Electrocatalytic hydrogen evolution reaction on reduced graphene oxide electrode decorated with cobaltphthalocyanine

被引:79
|
作者
Akyuz, Duygu [1 ]
Keskin, Bahadir [2 ]
Sahinturk, Utkan [3 ]
Koca, Atif [4 ]
机构
[1] Marmara Univ, Fac Sci & Letters, Dept Chem, TR-34722 Istanbul, Turkey
[2] Yildiz Tech Univ, Fac Arts & Sci, Dept Chem, TR-34210 Istanbul, Turkey
[3] Yildiz Tech Univ, Fac Chem Met, Dept Met & Mat Engn, TR-34210 Istanbul, Turkey
[4] Marmara Univ, Fac Engn, Dept Chem Engn, TR-34722 Istanbul, Turkey
关键词
Electrocatalyst; Hydrogen evolution reaction; Phthalocyanine; Click electrochemistry; Graphene Oxide; Reduced graphene oxide; VERSATILE BUILDING-BLOCKS; OXYGEN REDUCTION; CLICK ELECTROCHEMISTRY; PHTHALOCYANINE; PERFORMANCE; FILMS; NANOPARTICLES; MEMBRANE; PHOTOCATALYSTS; NANOCOMPOSITES;
D O I
10.1016/j.apcatb.2016.02.003
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
Electrocatalytic hydrogen evolution reaction (HER) on azido graphene oxide (GO-N-3) and reduced azido graphene oxide (RGO-N-3) electrodes decorated with the cobaltphthalocyanine complex bearing terminal alkyne moieties (TA-CoPc) was investigated. GCE/RGO-N-3 electrode was constructed with the electrochemical reduction of GO-N-3 coated on a glassy carbon electrode. Decoration of GCE/RGO-N-3 and GCE/GO-N-3 electrodes were performed with a new electrode modification technique, "click electrochemistry (CEC)", with which TA-CoPc complex was bonded to azido functional groups of GO-N-3 and RGO-N-3 on the electrodes. The modified GCE/RGO-N-3/TA-CoPc and GCE/GO-N-3/TA-CoPc electrodes were characterized with square wave voltammetry and electrochemical impedance spectroscopy (EIS), and then tested as heterogeneous electrocatalysts for HER. GCE/RGO-N-3/TA-CoPc electrode illustrates well electrocatalytic activity by decreasing the over-potential of the bare electrode about 340 mV and increasing the current density of the electrode about 15 fold at low pHs with absolutely high stability and reproducibility. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:217 / 226
页数:10
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