Vanadium Redox Flow Battery Using Electrocatalyst Decorated with Nitrogen-Doped Carbon Nanotubes Derived from Metal-Organic Frameworks

流动电池 碳纳米管 材料科学 氧化还原 化学工程 X射线光电子能谱 催化作用 电催化剂 无机化学 化学 电化学 纳米技术 电极 有机化学 冶金 物理化学 工程类 电解质
作者
Chanho Noh,Chang‐Soo Lee,Won Seok,Yongjin Chung,Jong Hak Kim,Yongchai Kwon
出处
期刊:Journal of The Electrochemical Society [The Electrochemical Society]
卷期号:165 (7): A1388-A1399 被引量:60
标识
DOI:10.1149/2.0621807jes
摘要

Highly porous zeolitic-imidazole frameworks (ZIFs) are synthesized to produce N-doped mesoporous carbon electrocatalysts via calcination. The N-doped carbon (m-NC) and carbon nanotubes (m-NCNT) are obtained from ZIF-8 and ZIF-67, while the core-shell structure of ZIF-8@ZIF-67 produced with ZIF-8 seeds (m-NC@NCNT) is prepared by hydrothermal method. Chemical and optical evaluations of the catalysts are characterized using BET, FT-IR, XPS, XRD, Raman spectroscopy and SEM/STEM and they are used as the catalysts for redox reactions of vanadium ions and redox flow battery (VRFB) performance. In the utilization, m-NC@NCNT and m-NCNT are effective for improving VO2+/VO2+ redox reaction, although m-NC does not influence that. Even in VRFB tests using the catalysts, charge/discharge potential and energy efficiency (EE) of m-NC@NCNT and m-NCNT are highest, not to mention excellent EE resilience after undergoing tougher cycling condition. These results are due to the large graphitic-N portion of the two catalysts. Namely, electrons produced by the graphitic-N are delocalized, forming pi-conjugated system and vanadium–nitrogen transition state. This state then promotes electron transfer during VO2+/VO2+ redox reaction and VRFB performance.
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