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High-Capacity Rechargeable Li/Cl2 Batteries with Graphite Positive Electrodes.
Zhu, Guanzhou; Liang, Peng; Huang, Cheng-Liang; Huang, Cheng-Chia; Li, Yuan-Yao; Wu, Shu-Chi; Li, Jiachen; Wang, Feifei; Tian, Xin; Huang, Wei-Hsiang; Jiang, Shi-Kai; Hung, Wei-Hsuan; Chen, Hui; Lin, Meng-Chang; Hwang, Bing-Joe; Dai, Hongjie.
Afiliação
  • Zhu G; Department of Chemistry and Bio-X, Stanford University, Stanford, California94305, United States.
  • Liang P; Department of Chemistry and Bio-X, Stanford University, Stanford, California94305, United States.
  • Huang CL; Department of Chemical Engineering, National Chung Cheng University, Chia-Yi62102, Taiwan.
  • Huang CC; Department of Electrical Engineering, National Chung Cheng University, Chia-Yi62102, Taiwan.
  • Li YY; Department of Chemical Engineering, National Chung Cheng University, Chia-Yi62102, Taiwan.
  • Wu SC; Department of Chemical Engineering, National Chung Cheng University, Chia-Yi62102, Taiwan.
  • Li J; Department of Chemistry and Bio-X, Stanford University, Stanford, California94305, United States.
  • Wang F; Department of Chemistry and Bio-X, Stanford University, Stanford, California94305, United States.
  • Tian X; Department of Chemistry and Bio-X, Stanford University, Stanford, California94305, United States.
  • Huang WH; Department of Chemistry and Bio-X, Stanford University, Stanford, California94305, United States.
  • Jiang SK; Graduate Institute of Applied Science and Technology, National Taiwan University of Science and Technology, Taipei10607, Taiwan.
  • Hung WH; National Synchrotron Radiation Research Center, Hsinchu30076, Taiwan.
  • Chen H; Department of Chemical Engineering, National Taiwan University of Science and Technology, Taipei10607, Taiwan.
  • Lin MC; Institute of Materials Science and Engineering, National Central University, Taoyuan City32001, Taiwan.
  • Hwang BJ; College of Electrical Engineering and Automation, Shandong University of Science and Technology, Qingdao, Shandong Province, 266590, P. R. China.
  • Dai H; College of Electrical Engineering and Automation, Shandong University of Science and Technology, Qingdao, Shandong Province, 266590, P. R. China.
J Am Chem Soc ; 144(49): 22505-22513, 2022 Dec 14.
Article em En | MEDLINE | ID: mdl-36450002
ABSTRACT
Developing new types of high-capacity and high-energy density rechargeable batteries is important to future generations of consumer electronics, electric vehicles, and mass energy storage applications. Recently, we reported ∼3.5 V sodium/chlorine (Na/Cl2) and lithium/chlorine (Li/Cl2) batteries with up to 1200 mAh g-1 reversible capacity, using either a Na or a Li metal as the negative electrode, an amorphous carbon nanosphere (aCNS) as the positive electrode, and aluminum chloride (AlCl3) dissolved in thionyl chloride (SOCl2) with fluoride-based additives as the electrolyte [Zhu et al., Nature, 2021, 596 (7873), 525-530]. The high surface area and large pore volume of aCNS in the positive electrode facilitated NaCl or LiCl deposition and trapping of Cl2 for reversible NaCl/Cl2 or LiCl/Cl2 redox reactions and battery discharge/charge cycling. Here, we report an initially low surface area/porosity graphite (DGr) material as the positive electrode in a Li/Cl2 battery, attaining high battery performance after activation in carbon dioxide (CO2) at 1000 °C (DGr_ac) with the first discharge capacity ∼1910 mAh g-1 and a cycling capacity up to 1200 mAh g-1. Ex situ Raman spectroscopy and X-ray diffraction (XRD) revealed the evolution of graphite over battery cycling, including intercalation/deintercalation and exfoliation that generated sufficient pores for hosting LiCl/Cl2 redox. This work opens up widely available, low-cost graphitic materials for high-capacity alkali metal/Cl2 batteries. Lastly, we employed mass spectrometry to probe the Cl2 trapped in the graphitic positive electrode, shedding light into the Li/Cl2 battery operation.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article