Hydrothermal synthesis of Co3O4 nanowire electrocatalysts for oxygen evolution reaction

被引:9
作者
Xu, Shuai [1 ]
Tong, Jinlin [1 ]
Liu, Yuan [1 ]
Hu, Wei [1 ]
Zhang, Ganbing [1 ]
Xia, Qinghua [1 ]
机构
[1] Hubei Univ, Key Lab Synth & Applicat Organ Funct Mol, Hubei Collaborat Innovat Ctr Adv Organ Chem Mat, Minist Educ, Wuhan 430062, Peoples R China
关键词
LITHIUM-ION BATTERIES; WATER OXIDATION; COBALT OXIDE; MESOPOROUS CO3O4; CATALYST; ELECTRODES; ARRAYS; CONVERSION; REDUCTION; HYDROXIDE;
D O I
10.1063/1.4961432
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Herein, we reported a well-controlled hydrothermal synthesis of Co3O4 nanowires using CoSO4 as a cobalt precursor and glycerol as a morphological directing agent. Scanning electron microscopy was employed to observe the growth of nanowires. As an important synthetic parameter, reaction time is spanned from 4 to 24 h, which played an important role in the morphology and properties of materials. When the reaction time was 4 h, the resulting Co3O4 nanoparticles assembled into some short nanorods. While increasing the reaction time, the nanorods grew into long nanowires with large aspect ratio, and then attached into bundles when the reaction time was extended up to 24 h. Electrochemical characterization shows that Co3O4 nanowires prepared by hydrothermal reaction for 12 h exhibited the highest catalytic activity for oxygen evolution reaction (OER) among all synthesized nanowires and nanoparticles using the similar method. The enhanced OER activity of the 12 h-prepared Co3O4 nanowires should be attributed to the increased electroactive surface area because observed from the cyclic voltammogram, the 12 h-prepared Co3O4 nanowires possessed the highest surface area among all tested samples. It was also illustrated that there existed a close correlation of the OER catalytic activity with the transition of oxidation state and the density of activity sites of the catalyst exposing to the electrolyte solution during the electrolysis. Though both Co3O4 nanowires and nanoparticles exhibited a considerable loss in OER activity during the stability testing, after polarization for 4 h at 1.7V (versus a reversible hydrogen electrode), the Co3O4 nanowires still produced the higher catalytic current than that of the Co3O4 nanoparticles showing a slightly higher stability than the particles because of the nanowire structure. Published by AIP Publishing.
引用
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页数:10
相关论文
共 35 条
[1]   Anodic electrodeposition of cobalt oxides from an alkaline bath containing Co-gluconate complexes on glassy carbon. An electroanalytical investigation [J].
Casella, Innocenzo G. ;
Di Fonzo, Daniela A. .
ELECTROCHIMICA ACTA, 2011, 56 (22) :7536-7540
[2]   Electrochemical characterization of porous nickel-cobalt oxide electrodes [J].
Castro, EB ;
Real, SG ;
Dick, LFP .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2004, 29 (03) :255-261
[3]   Electrodeposited Ni-Co-oxide electrodes: characterization and kinetics of the oxygen evolution reaction [J].
Castro, EB ;
Gervasi, CA .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2000, 25 (12) :1163-1170
[4]   Self-assembled Co3O4 porous nanostructures and their photocatalytic activity [J].
Chen, Youcun ;
Hu, Lin ;
Wang, Min ;
Min, Yulin ;
Zhang, Yuanguang .
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 2009, 336 (1-3) :64-68
[5]   Mechanism of Water Oxidation by Single-Site Ruthenium Complex Catalysts [J].
Concepcion, Javier J. ;
Tsai, Ming-Kang ;
Muckerman, James T. ;
Meyer, Thomas J. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2010, 132 (05) :1545-1557
[6]   Solar Energy Supply and Storage for the Legacy and Non legacy Worlds [J].
Cook, Timothy R. ;
Dogutan, Dilek K. ;
Reece, Steven Y. ;
Surendranath, Yogesh ;
Teets, Thomas S. ;
Nocera, Daniel G. .
CHEMICAL REVIEWS, 2010, 110 (11) :6474-6502
[7]   Water Oxidation Electrocatalyzed by an Efficient Mn3O4/CoSe2 Nanocomposite [J].
Gao, Min-Rui ;
Xu, Yun-Fei ;
Jiang, Jun ;
Zheng, Ya-Rong ;
Yu, Shu-Hong .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2012, 134 (06) :2930-2933
[8]   Efficient Water Oxidation Using Nanostructured α-Nickel-Hydroxide as an Electrocatalyst [J].
Gao, Minrui ;
Sheng, Wenchao ;
Zhuang, Zhongbin ;
Fang, Qianrong ;
Gu, Shuang ;
Jiang, Jun ;
Yan, Yushan .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2014, 136 (19) :7077-7084
[9]   A Bifunctional Nonprecious Metal Catalyst for Oxygen Reduction and Water Oxidation [J].
Gorlin, Yelena ;
Jaramillo, Thomas F. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2010, 132 (39) :13612-13614
[10]  
Hamdani M, 2010, INT J ELECTROCHEM SC, V5, P556