Dual-laser pulse-patterned α-Co(OH)2/rGO heterointerface for accelerated water oxidation and surface phase-transition via in-situ Raman spectroscopyopen access
- Authors
- Lee, Yeryeong; Theerthagiri, Jayaraman; Min, Ahreum; Moon, Cheol Joo; Choi, Myong Yong
- Issue Date
- Dec-2023
- Publisher
- John Wiley and Sons Inc
- Keywords
- dual-laser pulses; in situ electrochemical–Raman probes; oxygen evolution reaction; pulsed laser irradiation in liquids; α-Co(OH)<sub>2</sub>/rGO
- Citation
- EcoMat, v.5, no.12
- Indexed
- SCIE
SCOPUS
- Journal Title
- EcoMat
- Volume
- 5
- Number
- 12
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/68052
- DOI
- 10.1002/eom2.12417
- ISSN
- 2567-3173
2567-3173
- Abstract
- The dynamic surface reconstruction of electrodes is a legible sign to understand the deep phase-transition mechanistic and electrocatalytic origin during the oxygen evolution reaction (OER). Herein, we report a dual-laser pulse-patterned heterointerface of α-Co(OH)2 and reduced graphene oxide (rGO) nanosheets via pulsed laser irradiation in liquid (PLIL) to accelerate OER kinetics. α-Co(OH)2 was formed from the OH− ions generated during the PLIL of GO at neutral pH. Co2+ modulation in tetrahedral coordination sites benefits as an electrophilic surface for water oxidation. Few d-vacancies in Co2+ increase its affinity toward oxygen, lowering the energy barrier and generating many CoOOH and CoO2 active sites. rGO with an ordered π-conjugated system aids the surface adsorption of OOH*, O*, and OH* during OER. α-Co(OH)2 surface phase-transition and OER mechanistic steps occurred via phase-reconstruction to CoOOH and CoO2 reactive intermediates, uncovered using in situ electrochemical–Raman spectroscopy. Our findings in the dual-laser pulse strategy and the surface reconstruction correlation in active OER catalysts pave the path for paramount in multiple energy technologies. (Figure presented.). © 2023 The Authors. EcoMat published by The Hong Kong Polytechnic University and John Wiley & Sons Australia, Ltd.
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