首页> 外文期刊>Journal of Colloid and Interface Science >Silver chloride enwrapped silver grafted on nitrogen-doped reduced graphene oxide as a highly efficient visible-light-driven photocatalyst
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Silver chloride enwrapped silver grafted on nitrogen-doped reduced graphene oxide as a highly efficient visible-light-driven photocatalyst

机译:作为高效的可见光催化的光催化剂,氯化银掺杂在氮气掺杂的石墨烯氧化物上的覆盖物

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摘要

The visible-light-driven plasmonic photocatalyst silver chloride enwrapped silver/nitrogen-doped reduced graphene oxide (AgCl@Ag/N-rGO) was prepared by a facile hydrothermal-in situ oxidation method and characterized by Scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transform-infrared spectroscopy (FTIR), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS) and UV-vis diffuse reflectance spectroscopy (UV-vis DRS). The characterization results reveal that Ag nanoparticles (NPs) were first grafted on N-rGO via N-groups as anchor sites and then enwrapped by AgCl by in situ oxidation. Close interfacial contact favors efficient electron transfer, leading to high photoactivity and photostability for the degradation of various toxic organic pollutants. The photocatalytic performance of this photocatalyst was significantly higher than that of AgCl@Ag/rGO and other related photocatalysts due to the in situ introduction of N-groups. Additionally, the used catalyst can be recycled without an appreciable loss of catalytic activity. Based on electron spin resonance and cyclic voltammetry analyses, the electron transfer processes were confirmed to occur from plasmon-induced Ag NPs to AgCl and from N-rGO to Ag NPs, and pollutants could be oxidized through the loss of electrons to N-rGO by the interaction between the pollutants and N-rGO. The active species of superoxide anion radicals (O-2(center dot-), photogenerated holes (h(+)) and surface-adsorbed (OH)-O-center dot played roles in pollutant photodegradation. Accordingly, the plasmon-induced electron transfer processes elucidated photostability of AgCl@Ag/N-rGO. AgCl@Ag/N-rGO has a potential application in water purification due to its high photoactivity and photostability. (C) 2017 Elsevier Inc. All rights reserved.
机译:通过容易的水热原位氧化方法制备可见光驱动的等离子体光催化剂酰氯杂交银/氮掺杂的石墨烯(AgCl @ Ag / N-Rgo),并通过扫描电子显微镜(SEM),x -Ray衍射(XRD),傅里叶变换 - 红外光谱(FTIR),拉曼光谱,X射线光电子能谱(XPS)和UV-Vis弥射反射光谱(UV-Vis DRS)。表征结果显示,Ag纳米颗粒(NPS)首先通过N基团作为锚位移植在N-RGO上,然后通过原位氧化通过AgCl包裹。关闭界面接触利​​用高效的电子转移,导致各种有毒有机污染物的降解的高度光度和光稳定性。由于N组的原位引入,这种光催化剂的光催化性能显着高于AgCl @ Ag / Rgo和其他相关光催化剂。另外,可以再循环使用的催化剂而没有明显的催化活性丧失。基于电子自旋共振和循环伏安法分析,确认电子转移过程从等离子体诱导的Ag NPS发生至AgCl,从N-RGO到Ag NPS,并且可以通过对N-RGO的电子丢失来氧化污染物污染物与n-rgo之间的相互作用。超氧化物阴离子自由基的活性物种(O-2(中心点),光生孔(H(+))和表面吸附(OH)-O-中心点在污染物光降解中发挥作用。因此,等离子体诱导的电子转移过程阐明了AgCl @ Ag / N-Rgo的光稳定性。AgCl @ Ag / N-Rgo由于其高光度和光稳定性而具有水净化的潜在应用。(c)2017 Elsevier Inc.保留所有权利。

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