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Intrinsic glassy-metallic transport in an amorphous coordination polymer.
Xie, Jiaze; Ewing, Simon; Boyn, Jan-Niklas; Filatov, Alexander S; Cheng, Baorui; Ma, Tengzhou; Grocke, Garrett L; Zhao, Norman; Itani, Ram; Sun, Xiaotong; Cho, Himchan; Chen, Zhihengyu; Chapman, Karena W; Patel, Shrayesh N; Talapin, Dmitri V; Park, Jiwoong; Mazziotti, David A; Anderson, John S.
Afiliação
  • Xie J; Department of Chemistry, University of Chicago, Chicago, Illinois, USA.
  • Ewing S; Department of Chemistry, University of Chicago, Chicago, Illinois, USA.
  • Boyn JN; James Franck Institute, University of Chicago, Chicago, Illinois, USA.
  • Filatov AS; Department of Chemistry, University of Chicago, Chicago, Illinois, USA.
  • Cheng B; James Franck Institute, University of Chicago, Chicago, Illinois, USA.
  • Ma T; Department of Chemistry, University of Chicago, Chicago, Illinois, USA.
  • Grocke GL; Department of Chemistry, University of Chicago, Chicago, Illinois, USA.
  • Zhao N; Pritzker School of Molecular Engineering, University of Chicago, Chicago, Illinois, USA.
  • Itani R; Pritzker School of Molecular Engineering, University of Chicago, Chicago, Illinois, USA.
  • Sun X; Department of Chemistry, University of Chicago, Chicago, Illinois, USA.
  • Cho H; Department of Chemistry, University of Chicago, Chicago, Illinois, USA.
  • Chen Z; Department of Human Genetics, University of Chicago, Chicago, Illinois, USA.
  • Chapman KW; Department of Chemistry, University of Chicago, Chicago, Illinois, USA.
  • Patel SN; Department of Materials Science and Engineering, Korea Advanced Institute of Science and Technology, Dajeon, South Korea.
  • Talapin DV; Department of Chemistry, Stony Brook University, Stony Brook, New York, USA.
  • Park J; Department of Chemistry, Stony Brook University, Stony Brook, New York, USA.
  • Mazziotti DA; Pritzker School of Molecular Engineering, University of Chicago, Chicago, Illinois, USA.
  • Anderson JS; Department of Chemistry, University of Chicago, Chicago, Illinois, USA.
Nature ; 611(7936): 479-484, 2022 Nov.
Article em En | MEDLINE | ID: mdl-36289346
Conducting organic materials, such as doped organic polymers1, molecular conductors2,3 and emerging coordination polymers4, underpin technologies ranging from displays to flexible electronics5. Realizing high electrical conductivity in traditionally insulating organic materials necessitates tuning their electronic structure through chemical doping6. Furthermore, even organic materials that are intrinsically conductive, such as single-component molecular conductors7,8, require crystallinity for metallic behaviour. However, conducting polymers are often amorphous to aid durability and processability9. Using molecular design to produce high conductivity in undoped amorphous materials would enable tunable and robust conductivity in many applications10, but there are no intrinsically conducting organic materials that maintain high conductivity when disordered. Here we report an amorphous coordination polymer, Ni tetrathiafulvalene tetrathiolate, which displays markedly high electronic conductivity (up to 1,200 S cm-1) and intrinsic glassy-metallic behaviour. Theory shows that these properties are enabled by molecular overlap that is robust to structural perturbations. This unusual set of features results in high conductivity that is stable to humid air for weeks, pH 0-14 and temperatures up to 140 °C. These findings demonstrate that molecular design can enable metallic conductivity even in heavily disordered materials, raising fundamental questions about how metallic transport can exist without periodic structure and indicating exciting new applications for these materials.

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

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