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Rechargeable Na/Cl2 and Li/Cl2 batteries.
Zhu, Guanzhou; Tian, Xin; Tai, Hung-Chun; Li, Yuan-Yao; Li, Jiachen; Sun, Hao; Liang, Peng; Angell, Michael; Huang, Cheng-Liang; Ku, Ching-Shun; Hung, Wei-Hsuan; Jiang, Shi-Kai; Meng, Yongtao; Chen, Hui; Lin, Meng-Chang; Hwang, Bing-Joe; Dai, Hongjie.
Afiliação
  • Zhu G; Department of Chemistry and Bio-X, Stanford University, Stanford, CA, USA.
  • Tian X; Department of Chemistry and Bio-X, Stanford University, Stanford, CA, USA.
  • Tai HC; Department of Chemical Engineering, National Chung Cheng University, Chia-Yi, Taiwan.
  • Li YY; Department of Chemical Engineering, National Chung Cheng University, Chia-Yi, Taiwan.
  • Li J; Department of Chemistry and Bio-X, Stanford University, Stanford, CA, USA.
  • Sun H; Department of Chemistry and Bio-X, Stanford University, Stanford, CA, USA.
  • Liang P; Department of Chemistry and Bio-X, Stanford University, Stanford, CA, USA.
  • Angell M; Department of Chemistry and Bio-X, Stanford University, Stanford, CA, USA.
  • Huang CL; Department of Chemical Engineering, National Chung Cheng University, Chia-Yi, Taiwan.
  • Ku CS; National Synchrotron Radiation Research Center, Hsinchu, Taiwan.
  • Hung WH; Institute of Materials Science and Engineering, National Central University, Taoyuan City, Taiwan.
  • Jiang SK; Department of Chemical Engineering, National Taiwan University of Science and Technology, Taipei, Taiwan.
  • Meng Y; Department of Chemistry and Bio-X, Stanford University, Stanford, CA, USA.
  • Chen H; College of Electrical Engineering and Automation, Shandong University of Science and Technology, Qingdao, People's Republic of China.
  • Lin MC; College of Electrical Engineering and Automation, Shandong University of Science and Technology, Qingdao, People's Republic of China.
  • Hwang BJ; Department of Chemical Engineering, National Taiwan University of Science and Technology, Taipei, Taiwan.
  • Dai H; Department of Chemistry and Bio-X, Stanford University, Stanford, CA, USA. hdai1@stanford.edu.
Nature ; 596(7873): 525-530, 2021 08.
Article em En | MEDLINE | ID: mdl-34433941
Lithium-ion batteries (LIBs) are widely used in applications ranging from electric vehicles to wearable devices. Before the invention of secondary LIBs, the primary lithium-thionyl chloride (Li-SOCl2) battery was developed in the 1970s using SOCl2 as the catholyte, lithium metal as the anode and amorphous carbon as the cathode1-7. This battery discharges by lithium oxidation and catholyte reduction to sulfur, sulfur dioxide and lithium chloride, is well known for its high energy density and is widely used in real-world applications; however, it has not been made rechargeable since its invention8-13. Here we show that with a highly microporous carbon positive electrode, a starting electrolyte composed of aluminium chloride in SOCl2 with fluoride-based additives, and either sodium or lithium as the negative electrode, we can produce a rechargeable Na/Cl2 or Li/Cl2 battery operating via redox between mainly Cl2/Cl- in the micropores of carbon and Na/Na+ or Li/Li+ redox on the sodium or lithium metal. The reversible Cl2/NaCl or Cl2/LiCl redox in the microporous carbon affords rechargeability at the positive electrode side and the thin alkali-fluoride-doped alkali-chloride solid electrolyte interface stabilizes the negative electrode, both are critical to secondary alkali-metal/Cl2 batteries.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article