Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/8797
Title: Electrodeposited Organic-Inorganic Nanohybrid as Robust Bifunctional Electrocatalyst for Water Splitting
Authors: Jadhav, Rohit G.
Singh, Devraj
Das, Apurba Kumar
Issue Date: 2020
Publisher: American Chemical Society
Citation: Jadhav, R. G., Singh, D., Krivoshapkin, P. V., & Das, A. K. (2020). Electrodeposited organic-inorganic nanohybrid as robust bifunctional electrocatalyst for water splitting. Inorganic Chemistry, 59(11), 7469-7478. doi:10.1021/acs.inorgchem.0c00227
Abstract: Rational engineering of novel nanohybrid materials for sustainable and efficient energy conversion has gained extensive research interest. Cross-linked nanosheets of organic-inorganic nanohybrids (BSeF/Ni(OH)2) were fabricated by one-step reductive electrosynthesis and subsequently applied for electrocatalytic water electrolysis. The organic-inorganic nanohybrids consist of benzo[2,1,3]selenadiazole-5-carbonyl phenylalanine (BSeF) cross-linked with nickel ions (Ni-BSeF) and nickel hydroxides (Ni(OH)2), which provide abundant active sites and feasible charge transfer at the electrocatalytic interface. The resulting electrodeposited nanohybrid BSeF/Ni(OH)2 exhibits bifunctional electrocatalytic performance with 240 and 401 mV of overpotential at +100 and -100 mA cm-2 for oxygen evolution reaction (OER) and hydrogen evolution reaction (HER), respectively. The BSeF/Ni(OH)2 offers a longer electrocatalytic activity of 20 h for OER and HER at applied high current densities of +400 and -200 mA cm-2. Coupled with the high OER and HER activity, the two-electrode-based system of BSeF/Ni(OH)2 shows a low cell potential of 1.54 V at 10 mA cm-2. The electrocatalytic performance of Ni-BSeF and Ni(OH)2-based organic-inorganic nanohybrids provides an efficient way to develop a nanohybrid-based catalytic system for energy conversion. © 2020 American Chemical Society.
URI: https://doi.org/10.1021/acs.inorgchem.0c00227
https://dspace.iiti.ac.in/handle/123456789/8797
ISSN: 0020-1669
Type of Material: Journal Article
Appears in Collections:Department of Chemistry

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