TY - JOUR
T1 - Vanadium redox flow battery using electrocatalyst decorated with nitrogen-doped carbon nanotubes derived from metal-organic frameworks
AU - Noh, Chanho
AU - Lee, Chang Soo
AU - Chi, Won Seok
AU - Chung, Yongjin
AU - Kim, Jong Hak
AU - Kwon, Yongchai
N1 - Publisher Copyright:
© 2018 The Electrochemical Society.
PY - 2018
Y1 - 2018
N2 - 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 VO 2+ /VO 2 + 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 VO 2+ /VO 2 + redox reaction and VRFB performance.
AB - 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 VO 2+ /VO 2 + 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 VO 2+ /VO 2 + redox reaction and VRFB performance.
UR - http://www.scopus.com/inward/record.url?scp=85057651560&partnerID=8YFLogxK
U2 - 10.1149/2.0621807jes
DO - 10.1149/2.0621807jes
M3 - Article
AN - SCOPUS:85057651560
SN - 0013-4651
VL - 165
SP - A1388-A1399
JO - Journal of the Electrochemical Society
JF - Journal of the Electrochemical Society
IS - 7
ER -