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构建具有钴、磷和氮掺杂以及封装的钴/钴磷异质结的空心海胆状碳框架作为可充电锌空气电池的双功能电催化剂。

Construction of hollow urchin-like carbon frameworks with Co, P, and N doping and encapsulated Co/CoP heterojunction as bifunctional electrocatalysts for rechargeable Zn-air batteries.

作者信息

Liu Sa, Wang Luyuan, Wang Guoxiang, Zhu Ping, Long Zhouyang, Zhao Xinsheng

机构信息

School of Chemistry & Materials Science, Jiangsu Normal University, Xuzhou 221116, People's Republic of China.

School of Light Industry & Chemical Engineering, Dalian Polytechnic University, Dalian 116034, People's Republic of China.

出版信息

Nanoscale. 2025 Jun 19;17(24):14772-14780. doi: 10.1039/d5nr00625b.

Abstract

Controllable preparation of advanced electrocatalysts with well-designed architecture and desirable active sites for rechargeable Zn-air batteries (ZABs) is challenging. Herein, a hollow urchin-like bifunctional oxygen electrocatalyst (HCoPNC@Co/CoP-PNCNTs) was developed by assembling P, N-doped carbon nanotubes with confined Co/CoP heterojunctions on heteroatom-doped carbon hollow spheres polymerization/deposition, pyrolysis and topical phosphorization strategy. According to the analysis of experiments and theoretical calculations, the Co/CoP@NC core-shell structure at the top of each CNT was verified to facilitate the electron transfer and the conversion between the adsorbed intermediates, guaranteeing outstanding intrinsic catalytic activity. Meanwhile, the urchin-like hierarchical frameworks led to the formation of a desirable conductive and mass transport network, ensuring the efficient exposure of the electrocatalytic active sites and excellent structural stability. Therefore, the "framework-active sites" endowed HCoPNC@Co/CoP-PNCNTs with superior catalytic activities towards the oxygen reduction reaction (ORR, half-wave potential of 0.83 V) and oxygen evolution reaction (OER, overpotential of 350 mV@10 mA cm) in alkaline electrolyte. Expectedly, the as-assembled ZABs based on HCoPNC@Co/CoP-PNCNTs delivered a large peak power density of 250 mW cm and a robust charge-discharge cycling stability with negligible voltage decay for 110 h at 2 mA cm, illustrating its great practical application in advanced metal-air batteries.

摘要

可控制备具有精心设计的结构和理想活性位点的先进电催化剂用于可充电锌空气电池(ZABs)具有挑战性。在此,通过在杂原子掺杂的碳空心球上组装具有受限Co/CoP异质结的P、N掺杂碳纳米管,采用聚合/沉积、热解和局部磷化策略,开发了一种空心海胆状双功能氧电催化剂(HCoPNC@Co/CoP-PNCNTs)。根据实验分析和理论计算,证实了每个碳纳米管顶部的Co/CoP@NC核壳结构有助于电子转移和吸附中间体之间的转化,保证了优异的本征催化活性。同时,海胆状分级框架导致形成理想的导电和质量传输网络,确保电催化活性位点的有效暴露和优异的结构稳定性。因此,“框架-活性位点”赋予HCoPNC@Co/CoP-PNCNTs在碱性电解质中对氧还原反应(ORR,半波电位为0.83 V)和析氧反应(OER,在10 mA cm下过电位为350 mV)具有优异的催化活性。不出所料,基于HCoPNC@Co/CoP-PNCNTs组装的ZABs在2 mA cm下具有250 mW cm的大峰值功率密度和稳健的充放电循环稳定性,电压衰减可忽略不计,在110 h内保持稳定,说明了其在先进金属空气电池中的巨大实际应用价值。

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