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Bryan McCulloch

Researcher at University of California, Berkeley

Publications -  20
Citations -  1237

Bryan McCulloch is an academic researcher from University of California, Berkeley. The author has contributed to research in topics: Copolymer & Monomer. The author has an hindex of 9, co-authored 20 publications receiving 1128 citations. Previous affiliations of Bryan McCulloch include Lawrence Berkeley National Laboratory & Rohm and Haas.

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Block Copolymers for Organic Optoelectronics

TL;DR: In this paper, the authors describe both the synthesis and self-assembly of block copolymers for organic optoelectronics, and suggest that block-copolymer strategies previously employed for more classical, insulating polymer systems may be very useful in organic electronics.
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Effect of Interfacial Properties on Polymer–Nanocrystal Thermoelectric Transport

TL;DR: The electrical behavior of a conducting-polymer/inorganic-nanowire composite is explained with a model in which carrier transport occurs predominantly through a highly conductive volume of polymer that exists at the polymer- nanowire interface.
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Polymer Chain Shape of Poly(3-alkylthiophenes) in Solution Using Small-Angle Neutron Scattering

TL;DR: The chain shape of polymers affects many aspects of their behavior and is governed by their intramolecular interactions as mentioned in this paper, and it is clear that a hierarchy of structural features in these polymers controls charge transport.
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The relationship between morphology and performance of donor–acceptor rod–coil block copolymer solar cells

TL;DR: In this paper, self-assembled functional rod-coil block copolymers (poly(3-hexylthiophene)-b-poly(n-butyl acrylate-stat-acrylate perylene) containing electron donor (Poly(3hexyl thiophene)) and acceptor (perylene) moieties were synthesized, characterized, and studied in photovoltaic devices.
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Poly(3-alkylthiophene) diblock copolymers with ordered microstructures and continuous semiconducting pathways.

TL;DR: It is demonstrated that other, potentially more useful, nanostructures can be formed when these two interactions are more closely balanced, and careful design of the P3AT moiety allows for a balance between crystallization and microphase separation due to chemical dissimilarity between copolymer blocks.