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Open AccessDOI: 10.1016/S1872-5805(NCM2024-39-03-08)Original Research

Controllable construction of CoP nanoparticles anchored on a nitrogen-doped porous carbon as an electrocatalyst for highly efficient oxygen reduction in Zn-air batteries

YAN Xiao-li¹,WANG Kui¹,HAO Shu-wei¹,ZHOU Guang-da¹,YANG Hao-wei¹,ZHANG Hua¹,GUO Jun-jie¹

Key Laboratory of Interface Science and Engineering in Advanced Materials, Ministry of Education, College of Materials Science and Engineering, Taiyuan University of Technology, Taiyuan 030024, China

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Academic Research Journal
Published:January 15, 2025Edition:Vol 40, Issue 1 • pp. 100-112Citation:YAN Xiao-li et al. (2025), Academic Research Journal
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Key Takeaways & Executive Findings

  • • CoP nanoparticles anchored on nitrogen-doped porous carbon (CoP@NC) were synthesized via phosphating, retaining the dodecahedral structure of Co NPs. • The CoP@NC electrocatalyst exhibits remarkable ORR activity with a half-wave potential of 0.92 V in alkaline media. • Zinc-air batteries using CoP@NC as cathode achieve a high open-circuit voltage of 1.51 V and power density of 210.1 mW cm−2. • The synergistic coupling between CoP nanoparticles and nitrogen-doped carbon, along with efficient mass transport in the porous structure, enhances catalytic performance.
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Abstract

Exploring cost-efficient and highly-efficient noble metal-free catalysts for the oxygen reduction reactions (ORRs) involved in sustainable energy devices remains a great challenge. Transition-metal phosphides supported on heteroatom-doped carbons have shown potential as alternative candidates for precious metals because of their tunable electronic structures and higher catalytic performance. Phosphating was used to construct CoP nanoparticles (NPs) anchored on a nitrogen-doped porous carbon framework (CoP@NC) from Co NPs loaded on NC, using PH3 gas released from NaH2PO2 during heat treatment. The dodecahedral structure of Co NPs was retained in their transformation to CoP NPs. The CoP@NC electrocatalyst shows a remarkable ORR activity with a half-wave potential up to 0.92 V under alkaline conditions, which is attributed to the combined coupling between the well dispersed CoP nanoparticles on the nitrogen-doped carbon and the efficient mass transport in the porous structure. Zinc-air batteries assembled with the CoP@NC electrocatalyst as a cathode have a high open-circuit voltage of 1.51 V and power density of 210.1 mW cm−2. This work provides a novel strategy to develop low-cost catalysts with an excellent ORR performance to promote their practical use in metal-air batteries.

1. Introduction

The oxygen reduction reaction (ORR) is a key cathodic reaction in next-generation renewable energy conversion devices such as metal-air batteries[1–4]. However, the main challenge ORR face is lacking excellent catalysts, mainly due to the high energy barriers and sluggish kinetics caused by the four-electron/proton transfer pathway and intermediates adsorption/desorption in ORR[5–8]. Current commercially available platinum (Pt)-based catalysts hinder the large-scale and sustainable application of these devices by their low natural abundance, high-cost, and poor durability[2,9,10]. Therefore, the researchers focused their efforts on cost-effective precious-metal-free ORR catalysts to promote the commercial application of clean-energy devices [11–14].

Among various alternatives of Pt-based electrocatalysts, transition-metal phosphide (TMP) catalysts have attracted extensive interests due to their good conductivity, excellent stability, adjustable electronic structures and abundant bonding types[15–18]. Recent studies have shown that the synergy between the various active components can improve the catalytic activity of TMP catalysts[19–24]. For example, a composite of Co2P nanoparticle decorated N, P co-doped defective carbon materials (Co2P@CoNPG) exhibits excellent catalytic activity attributed to the synergistic effects of Co2P and Co-Nx active sites[25–29]. In addition, the powerful synergistic coupling between phosphides and defect-abundant carbon matrix can also enhance the catalytic activity of TMP catalysts[30]. CoP particles loaded on N, P-doped necklace-like carbon show excellent ORR activity due to the synergistic effects between CoP nanoparticles and carbon matrix[31]. Moreover, encapsulation of TMPs into carbon materials has been proved to further boost electrocatalytic activity and prevent the chemical corrosion[32–35]. Li et al. prepared a multifunctional Co-NC@CoP-NC

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Cite This Research Paper
YAN Xiao-li, WANG Kui, HAO Shu-wei, ZHOU Guang-da, YANG Hao-wei, ZHANG Hua, GUO Jun-jie (2025). Controllable construction of CoP nanoparticles anchored on a nitrogen-doped porous carbon as an electrocatalyst for highly efficient oxygen reduction in Zn-air batteries. SinoTechIntel Verified Research. https://doi.org/10.1016/S1872-5805(NCM2024-39-03-08)
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Frequently Asked Questions

What is the main innovation of this study?

The study presents a novel strategy to construct CoP nanoparticles anchored on nitrogen-doped porous carbon (CoP@NC) via phosphating, which retains the dodecahedral structure and achieves high ORR activity and battery performance.

What is the half-wave potential of the CoP@NC electrocatalyst?

The CoP@NC electrocatalyst exhibits a remarkable ORR activity with a half-wave potential up to 0.92 V under alkaline conditions.

How does the CoP@NC electrocatalyst perform in Zn-air batteries?

Zinc-air batteries assembled with CoP@NC as cathode show a high open-circuit voltage of 1.51 V and a power density of 210.1 mW cm−2.

What are the key factors contributing to the high catalytic performance?

The high performance is attributed to the combined coupling between well-dispersed CoP nanoparticles on nitrogen-doped carbon and efficient mass transport in the porous structure.

Why are transition-metal phosphides considered as alternatives to Pt-based catalysts?

Transition-metal phosphides offer good conductivity, excellent stability, adjustable electronic structures, and abundant bonding types, making them cost-effective and highly efficient alternatives to precious metals.

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