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形态调控的(111)面氧化铜纳米催化剂对4-硝基苯酚的显著面选择性还原

Remarkable Facet Selective Reduction of 4-Nitrophenol by Morphologically Tailored (111) Faceted CuO Nanocatalyst.

作者信息

Aditya Teresa, Jana Jayasmita, Singh Navin Kumar, Pal Anjali, Pal Tarasankar

机构信息

Department of Chemistry and Department of Civil Engineering, Indian Institute of Technology, Kharagpur 721302, India.

出版信息

ACS Omega. 2017 May 10;2(5):1968-1984. doi: 10.1021/acsomega.6b00447. eCollection 2017 May 31.

Abstract

In this work, we have disclosed the facile syntheses of morphologically diverse CuO nanoparticles using our laboratory designed modified hydrothermal reactor employing low-cost copper (II) acetate precursor compounds. The reaction conditions dovetail the effect of ethylene glycol (EG) and glucose to exclusively evolve the morphology tuned CuO nanomaterial at different pHs. The morphology tuning produces octahedron (Oh), dwarf hexapod (DHP), and elongated hexapod (EHP) CuO structures only with the optimized reagent concentrations. Interestingly, all of them were bestowed with a (111) facet, a superlative facet for facile nitroarene reduction. Thus, the morphology reliant catalytic reaction becomes evident. However, when used individually, EG and glucose evolve ill-defined CuO/CuO and CuO structures, respectively. We have observed that a change in pH of the medium at the onset of the reaction is obligatory for the evolution of tailor-made morphologically diverse CuO nanoparticles. However, preformed CuO particles do not suffer further structure/morphology changes under deliberate pH (6.0-9.0) change. With the as-obtained Oh, DHP, and EHP CuO structures, we further delve into the realm of catalysis to understand the splendor of the nanocatalyst, morphology and surface area dependence, facet selective reactivity, and other factors affecting the catalytic efficiency. The remarkable rate of catalysis of 4-nitrophenol (4-NP), evident from the catalyst activity parameter ( = 123.6 g s), to produce 4-aminophenol in the presence of a reducing agent like sodium borohydride (NaBH) of the as-prepared catalysts is evidence of the collaborative effects of the effective surface area, surface positive charge, and active (111) facet of the CuO nanocatalyst. We have also studied the effect of other common anions, namely, Cl, NO , NO , CO , and SO on the reduction process. To obtain a general consensus about facets, we compared (100) and (111) faceted CuO nanocatalysts not only for 4-NP reduction but also for the reduction of toxic chromium Cr(VI) in the presence of formic acid to further emphasize the importance of facet selectivity in catalysis and the versatility of the morphology tuned as-prepared CuO.

摘要

在这项工作中,我们利用实验室设计的改良水热反应器,使用低成本的醋酸铜(II)前驱体化合物,揭示了形态多样的氧化铜纳米颗粒的简便合成方法。反应条件与乙二醇(EG)和葡萄糖的作用相契合,以在不同pH值下专门生成形态可调的氧化铜纳米材料。形态调控仅在优化的试剂浓度下产生八面体(Oh)、矮六足体(DHP)和细长六足体(EHP)氧化铜结构。有趣的是,它们都具有(111)晶面,这是用于简便还原硝基芳烃的最佳晶面。因此,形态依赖的催化反应变得明显。然而,单独使用时,EG和葡萄糖分别生成定义不明确的CuO/CuO和CuO结构。我们观察到,反应开始时介质pH值的变化对于定制形态多样的氧化铜纳米颗粒的生成是必不可少的。然而,预先形成的氧化铜颗粒在有意改变pH值(6.0 - 9.0)的情况下不会进一步发生结构/形态变化。利用所获得的Oh、DHP和EHP氧化铜结构,我们进一步深入催化领域,以了解纳米催化剂的卓越性能、形态和表面积依赖性、晶面选择性反应性以及其他影响催化效率的因素。从催化剂活性参数( = 123.6 g s)可以明显看出,在像硼氢化钠(NaBH)这样的还原剂存在下,制备的催化剂对4 - 硝基苯酚(4 - NP)的催化速率显著,这证明了氧化铜纳米催化剂有效表面积、表面正电荷和活性(111)晶面的协同作用。我们还研究了其他常见阴离子,即Cl、NO 、NO 、CO 和SO 对还原过程的影响。为了对晶面达成普遍共识,我们不仅比较了(100)和(111)晶面的氧化铜纳米催化剂对4 - NP的还原,还比较了在甲酸存在下对有毒铬Cr(VI)的还原,以进一步强调晶面选择性在催化中的重要性以及形态可调的制备氧化铜的多功能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/405a/6641649/ddfb5223ae14/ao-2016-00447w_0015.jpg

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