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Author

Junping Du

Other affiliations: Imperial College London
Bio: Junping Du is an academic researcher from Chinese Academy of Sciences. The author has contributed to research in topics: Polymer & Conjugated system. The author has an hindex of 15, co-authored 18 publications receiving 1445 citations. Previous affiliations of Junping Du include Imperial College London.

Papers
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Journal ArticleDOI
TL;DR: The synthesis and polymerization of a novel thieno[3,2-b]thiophene-diketopyrrolopyrrole-based monomer is reported, which has a maximum hole mobility of 1.95 cm(2) V(-1) s(-1), which is the highest mobility from a polymer-based OFET reported to date.
Abstract: We report the synthesis and polymerization of a novel thieno[3,2-b]thiophene−diketopyrrolopyrrole-based monomer. Copolymerization with thiophene afforded a polymer with a maximum hole mobility of 1.95 cm2 V−1 s−1, which is the highest mobility from a polymer-based OFET reported to date. Bulk-heterojunction solar cells comprising this polymer and PC71BM gave a power conversion efficiency of 5.4%.

861 citations

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TL;DR: A series of transient absorption and photocurrent experiments as a function of excitation wavelength and temperature for two low-band-gap polymer/fullerene blends to study the mechanism of charge separation at the donor/acceptor interface provide key evidence for the role of excess energy in driving charge separation.
Abstract: The energetic driving force required to drive charge separation across donor/acceptor heterojunctions is a key consideration for organic optoelectronic devices. Herein we report a series of transient absorption and photocurrent experiments as a function of excitation wavelength and temperature for two low-band-gap polymer/fullerene blends to study the mechanism of charge separation at the donor/acceptor interface. For the blend that exhibits the smallest donor/acceptor LUMO energy level offset, the photocurrent quantum yield falls as the photon excitation energy is reduced toward the band gap, but the yield of bound, interfacial charge transfer states rises. This interplay between bound and free charge generation as a function of initial exciton energy provides key evidence for the role of excess energy in driving charge separation of direct relevance to the development of low-band-gap polymers for enhanced solar light harvesting.

189 citations

Journal ArticleDOI
TL;DR: A series of bitriazine derivatives were synthesized for the first time by the self-coupling reactions of the monocholoro-triazines in the presence of nickel catalyst and show excellent optoelectronic properties.

72 citations

Journal ArticleDOI
TL;DR: The role of PC70BM excitons in driving charge photogeneration in low bandgap polymer/fullerene bulk heterojunction solar cells has been studied in this article.
Abstract: The role of PC70BM excitons in driving charge photogeneration in low bandgap polymer/fullerene bulk heterojunction solar cells has been studied Both transient absorption spectroscopy of charge generation yields in blend films as a function of excitation energies and photocurrent quantum efficiency spectra of the corresponding devices indicate that charge generation in this system results primarily from direct optical excitation of PC70BM Blend composition studies of photocurrent density and photoluminescence quenching indicate that the efficiency of photocurrent generation is primarily determined by the limited efficiency of PC70BM exciton diffusion to the polymer due to the formation of PC70BM domains (≥5 nm) This limitation becomes more severe as the PC70BM content is increased above 50% Despite this limitation and despite the poor charge photogeneration from polymer excitons, organic solar cells fabricated using this photoactive blend layer yielded device photocurrents of 71 mA/cm2, maximal EQEs o

62 citations

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TL;DR: Several functionalized benzo[1,2-b:3,4-b':5,6-d'']trithiophenes have been synthesized and characterized and shows great promise as the donor constituent in donor-acceptor type copolymers for use in organic electronics.

61 citations


Cited by
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Journal ArticleDOI
TL;DR: School of Chemistry, Bio21 Institute, University of Melbourne, 30 Flemington Road, Victoria 3010, Australia; School of Materials Science and Engineering, Nanyang Technological University, Nastyang Avenue, Republic of Singapore 639798; Institute of Materials Research and Engineering (IMRE) and the Agency for Science, Technology and Research (A*STAR), 3 Research Link, Singapore 117602.
Abstract: A review was presented to demonstrate a historical description of the synthesis of light-emitting conjugated polymers for applications in electroluminescent devices. Electroluminescence (EL) was first reported in poly(para-phenylene vinylene) (PPV) in 1990 and researchers continued to make significant efforts to develop conjugated materials as the active units in light-emitting devices (LED) to be used in display applications. Conjugated oligomers were used as luminescent materials and as models for conjugated polymers in the review. Oligomers were used to demonstrate a structure and property relationship to determine a key polymer property or to demonstrate a technique that was to be applied to polymers. The review focused on demonstrating the way polymer structures were made and the way their properties were controlled by intelligent and rational and synthetic design.

2,378 citations

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TL;DR: In this paper, the state-of-the-art in organic field effect transistors (OFETs) are reviewed in light of requirements for demanding future applications, in particular active-matrix addressing for flexible organic light-emitting diode (OLED) displays.
Abstract: Over the past 25 years, organic field-effect transistors (OFETs) have witnessed impressive improvements in materials performance by 3–4 orders of magnitude, and many of the key materials discoveries have been published in Advanced Materials. This includes some of the most recent demonstrations of organic field-effect transistors with performance that clearly exceeds that of benchmark amorphous silicon-based devices. In this article, state-of-the-art in OFETs are reviewed in light of requirements for demanding future applications, in particular active-matrix addressing for flexible organic light-emitting diode (OLED) displays. An overview is provided over both small molecule and conjugated polymer materials for which field-effect mobilities exceeding > 1 cm2 V–1 s–1 have been reported. Current understanding is also reviewed of their charge transport physics that allows reaching such unexpectedly high mobilities in these weakly van der Waals bonded and structurally comparatively disordered materials with a view towards understanding the potential for further improvement in performance in the future.

1,992 citations

Journal ArticleDOI
TL;DR: The research community has made great progress in the field of bulk heterojunction (BHJ) polymer solar cells since its inception in 1995 as mentioned in this paper and the power conversion efficiency (PCE) has increased from 1% in the 1990s to over 8% just recently.
Abstract: The research on the polymer-based solar cells (PSCs) has attracted an increasing amount of attention in recent years because PSCs pose potential advantages over mainstream inorganic-based solar cells, such as significantly reduced material/fabrication costs, flexible substrates, and light weight of finished solar cells. The research community has made great progress in the field of bulk heterojunction (BHJ) polymer solar cells since its inception in 1995. The power conversion efficiency (PCE), a key parameter to assess the performance of solar cells, has increased from 1% in the 1990s to over 8% just recently. These great advances are mainly fueled by the development of conjugated polymers used as the electron-donating materials in BHJ solar cells. In this Perspective, we first briefly review the progress on the design of conjugated polymers for polymer solar cells in the past 16 years. Since a conjugated polymer can be arbitrarily divided into three constituting components—the conjugated backbone, the si...

1,403 citations

Journal ArticleDOI
TL;DR: This Perspective analyzes some of the most exciting strategies recently suggested in the design and structural organization of π-functional materials for transistor and solar cell applications and places emphasis on the interplay between molecular structure, self-assembling properties, nanoscale and mesoscale ordering, and device efficiency parameters.
Abstract: Organic electronics are broadly anticipated to impact the development of flexible thin-film device technologies. Among these, solution-processable π-conjugated polymers and small molecules are proving particularly promising in field-effect transistors and bulk heterojunction solar cells. This Perspective analyzes some of the most exciting strategies recently suggested in the design and structural organization of π-functional materials for transistor and solar cell applications. Emphasis is placed on the interplay between molecular structure, self-assembling properties, nanoscale and mesoscale ordering, and device efficiency parameters. A critical look at the various approaches used to optimize both materials and device performance is provided to assist in the identification of new directions and further advances.

1,301 citations

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TL;DR: The article reviews the current understanding of the physical mechanisms that determine the (opto)electronic properties of high-performance organic materials and highlights the capabilities of various experimental techniques for characterization, summarizes top-of-the-line device performance, and outlines recent trends in the further development of the field.
Abstract: Organic (opto)electronic materials have received considerable attention due to their applications in thin-film-transistors, light-emitting diodes, solar cells, sensors, photorefractive devices, and many others. The technological promises include low cost of these materials and the possibility of their room-temperature deposition from solution on large-area and/or flexible substrates. The article reviews the current understanding of the physical mechanisms that determine the (opto)electronic properties of high-performance organic materials. The focus of the review is on photoinduced processes and on electronic properties important for optoelectronic applications relying on charge carrier photogeneration. Additionally, it highlights the capabilities of various experimental techniques for characterization of these materials, summarizes top-of-the-line device performance, and outlines recent trends in the further development of the field. The properties of materials based both on small molecules and on conjug...

995 citations