journal article·2015-12-23

High-Capacity Te Anode Confined in Microporous Carbon for Long-Life Na-Ion Batteries

Juan Zhang, Ya-Xia Yin, Yu-Guo Guo

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Abstract

Sodium-ion batteries (SIBs) have attracted considerable attention as an alternative energy-storage technology in recent years. Developing advanced sodium storage anode materials with appropriate working potential, high capacity, and good cycling performance is very important. Herein, we demonstrate a nanostructured tellurium@carbon (nano-Te@C) composite by confining nano-Te molecules in the space of carbon micropores as an attractive anode material for SIBs. The nano-Te@C anode presents an appropriate redox potential in the range of 1.05-1.35 V (vs Na(+)/Na), which avoids the Na dendrite problem and achieves a high reversible capacity of 410 mA h g(-1) on the basis of a two-electron redox reaction mechanism. Notably, the nano-Te@C exhibits an admirable long-term cycling stability with a high capacity retention of 90% for 1000 cycles (i.e., ultralow capacity decay of 0.01% per cycle). The excellent electrochemical property of nano-Te@C benefits from the high electroactivity from the nanostructure design and the effective confinement of the microporous carbon host. In addition, a Na-ion full cell by using nano-Te@C as anode and Na2/3Ni1/3Mn2/3O2 as cathode is demonstrated for the first time and exhibits a remarkable capacity retention up to 95% after 150 cycles. The results put new insights for the development of advanced SIBs with long-cycle lifespan.
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Research context

OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · Advanced Battery Technologies Research

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

CAS Key Laboratory of Molecular Nanostructure and Nanotechnology, and Beijing National Laboratory for Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences (CAS), Beijing 100190, PR China

University of Chinese Academy of Sciences, Beijing 100049, PR China

Funding

Ministry of Science and Technology of the People's Republic of China · National Natural Science Foundation of China · Chinese Academy of Sciences

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