On the interface dipole at the pentacene-fullerene heterojunction : A theoretical study

• The electronic structure at organic/organic interfaces plays a key role, among others, in defining the quantum efficiency of organics-based photovoltaic cells. Here, we perform quantum-chemical and microelectrostatic calculations on molecular aggregates of various sizes and shapes to characterize the interfacial dipole moment at pentacene/C60 heterojunctions. The results show that the interfacial dipole mostly originates in polarization effects due to the asymmetry in the multipolar expansion of the electronic density distribution between the interacting molecules, rather than in a charge transfer from donor to acceptor. The local dipole is found to fluctuate in sign and magnitude over the interface and appears as a sensitive probe of the relative arrangements of the pentacene and C60 molecules (and of the resulting local electrical fields sensed by the molecular units).

Ämnesord

NATURVETENSKAP  -- Kemi -- Fysikalisk kemi (hsv//swe)

NATURAL SCIENCES  -- Chemical Sciences -- Physical Chemistry (hsv//eng)

Nyckelord

Electrical field

Electronic density distribution

Interacting molecules

Interface dipole

Interfacial dipoles

Molecular aggregate

Molecular units

Multipolar expansion

Organics

Pentacenes

Polarization effect

Sensitive probe

Theoretical study

Publikations- och innehållstyp

ref (ämneskategori)

art (ämneskategori)