Lukas Eng | Searcharxiv

arXiv2020

Optical-Field Driven Charge-Transfer Modulations near Composite Nanostructures

Optical activation of material properties illustrates the potentials held by tuning light-matter interactions with impacts ranging from basic science to technological applications. Here, we demonstrate for the first time that composite nanostructures providing nonlocal environments can be engineered to optically trigger photoinduced charge transfer dynamic (CTD) modulations in the solid state. The nanostructures herein explored lead to unprecedented out-of-phase behaviour between charge separation and recombination dynamics, along with linear CTD variations with the optical-field amplitude. Using transient absorption spectroscopy, up to 270 % increase in charge separation rate is obtained in organic semiconductor thin films. We provide evidences that composite nanostructures allow for surface photovoltages to be created, which kinetics vary with the composite architecture and last beyond optical pulse temporal characteristics. Furthermore, by generalizing Marcus theory framework, we explain why CTD modulations can only be unveiled when optic field effects are enhanced by nonlocal image dipole interactions. Demonstrating that composite nanostructures can be designed to use optical fields as CTD remote actuators opens the path for their use in practical and original applications ranging from photochemistry to optoelectronics.

cond-mat.mtrl-sci↗

arXiv2017

Epitaxial Growth of Pentacene on Alkali Halide Surfaces Studied by Kelvin Probe Force Microscopy

In the field of molecular electronics thin films of molecules adsorbed on insulating surfaces are used as the functional building blocks of electronic devices. A control of the structural and electronic properties of the thin films is required for a reliable operating mode of such devices. Here, noncontact atomic force and Kelvin probe force microscopies have been used to investigate the growth and electronic properties of pentacene on KBr(001) and KCl(001) surfaces. Mainly molecular islands of upright standing pentacene are formed, whereas a new phase of tilted molecules appear near step edges on some KBr samples. Local contact potential differences (LCPD) have been studied with both Kelvin experiments and density-functional theory calculations. Large LCPD are found between the substrate and the differently oriented molecules, which may be explained by a partial charge transfer from the pentacene to the surface. The monitoring of the changes of the pentacene islands during dewetting shows that multilayers build up at the expense of monolayers. Moreover, in the Kelvin images, previously unknown line defects appear, which unveil the epitaxial growth of pentacene crystals.

cond-mat.mes-hall↗