In-situ stabilization of tin nanoparticles in porous carbon matrix derived from metal organic framework: high capacity and high rate capability anodes for lithium-ion batteries

Shiva, Konda ; Jayaramulu, Kolleboyina ; Rajendra, H. B. ; Kumar Maji, Tapas ; Bhattacharyya, Aninda J. (2014) In-situ stabilization of tin nanoparticles in porous carbon matrix derived from metal organic framework: high capacity and high rate capability anodes for lithium-ion batteries Zeitschrift fur Anorganische und Allgemeine Chemie, 640 (6). pp. 1115-1118. ISSN 0044-2313

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Official URL: http://onlinelibrary.wiley.com/doi/10.1002/zaac.20...

Related URL: http://dx.doi.org/10.1002/zaac.201300621

Abstract

It is a formidable challenge to arrange tin nanoparticles in a porous matrix for the achievement of high specific capacity and current rate capability anode for lithium-ion batteries. This article discusses a simple and novel synthesis of arranging tin nanoparticles with carbon in a porous configuration for application as anode in lithium-ion batteries. Direct carbonization of synthesized three-dimensional Sn-based MOF: [K2Sn2(1,4-bdc)3](H2O) (1) (bdc = benzenedicarboxylate) resulted in stabilization of tin nanoparticles in a porous carbon matrix (abbreviated as Sn@C). Sn@C exhibited remarkably high electrochemical lithium stability (tested over 100 charge and discharge cycles) and high specific capacities over a wide range of operating currents (0.2–5 Ag-1). The novel synthesis strategy to obtain Sn@C from a single precursor as discussed herein provides an optimal combination of particle size and dispersion for buffering severe volume changes due to Li-Sn alloying reaction and provides fast pathways for lithium and electron transport.

Item Type:Article
Source:Copyright of this article belongs to John Wiley and Sons, Inc.
Keywords:Sn@C; Metal-organic Frameworks; Anode Materials; Specific Capacity; Rate Capability; Lithium-ion Battery
ID Code:109138
Deposited On:22 Dec 2017 10:15
Last Modified:22 Dec 2017 10:15

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