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首页> 外文期刊>Chemical engineering journal >Stable self-assembly AgI/UiO-66(NH2) heterojunction as efficient visible-light responsive photocatalyst for tetracycline degradation and mechanism insight
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Stable self-assembly AgI/UiO-66(NH2) heterojunction as efficient visible-light responsive photocatalyst for tetracycline degradation and mechanism insight

机译:稳定的自组装AGI / UIO-66(NH2)异质结像四环素降解和机制洞察力的高效可见光响应光催化剂

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摘要

UiO-66(NH2) is a fascinating visible-light responsive amino functionalized zirconium-MOF. However, its photocatalytic performance is less satisfactory because of the disappointing separation rate of electron-hole pairs and the poor solar energy utilization ability. In this research, an unique AgI/UiO-66(NH2) heterojunction was constructed via a facile ion exchange precipitation method to reinforce the photocatalytic performance of UiO-66(NH2). The photocatalytic performance was evaluated by degrading tetracycline (TC) under visible light. The optimal TC removal rate was obtained by AgI(30% wt)/UiO-66(NH2) which was 3.8-fold of UiO-66(NH2) and 2.1-fold of AgI. TOC removal rate of AgI(30% wt)/UiO-66(NH2) reached 65.6% after 40 min irradiation which was better than pure UiO-66(NH2) (16.2%) and AgI (22.4%). The detailed intermediates and pathway of TC degradation were also illustrated. According to the results of characterization, it was determined that Ag nanoparticles (small amount) were occurred in the initial stage of photocatalytic process, which resulted in the transformation from AgI/UiO-66(NH2) type II heterojunction to AgI/Ag/UiO-66(NH2) Z-scheme heterojunction. Benefiting from the novel heterojunction and the Surface Plasmon Resonance (SPR) Ag, the redox capacity of photogenerated electron-hole pairs was enhanced and the photocorrosion of AgI was significantly suppressed, resulting in the excellent photocatalytic performance of AgI/UiO-66(NH2) composites. Moreover, the SPR Ag also resulted in the expansion of light absorption range. Besides, considerable active sites and depressed recombination of electron-hole pairs also exerted vital influence on enhancing photocatalytic activity. This work illustrates the great application potential of AgI/UiO-66(NH2) heterostructure photocatalyst in water remediation and provides a new insight in optimizing UiO-66(NH2).
机译:UIO-66(NH2)是一种迷人的可见光响应氨基官能化锆MOF。然而,由于电子孔对的令人失望的分离率和太阳能利用能力差,其光催化性能不太令人满意。在该研究中,通过容易离子交换沉淀法构建独特的AGI / UIO-66(NH2)异质结,以增强UIO-66(NH2)的光催化性能。通过在可见光下降解四环素(TC)来评价光催化性能。通过AGI(30%wt)/ UIO-66(NH 2)获得最佳TC去除率,其为3.8倍的UIO-66(NH2)和2.1倍的AGI。在40分钟照射后Agi(30%wt)/ UiO-66(NH2)的TOC去除率达到65.6%,比纯UIO-66(NH2)和AGI(22.4%)更好。还说明了TC降解的详细中间体和途径。根据表征的结果,确定在光催化过程的初始阶段发生Ag纳米颗粒(少量),从Agi / UIO-66(NH2)II型异质结转转化为AGI / AG / UIO -66(NH2)Z方案异质结。从新型异质结和表面等离子体共振(SPR)Ag中受益,增强了光生电子 - 空穴对的氧化还原能力,并且显着抑制了AGI的光腐蚀,导致AGI / UIO-66(NH2)的优异光催化性能复合材料。此外,SPRAG也导致光吸收范围的膨胀。此外,相当大的活​​性位点和电子孔对的凹陷重组也对增强光催化活性的重要影响也施加了至关重要的影响。这项工作说明了AGI / UIO-66(NH2)异质结构光催化剂在水处理中的巨大应用潜力,并提供了在优化UIO-66(NH2)的新见解。

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