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Title: Ultrafast electron transfer at organic semiconductor interfaces: Importance of molecular orientation

Journal Article · · Journal of Physical Chemistry Letters
DOI:https://doi.org/10.1021/jz502253r· OSTI ID:1215420
 [1];  [2];  [3];  [4];  [2]
  1. Stanford Univ., Stanford, CA (United States); SLAC National Accelerator Laboratory, Menlo Park, CA (United States)
  2. SLAC National Accelerator Laboratory, Menlo Park, CA (United States)
  3. Soongsil Univ., Seoul (Korea)
  4. Stanford Univ., Stanford, CA (United States)

Much is known about the rate of photoexcited charge generation in at organic donor/acceptor (D/A) heterojunctions overaged over all relative arrangements. However, there has been very little experimental work investigating how the photoexcited electron transfer (ET) rate depends on the precise relative molecular orientation between D and A in thin solid films. This is the question that we address in this work. We find that the ET rate depends strongly on the relative molecular arrangement: The interface where the model donor compound copper phthalocyanine is oriented face-on with respect to the fullerene C60 acceptor yields a rate that is approximately 4 times faster than that of the edge-on oriented interface. Our results suggest that the D/A electronic coupling is significantly enhanced in the face-on case, which agrees well with theoretical predictions, underscoring the importance of controlling the relative interfacial molecular orientation.

Research Organization:
SLAC National Accelerator Laboratory (SLAC), Menlo Park, CA (United States)
Sponsoring Organization:
USDOE Office of Science (SC)
Grant/Contract Number:
2011-0031628; KUS-C1-015-21
OSTI ID:
1215420
Journal Information:
Journal of Physical Chemistry Letters, Vol. 6, Issue 1; ISSN 1948-7185
Publisher:
American Chemical SocietyCopyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 45 works
Citation information provided by
Web of Science

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Impact of interfacial molecular orientation on radiative recombination and charge generation efficiency journal July 2017
Spontaneous Exciton Dissociation at Organic Semiconductor Interfaces Facilitated by the Orientation of the Delocalized Electron–Hole Wavefunction journal March 2020
Recent Advances in Morphology Optimization for Organic Photovoltaics journal June 2018
Rationalizing Small-Molecule Donor Design toward High-Performance Organic Solar Cells: Perspective from Molecular Architectures journal August 2018
Electroluminochromic Materials and Devices Based on Metal Complexes journal October 2019
Influence of conjugation length on ultrafast electronic tunneling in organic semiconductor thin films journal January 2018
Ultrafast core-excited electron dynamics in model crystalline organic semiconductors journal January 2020
Attractive Dispersion Interactions Versus Steric Repulsion of tert -Butyl groups in the Crystal Packing of a D 3 h -Symmetric Tris(quinoxalinophenanthrophenazine) journal December 2015
Growing Ultra-flat Organic Films on Graphene with a Face-on Stacking via Moderate Molecule-Substrate Interaction journal June 2016
Luminescent ion pairs with tunable emission colors for light-emitting devices and electrochromic switches journal January 2017
Structure–Function Relationship of Organic Semiconductors: Detailed Insights From Time-Resolved EPR Spectroscopy journal February 2019