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SWNT Anchored with Carboxylated Polythiophene "Links" on High-Capacity Li-Ion Battery Anode Materials.
Kwon, Yo Han; Minnici, Krysten; Park, Jung Jin; Lee, Sujin R; Zhang, Guoyan; Takeuchi, Esther S; Takeuchi, Kenneth J; Marschilok, Amy C; Reichmanis, Elsa.
Afiliación
  • Park JJ; Department of Chemical and Biomolecular Engineering , Korea Advanced Institute of Science and Technology (KAIST) , 291 Daehak-ro, Yuseong-gu , Daejeon 305-701 , Republic of Korea.
  • Takeuchi ES; Energy Sciences Directorate , Brookhaven National Laboratory , Upton , New York 11973 , United States.
  • Marschilok AC; Energy Sciences Directorate , Brookhaven National Laboratory , Upton , New York 11973 , United States.
J Am Chem Soc ; 140(17): 5666-5669, 2018 05 02.
Article en En | MEDLINE | ID: mdl-29526097
ABSTRACT
Conjugated polymers possessing polar functionalities were shown to effectively anchor single-walled carbon nanotubes (SWNTs) to the surface of high-capacity anode materials and enable the formation of electrical networks. Specifically, poly[3-(potassium-4-butanoate) thiophene] (PPBT) served as a bridge between SWNT networks and various anode materials, including monodispersed Fe3O4 spheres (sFe3O4) and silicon nanoparticles (Si NPs). The PPBT π-conjugated backbone and carboxylate (COO-) substituted alkyl side chains, respectively, attracted the SWNT π-electron surface and chemically interacted with active material surface hydroxyl (-OH) species to form a carboxylate bond. Beneficially, this architecture effectively captured cracked/pulverized particles that typically form as a result of repeated active material volume changes that occur during charging and discharging. Thus, changes in electrode thickness were suppressed substantially, stable SEI layers were formed, electrode resistance was reduced, and enhanced electrode kinetics was observed. Together, these factors led to excellent electrochemical performance.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Am Chem Soc Año: 2018 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Am Chem Soc Año: 2018 Tipo del documento: Article