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用于性能增强型锌空气电池的相重构诱导NiS/NiFe O复合材料

Phase-Reconfiguration-Induced NiS/NiFe O Composite for Performance-Enhanced Zinc-Air Batteries.

作者信息

Shao Zhiyu, Zhu Qian, Sun Yu, Zhang Yuan, Jiang Yilan, Deng Shiqing, Zhang Wei, Huang Keke, Feng Shouhua

机构信息

State Key Laboratory of Inorganic Synthesis and Preparative, Chemistry Jilin Provincial International Cooperation Key Laboratory of Advanced Inorganic Solid Functional Materials, College of Chemistry, Jilin University, Qianjin Street 2699, Changchun, 130012, China.

School of Advanced Materials and Nanotechnology, Xidian University, Xi'an, 710126, China.

出版信息

Adv Mater. 2022 Apr;34(15):e2110172. doi: 10.1002/adma.202110172. Epub 2022 Mar 6.

Abstract

Constructing composite structures is an essential approach for obtaining multiple functionalities in a single entity. Available synthesis methods of the composites need to be urgently exploited; especially in situ construction. Here, a NiS/NiFe O composite through a local metal-S coordination at the interface is reported, which is derived from phase reconstruction in the highly defective matrix. X-ray absorption fine structure confirms that long-range order is broken via the local metal-S coordination and, by using electron energy loss spectroscopy, the introduction of NiS/NiFe O interfaces during the irradiation of plasma energy is identified. Density functional theory (DFT) calculations reveal that in situ phase reconfiguration is crucial for synergistically reducing energetic barriers and accelerating reaction kinetics toward catalyzing the oxygen evolution reaction (OER). As a result; it leads to an overpotential of 230 mV @10 mA cm for the OER and a half-wave potential of 0.81 V for the oxygen reduction reaction (ORR); as well as an excellent zinc-air battery (ZAB) performance with a power density of 148.5 mW cm . This work provides a new compositing strategy in terms of fast phase reconstruction of bifunctional catalysts.

摘要

构建复合结构是在单个实体中获得多种功能的重要方法。复合材料的现有合成方法亟待开发,尤其是原位构建方法。在此,报道了一种通过界面处局部金属 - 硫配位形成的NiS/NiFeO复合材料,它源自高度缺陷基质中的相重构。X射线吸收精细结构证实,通过局部金属 - 硫配位破坏了长程有序,并且利用电子能量损失谱确定了在等离子体能量辐照期间NiS/NiFeO界面的引入。密度泛函理论(DFT)计算表明,原位相重构对于协同降低能垒和加速催化析氧反应(OER)的反应动力学至关重要。结果,它导致OER在10 mA cm时过电位为230 mV,氧还原反应(ORR)的半波电位为0.81 V,以及具有148.5 mW cm功率密度的优异锌空气电池(ZAB)性能。这项工作在双功能催化剂的快速相重构方面提供了一种新的复合策略。

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