Enhancing Sodium‐Ion Storage Capacity and Stability in Metal–Organic Coordination Compounds by Bifunctional Coordinated Water Molecule

Redox‐active organic compounds have received much attention as high‐capacity electrodes for rechargeable batteries. However, the high solubility in organic electrolytes during charge and discharge processes hinders the practical exploitation of organic compounds. This study presents a cobalt‐based metal–organic coordination compound with bifunctional coordinated water (Co‐MOC‐H 2 O) for sodium‐ion storage. The coordinated water enhances interactions between sodium ions and nitrogen atoms in organic ligands through chelation, activating the inert sodium‐ion storage sites (C=N). Moreover, the stable hydrogen bonded framework formed by the coordinated water molecules prevents the active organic compounds from dissolving into the electrolyte, thereby enhancing cycling stability. With the bifunctional coordinated water molecules, the Co‐MOC‐H 2 O electrode delivers a high capacity of 403 mAh g −1 at 0.2 A g −1 over 600 cycles and exhibits a capacity retention of 77.9% at 2 A g −1 after 1100 cycles. This work highlights the crucial role of the coordinated water molecules in constructing high capacity and long‐life sodium‐ion storage materials.

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Publication Details

Journal
Energy & environment materials
Published
2024-11-23
DOI
https://doi.org/10.1002/eem2.12851
Citations
9
Primary Topic
Advanced Battery Materials and Technologies
Type
article
Field-Weighted Citation Impact
1.88

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article

Enhancing Sodium‐Ion Storage Capacity and Stability in Metal–Organic Coordination Compounds by Bifunctional Coordinated Water Molecule

Runhao Zhang, Jialong Jiang, Limin Zhou, Meihong Che et al.
9 citations
Energy & environment materials
Advanced Battery Materials and Technologies
1.88
article

Enhancing Sodium‐Ion Storage Capacity and Stability in Metal–Organic Coordination Compounds by Bifunctional Coordinated Water Molecule

Runhao Zhang, Jialong Jiang, Limin Zhou, Meihong Che, Tongrui Zhang, Wei Shi, Weibo Hua, Zhonghan Wu, Kai Zhang, Jun Chen, Yong Lu, Jiangtao Yu, Ziheng Zhang
article en
9 citations

Abstract

Redox‐active organic compounds have received much attention as high‐capacity electrodes for rechargeable batteries. However, the high solubility in organic electrolytes during charge and discharge processes hinders the practical exploitation of organic compounds. This study presents a cobalt‐based metal–organic coordination compound with bifunctional coordinated water (Co‐MOC‐H 2 O) for sodium‐ion storage. The coordinated water enhances interactions between sodium ions and nitrogen atoms in organic ligands through chelation, activating the inert sodium‐ion storage sites (C=N). Moreover, the stable hydrogen bonded framework formed by the coordinated water molecules prevents the active organic compounds from dissolving into the electrolyte, thereby enhancing cycling stability. With the bifunctional coordinated water molecules, the Co‐MOC‐H 2 O electrode delivers a high capacity of 403 mAh g −1 at 0.2 A g −1 over 600 cycles and exhibits a capacity retention of 77.9% at 2 A g −1 after 1100 cycles. This work highlights the crucial role of the coordinated water molecules in constructing high capacity and long‐life sodium‐ion storage materials.

Energy & environment materialsVol. 8(3)
Nankai University (CN), Nanjing University of Science and Technology (CN), Unité Matériaux et Transformations (FR), Collaborative Innovation Center of Chemical Science and Engineering Tianjin (CN), Xi'an Jiaotong University (CN)
National Natural Science Foundation of China, Natural Science Foundation of Jiangsu Province, National Key Research and Development Program of China, Fundamental Research Funds for the Central Universities, Tianjin Science and Technology Program
Clean water and sanitation
Openalex Percentile: Top 14%
Advanced Battery Materials and Technologies
1.88
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