Cobalt (II) phthalocyanine derived Co3O4@HCNFs as highly effective bifunctional electrocatalysts for iodide redox couple reduction (IRR) and oxygen reduction reaction (ORR)

Developing low-cost electrocatalysts for iodide redox couple reduction (IRR) and oxygen reduction reaction (ORR), applied in dye-sensitized solar cells (DSCs) and Zinc-air batteries (ZABs) is of crucial significance for the fields of energy conversion and energy storage. Herein, nitrogen-enriched hollow carbon nanofibers with opens at both ends (HCNFs) are first synthesized, which show decent catalytic activity for the IRR, and a power conversion efficiency (PCE) of 6.95 % is achieved by the corresponding DSCs. Cobalt (II) phthalocyanine derived Co 3 O 4 incorporated HCNFs (Co 3 O 4 @HCNFs) are further prepared to improve the catalytic activity, generating a high PCE of 8.36 %, indicating a photovoltaic enhancement of 20.3 % as compared with HCNFs. Similarly, Co 3 O 4 @HCNFs also exhibit excellent ORR performance, and the half-wave potential (E 1/2 ) is up to 0.827 V, with the limiting current density (J lim ) improved to 4.54 mA·cm −2 . In contrast, the E 1/2 and J lim of the pristine HCNFs are 0.630 V and 3.99 mA·cm −2 , respectively, much lower than those of Co 3 O 4 @HCNFs. The remarkable catalytic activity of Co 3 O 4 @HCNFs can be ascribed the introduced Co 3 O 4 , resulting in additional active sites of Co-N-C, and the synergistic effects between metals and carbon also accounts for the enhanced catalytic activity. Moreover, the specific hollow structure with opens at both ends is beneficial for mass diffusion to ensure sufficient contact between the electrolyte and the electrocatalysts, which is also a possible reason for the high catalytic activity of Co 3 O 4 @HCNFs. This work is expected to provide a feasible strategy for exploring low-cost and highly effective bifunctional IRR/ORR electrocatalysts for DSCs and ZABs. • Co 3 O 4 @HCNFs with opens at both ends are synthesized as catalysts for IRR and ORR. • The DSCs with Co 3 O 4 @HCNFs showed a PCE of 8.36 %, indicating an enhancement of 20.3 %. • Co 3 O 4 @HCNFs also exhibit excellent ORR performance compared with the pristine HCNFs.

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Journal
Next Materials
Published
2025-02-05
DOI
https://doi.org/10.1016/j.nxmate.2025.100518
Primary Topic
Electrochemical Analysis and Applications
Type
article
Field-Weighted Citation Impact
0.00

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article

Cobalt (II) phthalocyanine derived Co3O4@HCNFs as highly effective bifunctional electrocatalysts for iodide redox couple reduction (IRR) and oxygen reduction reaction (ORR)

Mingxing Wu, Jianing Guo, Wenyu Gong, Ziyu Guo
1 links
Next Materials
Electrochemical Analysis and Applications
article

Cobalt (II) phthalocyanine derived Co3O4@HCNFs as highly effective bifunctional electrocatalysts for iodide redox couple reduction (IRR) and oxygen reduction reaction (ORR)

Mingxing Wu, Jianing Guo, Wenyu Gong, Ziyu Guo
article en

Abstract

Developing low-cost electrocatalysts for iodide redox couple reduction (IRR) and oxygen reduction reaction (ORR), applied in dye-sensitized solar cells (DSCs) and Zinc-air batteries (ZABs) is of crucial significance for the fields of energy conversion and energy storage. Herein, nitrogen-enriched hollow carbon nanofibers with opens at both ends (HCNFs) are first synthesized, which show decent catalytic activity for the IRR, and a power conversion efficiency (PCE) of 6.95 % is achieved by the corresponding DSCs. Cobalt (II) phthalocyanine derived Co 3 O 4 incorporated HCNFs (Co 3 O 4 @HCNFs) are further prepared to improve the catalytic activity, generating a high PCE of 8.36 %, indicating a photovoltaic enhancement of 20.3 % as compared with HCNFs. Similarly, Co 3 O 4 @HCNFs also exhibit excellent ORR performance, and the half-wave potential (E 1/2 ) is up to 0.827 V, with the limiting current density (J lim ) improved to 4.54 mA·cm −2 . In contrast, the E 1/2 and J lim of the pristine HCNFs are 0.630 V and 3.99 mA·cm −2 , respectively, much lower than those of Co 3 O 4 @HCNFs. The remarkable catalytic activity of Co 3 O 4 @HCNFs can be ascribed the introduced Co 3 O 4 , resulting in additional active sites of Co-N-C, and the synergistic effects between metals and carbon also accounts for the enhanced catalytic activity. Moreover, the specific hollow structure with opens at both ends is beneficial for mass diffusion to ensure sufficient contact between the electrolyte and the electrocatalysts, which is also a possible reason for the high catalytic activity of Co 3 O 4 @HCNFs. This work is expected to provide a feasible strategy for exploring low-cost and highly effective bifunctional IRR/ORR electrocatalysts for DSCs and ZABs. • Co 3 O 4 @HCNFs with opens at both ends are synthesized as catalysts for IRR and ORR. • The DSCs with Co 3 O 4 @HCNFs showed a PCE of 8.36 %, indicating an enhancement of 20.3 %. • Co 3 O 4 @HCNFs also exhibit excellent ORR performance compared with the pristine HCNFs.

Next MaterialsVol. 7
Hebei Normal University (CN)
National Natural Science Foundation of China, Natural Science Foundation of Hebei Province
Clean water and sanitation
Openalex Percentile: Top 98%
Electrochemical Analysis and Applications
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