Spatial separation of photocarriers and selective adsorption on flower-like core-shell heterojunction of Cr(VI) imprinted polymer@BiOI for boosted photocatalytic Cr(VI) reduction

IF 5.5 3区 工程技术 Q1 ENGINEERING, CHEMICAL Journal of the Taiwan Institute of Chemical Engineers Pub Date : 2024-05-02 DOI:10.1016/j.jtice.2024.105525
Wei Guo , Wei Wei , Yue Tang , Rujing Shen , Xin Liu , Yihang Li , Ang Wei
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Abstract

Background

Constructing heterojunction photocatalyst is a well-established strategy for enhancing photocatalytic Cr(VI) reduction due to the heightened separation and transfer of photocarriers. Whereas, aimless and random transfer of photocarriers and low photocarrier utilization rate deriving from the weak interface interaction between heterojunction and Cr(VI) are still limited the photocatalytic reduction performance of Cr(VI).

Methods

Herein, a flower-like core-shell heterojunction photocatalyst was designed by wrapping a pyridine-based Cr(VI) imprinted polymer (PCIP) onto flower-like BiOI to achieve spatial separation of photocarriers and selective adsorption of Cr(VI), resulting in an outstanding photocatalytic reduction performance of Cr(VI).

Significant findings

In the core-shell heterojunction, photocarriers could be spatially separated, and then brought about high-efficient photocatalytic Cr(VI) reduction close to the selective adsorption sites of Cr(VI). After measurement, the optimal PCIP@BiOI core-shell heterojunction, polymerized for ≈30 min, exhibited a robust photocatalytic reduction performance of Cr(VI), without adding any free radical sacrifice agents. Within 1 h, the aqueous solution containing 100 mg/L of Cr(VI) could be completely removed, and the photocatalytic reduction rate constant of Cr(VI) was ≈20 times superior to BiOI. This study presents a methodology for designing core-shell heterojunction photocatalysts on the basis of inorganic/organic conjunction for environmental remediation of high concentrations of Cr(VI).

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光载体的空间分离以及六价铬印迹聚合物@BiOI花朵状核壳异质结上的选择性吸附促进光催化还原六价铬
背景由于光载体的分离和转移能力增强,构建异质结光催化剂是提高光催化还原六价铬性能的一种行之有效的策略。然而,由于异质结与六价铬之间的界面相互作用较弱,光载体的无目的随机转移和低光载体利用率仍然限制了六价铬的光催化还原性能。方法通过将吡啶基六价铬印迹聚合物(PCIP)包裹在花朵状生物氧化物上,设计了一种花朵状核壳异质结光催化剂,实现了光载体的空间分离和六价铬的选择性吸附,从而获得了优异的六价铬光催化还原性能。重要发现在核壳异质结中,光载体可以在空间上分离,然后在靠近六价铬选择性吸附位点的地方实现高效光催化还原六价铬。经测量,聚合≈30 分钟的最佳 PCIP@BiOI 核壳异质结在不添加任何自由基牺牲剂的情况下,对六价铬具有很强的光催化还原性。在 1 小时内,含 100 mg/L 六价铬的水溶液可被完全去除,六价铬的光催化还原速率常数是 BiOI 的≈20 倍。本研究提出了一种基于无机/有机结合设计核壳异质结光催化剂的方法,用于高浓度六价铬的环境修复。
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来源期刊
CiteScore
9.10
自引率
14.00%
发文量
362
审稿时长
35 days
期刊介绍: Journal of the Taiwan Institute of Chemical Engineers (formerly known as Journal of the Chinese Institute of Chemical Engineers) publishes original works, from fundamental principles to practical applications, in the broad field of chemical engineering with special focus on three aspects: Chemical and Biomolecular Science and Technology, Energy and Environmental Science and Technology, and Materials Science and Technology. Authors should choose for their manuscript an appropriate aspect section and a few related classifications when submitting to the journal online.
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