Abstract
The study of excited-state energy diffusion has had an important impact in the development and optimization of organic electronics. For instance, optimizing excited-state energy migration in the photoactive layer in an organic solar cell device has been shown to yield efficient solar energy conversion. Despite the crucial role that energy migration plays in molecular electronic device physics, there is still a great deal to be explored to establish how molecular orientation impacts energy diffusion mechanisms. In this work, we have synthesized a new library of solution-processable, Zn (alkoxycarbonyl)phenylporphyrins containing butyl (ZnTCB4PP), hexyl (ZnTCH4PP), 2-ethylhexyl (ZnTCEH4PP), and octyl (ZnTCO4PP) alkoxycarbonyl groups. We establish that, by varying the length of the peripheral alkyl chains on the metalloporphyrin macrocycle, preferential orientation and molecular self-assembly is observed in solution-processed thin films. The resultant arrangement of molecules consequently affects the electronic and photophysical characteristics of the metalloporphyrin thin films. The various molecular arrangements in the porphyrin thin films and their resultant impact were determined using UV-Vis absorption spectroscopy, steady-state and time-resolved fluorescence emission lifetimes, and X-ray diffraction in thin films. The films were doped with C60 quencher molecules and the change in fluorescence was measured to derive a relative quenching efficiency. Using emission decay, relative quenching efficiency, and dopant volume fraction as input, insights on exciton diffusion coefficient and exciton diffusion lengths were obtained from a Monte Carlo simulation. The octyl derivative (ZnTCO4PP) showed the strongest relative fluorescence quenching and, therefore, the highest exciton diffusion coefficient (5.29 × 10−3 cm2 s−1) and longest exciton diffusion length (~81 nm). The octyl derivative also showed the strongest out-of-plane stacking among the metalloporphyrins studied. This work demonstrates how molecular self-assembly can be used to modulate and direct exciton diffusion in solution-processable metalloporphyrin thin films engineered for optoelectronic and photonic applications.
Highlights
Introduction iationsAfter billions of years of evolution, nature has optimized the process of photosynthesis through which living organisms can harvest sunlight for sustenance [1,2]
When sunlight is absorbed by a chromophore or an array of chromophores, the energy captured is transferred to reaction centers for dissociation of charges [3,4]
This charge separation leads to the storage of chemical energy which is later used for metabolic activities [5]. These photophysical processes of absorption of light, migration of energy, and separation of charges have influenced the field of bio-inspired solar cell fabrication tremendously [6,7,8]
Summary
Introduction iationsAfter billions of years of evolution, nature has optimized the process of photosynthesis through which living organisms can harvest sunlight for sustenance [1,2]. When sunlight is absorbed by a chromophore or an array of chromophores, the energy captured is transferred to reaction centers for dissociation of charges [3,4]. This charge separation leads to the storage of chemical energy which is later used for metabolic activities [5]. These photophysical processes of absorption of light, migration of energy, and separation of charges have influenced the field of bio-inspired solar cell fabrication tremendously [6,7,8]. Porphyrins have been used as linkers in metal and covalent organic frameworks and for a wide
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