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Unique production strategy of Pt/C electrocatalysts via pulsed laser for hydrogen generation: Insights screening by DFT calculations

Authors
Jeong, YujeongTheerthagiri, JayaramanLee, Seung JunChitumalla, Ramesh KumarMoon, Cheol JooMin, AhreumKheawhom, SoorathepJang, JoonkyungChoi, Myong Yong
Issue Date
Jun-2024
Publisher
Elsevier Ltd
Keywords
DFT calculations; Electrocatalysis; Hydrogen production; Pt/C nanoarchitectures; Pulsed laser ablation in liquid
Citation
Electrochimica Acta, v.488
Indexed
SCIE
SCOPUS
Journal Title
Electrochimica Acta
Volume
488
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/70267
DOI
10.1016/j.electacta.2024.144218
ISSN
0013-4686
1873-3859
Abstract
Design and optimizing the components and structure of highly-active electrocatalysts is a prevalent approach for reducing the input electrical energy consumption and concurrently H2 fuel production. An efficient and sustainable method is a water-electrolyzer for H2 generation, but still restricted by the stable electrode materials. In this study, a green chemistry approach for one-pot production of Pt/C nanospherical with controllable ratios of Pt and C was demonstrated using simple pulsed laser ablation in liquid (PLAL) process, during which Pt target ablation in diverse solvents (water, methanol, ethanol, and 1-propanol) without external carbon source and reducing/capping agents. The carbon-rich solvents are acted as both C-source and solvent, which are decomposed during the PLAL process, producing C, H, and OH ions inside the cavitation bubble which condenses as C-shells on the Pt surface. The optimal Pt/C proportions have the highest electrochemical H2-evolution in acidic media with an overpotential of 59 mV at 10 mA/cm2, Tafel slope of 41 mV/dec, and j0 of 0.686 mA/cm2. The exceptional electrocatalytic concert of optimal Pt/C was further supported by the density functional theory. Optimized C-content in Pt/C reveals good dispersion and strong interaction of C with Pt can make efficient electron transfer, structural stability, and electrochemical durability, resulting in superior electrocatalytic performance in electrolyzer devices. © 2024 Elsevier Ltd
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