Chunhui Duan

ORCID: 0000-0002-6521-2149
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About
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Research Areas
  • Organic Electronics and Photovoltaics
  • Conducting polymers and applications
  • Perovskite Materials and Applications
  • Organic Light-Emitting Diodes Research
  • Thin-Film Transistor Technologies
  • Molecular Junctions and Nanostructures
  • Luminescence and Fluorescent Materials
  • Nanowire Synthesis and Applications
  • Crystallization and Solubility Studies
  • X-ray Diffraction in Crystallography
  • Semiconductor materials and interfaces
  • Reproductive Physiology in Livestock
  • Ruminant Nutrition and Digestive Physiology
  • Molecular Sensors and Ion Detection
  • Quantum Dots Synthesis And Properties
  • Porphyrin and Phthalocyanine Chemistry
  • Effects of Environmental Stressors on Livestock
  • Analytical Chemistry and Sensors
  • Magnetism in coordination complexes
  • Chalcogenide Semiconductor Thin Films
  • solar cell performance optimization
  • Photochemistry and Electron Transfer Studies
  • Epoxy Resin Curing Processes
  • Covalent Organic Framework Applications
  • Advanced biosensing and bioanalysis techniques

South China University of Technology
2016-2025

Hebei Agricultural University
2020-2025

State Key Laboratory of Luminescent Materials and Devices
2012-2022

Dalian University
2021-2022

Dalian University of Technology
2021-2022

Beijing National Laboratory for Molecular Sciences
2019-2021

Shanxi Agricultural University
2020

China Agricultural University
2020

State Key Laboratory of Animal Nutrition
2020

Huaibei Normal University
2020

Bulk heterojunction (BHJ) polymer solar cells (PSCs) that can be fabricated by solution processing techniques are under intense investigation in both academic institutions and industrial companies because of their potential to enable mass production flexible cost-effective alternative silicon-based cells. A combination novel development, nanoscale morphology control optimization has led over 8% power conversion efficiencies (PCEs) for BHJ PSCs with a conventional device structure. Attempts...

10.1039/c2ee22296e article EN Energy & Environmental Science 2012-01-01

Bulk-heterojunction polymer solar cells have emerged as an attractive type of cost-effective energy–electrical power transforming device. Recently, great progress in the development new photo-harvesting materials and device optimizations been achieved this field, resulting significant improvement conversion efficiencies from around 1% to higher than 8.0%. The rational design fine tailoring molecular structures donor polymers significantly contributed these prominent advances. Among all kinds...

10.1039/c2jm30470h article EN Journal of Materials Chemistry 2012-01-01

Organic light-emitting diodes (OLEDs) have been successfully developed and now entered the commercial marketplace. Besides impressive performance as displays, one of key advantages OLEDs is that they can potentially be made entirely by solution process thus are more suitable for low cost, large area flexible displays white lighting panels. To realize this, many efforts devoted on development processable materials charge transporting well electrode materials, which resulted in successful...

10.1021/cm101937p article EN Chemistry of Materials 2010-10-21

The majority of organic semiconductors have a low relative dielectric constant (εr < 6), which is an important limitation for solar cells (OSCs). A high would reduce the exciton binding energy, charge carrier recombination losses, and thereby enhance overall device performance OSCs. However, development organic/polymeric with higher constants > 6) has attracted very limited attention. Moreover, OSCs based on photovoltaic materials are still in their infancy. Herein, we report oligoethylene...

10.1039/c7ta10136h article EN Journal of Materials Chemistry A 2017-12-01

The effects of Au nanoparticles (NPs) incorporated into the active layer polymer solar cells (PSCs) with a newly synthesized donor are investigated in detail. Our work shows that localized surface plasmon resonance (LSPR) introduced by metallic NPs can experimentally and theoretically enhance light absorption PSCs because strong LSPR near field mainly distributes laterally along layer. understanding be applied to other NP organic cells. Meanwhile, our results show electrical properties...

10.1039/c1jm14150c article EN Journal of Materials Chemistry 2011-11-19

All-polymer solar cells (all-PSCs) composed of conjugated polymers as both donor and acceptor components in bulk heterojunction photoactive layers have attracted increasing attention. However, it is a big challenge to achieve optimal morphology polymer:polymer blends. In response, we report herein new strategy adjust the nanoscale organization for all-PSCs. Specifically, side chain engineering well-known naphthalene diimide (NDI)-based polymer N2200 modulated by introducing fraction linear...

10.1021/jacs.8b05038 article EN Journal of the American Chemical Society 2018-06-26

A new amino-functionalized polymer, PN<sub>4</sub>N, was developed and applied as an efficient interlayer to improve the cathode interface of fullerene/perovskite (CH<sub>3</sub>NH<sub>3</sub>PbI<sub>x</sub>Cl<sub>3−x</sub>) planar heterojunction solar cells.

10.1039/c4ta05352d article EN Journal of Materials Chemistry A 2014-01-01

Abstract High‐efficiency organic solar cells (OSCs) largely rely on polymer donors. Herein, we report a new building block BNT and relevant PBNT‐BDD featuring B‐N covalent bond for application in OSCs. The unit is synthesized only 3 steps, leading to the facile synthesis of PBNT‐BDD. When blended with nonfullerene acceptor Y6‐BO, afforded power conversion efficiency (PCE) 16.1 % an OSC, comparable benzo[1,2‐b:4,5‐b′]dithiophene (BDT)‐based counterpart. nonradiative recombination energy loss...

10.1002/anie.202016265 article EN Angewandte Chemie International Edition 2021-03-08

Abstract Benefiting from low cost and simple synthesis, polythiophene (PT) derivatives are one of the most popular donor materials for organic solar cells (OSCs). However, polythiophene‐based OSCs still suffer inferior power conversion efficiency (PCE) than those based on donor–acceptor (D–A)‐type conjugated polymers. Herein, a fluorinated derivative, namely P4T2F‐HD, is introduced to modulate miscibility morphology bulk heterojunction (BHJ)‐active layer, leading significant improvement OSC...

10.1002/adma.202008158 article EN Advanced Materials 2021-05-10

Abstract The power conversion efficiencies (PCEs) of organic solar cells (OSCs) have increased rapidly owing to the development non‐fullerene acceptors (NFAs). However, polymer donors lags behind significantly. Currently, are dominated by a handful thiophene‐substituted benzo[1,2‐b:4,5‐b']dithiophene (BDTT) polymers, which suffer from lengthy synthesis and high production cost. Compared with BDTT‐based oligothiophene‐based donor‐acceptor polymers feature much easier synthesis, were...

10.1002/aenm.202104050 article EN Advanced Energy Materials 2022-02-25

Suppressing the photon energy loss (Eloss ), especially non-radiative loss, is of importance to further improve device performance organic solar cells (OSCs). However, typical π-conjugated semiconductors possess a large singlet-triplet gap (ΔEST leading lower triplet state than charge transfer and contributing channel photocurrent by state. Herein, series polymer donors are developed introducing BNIDT block into PM6 backbone. The high electron affinity opposite resonance effect BN bond in...

10.1002/adma.202211871 article EN Advanced Materials 2023-02-03

Abstract Detecting short‐wavelength infrared (SWIR) light has underpinned several emerging technologies. However, the development of highly sensitive organic photodetectors (OPDs) operating in SWIR region is hindered by their poor external quantum efficiencies (EQEs) and high dark currents. Herein, high‐sensitivity SWIR‐OPDs with an efficient photoelectric response extending up to 1.3 µm reported. These OPDs utilize a new ultralow‐bandgap molecular semiconductor featuring quinoidal tricyclic...

10.1002/adma.202310811 article EN Advanced Materials 2024-02-15

Abstract Nonfused ring electron acceptors (NFREAs) are promising candidates for future commercialization of organic solar cells (OSCs) due to their simple synthesis. Still, the power conversion efficiencies (PCEs) NFREA‐based OSCs have large room improvement. In this work, by merging end group halogenation and side chain engineering, we developed four A–D–A'–D–A type NFREAs, which refer as EH‐4F, C4‐4F, EH‐4Cl, C4‐4Cl. Single crystal X‐ray diffraction revealed that multiple intermolecular...

10.1002/agt2.488 article EN cc-by Aggregate 2024-01-04

High concentrations of prolactin (PRL)-induced ovine ovarian granulosa cell (GCs) apoptosis and MAPK12 could aggravate the induced effect. However, molecular mechanisms that MAPK12-induced GC repressed steroid hormone secretion remain unclear. In this study, GCs in P group (GCs with high PRL concentration: 500 ng/mL PRL) P-10 infected by lentiviruses carrying overexpressed sequences MAPK12) were collected for whole-transcriptome analysis. Then, we applied miRNA mimics combined a...

10.3390/ijms26020576 article EN International Journal of Molecular Sciences 2025-01-11

To develop environmentally friendly solvent processed high performance polymer solar cells (PSCs), an alcohol soluble narrow-band-gap conjugated PCDTBT-N and C70 fullerene derivative PC71BM-N, which were functionalized with pendant tertiary amino groups, developed used as active layers in PSCs buffer metal–semiconductor interfaces. Though containing groups showed no photovoltaic properties regardless of the processing conditions, both PC71BM-N performed well to improve electron collection...

10.1039/c3ee41838c article EN Energy & Environmental Science 2013-01-01

A series of internal donor−acceptor type copolymers containing benzothiadiazole and four thiophene rings (bis(2,2′-dithienyl)benzothiadiazole) in their repeating units were synthesized characterized. The effect the position alkyl groups attached to different new polymers on optical, electrochemical, photovoltaic properties was investigated compared with poly(2,7-(9,9-dioctylfluorene)-alt-5,5-(4′,7′-di-2-thienylbenzo[c][1,2,5]thiadiazole)) (PFO-DBT). One polymers,...

10.1021/ma900601y article EN Macromolecules 2009-05-28

Two low-band-gap conjugated polymers, PSiFDCN and PSiFDTA, which consist of alternating silafluorene triphenylamine backbone different pendant acceptor groups (malononitrile 1,3-diethyl-2-thiobarbituric acid) with styrylthiophene as π-bridge, were synthesized characterized. By changing the in side chain, energy levels, absorption spectra, band gaps resulted polymers effectively tuned. As strength acceptors increases, gap reduces from 1.83 eV for to 1.74 PSiFDTA. Bulk heterojunction solar...

10.1021/ma100616f article EN Macromolecules 2010-05-19

Abstract One of the most important factors that limits efficiencies bulk‐heterojunction organic solar cells (OSCs) is modest open‐circuit voltage ( V oc ) due to their large loss caused by significant nonradiative recombination loss. To boost performance OSCs toward theoretical limit, developing high‐performance donor: acceptor systems featuring low with suppressed losses (&lt;0.30 V) desired. Herein, high based on a polymer donor benzodithiophene‐difluorobenzoxadiazole‐2‐decyltetradecyl...

10.1002/aenm.201801699 article EN Advanced Energy Materials 2018-07-29

A series of novel conjugated copolymers based on naphtho[1,2-c:5,6-c]bis(2-octyl-[1,2,3]triazole) (TZNT) are synthesized. These exhibit medium bandgaps ≈1.9 eV. One them demonstrates a high performance up to 6.10% power conversion efficiency in bulk-heterojunction (BHJ) solar-cell device. The can be further enhanced 7.11% when applied an inverted device architecture, using PF3 N-OX as interfacial modifier.

10.1002/adma.201301547 article EN Advanced Materials 2013-05-31

A series of narrow-band-gap donor−acceptor (D−A) conjugated polymers, with thiophene-substituted quinoxaline monomer 5,8-bis(5-bromothiophen-2-yl)-2,3-bis(5-octylthiophen-2-yl)quinoxaline (TTQx) or its cyclized phenazine derivative 8,11-bis(5-bromothiophen-2-yl)-2,5-dioctyldithieno[2,3-a:3′,2′-c]phenazine (TTPz) as acceptors, were synthesized via Suzuki coupling reaction. It was found that the copolymers based on TTQx exhibit obviously red-shifted absorbance compared to previously reported...

10.1021/ma1027164 article EN Macromolecules 2011-01-27
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