TY - JOUR
T1 - Solid State Dilution Controls Marcus Inverted Transport in Rectifying Molecular Junctions
AU - Kang, Hungu
AU - Kong, Gyu Don
AU - Yoon, Hyo Jae
N1 - Funding Information:
This research was supported by the NRF of Korea (NRF-2019R1A2C2011003 and NRF-2019R1A6A1A11044070).
Publisher Copyright:
© 2021 American Chemical Society.
PY - 2021/1/28
Y1 - 2021/1/28
N2 - Traditional Marcus theory accounts for electron transfer reactions in solutions, and the polarity of solvent molecule matters for them. How such an environment polarity affects electron transfer reactions in solid-state devices, however, remains uncertain. This paper describes how the Marcus inverted charge transport is influenced by solid-state molecular dilution in large-area tunneling junctions. A monolayer of 2,2′-bipyridyl terminated n-alkanethiolate (SC11BIPY), which rectifies currents via electron hopping within the inverted regime, is diluted with n-alkanethiolate (SCn) of different lengths (n = 8, 10, or 18) or at different surface mole fractions. The dilution introduces nonpolar environments within the monolayer, hinders stabilization of charged BIPY species upon electron hopping, and pushes the equilibrium of BIPY ⇄ BIPY•- process toward the reverse direction. Our work demonstrates that solid-state molecular dilution permits systematic control of the environment polarity of active component in nanoscale devices, much like solvent polarity control in solution, and their performances.
AB - Traditional Marcus theory accounts for electron transfer reactions in solutions, and the polarity of solvent molecule matters for them. How such an environment polarity affects electron transfer reactions in solid-state devices, however, remains uncertain. This paper describes how the Marcus inverted charge transport is influenced by solid-state molecular dilution in large-area tunneling junctions. A monolayer of 2,2′-bipyridyl terminated n-alkanethiolate (SC11BIPY), which rectifies currents via electron hopping within the inverted regime, is diluted with n-alkanethiolate (SCn) of different lengths (n = 8, 10, or 18) or at different surface mole fractions. The dilution introduces nonpolar environments within the monolayer, hinders stabilization of charged BIPY species upon electron hopping, and pushes the equilibrium of BIPY ⇄ BIPY•- process toward the reverse direction. Our work demonstrates that solid-state molecular dilution permits systematic control of the environment polarity of active component in nanoscale devices, much like solvent polarity control in solution, and their performances.
UR - http://www.scopus.com/inward/record.url?scp=85100279372&partnerID=8YFLogxK
U2 - 10.1021/acs.jpclett.0c03251
DO - 10.1021/acs.jpclett.0c03251
M3 - Article
C2 - 33464915
AN - SCOPUS:85100279372
SN - 1948-7185
VL - 12
SP - 982
EP - 988
JO - Journal of Physical Chemistry Letters
JF - Journal of Physical Chemistry Letters
IS - 3
ER -