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Sei Hum Jang

Researcher at University of Washington

Publications -  24
Citations -  1707

Sei Hum Jang is an academic researcher from University of Washington. The author has contributed to research in topics: Chromophore & Micelle. The author has an hindex of 19, co-authored 23 publications receiving 1594 citations. Previous affiliations of Sei Hum Jang include Purdue University & University of Southern California.

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Enhancement of aggregation-induced emission in dye-encapsulating polymeric micelles for bioimaging

TL;DR: Three amphiphilic block copolymers are employed to form polymeric micelles and function as nanocarriers to disperse hydrophobic aggregation‐induced emission (AIE) dyes, 1,1,2,3,4,5‐hexaphenylsilole (HPS) and/or bis(4‐(N‐(1‐naphthyl) phenylamino)‐phenyl)fumaronitrile (NPAFN)
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Rational Design of Dipolar Chromophore as an Efficient Dopant-Free Hole-Transporting Material for Perovskite Solar Cells

TL;DR: An electron donor-acceptor (D-A) substituted dipolar chromophore (BTPA-TCNE) is developed to serve as an efficient dopant-free hole-transporting material (HTM) for perovskite solar cells (PVSCs) by outperforming the control device with doped spiro-OMeTAD HTM.
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Nanoscale architectural control and macromolecular engineering of nonlinear optical dendrimers and polymers for electro-optics

TL;DR: In this article, the authors focused on using nanoscal polymers for high-performance electro-optic (EO) devices and developed highly efficient nonlinear optical dendrimers and polymers.
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Donor-Acceptor Thiolated Polyenic Chromophores Exhibiting Large Optical Nonlinearity and Excellent Photostability

TL;DR: In this paper, epoxyisophorone ring-opening chemistry was used to incorporate the butylthio group to the phenyltetraene bridge of highly efficient nonlinear optical chromophores in high overall yield.
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PH-dependent, thermosensitive polymeric nanocarriers for drug delivery to solid tumors

TL;DR: Doxorubicin-loaded micelles formed from a series of dual pH- and temperature-responsive block copolymers were stable at blood pH and showed increased drug release at acidic pH and displayed more potent anti-cancer activity than free doxorUBicin when tested in a tumor xenograft model in mice.