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Shedding light on rechargeable Na/Cl2 battery.
Zhu, Guanzhou; Liang, Peng; Huang, Cheng-Liang; Wu, Shu-Chi; Huang, Cheng-Chia; Li, Yuan-Yao; Jiang, Shi-Kai; Huang, Wei-Hsiang; Li, Jiachen; Wang, Feifei; Hwang, Bing-Joe; Dai, Hongjie.
Afiliación
  • Zhu G; Department of Chemistry and Bio-X, Stanford University, Stanford, CA 94305.
  • Liang P; Department of Chemistry and Bio-X, Stanford University, Stanford, CA 94305.
  • Huang CL; Department of Chemical Engineering, National Chung Cheng University, Chia-Yi 62102, Taiwan.
  • Wu SC; Department of Electrical Engineering, National Chung Cheng University, Chia-Yi 62102, Taiwan.
  • Huang CC; Department of Chemistry and Bio-X, Stanford University, Stanford, CA 94305.
  • Li YY; Department of Chemical Engineering, National Chung Cheng University, Chia-Yi 62102, Taiwan.
  • Jiang SK; Department of Chemical Engineering, National Chung Cheng University, Chia-Yi 62102, Taiwan.
  • Huang WH; Department of Chemical Engineering, National Taiwan University of Science and Technology, Taipei 10607, Taiwan.
  • Li J; National Synchrotron Radiation Research Center, Hsinchu 30076, Taiwan.
  • Wang F; Department of Chemistry and Bio-X, Stanford University, Stanford, CA 94305.
  • Hwang BJ; Department of Electrical and Electronic Engineering, The University of Hong Kong, Hong Kong 999077, China.
  • Dai H; Department of Chemical Engineering, National Taiwan University of Science and Technology, Taipei 10607, Taiwan.
Proc Natl Acad Sci U S A ; 120(39): e2310903120, 2023 Sep 26.
Article en En | MEDLINE | ID: mdl-37729201
ABSTRACT
Advancing new ideas of rechargeable batteries represents an important path to meeting the ever-increasing energy storage needs. Recently, we showed rechargeable sodium/chlorine (Na/Cl2) (or lithium/chlorine Li/Cl2) batteries that used a Na (or Li) metal negative electrode, a microporous amorphous carbon nanosphere (aCNS) positive electrode, and an electrolyte containing dissolved aluminum chloride and fluoride additives in thionyl chloride [G. Zhu et al., Nature 596, 525-530 (2021) and G. Zhu et al., J. Am. Chem. Soc. 144, 22505-22513 (2022)]. The main battery redox reaction involved conversion between NaCl and Cl2 trapped in the carbon positive electrode, delivering a cyclable capacity of up to 1,200 mAh g-1 (based on positive electrode mass) at a ~3.5 V discharge voltage [G. Zhu et al., Nature 596, 525-530 (2021) and G. Zhu et al., J. Am. Chem. Soc. 144, 22505-22513 (2022)]. Here, we identified by X-ray photoelectron spectroscopy (XPS) that upon charging a Na/Cl2 battery, chlorination of carbon in the positive electrode occurred to form carbon-chlorine (C-Cl) accompanied by molecular Cl2 infiltrating the porous aCNS, consistent with Cl2 probed by mass spectrometry. Synchrotron X-ray diffraction observed the development of graphitic ordering in the initially amorphous aCNS under battery charging when the carbon matrix was oxidized/chlorinated and infiltrated with Cl2. The C-Cl, Cl2 species and graphitic ordering were reversible upon discharge, accompanied by NaCl formation. The results revealed redox conversion between NaCl and Cl2, reversible graphitic ordering/amorphourization of carbon through battery charge/discharge, and probed trapped Cl2 in porous carbon by XPS.
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