Volume 63, Issue 51 e202412287
Research Article

Stable Dendrite-Free Room Temperature Sodium-Sulfur Batteries Enabled by a Novel Sodium Thiotellurate Interface

Wanjie Gao

Wanjie Gao

Confucius Energy Storage Lab, School of Energy and Environment, Southeast University, 211189 Nanjing, Jiangsu, China

Contribution: Software (lead), Validation (lead), Visualization (lead), Writing - original draft (lead), Writing - review & editing (lead)

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Prof. Laisuo Su

Prof. Laisuo Su

Department of Materials Science and Engineering, University of Texas at Dallas, 75080 Richardson, Texas, USA

Contribution: Software (supporting)

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Yueheng Yu

Yueheng Yu

Confucius Energy Storage Lab, School of Energy and Environment, Southeast University, 211189 Nanjing, Jiangsu, China

Contribution: Visualization (supporting)

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Yuhan Lu

Yuhan Lu

Confucius Energy Storage Lab, School of Energy and Environment, Southeast University, 211189 Nanjing, Jiangsu, China

Contribution: Visualization (supporting)

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Xi Liu

Xi Liu

Confucius Energy Storage Lab, School of Energy and Environment, Southeast University, 211189 Nanjing, Jiangsu, China

Contribution: Visualization (supporting)

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Yi Peng

Yi Peng

Confucius Energy Storage Lab, School of Energy and Environment, Southeast University, 211189 Nanjing, Jiangsu, China

Contribution: Visualization (supporting)

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Xiaosong Xiong

Xiaosong Xiong

Confucius Energy Storage Lab, School of Energy and Environment, Southeast University, 211189 Nanjing, Jiangsu, China

Contribution: Visualization (supporting)

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Prof. Jiarui He

Corresponding Author

Prof. Jiarui He

Confucius Energy Storage Lab, School of Energy and Environment, Southeast University, 211189 Nanjing, Jiangsu, China

Contribution: Funding acquisition (lead), Writing - original draft (supporting), Writing - review & editing (supporting)

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Prof. Yuanfu Chen

Corresponding Author

Prof. Yuanfu Chen

School of Integrated Circuit Science and Engineering, State Key Laboratory of Electronic Thin Films and Integrated Devices, University of Electronic Science and Technology of China, 610054 Chengdu, Sichuan, PR China

Contribution: Funding acquisition (lead), Visualization (supporting), Writing - original draft (supporting)

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Prof. Yuping Wu

Corresponding Author

Prof. Yuping Wu

Confucius Energy Storage Lab, School of Energy and Environment, Southeast University, 211189 Nanjing, Jiangsu, China

Contribution: Funding acquisition (lead), Writing - original draft (supporting), Writing - review & editing (supporting)

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First published: 29 August 2024
Citations: 14

Graphical Abstract

Novel sodium thiotellurate (Na2TeS3) interfaces are constructed both on the cathode and anode for Na−S batteries to simultaneously address the Na dendritic growth and polysulfide shuttling. Benefiting from this rational design, an anode-free cell fabricated with the Na2S/Na2Te@C cathode delivers an ultrahigh initial discharge capacity of 634 mAh g−1 at 0.1 C under practically necessary conditions, which could pave a new path to design high-performance cathodes for anode-free RT Na−S batteries.

Abstract

The practical application of room-temperature sodium-sulfur (RT Na−S) batteries is severely hindered by inhomogeneous sodium deposition and notorious sodium polysulfides (NaPSs) shuttling. Herein, novel sodium thiotellurate (Na2TeS3) interfaces are constructed both on the cathode and anode for Na−S batteries to simultaneously address the Na dendritic growth and polysulfides shuttling. On the cathode side, a heterostructural sodium sulfide/sodium telluride embedded in a carbon matrix (Na2S/Na2Te@C) is rationally designed through a facile carbothermal reaction, where the Na2TeS3 interface will be in situ chemically obtained. Such an interface provides abundant electron/ion diffusion channels and ensures rich catalytic surfaces toward Na−S redox, which could significantly improve the utilization of active material and alleviate polysulfides shuttling in the cathode. On the anode side, the inevitable formation of soluble polytellurosulfides species will migrate on Na anode surface, finally constructing a compact and smooth solid-electrolyte Na2TeS3 interphase (SEI) layer. Such electrochemical formed Na2TeS3 interface can significantly enhance ionic transport and stabilize Na deposition, thus realizing dendrite-free Na-metal plating/stripping. Benefitting from these advantages, an anode-free cell fabricated with the Na2S/Na2Te@C cathode exhibits an ultrahigh initial discharge capacity of 634 mAh g−1 at 0.1 C, which could pave a new path to design high-performance cathodes for anode-free RT Na−S batteries.

Conflict of Interests

The authors declare no conflict of interest.

Data Availability Statement

The data that support the findings of this study are available from the corresponding author upon reasonable request.

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