p–d orbital hybridization induced by transition metal atom sites for room-temperature sodium–sulfur batteries

For energy storage applications involving sulfur redox reactions, uniformly dispersed metal sites in sulfur hosts serve as an effective approach to facilitate electron transfer during charge and discharge cycles. In this study, we exploited a facile method to construct transitional single-atom catalysts to overcome the kinetic limitations for electron transportation in room-temperature sodium-sulfur batteries. By the synergistic effect of polysulfide adsorption and p-d orbital hybridization between catalysts and intermediates, electron-donating and electron-capturing capabilities of different atomic sites towards sulfur redox reactions are systematically revealed. Remarkably, atomic Mn-N<sub>4</sub> active moiety structures possess abundant unfilled antibonding orbitals, promoting p-d hybridization and leading to superior sulfur conversion reactions. This work establishes a design paradigm for single-atom catalysts in metal-sulfur batteries by linking atomic-scale electronic features to macroscopic performance. This atomic-level engineering strategy paves the way for high-energy-density room-temperature sodium-sulfur batteries, with potential extensions to other multivalent sulfur-based energy storage systems.

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Publication Details

Journal
National Science Review
Published
2025-06-11
DOI
https://doi.org/10.1093/nsr/nwaf241
Citations
8
Primary Topic
Advanced Battery Materials and Technologies
Type
article
Field-Weighted Citation Impact
5.84

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article

p–d orbital hybridization induced by transition metal atom sites for room-temperature sodium–sulfur batteries

Le Pang, Guoxiu Wang, Ailing Song, Bing Sun et al.
8 citations
National Science Review
Advanced Battery Materials and Technologies
5.84
article

p–d orbital hybridization induced by transition metal atom sites for room-temperature sodium–sulfur batteries

Le Pang, Guoxiu Wang, Ailing Song, Bing Sun, Hongxia Wang, Hao Tian, Wei‐Hong Lai, Chung‐Li Dong, Cheng‐Chieh Yang, Sean C. Smith, Yunxiao Wang, Xin Tan, Yaojie Lei, Tao Huang, Xiaoyue Zhang, Hao Liu, Chi‐Liang Chen, Yong Chen
article en
8 citations

Abstract

For energy storage applications involving sulfur redox reactions, uniformly dispersed metal sites in sulfur hosts serve as an effective approach to facilitate electron transfer during charge and discharge cycles. In this study, we exploited a facile method to construct transitional single-atom catalysts to overcome the kinetic limitations for electron transportation in room-temperature sodium-sulfur batteries. By the synergistic effect of polysulfide adsorption and p-d orbital hybridization between catalysts and intermediates, electron-donating and electron-capturing capabilities of different atomic sites towards sulfur redox reactions are systematically revealed. Remarkably, atomic Mn-N<sub>4</sub> active moiety structures possess abundant unfilled antibonding orbitals, promoting p-d hybridization and leading to superior sulfur conversion reactions. This work establishes a design paradigm for single-atom catalysts in metal-sulfur batteries by linking atomic-scale electronic features to macroscopic performance. This atomic-level engineering strategy paves the way for high-energy-density room-temperature sodium-sulfur batteries, with potential extensions to other multivalent sulfur-based energy storage systems.

National Science ReviewVol. 12(7)
Tamkang University (TW), University of Technology Sydney (AU), Australian National University (AU), Wenzhou University (CN), University of Shanghai for Science and Technology (CN), Queensland University of Technology (AU), Fudan University (CN), Yanshan University (CN), Materials Design (France) (FR)
Australian Research Council
Openalex Percentile: Top 4%
Advanced Battery Materials and Technologies
5.84
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