Layered Bimetallic Metal‐Organic Material Derived Cu2SnS3/SnS2/C Composite for Anode Applications in Lithium‐Ion Batteries
Here, we report the synthesis of a bimetallic 2D interpenetrated metal‐organic material (MOM) and its use as a sacrificial precursor for the formation of a Cu2SnS3/SnS2/C composite. The one‐step sulfurisation of the novel Sn/Cu‐MOM represents a facile method for the preparation of an effective anode...
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Veröffentlicht in: | ChemElectroChem 2018-12, Vol.5 (23), p.3764-3770 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Here, we report the synthesis of a bimetallic 2D interpenetrated metal‐organic material (MOM) and its use as a sacrificial precursor for the formation of a Cu2SnS3/SnS2/C composite. The one‐step sulfurisation of the novel Sn/Cu‐MOM represents a facile method for the preparation of an effective anode material for Li‐ion battery applications. The Cu2SnS3/SnS2/C composite was characterised by XRD, TGA, TEM and SEM. Electrochemical analysis was conducted on SnCu2SnS3/SnS2/C anodes in half cell configurations between 0–3 V and 0–1 V. Anodes cycled between 0–1 V exhibited markedly more stable capacity retention (315 mAh/g after 100 cycles), as only alloying of the Li with Sn took place within this potential window, compared to a combination of conversion and alloying for the wider potential range. This stability of the Li alloying based capacity was further enhanced by replacing the planar Cu foil with a rough dendritic Cu foil as the current collector, resulting in an improved capacity retention of 84 % after 100 cycles.
Boost from precursor chemistry: a bimetallic 2D interpenetrated metal‐organic material is used as sacrificial precursor for the formation of a Cu2SnS3/SnS2/C composite as anode for Li‐ion batteries. The anodes are cycled in potential ranges between 0–3 V and 0–1 V in half cell configuration. In the wider potential range, conversion and alloying of Li with Sn takes place while in the smaller potential window only alloying is observed, leading to a more stable capacity retention. |
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ISSN: | 2196-0216 2196-0216 |
DOI: | 10.1002/celc.201800989 |