Layered metal-organic framework based on tetracyanonickelate as a cathode material for in situ Li-ion storage

Prussian blue analogs (PBAs) formed with hexacyanide linkers have been studied for decades. The framework crystal structure of PBAs mainly benefits from the six-fold coordinated cyano functional groups. In this study, in-plane tetracyanonickelate was utilized to engineer an organic linker and design...

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Veröffentlicht in:RSC advances 2019-07, Vol.9 (37), p.21363-21370
Hauptverfasser: Zhang, Kaiqiang, Lee, Tae Hyung, Bubach, Bailey, Ostadhassan, Mehdi, Jang, Ho Won, Choi, Ji-Won, Shokouhimehr, Mohammadreza
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Sprache:eng
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Zusammenfassung:Prussian blue analogs (PBAs) formed with hexacyanide linkers have been studied for decades. The framework crystal structure of PBAs mainly benefits from the six-fold coordinated cyano functional groups. In this study, in-plane tetracyanonickelate was utilized to engineer an organic linker and design a family of four-fold coordinated PBAs (FF-PBAs; Fe Ni(CN) , MnNi(CN) , Fe Ni(CN) , CuNi(CN) , CoNi(CN) , ZnNi(CN) , and NiNi(CN) ), which showed an interesting two-dimensional (2D) crystal structure. It was found that these FF-PBAs could be utilized as cathode materials of Li-ion batteries, and the Ni/Fe system exhibited superior electrochemical properties compared to the others with a capacity of 137.9 mA h g at a current density of 100 mA g . Furthermore, after a 5000-cycle long-term repeated charge/discharge measurement, the Ni/Fe system displayed a capacity of 60.3 mA h g with a coulombic efficiency of 98.8% at a current density of 1000 mA g . In addition, the capacity of 86.1% was preserved at 1000 mA g as compared with that at 100 mA g , implying a good rate capability. These potential capacities can be ascribed to an reduction of Li in the interlayer of Ni/Fe instead of the formation of other compounds with the host material according to XRD characterization. These specially designed FF-PBAs are expected to inspire new concepts in electrochemistry and other applications requiring 2D materials.
ISSN:2046-2069
2046-2069
DOI:10.1039/c9ra03975a