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Photo-electroactive p-n heterojunction catalyst with dual Co sites for high-performance light-enhanced zinc-air batteriesopen access

Authors
Lu, TuoXu, NengnengZhou, BenjiGuo, LiyuanWen, XiaodanLou, ShuaifengLiu, GuichengYang, WoochulYang, NianjunSafari, MomoHuang, HaitaoQiao, Jinli
Issue Date
Jan-2026
Publisher
Elsevier B.V.
Keywords
Bifunctional oxygen electrode; Carbon nanofiber/carbon nitride; Dual active Co sites; Light-enhanced Zn–air battery; P-n heterojunction
Citation
eScience, v.6, no.1, pp 1 - 11
Pages
11
Indexed
SCIE
SCOPUS
Journal Title
eScience
Volume
6
Number
1
Start Page
1
End Page
11
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/62685
DOI
10.1016/j.esci.2025.100450
ISSN
2097-2431
2667-1417
Abstract
Highly electrocatalytic and durable Co-Nx-C frameworks containing carbon nanofibers (CNFs)/carbon nitrides (CNs) are vital materials for rechargeable zinc–air batteries (RZABs). However, the existing Co-Nx-C frameworks experience severe agglomeration during synthesis and limited active site accessibility/mechanical robustness. In this work, a photo-enhanced bifunctional catalyst with a type II p-n heterojunction (g–C<inf>3</inf>N<inf>4</inf>–Co@CNT/Co–N<inf>4</inf>/C@CNF) is achieved through a combined “electrospinning + calcination + ball milling” approach. The composite integrates graphitic carbon nitride (g-C<inf>3</inf>N<inf>4</inf>) nanosheets with dual active Co sites (nanoparticles and Co–N<inf>4</inf> single atoms) anchored on conductive carbon nanofibers. This architecture enables efficient charge separation, enhanced light absorption, and accelerated oxygen redox kinetics. DFT calculations reveal that g-C<inf>3</inf>N<inf>4</inf> modulates the electronic structure and lowers the reaction free-energy barriers, leading the d-band center closer to the Fermi level. Under light irradiation, the g–C<inf>3</inf>N<inf>4</inf>–Co@CNT/Co–N<inf>4</inf>/C@CNF exhibits outstanding ORR/OER catalytic performance, with a small overpotential gap of 0.684 V (E<inf>1/2</inf> = 0.930 V, E<inf>j:10</inf> = 1.614 V). In practical application: 1) light-enhanced liquid ZABs with g–C<inf>3</inf>N<inf>4</inf>–Co@CNT/Co–N<inf>4</inf>/C@CNF photoactive catalysts manifest a peak power density of 310 mW cm−2 and a long cycle life exceeding 1100 h. 2) Light-enhanced flexible ZABs also can reach a peak power density of 96 mW cm−2 and tolerate a wide range of bending angles (0°–180°–0°) during harsh operation. This work offers a new platform for designing efficient photo-electrocatalysts and advancing next-generation solar–electrochemical energy conversion systems. © 2025 The Authors.
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