Surface amending effect of N-doped carbon-embedded NiO films for multirole electrochromic energy-storage devices

被引:38
作者
Kim, Kue-Ho [1 ]
Jeong, Seock-Joon [1 ]
Koo, Bon-Ryul [2 ]
Ahn, Hyo-Jin [1 ,2 ]
机构
[1] Seoul Natl Univ Sci & Technol, Dept Mat Sci & Engn, Seoul 01811, South Korea
[2] Seoul Natl Univ Sci & Technol, Program Mat Sci & Engn, Convergence Inst Biomed Engn & Biomat, Seoul 01811, South Korea
基金
新加坡国家研究基金会;
关键词
Nickel oxide films; Multirole electrodes; N-doped carbon; Electrical properties; Sol-gel method; THIN-FILMS; OPTICAL-PROPERTIES; SMART WINDOWS; QUANTUM DOTS; NICKEL-OXIDE; WO3; FILMS; GENERATION; PERFORMANCE; ARRAYS; SIZE;
D O I
10.1016/j.apsusc.2020.147902
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
We synthesize N-doped carbon-embedded porous NiO electrodes using an amide-condensation reaction assisted sol-gel method for multirole electrochromic (EC) energy-storage devices. By adjusting the amount of oleylamine added to the sol solution, we simultaneously developed N-doped carbon-embedded NiO films with an optimized surface pore structure. NiO films fabricated using 2.5 wt% oleylamine (2.5OL-NiO) exhibited superior EC energy-storage performance outcomes, specifically with regard to the switching speed (coloration speed of 3.2 s and bleaching speed of 2.7 s), coloration efficiency (CE) value (48.5 cm(2)/C), and the specific capacitance (235.8 F/g at a current density of 2 A/g). These attractive EC energy-storage performance outcomes are primarily due to the enhanced electrochemical activity with the optimized surface pore structure. This porous film morphology was developed using evaporated H2O molecules generated from an amide condensation reaction. A second cause was the improved electrical conductivity due to the highly conductive N-doped carbon formed by means of multimeric amide condensation, which provides preferred electron pathways. Accordingly, we believe that our results present a promising electrode design strategy by which to realize multirole EC energy-storage devices.
引用
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页数:8
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