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Title: Long-Range Resonant Charge Transport through Open-Shell Donor–Acceptor Macromolecules

Journal Article · · Journal of the American Chemical Society
 [1];  [1]; ORCiD logo [2];  [3]; ORCiD logo [2];  [2]; ORCiD logo [2];  [4]; ORCiD logo [1]; ORCiD logo [5]; ORCiD logo [6]; ORCiD logo [2]; ORCiD logo [1]
  1. Univ. of Miami, FL (United States)
  2. Georgia Institute of Technology, Atlanta, GA (United States)
  3. Mississippi State Univ., Mississippi State, MS (United States)
  4. Andrés Bello Univ. (Chile)
  5. Univ. of Georgia, Athens, GA (United States)
  6. Univ. of Rochester, NY (United States)

A grand challenge in molecular electronics is the development of molecular materials that can facilitate efficient longrange charge transport. Research spanning more than two decades has been fueled by the prospects of creating a new generation of miniaturized electronic technologies based on molecules whose synthetic tunability offers tailored electronic properties and functions unattainable with conventional electronic materials. However, current design paradigms produce molecules that exhibit off-resonant transport under low bias, which limits the conductance of molecular materials to unsatisfactorily low levels several orders of magnitude below the conductance quantum 1 G0 and often results in an exponential decay in conductance with length. Here, we demonstrate a chemically robust, air-stable, and highly tunable molecular wire platform comprised of open-shell donor−acceptor macromolecules that exhibit remarkably high conductance close to 1 G0 over a length surpassing 20 nm under low bias, with no discernible decay with length. Single-molecule transport measurements and ab initio calculations show that the ultralong-range resonant transport arises from extended π-conjugation, a narrow bandgap, and diradical character, which synergistically enables excellent alignment of frontier molecular orbitals with the electrode Fermi energy. The implementation of this long-sought-after transport regime within molecular materials offers new opportunities for the integration of manifold properties within emerging nanoelectronic technologies.

Research Organization:
Univ. of Miami, Coral Gables, FL (United States); Univ. of Miami, FL (United States)
Sponsoring Organization:
National Science Foundation (NSF); USDOE Office of Science (SC), Basic Energy Sciences (BES)
Grant/Contract Number:
SC0024924
OSTI ID:
2563762
Journal Information:
Journal of the American Chemical Society, Journal Name: Journal of the American Chemical Society Journal Issue: 24 Vol. 147; ISSN 0002-7863; ISSN 1520-5126
Publisher:
American Chemical Society (ACS)Copyright Statement
Country of Publication:
United States
Language:
English

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