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无表面活性剂制备及电荷载流子分离改善诱导暴露{001}面的独特八边形BiOCl纳米片光催化活性增强

Surfactant free fabrication and improved charge carrier separation induced enhanced photocatalytic activity of {001} facet exposed unique octagonal BiOCl nanosheets.

作者信息

Haider Zeeshan, Zheng Jin You, Kang Young Soo

机构信息

Korea Center for Artificial Photosynthesis and Department of Chemistry, Sogang University, Seoul 121-742, Republic of Korea.

出版信息

Phys Chem Chem Phys. 2016 Jul 20;18(29):19595-604. doi: 10.1039/c6cp01740a.

Abstract

Unique octagonal shaped BiOCl nanosheets (NS) dominantly exposed with high energy {001} crystal facets have been fabricated via a simple hydrothermal route without using organic surfactants. The dynamics of photogenerated charge carriers have been studied by time-resolved photoluminescence spectroscopy. The fitting parameters of the decay kinetics were used to calculate both the intensity weighted average lifetime (〈τ〉int.), as well as the amplitude weighted average lifetime (〈τ〉amp.) of the photogenerated charge carriers. The 〈τ〉int. and 〈τ〉amp. values for {001} BiOCl NS, i.e., 17.23 ns and 1.94 ns, respectively, were observed to be significantly higher than the corresponding values obtained for pristine BiOCl such as 2.52 ns and 1.07 ns, respectively. Significant quenching of the PL emission intensity of {001} BiOCl NS reflected the enhanced separation of the photogenerated charge carriers. Reduced thickness and in situ iodine doping was favorable to minimize the recombination tendency. The photocatalytic activity was monitored via the photodegradation of RhB under visible light illumination (λ > 400 nm). {001} BiOCl NS exhibited superior performance when compared to pristine BiOCl in terms of the rapid degradation kinetics and higher photonic efficiency. The photocatalytic efficiency of {001} BiOCl NS was 2.8 times higher than pristine BiOCl. Iodine doping induced extended the optical absorption in the visible region and improved the separation of the photogenerated charge carriers, which played an important role to enhance the photocatalytic activity. The photodegradation mechanism was systematically studied using various radical quenchers and it was revealed that photogenerated holes (h(+)) and superoxide radicals (˙O(2-)) actively participated whereas hydroxyl (OH˙) radicals had a negligible contribution in the photodegradation of RhB. {001} BiOCl NS has shown a higher photocurrent density and lower charge transfer resistance analyzed through photoelectrochemical and electrochemical impedance measurements. This study highlights the fabrication of unique octagonal BiOCl NS with improved separation of charge carriers across high energy crystal facts to design a highly efficient photocatalyst.

摘要

通过一种简单的水热法,在不使用有机表面活性剂的情况下制备出了主要暴露高能{001}晶面的独特八边形BiOCl纳米片(NS)。通过时间分辨光致发光光谱研究了光生载流子的动力学。利用衰减动力学的拟合参数计算了光生载流子的强度加权平均寿命(〈τ〉int.)和幅度加权平均寿命(〈τ〉amp.)。观察到{001} BiOCl NS的〈τ〉int.和〈τ〉amp.值分别为17.23 ns和1.94 ns,显著高于原始BiOCl相应的值,分别为2.52 ns和1.07 ns。{001} BiOCl NS的PL发射强度显著猝灭,反映了光生载流子分离的增强。减小厚度和原位碘掺杂有利于最小化复合趋势。通过在可见光照射(λ>400 nm)下对RhB的光降解来监测光催化活性。与原始BiOCl相比,{001} BiOCl NS在快速降解动力学和更高的光子效率方面表现出优异的性能。{001} BiOCl NS的光催化效率比原始BiOCl高2.8倍。碘掺杂诱导了可见光区域的光吸收扩展,并改善了光生载流子的分离,这对提高光催化活性起到了重要作用。使用各种自由基猝灭剂系统地研究了光降解机理,结果表明光生空穴(h(+))和超氧自由基(˙O(2-))积极参与,而羟基(OH˙)自由基在RhB的光降解中贡献可忽略不计。通过光电化学和电化学阻抗测量分析,{001} BiOCl NS显示出更高的光电流密度和更低的电荷转移电阻。这项研究突出了制备具有独特八边形的BiOCl NS,通过高能晶体面改善电荷载流子的分离,以设计一种高效的光催化剂。

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