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Synthesis of nanoporous PdAg nanoalloy for hydrogen generation from formic acid at room temperature

机译:在室温下由甲酸合成纳米多孔PdAg纳米合金用于制氢

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A new one pot, surfactant-free, room temperature synthetic route based on coreduction of Pd2+ and Ag+ salt by ascorbic acid has been developed for the synthesis of PdxAg1-x nanoparticles (NPs). The nanoporous structure of the PdxAg1-x nanoalloy having spherical ligaments is confirmed by XRD, FESEM, EDX, TEM, HRTEM, SAED and XPS studies. The nitrogen adsorption-desorption isotherm (BET) of PdxAg1-x NPs can be classified as type V which is characteristic of a solid with mesopores. Some of the PdxAg1-x nanoporous nanoalloy catalyst thus prepared exhibit high activity towards H-2 generation with an extremely high selectivity and stability in formic acid (FA) dehydrogenation. The catalytic activity towards H2 generation from FA followed the trend of Pd0.5Ag0.5 > Pd0.6Ag0.4 > Pd0.67Ag0.33 > Pd0.75Ag0.25 approximate to Pd. Rate of FA decomposition closely follow the first order kinetics. The recycle test results of the Pd0.5Ag0.5 nanocatalyst show no significant decrease in catalytic activity over five cycles. The catalysts can be regenerated by simply rinsing with water followed by drying at room temperature. It is believed that this low cost, selective and efficient CO-free H2 generation system at room temperature will promote its application in different devices like FA driven fuel cells. Copyright (C) 2015, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
机译:已经开发了一种新的无罐,无表面活性剂的室温合成路线,该路线基于抗坏血酸对Pd2 +和Ag +盐的共轭反应,用于合成PdxAg1-x纳米粒子(NPs)。 XRD,FESEM,EDX,TEM,HRTEM,SAED和XPS研究证实了具有球形韧带的PdxAg1-x纳米合金的纳米孔结构。 PdxAg1-x NP的氮吸附-解吸等温线(BET)可以归类为V型,这是具有中孔的固体的特征。如此制备的某些PdxAg1-x纳米多孔纳米合金催化剂在甲酸(FA)脱氢中具有极高的选择性和稳定性,从而对H-2生成表现出高活性。 FA对H2生成的催化活性遵循Pd0.5Ag0.5> Pd0.6Ag0.4> Pd0.67Ag0.33> Pd0.75Ag0.25近似于Pd的趋势。 FA分解速率紧密遵循一级动力学。 Pd0.5Ag0.5纳米催化剂的循环测试结果表明,在五个循环中,催化活性均没有明显降低。只需用水冲洗,然后在室温下干燥,即可再生催化剂。可以相信,这种低成本,选择性和高效的,室温下无CO的H2生成系统将促进其在FA驱动的燃料电池等不同设备中的应用。 Hydrogen Energy Publications,LLC版权所有(C)2015。由Elsevier Ltd.出版。保留所有权利。

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