Polarized Metal Organic Framework Nanoreactors for Rechargeable Sodium–Chlorine Batteries

Rechargeable sodium–chlorine (Na–Cl2) batteries have attracted attention for next-generation energy storage. However, their application is hindered by poor cycling stability, primarily caused by sluggish reaction kinetics and uneven NaCl nucleation. Herein, we prepared a series of polarized metal organic frameworks (MOFs) and verified that polar groups anchored on the penetrated porous skeletons can act as confined nanoreactors, enhancing the Cl–/Na+ adsorption capability and simultaneously repulsing the formed Cl2, finally boosting the uniform deposition/exfoliation of NaCl nanocrystals and reversible reaction between NaCl and Cl2. The Na–Cl2@UiO-66-SO3H battery demonstrates a polarization of 0.27 V, along with cycling for 600 cycles at 10,000 mA g–1, and even operates at a current density of 20,000 mA g–1. Moreover, this sodium–chlorine battery shows performance at low temperature, increased areal capacity, and capacity scaling in large-format pouch cells.

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Publication Details

Journal
ACS Energy Letters
Published
2026-04-15
DOI
https://doi.org/10.1021/acsenergylett.6c00458
Primary Topic
Thermal Expansion and Ionic Conductivity
Type
article
Field-Weighted Citation Impact
0.00

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article

Polarized Metal Organic Framework Nanoreactors for Rechargeable Sodium–Chlorine Batteries

Yecan Pi, Luxu Wang, Boman Li, Wenhua Li et al.
ACS Energy Letters
Thermal Expansion and Ionic Conductivity
article

Polarized Metal Organic Framework Nanoreactors for Rechargeable Sodium–Chlorine Batteries

Yecan Pi, Luxu Wang, Boman Li, Wenhua Li, Huan Pang, Bin He, Wanchang Feng, Yawei Li, Mohsen Shakouri
article en

Abstract

Rechargeable sodium–chlorine (Na–Cl2) batteries have attracted attention for next-generation energy storage. However, their application is hindered by poor cycling stability, primarily caused by sluggish reaction kinetics and uneven NaCl nucleation. Herein, we prepared a series of polarized metal organic frameworks (MOFs) and verified that polar groups anchored on the penetrated porous skeletons can act as confined nanoreactors, enhancing the Cl–/Na+ adsorption capability and simultaneously repulsing the formed Cl2, finally boosting the uniform deposition/exfoliation of NaCl nanocrystals and reversible reaction between NaCl and Cl2. The Na–Cl2@UiO-66-SO3H battery demonstrates a polarization of 0.27 V, along with cycling for 600 cycles at 10,000 mA g–1, and even operates at a current density of 20,000 mA g–1. Moreover, this sodium–chlorine battery shows performance at low temperature, increased areal capacity, and capacity scaling in large-format pouch cells.

ACS Energy LettersVol. 11(5)
Huzhou Normal University (CN), University of Saskatchewan (CA), Advanced Energy Materials (United States) (US), Materials Technology (United Kingdom) (GB), Yangzhou University (CN), Canadian Light Source (Canada) (CA)
National Natural Science Foundation of China, Basic Research Program of Jiangsu Province
Openalex Percentile: Top 28%
Thermal Expansion and Ionic Conductivity
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