Reduced graphene oxide supported chromium oxide hybrid as high efficient catalyst for oxygen reduction reaction

被引:31
|
作者
Wen, Changlan [1 ]
Gao, Xueping [2 ]
Huang, Taizhong [1 ]
Wu, Xiaoying [1 ]
Xu, Luping [3 ]
Yu, Jiemei [1 ]
Zhang, Haitao [1 ]
Zhang, Zhaoliang [1 ]
Han, Jitian [4 ]
Ren, Hao [1 ]
机构
[1] Univ Jinan, Sch Chem & Chem Engn, Shandong Prov Key Lab Fluorine Chem & Chem Mat, Jinan 250022, Peoples R China
[2] Shandong Univ, Sch Mat Sci & Engn, Jinan 250061, Peoples R China
[3] Xian Modern Chem Res Inst, Xian 710065, Peoples R China
[4] Shandong Univ, Sch Energy & Power Engn, Jinan 250061, Peoples R China
基金
高等学校博士学科点专项科研基金; 中国国家自然科学基金;
关键词
Oxygen reduction reaction; Electrocatalysis; Reduced graphene oxide; Chromium oxides; METAL-FREE ELECTROCATALYST; NITROGEN-DOPED GRAPHENE; COBALT OXIDE; BIFUNCTIONAL ELECTROCATALYST; VANADIUM CARBIDE; NANOPARTICLES; EVOLUTION; PERFORMANCE; COMPOSITES; CARBON;
D O I
10.1016/j.ijhydene.2016.05.051
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
Reduced graphene oxide (rGO) supported nano-chromium oxide (Cr2O3/rGO) catalyst for oxygen reduction reaction (ORR) has been successfully synthesized by the pyrolysis of chromium-urea coordination compound. The structure and morphology of the hybrid are investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM) and high resolution transmission electron microscopy (HRTEM) tests. XRD tests reveal that the Cr2O3 with hexagonal structure is obtained. SEM and TEM tests show that the nano-Cr2O3 is supported by rGO sheet. The cyclic voltammetry, tafel, linear scanning voltammetry and current-time chronoamperometric tests prove that the obtained Cr2O3/rGO hybrid has a remarkable catalytic activity and good stability for oxygen reduction. Both the rotating disc electrode and rotating ring disc electrode tests approve that the ORR major happens through 4-electron reaction style. The Cr2O3/rGO hybrid is a promising low cost and high performances catalyst for ORR of alkaline electrolyte. (C) 2016 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:11099 / 11107
页数:9
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