Controlled synthesis of CeOx-NiCo2O4 nanocomposite with 3D umbrella-shaped hierarchical structure: A sharp-tip enhanced electrocatalyst for efficient oxygen evolution reaction over a broad pH region

被引:9
|
作者
Ji, Jindong [1 ]
Xu, Jingjing [1 ]
Fan, Guoli [1 ]
Guo, Tao [2 ]
Yang, Lan [1 ]
Li, Feng [1 ,3 ]
机构
[1] Beijing Univ Chem Technol, State Key Lab Chem Resource Engn, POB 98, Beijing 100029, Peoples R China
[2] Xian Modern Chem Res Inst, State Key Lab Fluorine & Nitrogen Chem, Xian 710065, Shaanxi, Peoples R China
[3] Beijing Univ Chem Technol, Beijing Adv Innovat Ctr Soft Matter Sci & Engn, Beijing 100029, Peoples R China
基金
中国国家自然科学基金;
关键词
CeOx-NiCo2O4; nanocomposite; Umbrella-shaped hierarchical structure; Bubble adhesion force; Oxygen evolution reaction; Acid-alkali resistance; HIGHLY-EFFICIENT; DESIGNED FORMATION; WATER OXIDATION; NICO2O4; NANOSHEETS; NANOCAGES; CATALYST; BATTERY; OXIDE;
D O I
10.1016/j.electacta.2021.138345
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Simultaneously improve the activity and durability of complex metal oxides based OER electrocatalyst is crucial important for the conversion and storage of renewable energy, and is still confronted with significant challenges because of their easy dissolution and surface reconstruction in alkaline or acid electrolyte, as well as poor electrical conductivity. Herein, CeOx-NiCo2O4-U/NF electrocatalyst with umbrella-shaped hierarchical structure was synthesized through a three-step processes including the surfactant induced in-situ fabrication of umbrella-shaped nickel-cobalt complex hydroxide precursor on nickel foam, calcination treatment, and potentiostatic electro-deposition of CeOx. Owing to the co-existence of multiple redox couples, synergistic effect between active sites, enriched quantity of surface oxygen defects, multiple electron transport channels, sharp-tip effects originated from the umbrella-shaped hierarchical structure, the as-prepared CeOx-NiCo2O4-U/NF electrocatalyst exhibited advanced OER activity with a small overpotential of 219 mV at 10 mA cm(-2) and Tafel slope of 67 mV dec(-1) in 1.0 M KOH solution, and 328 mV in 0.05 M H2SO4 solution with a Tafel slope of 96 mV dec(-1), much lower than those of reported nickel- or cobalt-based OER catalyst. Moreover, due to the in-situ fabrication strategy and excellent acid-alkali resistance of NiCo2O4 and CeOx components, the as-prepared CeOx-NiCo2O4-U/NF electrocatalyst exhibited long-term structure and chemical stability over a broad pH region. Furthermore, the synthetic strategy presented here offers a new method for the rational design and synthesis of complex metal oxides based electrocatalyst for energy conversion and storage applications with excellent catalytic performance and long-term stability. (C) 2021 Elsevier Ltd. All rights reserved.
引用
收藏
页数:10
相关论文
共 4 条
  • [1] Hierarchical Ni3S2 nanosheets coated on Co3O4 nanoneedle arrays on 3D nickel foam as an efficient electrocatalyst for the oxygen evolution reaction
    Gong, Yaqiong
    Xu, Zhoufeng
    Pan, Hailong
    Lin, Yu
    Yang, Zhi
    Du, Xiaoqiang
    JOURNAL OF MATERIALS CHEMISTRY A, 2018, 6 (12) : 5098 - 5106
  • [2] In-situ transformation of Co(OH)2 into NH4CoPO4·H2O on Co foil: 3D self-supported electrocatalyst with asymmetric local atomic and electronic structure for enhanced oxygen evolution reaction
    Quande Che
    Xiaobin Xie
    Qian Ma
    Junpeng Wang
    Yuanna Zhu
    Ruixia Shi
    Ping Yang
    Journal of Energy Chemistry, 2020, 51 (12) : 167 - 174
  • [3] In-situ transformation of Co(OH)2 into NH4CoPO4•H2O on Co foil: 3D self-supported electrocatalyst with asymmetric local atomic and electronic structure for enhanced oxygen evolution reaction
    Che, Quande
    Xie, Xiaobin
    Ma, Qian
    Wang, Junpeng
    Zhu, Yuanna
    Shi, Ruixia
    Yang, Ping
    JOURNAL OF ENERGY CHEMISTRY, 2020, 51 : 167 - 174
  • [4] In-situ transformation of Co(OH)2 into NH4CoPO4•H2O on Co foil: 3D self-supported electrocatalyst with asymmetric local atomic and electronic structure for enhanced oxygen evolution reaction
    Che, Quande
    Xie, Xiaobin
    Ma, Qian
    Wang, Junpeng
    Zhu, Yuanna
    Shi, Ruixia
    Yang, Ping
    Che, Quande (mse_cheqd@ujn.edu.cn), 1600, Elsevier B.V., Netherlands (51): : 167 - 174