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Experimental insights and DFT analysis of metal-free DNA nanocatalyst with enhanced hydrogen evolution via phosphate-mediated proton acceptance

Authors
SATHISH, PANNEER SELVAMKamalakannan, ShanmugasundaramMaiyelvaganan, K. RudharachariPrakash, MuthuramalingamGopi, SivalingamMahajan, HansaYun, KyusikCho, Sungbo
Issue Date
Jan-2024
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Keywords
DNA; Theobroma cacao; Density functional theory; Proton acceptor
Citation
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, v.51, pp 1558 - 1576
Pages
19
Journal Title
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume
51
Start Page
1558
End Page
1576
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/90246
DOI
10.1016/j.ijhydene.2023.09.254
ISSN
0360-3199
1879-3487
Abstract
Although platinum is widely recognized as a benchmark catalyst for realizing highly efficient hydrogen evolution reactions, its practical application is hindered by the scarcity and high cost of Pt. In this regard, metal-free organic catalysts are considered vital alternatives for producing H2 in green energy applications. In this study, we prepare binder-free electrocatalysts by combining salmon DNA with activated carbon (AC) (cacao pods) for H2 production. The AC-DNA (0.025 M DNA) sample requires an overpotential (h) of 106 mV to generate a current density of 10 mA cm-2, with a Tafel slope of 96 mV dec-1, in 0.5 M H2SO4. The phosphate-mediated proton acceptance of DNA facilitates the hydrogen evolution reaction (HER) in the presence of AC, resulting in excellent durability over 40 h at 10 mA cm-2 (h10 = 106 mV) and 100 mA cm-2 (h100 = 271 mV). In addition, the electro-catalyst exhibits a faradaic efficiency of 96.9%. The proton acceptance facilitated by the phosphate group in DNA achieves outstanding performance with a turnover frequency of 2.76 s-1 and an exchange current density of 2.08 x 10-3 A cm-2. Theoretical calculations support the in-depth H2 evolution mechanism at the DNA-anchored AC samples via proton capturing of phosphate groups during water splitting.(c) 2023 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
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