A new nickel coordination polymer electrode material for hybrid supercapacitors
Battery-type electrode materials store charge through chemical reactions, leading to low power densities and rendering it difficult to reach the performance levels associated with capacitors. This study introduces a coordination polymer electrode material for hybrid supercapacitors, specifically, poly[[tri-μ-ethanolato-di-μ<sub>3</sub>-sulfido-hexakis(μ<sub>4</sub>-2-sulfidobenzoato)dinickel(II)tetranickel(III)dipotassium(I)[potassium(I)/sodium(I)(0.60/0.40)]] quaterhydrate], {[Ni<sup>III</sup><sub>4</sub>Ni<sup>II</sup><sub>2</sub>K<sub>2.60</sub>Na<sub>0.40</sub>(C<sub>2</sub>H<sub>5</sub>O)<sub>3</sub>(C<sub>7</sub>H<sub>4</sub>O<sub>2</sub>S)<sub>6</sub>S<sub>2</sub>]·0.25H<sub>2</sub>O}<sub>n</sub> or Ni-mba-K(Na), where H<sub>2</sub>mba is 2-mercaptobenzoic acid, (1). As a hybrid capacitor electrode material, Ni-mba-K(Na) exhibits the characteristics of battery-type electrode materials but demonstrates a capacitor-level power density and cycling stability. The microstructure, element composition, phase structure and thermodynamic stability of Ni-mba-K(Na) are characterized through techniques such as crystal structure determination and X-ray photoelectron spectroscopy. Single-crystal X-ray diffraction shows that compound (1) consists of a hexanuclear nickel cluster, two mononuclear K nodes and a mononuclear K<sub>0.60</sub>/Na<sub>0.40</sub> shared node, resulting in the formation of a complex covalent three-dimensional network. Due to this novel structure, Ni-mba-K(Na) exhibits supercapacitor performance that combines high energy density and high power density.
Authors
- Xinhua Li (ORCID: https://orcid.org/0000-0002-7899-4370)
- Xihao Lin
- Yihuo Wu
- Hongping Xiao
Institutions
- Wenzhou University (CN)
Publication Details
- Journal
- Acta Crystallographica Section C Structural Chemistry
- Published
- 2026-02-25
- DOI
- https://doi.org/10.1107/s205322962600207x
- Primary Topic
- Supercapacitor Materials and Fabrication
- Type
- article
- Field-Weighted Citation Impact
- 0.00