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Stephen Barlow

Researcher at Georgia Institute of Technology

Publications -  301
Citations -  22649

Stephen Barlow is an academic researcher from Georgia Institute of Technology. The author has contributed to research in topics: Doping & Dopant. The author has an hindex of 64, co-authored 278 publications receiving 19520 citations. Previous affiliations of Stephen Barlow include University of Colorado Boulder.

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Journal ArticleDOI

Phosphonic Acids for Interfacial Engineering of Transparent Conductive Oxides

TL;DR: This review surveys the literature on TCO modification with phosphonic acids (PAs), which has increasingly been used to engineer these interfacial properties in organic-semiconductor devices and discusses the relevance of TCO surface modification to organic electronics.
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Two-photon absorption at telecommunications wavelengths in a dipolar chromophore with a pyrrole auxiliary donor and thiazole auxiliary acceptor.

TL;DR: Three new dipolar chromophores based on a diaklyaminophenyl donor, a pyrrole auxiliary donors, a thiazole auxiliary acceptor, and strong heterocyclic acceptors have been synthesized.
Book ChapterDOI

Two-Photon Absorbing Materials and Two-Photon-Induced Chemistry

TL;DR: Two-photon absorption has been extensively studied from both fundamental and application points of view as discussed by the authors, and a survey of the properties of these classes of materials can be found in this paper.
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Dithienopyrrole-based donor–acceptor copolymers: low band-gap materials for charge transport, photovoltaics and electrochromism

TL;DR: A series of highly soluble donor-acceptor (D-A) copolymers containing N-(3,4,5-tri-n-decyloxyphenyl)-dithieno[3,2-b:2′,3′-d]pyrrole (DTP) or N-(2-decyltetradecyl)-ditieno [3, 2-b] as donor and three different acceptors, 4,7-dittien-2-yl-[2,1,3]-benzothiad
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Electron Affinities of 1,1-Diaryl-2,3,4,5-tetraphenylsiloles: Direct Measurements and Comparison with Experimental and Theoretical Estimates

TL;DR: The experimental and theoretical characterization of the electronic structure of four 1,1-diaryl-2,3,4,5-tetraphenylsiloles and the reorganization energies for the electron-transfer reactions between these siloles and their radical anions are presented.