Orientation and morphology control in acid-catalyzed covalent organic framework thin films†
ab
Kirt A.
Page,
abc
Alexander
Reidell,
ab
Cheri M.
Hampton,
ab
W. Joshua
Kennedy,
a
Tobin J.
Marks,
d
Antonio
Facchetti,
dh
Jun
Lou,
f
Luke A.
Baldwin
a
and
Nicholas R.
Glavin
*a
Abstract
As thin films of semiconducting covalent organic frameworks (COFs) are demonstrating utility for ambipolar electronics, channel materials in organic electrochemical transistors (OECTs), and broadband photodetectors, control and modulation of their thin film properties is paramount. In this work, an interfacial growth technique is utilized to synthesize imine TAPB-PDA COF films at both the liquid–liquid interface as well as at the liquid–solid interface on a Si/SiO2 substrate. The concentration of acetic acid catalyst in the aqueous phase is shown to significantly influence the thin film morphology of the liquid–solid growth, with concentrations below 1 M resulting in no film nucleation, concentrations of 1–4 M enabling smooth film formation, and concentrations greater than 4 M resulting in films with a higher density of particulates on the surface. Importantly, while the films grown at the liquid–liquid interface are mixed-orientation, those grown directly at the liquid–solid interface on the Si/SiO2 surface have highly oriented COF layers aligned parallel to the substrate surface. Moreover, this liquid–solid growth process affords TAPB-PDA COF thin films with p-type charge transport having a transconductance of 10 μS at a gate voltage of −0.9 V in an OECT device structure.
- This article is part of the themed collection: Nanoscale 2024 Emerging Investigators
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