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Fabrication of recoverable Bi2O2S/Bi5O7I/ZA hydrogel beads for enhanced photocatalytic Hg0 removal in the presence of H2O2
Separation and Purification Technology ( IF 8.1 ) Pub Date : 2024-11-19 , DOI: 10.1016/j.seppur.2024.130597 Haixing Du, Anchao Zhang, Qianqian Zhang, Yihong Sun, Haowei Zhu, Hua Wang, Zengqiang Tan, Xinmin Zhang, Guoyan Chen
Separation and Purification Technology ( IF 8.1 ) Pub Date : 2024-11-19 , DOI: 10.1016/j.seppur.2024.130597 Haixing Du, Anchao Zhang, Qianqian Zhang, Yihong Sun, Haowei Zhu, Hua Wang, Zengqiang Tan, Xinmin Zhang, Guoyan Chen
The effective removal of elemental mercury (Hg0) is a global challenge due to its toxicity and bioaccumulation threat to public health and ecosystems. Photocatalytic technology by visible light-driven photocatalysts is promising for Hg0 removal. However, effective separation of photocatalyst powders from reaction solution limits its widespread use. To solve the problem, we report for the first time the successful fabrication of recoverable Bi2O2S/Bi5O7I/ZA hydrogel beads for enhanced photocatalytic Hg0 removal in the presence of H2O2. Characterization techniques such as XRD, TEM, EDS, XPS, UV–vis DRS, PL, etc. are employed to understand the physicochemical properties and photoelectric performance of the photocatalysts. The serial BOSI photocatalysts all outperform the single component, which is attributed to the formation of a heterojunction between Bi5O7I and Bi2O2S. The coupling of 2-BOSI-ZA beads with H2O2 shows favorable synergistic effect, with Hg0 removal efficiency in the following order: H2O2 + 2-BOSI-ZA < 2-BOSI-ZA + FSL < H2O2 + 2-BOSI-ZA + FSL. TPC, EIS, and PL tests confirm that the introduction of Bi2O2S effectively suppresses charge carrier recombination. ESR and free radicals capture experiments demonstrate that the main species responsible for removal of Hg0 are •O2– and •OH. Density functional theory calculations exhibit that the internal electric field (IEF) between Bi5O7I and Bi2O2S contributes to the spatial charge separation of the heterojunction. The IEF leads to an S-scheme carrier transfer mechanism at the Bi2O2S/Bi5O7I interface that benefits the carrier separation on Bi5O7I, resulting in an enhanced photocatalytic performance. This work can provide further inspiration for designing hydrogel photocatalysts with an excellent activity in conjunction with oxidants in the field of mercury pollution control.
中文翻译:
制备可回收的 Bi2O2S/Bi5O7I/ZA 水凝胶珠,用于在 H2O2 存在下增强光催化 Hg0 去除
有效去除元素汞 (Hg 0) 是一项全球性挑战,因为其毒性和生物积累对公共卫生和生态系统构成威胁。可见光驱动光催化剂的光催化技术有望去除Hg 0。然而,光催化剂粉末与反应溶液的有效分离限制了其广泛使用。为了解决这个问题,我们首次报道了在 H2O2 存在下成功制造可回收的 Bi2O2S/Bi5O7I/ZA 水凝胶珠,用于增强光催化 Hg0 去除。采用 XRD、TEM、EDS、XPS、UV-vis DRS、PL 等表征技术来了解光催化剂的物理化学性质和光电性能。系列BOSI光催化剂的性能都优于单一组分,这归因于Bi5O7I和Bi2O2S之间异质结的形成。2-BOSI-ZA 珠子与 H2O2 的偶联显示出良好的协同效应,Hg0 去除效率按以下顺序排列:H2O2 + 2-BOSI-ZA < 2-BOSI-ZA + FSL < H2O2 + 2-BOSI-ZA + FSL。TPC、EIS 和 PL 测试证实,Bi2O2S 的引入有效抑制了电荷载流子复合。ESR 和自由基捕获实验表明,负责去除 Hg0 的主要物质是 •O2– 和 •OH。 密度泛函理论计算表明,Bi5O7I 和 Bi2O2S 之间的内电场 (IEF) 有助于异质结的空间电荷分离。IEF 导致 Bi2O2S/Bi5O7I 界面的 S 型载流子转移机制,有利于 Bi5O7I 上的载流子分离,从而增强光催化性能。这项工作可以为在汞污染控制领域设计具有优异活性的水凝胶光催化剂提供进一步的灵感。
更新日期:2024-11-19
中文翻译:
制备可回收的 Bi2O2S/Bi5O7I/ZA 水凝胶珠,用于在 H2O2 存在下增强光催化 Hg0 去除
有效去除元素汞 (Hg 0) 是一项全球性挑战,因为其毒性和生物积累对公共卫生和生态系统构成威胁。可见光驱动光催化剂的光催化技术有望去除Hg 0。然而,光催化剂粉末与反应溶液的有效分离限制了其广泛使用。为了解决这个问题,我们首次报道了在 H2O2 存在下成功制造可回收的 Bi2O2S/Bi5O7I/ZA 水凝胶珠,用于增强光催化 Hg0 去除。采用 XRD、TEM、EDS、XPS、UV-vis DRS、PL 等表征技术来了解光催化剂的物理化学性质和光电性能。系列BOSI光催化剂的性能都优于单一组分,这归因于Bi5O7I和Bi2O2S之间异质结的形成。2-BOSI-ZA 珠子与 H2O2 的偶联显示出良好的协同效应,Hg0 去除效率按以下顺序排列:H2O2 + 2-BOSI-ZA < 2-BOSI-ZA + FSL < H2O2 + 2-BOSI-ZA + FSL。TPC、EIS 和 PL 测试证实,Bi2O2S 的引入有效抑制了电荷载流子复合。ESR 和自由基捕获实验表明,负责去除 Hg0 的主要物质是 •O2– 和 •OH。 密度泛函理论计算表明,Bi5O7I 和 Bi2O2S 之间的内电场 (IEF) 有助于异质结的空间电荷分离。IEF 导致 Bi2O2S/Bi5O7I 界面的 S 型载流子转移机制,有利于 Bi5O7I 上的载流子分离,从而增强光催化性能。这项工作可以为在汞污染控制领域设计具有优异活性的水凝胶光催化剂提供进一步的灵感。