Issue 13, 2024

Bimetallic Ni2−xCoxP carbon nanofibers network: solid–solution alloy nano-architecture as efficient electrocatalyst for water splitting

Abstract

The design of efficient and cost-effective electrocatalysts with steady capability has attracted much attention in the field of water splitting in recent years. In this paper, Ni2−xCoxP/CNFs (x = 0, 0.67, 1, 1.33 and 2), where the ultrafine Ni2−xCoxP nanoparticles are encapsulated in carbon nanofibers, are synthesized using a facile electrospinning method followed by thermal treatment. The space confinement by the carbon matrix with a high length-to-diameter ratio (>1000) and excellent conductivity produces ultrafine Ni2−xCoxP with abundant active sites. Moreover, engineering of Ni2−xCoxP/CNFs can induce electronic modulation and consequently optimize the adsorption of H on the electrocatalyst surface to promote HER performance, as well as to reduce the energy barrier of the potential-limiting step. The optimal Ni2−xCoxP/CNFs exhibit superior electrocatalytic performance with low overpotentials of about 271 mV for OER and about 118.76 mV for HER at 10 mA cm−2 with excellent long-term durability in 1.0 M KOH solutions, performing as one of the best non-noble-metal electrocatalysts so far. Furthermore, the two-electrode electrolyser delivers a high efficiency and remarkable long-term durability for overall water splitting. This work provides new insights into the development of nanofiber-structured electrocatalysts.

Graphical abstract: Bimetallic Ni2−xCoxP carbon nanofibers network: solid–solution alloy nano-architecture as efficient electrocatalyst for water splitting

Supplementary files

Article information

Article type
Paper
Submitted
08 Mar 2024
Accepted
19 May 2024
First published
21 May 2024

Green Chem., 2024,26, 7789-7798

Bimetallic Ni2−xCoxP carbon nanofibers network: solid–solution alloy nano-architecture as efficient electrocatalyst for water splitting

M. Ding, Z. Wei, W. Zhao, Q. Lu, C. Lu, M. Zhou, D. Liu and H. Yang, Green Chem., 2024, 26, 7789 DOI: 10.1039/D4GC01098A

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