Date of Award

Fall 9-5-2025

Degree Type

Dissertation

Degree Name

Doctor of Philosophy (PhD)

Department

Chemistry

First Advisor

Jacob Ciszek

Abstract

Interlayers are used at the metal-on-organic interfaces of organic semiconductor devices to alleviate complications due to thermal metal deposition. Common methods of depositing interlayers include spin-coating, atomic layer deposition, and thermal deposition. These techniques have unintended drawbacks and limitations including by-product formation, solution degrading underlying layers, and limited compatible materials. Reactive installation of interlayers provides a way to modify the metal-organic interface while avoiding issues of the other techniques and providing secondary benefits. However, this method has yet to be utilized at the cathode-electron transport layer (ETL) interface within organic light-emitting devices (OLEDs). The reactive nitrogen of TPBi (2,2',2''-(1,3,5-benzinetriyl)-tris(1-phenyl-1-H-benzimidazole)) allowed for various reactions to occur on the surface, including a ring opening with propylene oxide and acid-base reaction with trifluoroacetic acid. The addition of propylene oxide to the surface of thin film TPBi introduced a controllable oxygen-rich interlayer, confirmed by high-resolution X-ray photoelectron spectroscopy (XPS) and energy dispersive X-ray spectroscopy (EDX). The presence of propylene oxide lowered the contact angle and increased the wettability of TPBi while not negatively affecting a bottom-emission OLED. The reactive nitrogen of TPBi also acted as a base for deprotonation of trifluoroacetic acid leaving a carboxylate interlayer seen on polarization modulation infrared reflection-absorption spectroscopy (PM-IRRAS). The carboxylate layer on the surface acted as a metal binder with an aluminum cathode, as shown in XPS and PM-IRRAS. While this work is targeted at the metal-on-organic interfaces of the ETL and cathode in OLEDS, it could be applied to a wide range of organic semiconductor devices for targeted interfacial modifications.

Available for download on Sunday, February 06, 2028

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