Charge-Tunable Bismuth-Hydroxamate Metal–Organic Frameworks for Photocatalytic Cr(VI) Mitigation

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-10-15 DOI:10.1021/acs.cgd.4c0117210.1021/acs.cgd.4c01172
Chaozhi Xiong, Zhen-Wu Shao, Zhiyuan Zhang, Yue Dong, Li Xiong, Yuqing Qiu, Xiangping Duan, Yuxin Liu and Chong Liu*, 
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Abstract

This study presents three bismuth-hydroxamate metal–organic frameworks (MOFs), namely, SUM-90A/B/C (SUM = Sichuan University Materials), prepared from Bi3+ and the same bridging ligand (1,4-benzenedihydroxamic acid). By varying the synthetic conditions, the charge states of the framework backbones and the coordination environments of the Bi3+ centers were finetuned, resulting in distinct structures and properties. The performances of MOFs as heterogeneous photocatalysts for Cr(VI) mitigation were comparatively studied, using both theoretical and experimental methods, and they exhibited remarkable kinetic stability in aqueous media and varied electronic structures. Specifically, SUM-90C, with an experimental band gap of 1.92 eV, was identified as a promising photocatalyst that could effectively convert Cr(VI) within 4 h and retain 96% of its capability over 3 cycles.

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用于光催化缓解六价铬的电荷可调铋羟肟酸金属有机框架
本研究介绍了由 Bi3+ 和相同桥接配体(1,4-苯二羟肟酸)制备的三种铋羟肟酸金属有机框架(MOFs),即 SUM-90A/B/C(SUM = 四川大学材料学院)。通过改变合成条件,对框架骨架的电荷状态和 Bi3+ 中心的配位环境进行了微调,从而获得了不同的结构和性能。利用理论和实验方法,对 MOFs 作为异相光催化剂用于缓解六价铬的性能进行了比较研究,结果表明它们在水介质中具有显著的动力学稳定性和不同的电子结构。具体而言,实验带隙为 1.92 eV 的 SUM-90C 被认为是一种很有前景的光催化剂,它能在 4 小时内有效转化六价铬,并在 3 个周期内保持 96% 的转化能力。
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4.30%
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567
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