Efficient and stable HER electrocatalyst using Pt-nanoparticles@poly(3,4 ethylene dioxythiophene) modified sulfonated graphene nanocomposite

被引:19
作者
Abdolmaleki, A. [1 ]
Mohamadi, Z. [1 ]
Ensafi, Ali A. [1 ]
Atashbar, N. Zandi [1 ]
Rezaei, B. [1 ]
机构
[1] Isfahan Univ Technol, Dept Chem, Esfahan 8415683111, Iran
关键词
Pt-nanoparticles Poly(3,4-ethylene dioxythiophene); Sulfonated graphene nanosheets; Electrocatalysis; Hydrogen evolution reaction; HYDROGEN EVOLUTION REACTION; OXYGEN REDUCTION REACTION; FUNCTIONALIZED GRAPHITE; CARBON NANOTUBES; HIGHLY EFFICIENT; EDGE; NANOPARTICLES; OXIDE; WATER; ACID;
D O I
10.1016/j.ijhydene.2018.03.142
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
The green production of hydrogen by electrochemical water splitting has been recently paid attention. It is more focused to research about the preparation of efficient electrocatalysts, which catalyze hydrogen evolution reaction (HER) in acidic media at low over potential. Platinum is known as an ideal option, but its rarity and high-cost limit its application in practical industrial plants. Hence, minimizing the level of it can be a solution. It can be achieved by the decoration of platinum nanoparticles (PtNPs) on the different composites such as poly(3,4-ethylene dioxythiophene, PEDOT) and sulfonated graphene nanosheets (SG) in this work. Accordingly, the successful preparation and HER electrocatalytic manner of this nanocomposite were main objectives in the present report. The related characterization and performance were monitored using various analytical and electrochemical techniques. The low charge transfer resistance (around 50 0), low over potential (-0.040 V vs. RHE), and stable manner (until 500 cycles) resulted in this HER electrocatalyst. It was controlled by Tafel reaction with electrochemical adsorption desorption because of kinetic factors including Tafel slope (28.4 mV dec(-1)), charge transfer coefficient of 2.0, and exchange current of 7.27 mA cm(-2). (C) 2018 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:8323 / 8332
页数:10
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