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固液界面配位化学助力无定形磷酸锰实现高容量铵存储。

Solid-Liquid Interfacial Coordination Chemistry Enables High-Capacity Ammonium Storage in Amorphous Manganese Phosphate.

作者信息

Yang Duo, Song Yu, Zhang Ming-Yue, Qin Zengming, Liu Jie, Liu Xiao-Xia

机构信息

Department of Chemistry, Northeastern University, 3-11, Wenhua Road, Heping district, Shenyang, 110819, China.

School of Resources and Civil Engineering, Northeastern University, 3-11, Wenhua Road, Heping district, Shenyang, 110819, China.

出版信息

Angew Chem Int Ed Engl. 2022 Sep 12;61(37):e202207711. doi: 10.1002/anie.202207711. Epub 2022 Aug 3.

Abstract

Ammonium (NH ) ion as charge carrier is attracting attention in aqueous batteries. Yet, most NH host materials are still limited by the relatively low capacities. Here, we fabricated a manganese phosphate (MP-20) for NH ion storage. MP-20 displays a high capacity of 299.6 mAh g at 1 A g in ammonium acetate (NH Ac) electrolyte, outperforming other reported NH host materials. Spectroscopy studies suggest a new NH /H co-insertion mechanism. We surprisingly discover that the NH Ac electrolyte plays an important role in improving the charge storage capability of the materials. Experimental and computational results indicate acetate ions can form coordination bonds with the Mn atoms, tailoring the electronic structure of the Mn atoms and the surrounding O atoms, and therefore facilitating the NH storage process. Our findings provide a new NH host material and propose the important role of the electrolyte-electrode coordination effect in aqueous ammonium batteries.

摘要

铵根离子(NH₄⁺)作为电荷载体在水系电池中备受关注。然而,大多数铵根离子宿主材料的容量仍然相对较低。在此,我们制备了一种用于铵根离子存储的磷酸锰(MP - 20)。在醋酸铵(NH₄Ac)电解液中,MP - 20在1 A g⁻¹电流密度下展现出299.6 mAh g⁻¹的高容量,优于其他已报道的铵根离子宿主材料。光谱研究表明存在一种新的NH₄⁺/H⁺共嵌入机制。我们意外地发现,NH₄Ac电解液在提高材料的电荷存储能力方面起着重要作用。实验和计算结果表明,醋酸根离子可以与锰原子形成配位键,调整锰原子及其周围氧原子的电子结构,从而促进铵根离子的存储过程。我们的研究结果提供了一种新型的铵根离子宿主材料,并揭示了电解液 - 电极配位效应在水系铵电池中的重要作用。

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