In situ construction of a Sillén–Aurivillius layered perovskite-based 0D/2D homologous Schottky junction for efficient piezo-photocatalytic activity†

IF 4.4 3区 化学 Q2 CHEMISTRY, PHYSICAL Catalysis Science & Technology Pub Date : 2023-08-02 DOI:10.1039/D3CY00876B
Jian Yang, Yali Xue, Chuang Han, Xiaorui Zhang, Ke Sa, Jin Jia, Hanlin Ye and Yujun Liang
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Abstract

The interface shielding effect resulting from the accumulation of charge carriers and the relatively weak driving force provided by the single built-in electric field in conventional heterojunctions seriously hamper the rapid and continuous charge separation. Herein, focusing on Sillén–Aurivillius perovskite-type bismuth tantalum oxyhalides, an ingenious 0D/2D Bi/Bi4TaO8Cl0.5Br0.5 (BTOCB) piezoelectric homologous Schottky heterojunction is judiciously designed and fabricated via in situ deposition of Bi nanodots on the surfaces of BTOCB solid solution nanosheets and shows mainly exposed (001) facets and strong piezoelectricity. Rietveld refinements confirm the substitution of Cl and Br in the lattice, and the band structure is regulated by solid solution engineering. Meanwhile, the introduction of Bi improves visible light absorption and creates an internal electric field at the heterointerface. Under the synergetic action of illumination and ultrasonic vibration, the unique multi-internal electric field modulation derived from the piezoelectric polarization and Schottky junction can break the heterointerface shielding effect and deliver powerful driving force for impactful spatial photocarrier migration and separation. As a result, the as-prepared Bi/BTOCB Schottky junction exhibits outstanding piezo-photocatalyst performance for tetracycline (TC) degradation. Lastly, the possible degradation pathway of TC is proposed, and the toxicity of intermediates is also analyzed. This study demonstrates a strategy of multi-field modulation in optimizing photogenerated carrier behaviors and gives deep insights into the design of high-performance piezo-photocatalysts.

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原位构建基于sill - aurivillius层状钙钛矿的0D/2D同源肖特基结,具有高效的压电光催化活性†
传统异质结中载流子的积累所产生的界面屏蔽效应和单一内置电场提供的相对较弱的驱动力严重阻碍了电荷的快速连续分离。本文以sill - aurivillius钙钛矿型铋钽氧化卤化物为研究对象,在BTOCB固溶体纳米片表面原位沉积Bi纳米点,设计并制备了一种新颖的0D/2D Bi/Bi4TaO8Cl0.5Br0.5 (BTOCB)压电同源肖特基异质结,该异质结主要表现为暴露(001)面和强压电性。Rietveld细化证实了Cl和Br在晶格中的取代作用,并通过固溶体工程调节了能带结构。同时,铋的引入提高了可见光的吸收,并在异质界面处产生了一个内部电场。在照明和超声振动的协同作用下,压电极化和肖特基结产生的独特的多内电场调制可以打破异质界面屏蔽效应,为有影响的空间光载流子迁移和分离提供强大的驱动力。结果表明,制备的Bi/BTOCB肖特基结在四环素(TC)降解中表现出优异的压电光催化剂性能。最后,提出了TC可能的降解途径,并对中间体的毒性进行了分析。本研究展示了一种多场调制优化光生载流子行为的策略,并为高性能压电光催化剂的设计提供了深刻的见解。
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来源期刊
Catalysis Science & Technology
Catalysis Science & Technology CHEMISTRY, PHYSICAL-
CiteScore
8.70
自引率
6.00%
发文量
587
审稿时长
1.5 months
期刊介绍: A multidisciplinary journal focusing on cutting edge research across all fundamental science and technological aspects of catalysis. Editor-in-chief: Bert Weckhuysen Impact factor: 5.0 Time to first decision (peer reviewed only): 31 days
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