Isolated Metalloid Tellurium Atomic Cluster on Nitrogen‐Doped Carbon Nanosheet for High‐Capacity Rechargeable Lithium‐CO2 Battery

Author:

Wang Ke1,Liu Dongyu2,Liu Limin1,Li Xinyang1,Wu Hu1,Sun Zongjie1,Li Mingtao3,Vasenko Andrey S.2,Ding Shujiang1,Wang Fengmei4,Xiao Chunhui1ORCID

Affiliation:

1. Xi'an Key Laboratory of Sustainable Energy Materials Chemistry School of Chemistry Energy Storage Materials and Chemistry of Shaanxi University Engineering Research Center Xi'an Jiaotong University 28 Xianning West Road Xi'an Shaanxi 710049 China

2. National Research University Higher School of Economics (HSE University) 20 Myasnitskaya Str.  Moscow 101000 Russia

3. International Research Center for Renewable Energy (IRCRE) State Key Laboratory of Multiphase Flow in Power Engineering (MFPE) Xi'an Jiaotong University 28 Xianning West Road Xi'an Shaanxi 710049 China

4. State Key Laboratory of Chemical Resource Engineering Beijing Advanced Innovation Center for Soft Matter Science and Engineering Beijing University of Chemical Technology Beijing 100029 China

Abstract

AbstractRechargeable Li‐CO2 battery represents a sustainable technology by virtue of CO2 recyclability and energy storage capability. Unfortunately, the sluggish mass transport and electron transfer in bulky high‐crystalline discharge product of Li2CO3, severely hinder its practical capacity and rechargeability. Herein, a heterostructure of isolated metalloid Te atomic cluster anchored on N‐doped carbon nanosheets is designed (TeAC@NCNS) as a metal‐free cathode for Li‐CO2 battery. X‐ray absorption spectroscopy analysis demonstrates that the abundant and dispersed Te active centers can be stabilized by C atoms in form of the covalent bond. The fabricated battery shows an unprecedented full‐discharge capacity of 28.35 mAh cm−2 at 0.05 mA cm−2 and long‐term cycle life of up to 1000 h even at a high cut‐off capacity of 1 mAh cm−2. A series of ex situ characterizations combined with theoretical calculations demonstrate that the abundant Te atomic clusters acting as active centers can drive the electron redistribution of carbonate via forming TeO bonds, giving rise to poor‐crystalline Li2CO3 film during the discharge process. Moreover, the efficient electron transfer between the Te centers and intermediate species is energetically beneficial for nucleation and accelerates the decomposition of Li2CO3 on the TeAC@NCNS during the discharge/charge process.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Physics and Astronomy,General Engineering,Biochemistry, Genetics and Molecular Biology (miscellaneous),General Materials Science,General Chemical Engineering,Medicine (miscellaneous)

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