mof衍生的ZnO/PANI s型异质结用于光催化苯酚矿化和H2O2生成

IF 10.8 2区 化学 Q1 CHEMISTRY, PHYSICAL
Bowen Liu , Jianjun Zhang , Han Li , Bei Cheng , Chuanbiao Bie
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引用次数: 0

摘要

废水中持久性有机污染物的完全矿化仍然是一个艰巨的挑战。在这里,我们报道了通过原位氧化聚合合成zif -8衍生的ZnO/聚苯胺(PANI) s型异质结的合理设计。进一步的表征证实了ZnO/PANI异质结中的S-scheme电荷转移机制。在模拟太阳照射下,优化后的复合材料在60 min内实现了苯酚的完全矿化,同时以0.75 mmol∙L−1·h−1的速率生成H2O2。机理研究证实,s型异质结保持了很强的氧化还原电位,推动了活性氧的形成,用于H2O2的产生和苯酚的降解。这项工作建立了mof衍生的无机/有机s -方案异质结的通用设计范式,有效地将太阳能驱动的能量转换与环境修复相结合。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
MOF-derived ZnO/PANI S-scheme heterojunction for efficient photocatalytic phenol mineralization coupled with H2O2 generation
Complete mineralization of persistent organic pollutants in wastewater remains a formidable challenge. Here, we report the rational design of a ZIF-8-derived ZnO/polyaniline (PANI) S-scheme heterojunction synthesized via in situ oxidative polymerization. Advanced characterizations confirm the S-scheme charge transfer mechanism within the ZnO/PANI heterojunction. The optimized composite achieves complete phenol mineralization within 60 min while concurrently generating H2O2 at a rate of 0.75 mmol∙L−1·h−1 under simulated solar irradiation. Mechanistic studies verify that the S-scheme heterojunction retains strong redox potentials, driving the formation of reactive oxygen species for H2O2 production and phenol degradation. This work establishes a universal design paradigm for MOF-derived inorganic/organic S-scheme heterojunctions, effectively coupling solar-driven energy conversion with environmental remediation.
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来源期刊
物理化学学报
物理化学学报 化学-物理化学
CiteScore
16.60
自引率
5.50%
发文量
9754
审稿时长
1.2 months
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