These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

155 related articles for article (PubMed ID: 32089763)

  • 1. Relation between the Electronic Properties of Regioregular Donor-Acceptor Terpolymers and Their Binary Copolymers.
    Heintges GHL; Bolduc A; Meskers SCJ; Janssen RAJ
    J Phys Chem C Nanomater Interfaces; 2020 Feb; 124(6):3503-3516. PubMed ID: 32089763
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Conjugated Donor-Acceptor Terpolymers Toward High-Efficiency Polymer Solar Cells.
    Dang D; Yu D; Wang E
    Adv Mater; 2019 May; 31(22):e1807019. PubMed ID: 30701605
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Contrasting performance of donor-acceptor copolymer pairs in ternary blend solar cells and two-acceptor copolymers in binary blend solar cells.
    Khlyabich PP; Rudenko AE; Burkhart B; Thompson BC
    ACS Appl Mater Interfaces; 2015 Feb; 7(4):2322-30. PubMed ID: 25590225
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Bi-diketopyrrolopyrrole (Bi-DPP) as a novel electron accepting compound in low band gap π-conjugated donor-acceptor copolymers/oligomers.
    Ahner J; Nowotny J; Schubert US; Hager MD
    Des Monomers Polym; 2017; 20(1):210-220. PubMed ID: 29491794
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Theoretical study on the correlation between band gap, bandwidth, and oscillator strength in fluorene-based donor-acceptor conjugated copolymers.
    Hung YC; Jiang JC; Chao CY; Su WF; Lin ST
    J Phys Chem B; 2009 Jun; 113(24):8268-77. PubMed ID: 19473008
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A Very Low Band Gap Diketopyrrolopyrrole-Porphyrin Conjugated Polymer.
    Bucher L; Tanguy L; Fortin D; Desbois N; Harvey PD; Sharma GD; Gros CP
    Chempluschem; 2017 Apr; 82(4):625-630. PubMed ID: 31961580
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Donor-pi-acceptor conjugated copolymers for photovoltaic applications: tuning the open-circuit voltage by adjusting the donor/acceptor ratio.
    Peng Q; Park K; Lin T; Durstock M; Dai L
    J Phys Chem B; 2008 Mar; 112(10):2801-8. PubMed ID: 18281978
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Enhancing the photocurrent in diketopyrrolopyrrole-based polymer solar cells via energy level control.
    Li W; Roelofs WS; Wienk MM; Janssen RA
    J Am Chem Soc; 2012 Aug; 134(33):13787-95. PubMed ID: 22812425
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Donor-acceptor-type copolymers based on a naphtho[1,2-c:5,6-c]bis(1,2,5-thiadiazole) scaffold for high-efficiency polymer solar cells.
    Liu LQ; Zhang GC; Liu P; Zhang J; Dong S; Wang M; Ma YG; Yip HL; Huang F
    Chem Asian J; 2014 Aug; 9(8):2104-12. PubMed ID: 24737596
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Computational Study of New Small Molecules based Thiophene as Donor Materials for Bulk Heterojunction Photovoltaic Cells.
    Zouitina S; Aboulouard A; Ghazali AE; Tounsi A; Idrissi ME
    J Fluoresc; 2023 Mar; 33(2):553-563. PubMed ID: 36454428
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Diketopyrrolopyrrole-based π-bridged donor-acceptor polymer for photovoltaic applications.
    Li W; Lee T; Oh SJ; Kagan CR
    ACS Appl Mater Interfaces; 2011 Oct; 3(10):3874-83. PubMed ID: 21888419
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The effect of different aromatic conjugated bridges on optoelectronic properties of diketopyrrolopyrrole-based donor materials for organic photovoltaics.
    Shafiq UrRehman ; Alam A; Bibi S; Sadaf S; Khan SR; Shoaib M; Khan AQ; Khan M; UrRehman W
    J Mol Model; 2020 May; 26(6):154. PubMed ID: 32451633
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Structure-Function Relationships in PMA and PMAT Series Copolymers for Polymer Solar Cells.
    Chen JH; Liu CK; Chang WC; Sah PT; Chan LH
    Polymers (Basel); 2018 Apr; 10(4):. PubMed ID: 30966419
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Enhanced performance of organic photovoltaic cells fabricated with a methyl thiophene-3-carboxylate-containing alternating conjugated copolymer.
    Cho MJ; Seo J; Kim KH; Choi DH; Prasad PN
    Macromol Rapid Commun; 2012 Jan; 33(2):146-51. PubMed ID: 22121017
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Universal correlation between fibril width and quantum efficiency in diketopyrrolopyrrole-based polymer solar cells.
    Li W; Hendriks KH; Furlan A; Roelofs WS; Wienk MM; Janssen RA
    J Am Chem Soc; 2013 Dec; 135(50):18942-8. PubMed ID: 24279503
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A 9.16% Power Conversion Efficiency Organic Solar Cell with a Porphyrin Conjugated Polymer Using a Nonfullerene Acceptor.
    Tanguy L; Malhotra P; Singh SP; Brisard G; Sharma GD; Harvey PD
    ACS Appl Mater Interfaces; 2019 Aug; 11(31):28078-28087. PubMed ID: 31294545
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular design of photovoltaic materials for polymer solar cells: toward suitable electronic energy levels and broad absorption.
    Li Y
    Acc Chem Res; 2012 May; 45(5):723-33. PubMed ID: 22288572
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Intrinsic Properties of Two Benzodithiophene-Based Donor--Acceptor Copolymers Used in Organic Solar Cells: A Quantum-Chemical Approach.
    Kastinen T; Niskanen M; Risko C; Cramariuc O; Hukka TI
    J Phys Chem A; 2016 Feb; 120(7):1051-64. PubMed ID: 26840559
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Regioregular copolymers of 3-alkoxythiophene and their photovoltaic application.
    Shi C; Yao Y; Yang Y; Pei Q
    J Am Chem Soc; 2006 Jul; 128(27):8980-6. PubMed ID: 16819895
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Donor-acceptor conjugated polymers based on multifused ladder-type arenes for organic solar cells.
    Wu JS; Cheng SW; Cheng YJ; Hsu CS
    Chem Soc Rev; 2015 Mar; 44(5):1113-54. PubMed ID: 25322211
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.