TY - JOUR
T1 - Electrospun cobalt-ZIF micro-fibers for efficient water oxidation under unique pH conditions
AU - Sankar, S. Sam
AU - Ede, Sivasankara Rao
AU - Anantharaj, S.
AU - Karthick, K.
AU - Sangeetha, K.
AU - Kundu, Subrata
N1 - Funding Information:
All the authors wish to acknowledge the Director, CSIR-CECRI, for his continuous support and encouragement. S. S. S. and K. K. wish to acknowledge UGC for Junior Research Fellowship (JRF) and Senior Research Fellowship (SRF) awards, respectively, and S. A. and S. R. Ede for the award of SRF from the CSIR and K. S. for DST Inspire Fellowship, respectively. S. Kundu wishes to acknowledge the Department of Science and Technology (DST) for EMR research funding of number # EMR/2017/000860 on 11th May 2018 with institute OM number 18-29-03/ (27/2018)–TTBD-CSIR-CECRI on 29/10/ 2018. The contributions from the Central Instrumentation Facility (CIF) are greatly appreciated.
Publisher Copyright:
© 2019 The Royal Society of Chemistry.
PY - 2019
Y1 - 2019
N2 - One dimensional (1D) materials are highly desirable in current platforms of materials chemistry owing to their unique physico-chemical properties. Herein, we report an effective way to synthesize 1D Co-ZIF microfibers using an electrospinning method, where a zeolitic imidazole framework (ZIF) with CoCl 2 ·6H 2 O was prepared as the precursor for electrospinning. The synthesized microfibers were labeled after their post-spinning processing temperature as Co-ZIF-RT (without annealing), Co-ZIF-350 (annealed at 350 °C in air and a N 2 atmosphere) and Co-ZIF-550 (annealed at 550 °C in air and a N 2 atmosphere). All five microfibers were evaluated for the first time in electrocatalytic oxygen evolution reaction (OER) studies both in 0.5 M H 2 SO 4 and 1 M KOH electrolytes. For the OER in 0.5 M H 2 SO 4 , Co-ZIF-550-N 2 delivered a superior activity and required an overpotential of 405 mV at a current density of 10 mA cm -2 with a Tafel slope value of 281 mV dec -1 . For the OER in 1 M KOH, Co-ZIF-350-air gave better activity and required an overpotential of 370 mV and a lower Tafel slope value of 55 mV dec -1 . Fabricated materials showing promising activity for the OER both in acid and alkali implied that they can be adapted as a cost-efficient, cheaper alternative to commercially available IrO 2 /C electrocatalysts. Moreover, in the future, the same synthetic protocol can be easily extended to the fabrication of other active metals incorporating ZIFs and the zeolite derived networks can also be utilized for other energy related applications.
AB - One dimensional (1D) materials are highly desirable in current platforms of materials chemistry owing to their unique physico-chemical properties. Herein, we report an effective way to synthesize 1D Co-ZIF microfibers using an electrospinning method, where a zeolitic imidazole framework (ZIF) with CoCl 2 ·6H 2 O was prepared as the precursor for electrospinning. The synthesized microfibers were labeled after their post-spinning processing temperature as Co-ZIF-RT (without annealing), Co-ZIF-350 (annealed at 350 °C in air and a N 2 atmosphere) and Co-ZIF-550 (annealed at 550 °C in air and a N 2 atmosphere). All five microfibers were evaluated for the first time in electrocatalytic oxygen evolution reaction (OER) studies both in 0.5 M H 2 SO 4 and 1 M KOH electrolytes. For the OER in 0.5 M H 2 SO 4 , Co-ZIF-550-N 2 delivered a superior activity and required an overpotential of 405 mV at a current density of 10 mA cm -2 with a Tafel slope value of 281 mV dec -1 . For the OER in 1 M KOH, Co-ZIF-350-air gave better activity and required an overpotential of 370 mV and a lower Tafel slope value of 55 mV dec -1 . Fabricated materials showing promising activity for the OER both in acid and alkali implied that they can be adapted as a cost-efficient, cheaper alternative to commercially available IrO 2 /C electrocatalysts. Moreover, in the future, the same synthetic protocol can be easily extended to the fabrication of other active metals incorporating ZIFs and the zeolite derived networks can also be utilized for other energy related applications.
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U2 - 10.1039/c8cy02620c
DO - 10.1039/c8cy02620c
M3 - Article
AN - SCOPUS:85064711580
SN - 2044-4753
VL - 9
SP - 1847
EP - 1856
JO - Catalysis Science and Technology
JF - Catalysis Science and Technology
IS - 8
ER -