MOF-derived Cu-Pd/nanoporous carbon composite as an efficient catalyst for hydrogen evolution reaction: A comparison between hydrothermal and electrochemical synthesis

被引:60
作者
Mandegarzad, Sakineh [1 ]
Raoof, Jahan Bakhsh [1 ]
Hosseini, Sayed Reza [2 ]
Ojani, Reza [1 ]
机构
[1] Univ Mazandaran, Fac Chem, Dept Analyt Chem, Electroanalyt Chem Res Lab, Babol Sar 4741695447, Iran
[2] Univ Mazandaran, Fac Chem, Nanochem Res Lab, Babol Sar 4741695447, Iran
关键词
Electrosynthesis; Hydrothermal; Direct carbonization; Cu-Pd bimetallic nanoparticles; Galvanic replacement; Hydrogen evolution reaction; METAL-ORGANIC FRAMEWORKS; NANOPOROUS CARBON; OXYGEN REDUCTION; ELECTROCATALYST; NANOPARTICLES; ELECTRODE; FABRICATION; HYBRID;
D O I
10.1016/j.apsusc.2017.12.034
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this study, a novel catalyst based on Cu-Pd bimetallic nanoparticles supported on nanoporous carbon composite (NPCC) is successfully fabricated through three-step process and used as an electrocatalyst towards hydrogen evolution reaction (HER). At the first step, MOF-199 is synthesized via two distinct strategies; (1) hydrothermal (HT) and (2) electrochemical (EC). Next, the synthesized MOF-199 is used as a template in order to prepare Cu/NPCC by direct carbonization under N-2 atmosphere followed by galvanic replacement reaction of Cu metals by PdII ions. All the prepared materials are characterized by X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDS), scanning electron microscopy (SEM), and nitrogen adsorption/desorption measurements. The effect of synthesis method of MOF-199 on the electrocatalytic activity of the final product towards HER is investigated. The electrochemical measurements indicate that Cu-Pd/NPCC derived from the MOF prepared by EC method (Cu-Pd/NPCC/EC) exhibits an enhanced catalytic activity towards HER in H2SO4 solution than the Cu-Pd/NPCC/HT. This improvement may be attributed to using of supporting electrolyte in the preparation of Cu-Pd/NPCC/EC. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:451 / 459
页数:9
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