3D Core-Shell NiFeCr Catalyst on a Cu Nanoarray for Water Oxidation: Synergy between Structural and Electronic Modulation

被引:111
作者
Fan, Lizhou [1 ]
Zhang, Peili [2 ,3 ]
Zhang, Biaobiao [1 ]
Daniel, Quentin [1 ]
Timmer, Brian J. J. [1 ]
Zhang, Fuguo [1 ]
Sun, Licheng [1 ,2 ,3 ]
机构
[1] KTH Royal Inst Technol, Dept Chem, S-10044 Stockholm, Sweden
[2] DUT, DUT KTH Joint Educ, Inst Artificial Photosynth, State Key Lab Fine Chem, Dalian 116024, Peoples R China
[3] DUT, Res Ctr Mol Devices, Dalian 116024, Peoples R China
基金
瑞典研究理事会; 中国国家自然科学基金;
关键词
DOUBLE-HYDROXIDE NANOSHEETS; EFFICIENT OXYGEN-EVOLUTION; HIGH-PERFORMANCE; REACTION DYNAMICS; REDOX STATES; ANATASE TIO2; ELECTROCATALYSTS; NANOTUBES; ALKALINE;
D O I
10.1021/acsenergylett.8b01897
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
Low cost transition metal-based electrocatalysts for water oxidation and understanding their structure-activity relationship are greatly desired for clean and sustainable chemical fuel production. Herein, a core-shell (CS) NiFeCr metal/metal hydroxide catalyst was fabricated on a 3D Cu nanoarray by a simple electrodeposition-activation method. A synergistic promotion effect between electronic structure modulation and nanostructure regulation was presented on a CS-NiFeCr oxygen evolution reaction (OER) catalyst: the 3D nanoarchitecture facilitates the mass transport process, the in situ formed interface metal/metal hydroxide heterojunction accelerates the electron transfer, and the electronic structure modulation by Cr incorporation improves the reaction kinetics. Benefiting from the synergy between structural and electronic modulation, the catalyst shows excellent activity toward water oxidation under alkaline conditions: overpotential of 200 mV at 10 mA/cm(2) current density and Tafel slope of 28 mV/dec. This work opens up a new window for understanding the structure-activity relationship of OER catalysts and encourages new strategies for development of more advanced OER catalysts.
引用
收藏
页码:2865 / 2874
页数:19
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