太阳能转换和载流子分离,为推进光催化废水修复提供了一种可靠的策略和有前途的方案。

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