TY - JOUR
T1 - Zinc-Based Metal–Organic Frameworks for High-Performance Supercapacitor Electrodes
T2 - Mechanism Underlying Pore Generation
AU - Umezawa, Shigeyuki
AU - Douura, Takashi
AU - Yoshikawa, Koji
AU - Tanaka, Daisuke
AU - Stolojan, Vlad
AU - Silva, S. Ravi P.
AU - Yoneda, Mika
AU - Gotoh, Kazuma
AU - Hayashi, Yasuhiko
N1 - Funding Information:
This work was partially supported by a Grant‐in‐Aid for Scientific Research (KAKENHI) from the Japan Society for the Promotion of Science (JSPS) (grant number 19H05332). The authors acknowledge Prof. Soshi Shiraishi at Gunma University for comprehensive support; Mr. Kohei Komatsubara at Okayama University for experimental support and literature research; Mr. Shota Takamiya, Mr. Shinya Sakane, and Mr. Takumi Fujita at Seiwa Electric Mfg. Co. Ltd., for experimental support; and Dr. Takashi Nishimura at Osaka Research Institute of Industrial Science and Technology (ORIST) for experimental support. We would like to thank Editage ( https://www.editage.com/ ) and Enago ( https://www.enago.com/ ) for their English language editing services.
Publisher Copyright:
© 2022 Zhengzhou University.
PY - 2022
Y1 - 2022
N2 - Heat treatment of metal–organic frameworks (MOFs) has provided a wide variety of functional carbons coordinated with metal compounds. In this study, two kinds of zinc-based MOF (ZMOF), C16H10O4Zn (ZMOF1) and C8H4O4Zn (ZMOF2), were prepared. ZMOF1 and ZMOF2 were carbonized at 1000 °C, forming CZMOF1 and CZMOF2, respectively. The specific surface area (SBET) of CZMOF2 was ~2700 m2 g−1, much higher than that of CZMOF1 (~1300 m2 g−1). A supercapacitor electrode based on CZMOF2 achieved specific capacitances of 360, 278, and 221 F g−1 at 50, 250, and 1000 mA g−1 in an aqueous electrolyte (H2SO4), respectively, the highest values reported to date for ZMOF-derived electrodes under identical conditions. The practical applicability of the CZMOF-based supercapacitor was verified in non-aqueous electrolytes. The initial capacitance retention was 78% after 100 000 charge/discharge cycles at 10 A g−1. Crucially, the high capacitance of CZMOF2 arises from pore generation during carbonization. Below 1000 °C, pore generation is dominated by the Zn/C ratio of ZMOFs, as carbon atoms reduce the zinc oxides formed during carbonization. Above 1000 °C, a high O/C ratio becomes essential for pore generation because the oxygen functional groups are pyrolyzed. These findings will provide insightful information for other metal-based MOF-derived multifunctional carbons.
AB - Heat treatment of metal–organic frameworks (MOFs) has provided a wide variety of functional carbons coordinated with metal compounds. In this study, two kinds of zinc-based MOF (ZMOF), C16H10O4Zn (ZMOF1) and C8H4O4Zn (ZMOF2), were prepared. ZMOF1 and ZMOF2 were carbonized at 1000 °C, forming CZMOF1 and CZMOF2, respectively. The specific surface area (SBET) of CZMOF2 was ~2700 m2 g−1, much higher than that of CZMOF1 (~1300 m2 g−1). A supercapacitor electrode based on CZMOF2 achieved specific capacitances of 360, 278, and 221 F g−1 at 50, 250, and 1000 mA g−1 in an aqueous electrolyte (H2SO4), respectively, the highest values reported to date for ZMOF-derived electrodes under identical conditions. The practical applicability of the CZMOF-based supercapacitor was verified in non-aqueous electrolytes. The initial capacitance retention was 78% after 100 000 charge/discharge cycles at 10 A g−1. Crucially, the high capacitance of CZMOF2 arises from pore generation during carbonization. Below 1000 °C, pore generation is dominated by the Zn/C ratio of ZMOFs, as carbon atoms reduce the zinc oxides formed during carbonization. Above 1000 °C, a high O/C ratio becomes essential for pore generation because the oxygen functional groups are pyrolyzed. These findings will provide insightful information for other metal-based MOF-derived multifunctional carbons.
KW - metal–organic frameworks
KW - pore generation
KW - porous carbons
KW - supercapacitor
KW - zinc oxides
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U2 - 10.1002/eem2.12320
DO - 10.1002/eem2.12320
M3 - Article
AN - SCOPUS:85128582541
SN - 2575-0348
JO - Energy and Environmental Materials
JF - Energy and Environmental Materials
ER -