Tin-Coated Viral Nanoforests as Sodium-Ion Battery Anodes

Designed as a high-capacity alloy host for Na-ion chemistry, a forest of Sn nanorods with a unique core–shell structure was synthesized on viral scaffolds, which were genetically engineered to ensure a nearly vertical alignment upon self-assembly onto a metal substrate. The interdigital spaces thus...

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Bibliographic Details
Published inACS nano Vol. 7; no. 4; pp. 3627 - 3634
Main Authors Liu, Yihang, Xu, Yunhua, Zhu, Yujie, Culver, James N, Lundgren, Cynthia A, Xu, Kang, Wang, Chunsheng
Format Journal Article
LanguageEnglish
Published United States American Chemical Society 23.04.2013
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Summary:Designed as a high-capacity alloy host for Na-ion chemistry, a forest of Sn nanorods with a unique core–shell structure was synthesized on viral scaffolds, which were genetically engineered to ensure a nearly vertical alignment upon self-assembly onto a metal substrate. The interdigital spaces thus formed between individual rods effectively accommodated the volume expansion and contraction of the alloy upon sodiation/desodiation, while additional carbon-coating engineered over these nanorods further suppressed Sn aggregation during extended electrochemical cycling. Due to the unique nanohierarchy of multiple functional layers, the resultant 3D nanoforest of C/Sn/Ni/TMV1cys, binder-free composite electrode already and evenly assembled on a stainless steel current collector, exhibited supreme capacity utilization and cycling stability toward Na-ion storage and release. An initial capacity of 722 mA·h (g Sn)−1 along with 405 mA·h (g Sn)−1 retained after 150 deep cycles demonstrates the longest-cycling nano-Sn anode material for Na-ion batteries reported in the literature to date and marks a significant performance improvement for neat Sn material as alloy host for Na-ion chemistry.
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ISSN:1936-0851
1936-086X
DOI:10.1021/nn400601y