共 44 条
Uniformly mesoporous NiO/NiFe2O4 biphasic nanorods as efficient oxygen evolving catalyst for water splitting
被引:126
作者:

Liu, Guang
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Taiyuan Univ Technol, Res Inst Special Chem, Taiyuan 030024, Shanxi, Peoples R China
Nankai Univ, Key Lab Adv Energy Mat Chem MOE, Tianjin 300071, Peoples R China Taiyuan Univ Technol, Res Inst Special Chem, Taiyuan 030024, Shanxi, Peoples R China

Gao, Xusheng
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Taiyuan Univ Technol, Res Inst Special Chem, Taiyuan 030024, Shanxi, Peoples R China Taiyuan Univ Technol, Res Inst Special Chem, Taiyuan 030024, Shanxi, Peoples R China

Wang, Kaifang
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Taiyuan Univ Technol, Res Inst Special Chem, Taiyuan 030024, Shanxi, Peoples R China Taiyuan Univ Technol, Res Inst Special Chem, Taiyuan 030024, Shanxi, Peoples R China

He, Dongying
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Taiyuan Univ Technol, Res Inst Special Chem, Taiyuan 030024, Shanxi, Peoples R China Taiyuan Univ Technol, Res Inst Special Chem, Taiyuan 030024, Shanxi, Peoples R China

Li, Jinping
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Taiyuan Univ Technol, Res Inst Special Chem, Taiyuan 030024, Shanxi, Peoples R China Taiyuan Univ Technol, Res Inst Special Chem, Taiyuan 030024, Shanxi, Peoples R China
机构:
[1] Taiyuan Univ Technol, Res Inst Special Chem, Taiyuan 030024, Shanxi, Peoples R China
[2] Nankai Univ, Key Lab Adv Energy Mat Chem MOE, Tianjin 300071, Peoples R China
关键词:
Water splitting;
Oxygen evolving;
Electrocatalyst;
NiO/NiFe2O4;
Mesoporous;
IN-SITU;
EVOLUTION CATALYST;
ELECTROCATALYSTS;
OXIDATION;
NANOSHEETS;
HYDROXIDE;
FILM;
PHOSPHATE;
D O I:
10.1016/j.ijhydene.2016.07.268
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:
Development of efficient, stable and earth-abundant metal oxide electrocatalysts is crucial to improve the efficacy of water electrolysis for harvest and storage solar energy. In this work, we report the synthesis, structural characterization and electrocatalytic water oxidation performances of mesoporous NiO/NiFe2O4 nanorods. It is found that different calcination temperature of NiFe-based coordination polymer leads to various structural composites and completely preserves the original nanorod-like morphology of coordination polymer precursor. The nanorods obtained at 350 degrees C identified as NiO/NiFe2O4 have the largest surface area of 191.5 m(2) g(-1) with an average pore size of 6.4 nm. When used as oxygen evolving catalyst in water splitting, NiO/NiFe2O4 nanorods are found to exhibit the highest electrocatalytic water oxidation activity in basic media compared to the composites obtained at other temperatures, even much better than those of individual NiO or NiFe2O4 as well as commercial RuO2 and IrO2. The current density of 10 mA cm(-2) is met at an overpotential of 302 mV with a Tafel slope of 42 mV dec(-1). The excellent electrocatalytic performance could be attributed to the synergetic benefits of biphasic NiO/NiFe2O4 mesoporous structure and large surface area, which offer pathways for easy accessibility of electrolytes and fast mass/charge transportation. (C) 2016 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
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页码:17976 / 17986
页数:11
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Univ Delaware, Ctr Catalyt Sci & Technol, Dept Chem & Biomol Engn, Newark, DE 19716 USA Univ Delaware, Ctr Catalyt Sci & Technol, Dept Chem & Biomol Engn, Newark, DE 19716 USA

Gu, Shuang
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Univ Delaware, Ctr Catalyt Sci & Technol, Dept Chem & Biomol Engn, Newark, DE 19716 USA Univ Delaware, Ctr Catalyt Sci & Technol, Dept Chem & Biomol Engn, Newark, DE 19716 USA

Jiang, Jun
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Univ Delaware, Ctr Catalyt Sci & Technol, Dept Chem & Biomol Engn, Newark, DE 19716 USA Univ Delaware, Ctr Catalyt Sci & Technol, Dept Chem & Biomol Engn, Newark, DE 19716 USA

Yan, Yushan
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Univ Delaware, Ctr Catalyt Sci & Technol, Dept Chem & Biomol Engn, Newark, DE 19716 USA Univ Delaware, Ctr Catalyt Sci & Technol, Dept Chem & Biomol Engn, Newark, DE 19716 USA
[10]
A mini review of NiFe-based materials as highly active oxygen evolution reaction electrocatalysts
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Gong, Ming
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Dai, Hongjie
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NANO RESEARCH,
2015, 8 (01)
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Gong, Ming
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Stanford Univ, Dept Chem, Stanford, CA 94305 USA Stanford Univ, Dept Chem, Stanford, CA 94305 USA

Dai, Hongjie
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Stanford Univ, Dept Chem, Stanford, CA 94305 USA Stanford Univ, Dept Chem, Stanford, CA 94305 USA