{"title":"Two polymolybdate-based hybrid compounds constructed from monodentate imidazolated naphthalene ligand with capacitive performance","authors":"Ya−shuang Zhu, Xin−yu Zhao, Wei Zhang, Xiang Wang","doi":"10.1007/s11243-024-00625-3","DOIUrl":null,"url":null,"abstract":"<div><p>The development of polyoxometalate-based hybrid compounds offered a hopeful opportunity to develop capacitor electrode materials. Herein, two new polyoxometalate-based hybrid compounds, [Cu(4 − INCN)<sub>2</sub>(ε − Mo<sub>8</sub>O<sub>26</sub>)<sub>0.5</sub>] (<b>1</b>) and [Zn(H<sub>2</sub>O)(4 − INCN)<sub>3</sub>(β − Mo<sub>8</sub>O<sub>26</sub>)<sub>0.5</sub>], were synthesized under hydrothermal condition by using 4 − imidazol − 1 − yl − naphthalene − 1 − carbonitrile (4 − INCN) as N-donor ligand. The [ε − Mo<sub>8</sub>O<sub>26</sub>]<sup>4−</sup> and [β − Mo<sub>8</sub>O<sub>26</sub>]<sup>4−</sup> anions were involved in the structures of two compounds, respectively. Compound <b>1</b> displayed a two-dimensional layer structure, where the [ε − Mo<sub>8</sub>O<sub>26</sub>]<sup>4−</sup> anions were gathered by Cu (II) ions to produce a two-dimensional structure with the 4 − INCN as monodentate organic ligands hanged on the both sides. In the structure of compound <b>2</b>, the aggregation of [β − Mo<sub>8</sub>O<sub>26</sub>]<sup>4−</sup> and Zn (II) ions resulted in a one-dimensional chain, which was decorated by the 4-INCN ligands through coordination with Zn (II) ions. Two compounds as electrode materials provided specific capacitances of 1092 F g<sup>–1</sup> for <b>1</b> and 731 F g<sup>–1</sup> for <b>2</b> at the current densities of 1 A g<sup>–1</sup>, and showed excellent capacitance retention rates after 1000 cycles. These findings provided a possible approach in the preparation of POM-based hybrid compounds employed as capacitor electrode materials.</p></div>","PeriodicalId":803,"journal":{"name":"Transition Metal Chemistry","volume":"50 3","pages":"313 - 322"},"PeriodicalIF":1.6000,"publicationDate":"2024-12-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Transition Metal Chemistry","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s11243-024-00625-3","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 0
Abstract
The development of polyoxometalate-based hybrid compounds offered a hopeful opportunity to develop capacitor electrode materials. Herein, two new polyoxometalate-based hybrid compounds, [Cu(4 − INCN)2(ε − Mo8O26)0.5] (1) and [Zn(H2O)(4 − INCN)3(β − Mo8O26)0.5], were synthesized under hydrothermal condition by using 4 − imidazol − 1 − yl − naphthalene − 1 − carbonitrile (4 − INCN) as N-donor ligand. The [ε − Mo8O26]4− and [β − Mo8O26]4− anions were involved in the structures of two compounds, respectively. Compound 1 displayed a two-dimensional layer structure, where the [ε − Mo8O26]4− anions were gathered by Cu (II) ions to produce a two-dimensional structure with the 4 − INCN as monodentate organic ligands hanged on the both sides. In the structure of compound 2, the aggregation of [β − Mo8O26]4− and Zn (II) ions resulted in a one-dimensional chain, which was decorated by the 4-INCN ligands through coordination with Zn (II) ions. Two compounds as electrode materials provided specific capacitances of 1092 F g–1 for 1 and 731 F g–1 for 2 at the current densities of 1 A g–1, and showed excellent capacitance retention rates after 1000 cycles. These findings provided a possible approach in the preparation of POM-based hybrid compounds employed as capacitor electrode materials.
期刊介绍:
Transition Metal Chemistry is an international journal designed to deal with all aspects of the subject embodied in the title: the preparation of transition metal-based molecular compounds of all kinds (including complexes of the Group 12 elements), their structural, physical, kinetic, catalytic and biological properties, their use in chemical synthesis as well as their application in the widest context, their role in naturally occurring systems etc.
Manuscripts submitted to the journal should be of broad appeal to the readership and for this reason, papers which are confined to more specialised studies such as the measurement of solution phase equilibria or thermal decomposition studies, or papers which include extensive material on f-block elements, or papers dealing with non-molecular materials, will not normally be considered for publication. Work describing new ligands or coordination geometries must provide sufficient evidence for the confident assignment of structural formulae; this will usually take the form of one or more X-ray crystal structures.