NiCo2O4/P,N-Doped Carbon with Engineered Interface to Improve the Rechargeability of Zn-Air Batteries at High Energy Demands

IF 4.7 4区 材料科学 Q2 ELECTROCHEMISTRY
Alexander Suárez-Barajas, Minerva Guerra-Balcázar, Carlos M. Ramos-Castillo, Lorena Álvarez-Contreras, Noé Arjona
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Abstract

The search for cost-effective, high-performance bifunctional catalysts for Zn-air batteries (ZABs) requires extensive research into precious-metal-free materials. This study provides insight into the synergy between nickel cobaltite and P,N-doped carbon modified through interface engineering by inducing oxygen vacancies in the spinel and non-metallic heteroatoms in the carbon material. NiCo2O4 with various oxygen vacancy levels was synthesized via an ethylene glycol-assisted solvothermal route. This resulted in significant changes in the structural and morphological properties, such as reduced crystallite size, lattice distortion, and increased oxygen vacancies, as observed from the physicochemical results. This was further verified by X-ray photoelectron spectroscopy (XPS) and high-resolution transmission electron microscopy (HR-TEM), which showed a homogeneous dispersion of nickel cobaltite nanorods on the carbonaceous matrix, along with an increased concentration of pyridinic nitrogen and the formation of P−N and P−C bonds, both of which enhance electrocatalytic activity. NiCo2O4DI/P,N−C exhibited superior discharge polarization behavior, achieving power and current densities of 124.4 mW cm−2 and 215.8 mA cm−2. Stability tests revealed that the catalyst had excellent performance, lasting up to 100 h, while Pt-IrO2/C lasted only up to 21 h. These results demonstrate the great potential of tailoring surface defects and heteroatom doping via interface engineering, resulting in high-performance precious-metal-free electrocatalysts for long-lasting and high-efficiency ZABs.

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NiCo2O4/P, n掺杂碳与工程界面改善高能量需求下锌空气电池的可充电性
寻找成本效益高、高性能的锌空气电池(ZABs)双功能催化剂需要对无贵金属材料进行广泛的研究。本研究通过界面工程诱导尖晶石中的氧空位和碳材料中的非金属杂原子,揭示了钴酸镍与P, n掺杂碳之间的协同作用。采用乙二醇辅助溶剂热法合成了不同氧空位度的NiCo2O4。这导致了结构和形态特性的显著变化,如晶体尺寸减小,晶格畸变和氧空位增加,从物理化学结果中观察到。x射线光电子能谱(XPS)和高分辨率透射电子显微镜(HR-TEM)进一步证实了这一点,结果表明碳质基质上钴酸镍纳米棒均匀分散,吡啶氮浓度增加,P−N和P−C键的形成,两者都增强了电催化活性。NiCo2O4DI/P,N−C表现出优异的放电极化行为,功率和电流密度分别为124.4 mW cm−2和215.8 mA cm−2。稳定性测试表明,Pt-IrO2/C催化剂具有优异的性能,持续时间长达100小时,而Pt-IrO2/C仅持续时间长达21小时。这些结果表明,通过界面工程剪裁表面缺陷和杂原子掺杂具有巨大的潜力,从而产生高性能的无贵金属电催化剂,用于长效和高效的ZABs。
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来源期刊
CiteScore
8.60
自引率
5.30%
发文量
223
期刊介绍: Electrochemical energy storage devices play a transformative role in our societies. They have allowed the emergence of portable electronics devices, have triggered the resurgence of electric transportation and constitute key components in smart power grids. Batteries & Supercaps publishes international high-impact experimental and theoretical research on the fundamentals and applications of electrochemical energy storage. We support the scientific community to advance energy efficiency and sustainability.
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