| Year |
Citation |
Score |
| 2020 |
Zeng M, Ren A, Wu W, Zhao Y, Zhan C, Yao J. Lanthanide MOFs for inducing molecular chirality of achiral stilbazolium with strong circularly polarized luminescence and efficient energy transfer for color tuning Chemical Science. 11: 9154-9161. DOI: 10.1039/D0Sc02856H |
0.332 |
|
| 2020 |
Chang Y, Lau T, Chow PCY, Wu N, Su D, Zhang W, Meng H, Ma C, Liu T, Li K, Zou X, Wong KS, Lu X, Yan H, Zhan C. A 16.4% efficiency organic photovoltaic cell enabled using two donor polymers with their side-chains oriented differently by a ternary strategy Journal of Materials Chemistry A. 8: 3676-3685. DOI: 10.1039/C9Ta13293G |
0.353 |
|
| 2020 |
Chai G, Chang Y, Peng Z, Jia Y, Zou X, Yu D, Yu H, Chen Y, Chow PCY, Wong KS, Zhang J, Ade H, Yang L, Zhan C. Enhanced hindrance from phenyl outer side chains on nonfullerene acceptor enables unprecedented simultaneous enhancement in organic solar cell performances with 16.7% efficiency Nano Energy. 76: 105087. DOI: 10.1016/J.Nanoen.2020.105087 |
0.394 |
|
| 2020 |
Li X, Li K, Su D, Shen F, Huo S, Fu H, Zhan C. Design a thieno[3,2-b]thiophene bridged nonfullerene acceptor to increase open-circuit voltage, short-circuit current-density and fill factor via the ternary strategy Chinese Chemical Letters. 31: 1243-1247. DOI: 10.1016/J.Cclet.2019.10.029 |
0.302 |
|
| 2020 |
Li K, Wu Y, Li X, Fu H, Zhan C. 17.1%-Efficiency organic photovoltaic cell enabled with two higher-LUMO-level acceptor guests as the quaternary strategy Science China-Chemistry. 63: 490-496. DOI: 10.1007/S11426-019-9668-8 |
0.365 |
|
| 2020 |
Zhang W, Huang J, Xu J, Han M, Su D, Wu N, Zhang C, Xu A, Zhan C. Phthalimide Polymer Donor Guests Enable over 17% Efficient Organic Solar Cells via Parallel‐Like Ternary and Quaternary Strategies Advanced Energy Materials. 10: 2001436. DOI: 10.1002/Aenm.202001436 |
0.344 |
|
| 2019 |
Meng H, Li Y, Pang B, Li Y, Xiang Y, Guo L, Li X, Zhan C, Huang J. Effects of Halogenation in B←N Embedded Polymer Acceptors on Performance of All-polymer Solar Cells. Acs Applied Materials & Interfaces. PMID 31856566 DOI: 10.1021/Acsami.9B20214 |
0.346 |
|
| 2019 |
Li Y, Meng H, Liu T, Xiao Y, Tang Z, Pang B, Li Y, Xiang Y, Zhang G, Lu X, Yu G, Yan H, Zhan C, Huang J, Yao J. 8.78% Efficient All-Polymer Solar Cells Enabled by Polymer Acceptors Based on a B←N Embedded Electron-Deficient Unit. Advanced Materials (Deerfield Beach, Fla.). e1904585. PMID 31532877 DOI: 10.1002/Adma.201904585 |
0.391 |
|
| 2019 |
Li W, Liu W, Zhang X, Yan D, Liu F, Zhan C. Quaternary Solar Cells with 12.5% Efficiency Enabled with Non-Fullerene and Fullerene Acceptor Guests to Improve Open Circuit Voltage and Film Morphology. Macromolecular Rapid Communications. e1900353. PMID 31531913 DOI: 10.1002/Marc.201900353 |
0.37 |
|
| 2019 |
Li F, Zhang C, Huang J, Fan H, Wang H, Wang P, Zhan C, Liu C, Li X, Yang L, Song Y, Jiang K. Cation-Exchange Approach for Fabrication of Efficient Methylammonium Tin Iodide Perovskite Solar Cells. Angewandte Chemie (International Ed. in English). PMID 30884017 DOI: 10.1002/Anie.201902418 |
0.346 |
|
| 2019 |
Meng H, Li Y, Pang B, Li Y, Zhan C, Huang J. Fullerene-free polymer solar cells enabled with a PhI-based wide band gap donor polymer: promoting efficiencies via acceptor screening and device engineering Journal of Materials Chemistry C. 7: 8442-8449. DOI: 10.1039/C9Tc01932D |
0.316 |
|
| 2019 |
Pan M, Lau T, Tang Y, Wu Y, Liu T, Li K, Chen M, Lu X, Ma W, Zhan C. 16.7%-efficiency ternary blended organic photovoltaic cells with PCBM as the acceptor additive to increase the open-circuit voltage and phase purity Journal of Materials Chemistry A. 7: 20713-20722. DOI: 10.1039/C9Ta06929A |
0.342 |
|
| 2019 |
Chang Y, Lau T, Pan M, Lu X, Yan H, Zhan C. The synergy of host–guest nonfullerene acceptors enables 16%-efficiency polymer solar cells with increased open-circuit voltage and fill-factor Materials Horizons. 6: 2094-2102. DOI: 10.1039/C9Mh00844F |
0.366 |
|
| 2019 |
Liu T, Luo Z, Chen Y, Yang T, Xiao Y, Zhang G, Ma R, Lu X, Zhan C, Zhang M, Yang C, Li Y, Yao J, Yan H. A nonfullerene acceptor with a 1000 nm absorption edge enables ternary organic solar cells with improved optical and morphological properties and efficiencies over 15% Energy & Environmental Science. 12: 2529-2536. DOI: 10.1039/C9Ee01030K |
0.342 |
|
| 2019 |
Shen F, Yan D, Li W, Meng H, Huang J, Li X, Xu J, Zhan C. Quaternary polymer solar cells with over 13% efficiency enabled by improving film-morphologies via binary mixed fullerene additive Materials Chemistry Frontiers. 3: 301-307. DOI: 10.1039/C8Qm00571K |
0.397 |
|
| 2019 |
Su D, Pan M, Liu Z, Lau T, Li X, Shen F, Huo S, Lu X, Xu A, Yan H, Zhan C. A Trialkylsilylthienyl Chain-Substituted Small-Molecule Acceptor with Higher LUMO Level and Reduced Band Gap for Over 16% Efficiency Fullerene-Free Ternary Solar Cells Chemistry of Materials. 31: 8908-8917. DOI: 10.1021/Acs.Chemmater.9B02943 |
0.306 |
|
| 2019 |
Chang Y, Zhang X, Tang Y, Gupta M, Su D, Liang J, Yan D, Li K, Guo X, Ma W, Yan H, Zhan C. 14%-efficiency fullerene-free ternary solar cell enabled by designing a short side-chain substituted small-molecule acceptor Nano Energy. 64: 103934. DOI: 10.1016/J.Nanoen.2019.103934 |
0.395 |
|
| 2019 |
Li X, Meng H, Shen F, Su D, Huo S, Shan J, Huang J, Zhan C. Semitransparent fullerene-free polymer solar cell with 44% AVT and 7% efficiency based on a new chlorinated small molecule acceptor Dyes and Pigments. 166: 196-202. DOI: 10.1016/J.Dyepig.2019.03.024 |
0.391 |
|
| 2019 |
Li K, Wu Y, Tang Y, Pan M, Ma W, Fu H, Zhan C, Yao J. Ternary Blended Fullerene‐Free Polymer Solar Cells with 16.5% Efficiency Enabled with a Higher‐LUMO‐Level Acceptor to Improve Film Morphology Advanced Energy Materials. 9: 1901728. DOI: 10.1002/Aenm.201901728 |
0.332 |
|
| 2018 |
Ye T, Jin S, Kang C, Tian C, Zhang X, Zhan C, Lu S, Kan Z. Comparison Study of Wide Bandgap Polymer (PBDB-T) and Narrow Bandgap Polymer (PBDTTT-EFT) as Donor for Perylene Diimide Based Polymer Solar Cells. Frontiers in Chemistry. 6: 613. PMID 30619822 DOI: 10.3389/Fchem.2018.00613 |
0.362 |
|
| 2018 |
Yan D, Xin J, Li W, Liu S, Wu H, Ma W, Yao J, Zhan C. 13%-Efficiency Quaternary Polymer Solar Cell with Nonfullerene and Fullerene as Mixed Electron Acceptor Materials. Acs Applied Materials & Interfaces. PMID 30525389 DOI: 10.1021/Acsami.8B17246 |
0.38 |
|
| 2018 |
Gupta M, Yan D, Yao J, Zhan C. Organophosphorus Derivatives as Cathode Interfacial Layer Materials For Highly Efficient Fullerene-Free Polymer Solar Cells. Acs Applied Materials & Interfaces. PMID 30260622 DOI: 10.1021/Acsami.8B09313 |
0.357 |
|
| 2018 |
Tang JH, Cai Z, Yan D, Tang K, Shao JY, Zhan C, Wang D, Zhong YW, Wan LJ, Yao J. A Molecular Quadripod as a Noncovalent Interfacial Coupling Reagent for Forming Immobilized Coordination Assemblies. Journal of the American Chemical Society. PMID 30220199 DOI: 10.1021/Jacs.8B07777 |
0.322 |
|
| 2018 |
Gupta M, Yan D, Xu J, Yao J, Zhan C. Tetraphenylphosphonium Bromide as Cathode Buffer Layer Material for Highly Efficient Polymer Solar Cells. Acs Applied Materials & Interfaces. PMID 29359553 DOI: 10.1021/Acsami.7B17870 |
0.359 |
|
| 2018 |
Shen F, Xu J, Li X, Zhan C. Nonfullerene small-molecule acceptors with perpendicular side-chains for fullerene-free solar cells Journal of Materials Chemistry. 6: 15433-15455. DOI: 10.1039/C8Ta04718A |
0.394 |
|
| 2018 |
Gupta M, Yan D, Yao J, Zhan C. Improved fullerene-free polymer solar cells using a rationally designed binary mixed solution of an electron extracting layer Materials Chemistry Frontiers. 2: 1876-1883. DOI: 10.1039/C8Qm00311D |
0.335 |
|
| 2018 |
Li Y, Meng H, Yan D, Li Y, Pang B, Zhang K, Luo G, Huang J, Zhan C. Synthesis of B←N embedded indacenodithiophene chromophores and effects of bromine atoms on photophysical properties and energy levels Tetrahedron. 74: 4308-4314. DOI: 10.1016/J.Tet.2018.06.035 |
0.332 |
|
| 2018 |
Huang J, Li Y, Wang Y, Meng H, Yan D, Jiang B, Wei Z, Zhan C. A Lewis acid-base chemistry approach towards narrow bandgap dye molecules Dyes and Pigments. 153: 1-9. DOI: 10.1016/J.Dyepig.2018.02.003 |
0.304 |
|
| 2018 |
Li W, Yan D, Liu F, Russell T, Zhan C, Yao J. High-efficiency quaternary polymer solar cells enabled with binary fullerene additives to reduce nonfullerene acceptor optical band gap and improve carriers transport Science China Chemistry. 61: 1609-1618. DOI: 10.1007/S11426-018-9320-3 |
0.386 |
|
| 2018 |
Yan D, Liu W, Yao J, Zhan C. Fused‐Ring Nonfullerene Acceptor Forming Interpenetrating J‐Architecture for Fullerene‐Free Polymer Solar Cells Advanced Energy Materials. 8: 1800204. DOI: 10.1002/Aenm.201800204 |
0.322 |
|
| 2017 |
Xu J, Liu W, Geng Y, Deng K, Zhan C, Zeng Q. An STM/STS study of site-selective adsorption of C70 molecules onto arc-shaped BODIPY molecular-networks. Nanoscale. PMID 28150825 DOI: 10.1039/C6Nr08234C |
0.311 |
|
| 2017 |
Liu W, Li W, Yao J, Zhan C. Achieving high short-circuit current and fill-factor via increasing quinoidal character on nonfullerene small molecule acceptor Chinese Chemical Letters. 29: 381-384. DOI: 10.1016/J.Cclet.2017.11.018 |
0.409 |
|
| 2017 |
Liu W, Yao J, Zhan C. Tailoring the photophysical and photovoltaic properties of boron-difluorodipyrromethene dimers Chinese Chemical Letters. 28: 875-880. DOI: 10.1016/J.Cclet.2017.01.013 |
0.407 |
|
| 2017 |
Liu W, Yao J, Zhan C. A Novel BODIPY‐Based Low‐Band‐Gap Small‐Molecule Acceptor for Efficient Non‐fullerene Polymer Solar Cells Chinese Journal of Chemistry. 35: 1813-1823. DOI: 10.1002/Cjoc.201700542 |
0.329 |
|
| 2016 |
Li W, Zhang X, Zhang X, Yao J, Zhan C. High-Performance Solution-Processed Single-Junction Polymer Solar Cell Achievable by Post-Treatment of PEDOT:PSS Layer with Water-Containing Methanol. Acs Applied Materials & Interfaces. PMID 28001036 DOI: 10.1021/Acsami.6B12389 |
0.332 |
|
| 2016 |
Sun MJ, Zhang X, Zhong YW, Zhan C, Yao J. Tunable Self-Assembly and Morphology-Dependent Photoconductivity of a Donor-Acceptor-Structured Diruthenium Complex. Inorganic Chemistry. 55: 13007-13013. PMID 27989151 DOI: 10.1021/Acs.Inorgchem.6B02532 |
0.32 |
|
| 2016 |
Tang A, Zhan C, Yao J, Zhou E. Design of Diketopyrrolopyrrole (DPP)-Based Small Molecules for Organic-Solar-Cell Applications. Advanced Materials (Deerfield Beach, Fla.). PMID 27859743 DOI: 10.1002/Adma.201600013 |
0.372 |
|
| 2016 |
Jiang B, Yao J, Zhan C. Modulating PCBM-Acceptor Crystallinity and Organic Solar Cell Performance by Judiciously Designing Small-Molecule Mainchain End-Capping Units. Acs Applied Materials & Interfaces. PMID 27618875 DOI: 10.1021/Acsami.6B08407 |
0.373 |
|
| 2016 |
Zhang X, Li W, Yao J, Zhan C. High-Efficiency Nonfullerene Polymer Solar Cells Enabling by Integration of Film-Morphology Optimization, Donor Selection, and Interfacial Engineering. Acs Applied Materials & Interfaces. PMID 27246160 DOI: 10.1021/Acsami.6B03926 |
0.355 |
|
| 2016 |
Yao J, Chen Y, Zhan C. Understanding Solvent Manipulation of Morphology in Bulk-Heterojunction Organic Solar Cells. Chemistry, An Asian Journal. PMID 27123789 DOI: 10.1002/Asia.201600374 |
0.351 |
|
| 2016 |
Huang J, Zhang S, Jiang B, Chen Y, Zhang X, Fan Z, Yu D, Lin Z, Yao J, Zhan C. Terminal moiety-driven electrical performance of asymmetric small-molecule-based organic solar cells Journal of Materials Chemistry. 4: 15688-15697. DOI: 10.1039/C6Ta07450B |
0.328 |
|
| 2016 |
Jiang B, Zhang X, Zheng Y, Yu G, Yao J, Zhan C. A comparative study of photovoltaic performance between non-fullerene and fullerene based organic solar cells Rsc Advances. 6: 43715-43718. DOI: 10.1039/C6Ra08827A |
0.37 |
|
| 2016 |
Wu Q, Li L, Hai J, Zhang X, Lu Z, Yang J, Liu Y, Zhang L, Zhan C. Edge-to-face stacking non-fullerene small molecule acceptor for bulk heterojunction solar cells Dyes and Pigments. 132: 41-47. DOI: 10.1016/J.Dyepig.2016.04.040 |
0.418 |
|
| 2016 |
Zhang X, Yao J, Zhan C. Synthesis and photovoltaic properties of low bandgap dimeric perylene diimide based non-fullerene acceptors Science China Chemistry. 59: 209-217. DOI: 10.1007/S11426-015-5485-8 |
0.391 |
|
| 2016 |
Zhang X, Yao J, Zhan C. Boosting Organic Solar Cell Electrical Performance by Introducing Large Aromatics onto Small‐Molecule Peripheral Side‐Chains Advanced Materials Interfaces. 3: 1600323. DOI: 10.1002/Admi.201600323 |
0.412 |
|
| 2015 |
Cui BB, Mao Z, Chen Y, Zhong YW, Yu G, Zhan C, Yao J. Tuning of resistive memory switching in electropolymerized metallopolymeric films. Chemical Science. 6: 1308-1315. PMID 29560217 DOI: 10.1039/C4Sc03345K |
0.306 |
|
| 2015 |
Chen Y, Zhang X, Zhan C, Yao J. Origin of effects of additive solvent on film-morphology in solution-processed nonfullerene solar cells. Acs Applied Materials & Interfaces. 7: 6462-71. PMID 25761629 DOI: 10.1021/Am507581W |
0.363 |
|
| 2015 |
Zhang X, Yao J, Zhan C. A selenophenyl bridged perylene diimide dimer as an efficient solution-processable small molecule acceptor. Chemical Communications (Cambridge, England). 51: 1058-61. PMID 25435375 DOI: 10.1039/C4Cc08457H |
0.377 |
|
| 2015 |
Zhan C, Zhang X, Yao J. New advances in non-fullerene acceptor based organic solar cells Rsc Advances. 5: 93002-93026. DOI: 10.1039/C5Ra17715D |
0.35 |
|
| 2015 |
Liu W, Yao J, Zhan C. Performance enhancement of BODIPY dimer-based small-molecule solar cells using a visible-photon-capturing diketopyrrolopyrrole π-bridge Rsc Advances. 5: 74238-74241. DOI: 10.1039/C5Ra16725F |
0.376 |
|
| 2015 |
Su MJ, Huang JH, Zhang LP, Zhang QQ, Zhan CL, Zhou XQ, Yang LM, Song Y, Jiang KJ. Small molecular thienoquinoidal dyes as electron donors for solution processable organic photovoltaic cells Rsc Advances. 5: 76666-76669. DOI: 10.1039/C5Ra15956C |
0.369 |
|
| 2015 |
Zhang X, Zhan C, Yao J. Non-fullerene organic solar cells with 6.1% efficiency through fine-tuning parameters of the film-forming process Chemistry of Materials. 27: 166-173. DOI: 10.1021/Cm504140C |
0.327 |
|
| 2015 |
Tang A, Zhan C, Yao J. Series of Quinoidal Methyl-Dioxocyano-Pyridine Based π-Extended Narrow-Bandgap Oligomers for Solution-Processed Small-Molecule Organic Solar Cells Chemistry of Materials. 27: 4719-4730. DOI: 10.1021/Acs.Chemmater.5B01350 |
0.417 |
|
| 2015 |
Chen Y, Zhang X, Zhan C, Yao J. In-depth understanding of photocurrent enhancement in solution-processed small-molecule: Perylene diimide non-fullerene organic solar cells Physica Status Solidi (a) Applications and Materials Science. 212: 1961-1968. DOI: 10.1002/Pssa.201532102 |
0.382 |
|
| 2015 |
Tang A, Zhan C, Yao J. Comparative Study of Effects of Terminal Non-Alkyl Aromatic and Alkyl Groups on Small-Molecule Solar Cell Performance Advanced Energy Materials. 5. DOI: 10.1002/Aenm.201500059 |
0.415 |
|
| 2014 |
Liu W, Tang A, Chen J, Wu Y, Zhan C, Yao J. Photocurrent enhancement of BODIPY-based solution-processed small-molecule solar cells by dimerization via the meso position. Acs Applied Materials & Interfaces. 6: 22496-505. PMID 25427221 DOI: 10.1021/Am506585U |
0.352 |
|
| 2014 |
Huang J, Wang X, Zhang X, Niu Z, Lu Z, Jiang B, Sun Y, Zhan C, Yao J. Additive-assisted control over phase-separated nanostructures by manipulating alkylthienyl position at donor backbone for solution-processed, non-fullerene, all-small-molecule solar cells. Acs Applied Materials & Interfaces. 6: 3853-62. PMID 24559327 DOI: 10.1021/Am406050J |
0.326 |
|
| 2014 |
Zhang S, Wang X, Tang A, Huang J, Zhan C, Yao J. Tuning morphology and photovoltaic properties of diketopyrrolopyrrole-based small-molecule solar cells by taloring end-capped aromatic groups. Physical Chemistry Chemical Physics : Pccp. 16: 4664-71. PMID 24468710 DOI: 10.1039/C3Cp54548B |
0.371 |
|
| 2014 |
Tang A, Lu Z, Bai S, Huang J, Chen Y, Shi Q, Zhan C, Yao J. Photocurrent enhancement in diketopyrrolopyrrole solar cells by manipulating dipolar anchoring terminals on alkyl-chain spacers. Chemistry, An Asian Journal. 9: 883-92. PMID 24353042 DOI: 10.1002/Asia.201301416 |
0.357 |
|
| 2014 |
Chen Y, Tang A, Zhang X, Lu Z, Huang J, Zhan C, Yao J. A new solution-processed diketopyrrolopyrrole donor for non-fullerene small-molecule solar cells Journal of Materials Chemistry. 2: 1869-1876. DOI: 10.1039/C3Ta14335J |
0.41 |
|
| 2014 |
Zhang X, Jiang B, Zhang X, Tang A, Huang J, Zhan C, Yao J. Cooperatively Tuning Phase Size and Absorption of Near IR Photons in P3HT:Perylene Diimide Solar Cells by Bay-Modifications on the Acceptor Journal of Physical Chemistry C. 118: 24212-24220. DOI: 10.1021/Jp5093674 |
0.379 |
|
| 2014 |
Lu Z, Jiang B, Zhang X, Tang A, Chen L, Zhan C, Yao J. Perylene–Diimide Based Non-Fullerene Solar Cells with 4.34% Efficiency through Engineering Surface Donor/Acceptor Compositions Chemistry of Materials. 26: 2907-2914. DOI: 10.1021/Cm5006339 |
0.317 |
|
| 2014 |
Wang X, Huang J, Niu Z, Zhang X, Sun Y, Zhan C. Dimeric naphthalene diimide based small molecule acceptors: synthesis, characterization, and photovoltaic properties Tetrahedron. 70: 4726-4731. DOI: 10.1016/J.Tet.2014.05.058 |
0.366 |
|
| 2014 |
Niu Z, Wang X, Huang J, Tang A, Sun Y, Zhan C. A Solution‐Processed Small‐Molecule Diketopyrrolopyrrole Dimer for Organic Solar Cells Asian Journal of Organic Chemistry. 3: 948-952. DOI: 10.1002/Ajoc.201402048 |
0.399 |
|
| 2013 |
Zhang X, Lu Z, Ye L, Zhan C, Hou J, Zhang S, Jiang B, Zhao Y, Huang J, Zhang S, Liu Y, Shi Q, Liu Y, Yao J. A potential perylene diimide dimer-based acceptor material for highly efficient solution-processed non-fullerene organic solar cells with 4.03% efficiency. Advanced Materials (Deerfield Beach, Fla.). 25: 5791-7. PMID 23925952 DOI: 10.1002/Adma.201300897 |
0.382 |
|
| 2013 |
Yu X, Zhan C, Ding X, Zhang S, Zhang X, Liu H, Chen L, Wu Y, Fu H, He S, Huang Y, Yao J. Chromism based on supramolecular H-bonds. Physical Chemistry Chemical Physics : Pccp. 15: 11960-5. PMID 23770931 DOI: 10.1039/C3Cp51268A |
0.356 |
|
| 2013 |
Zhang S, Jiang B, Zhan C, Huang J, Zhang X, Jia H, Tang A, Chen L, Yao J. Phenyl-1,3,5-trithienyl-diketopyrrolopyrrole: a molecular backbone potentially affording high efficiency for solution-processed small-molecule organic solar cells through judicious molecular design. Chemistry, An Asian Journal. 8: 2407-16. PMID 23766286 DOI: 10.1002/Asia.201300371 |
0.349 |
|
| 2013 |
Lu Z, Zhang X, Zhan C, Jiang B, Zhang X, Chen L, Yao J. Impact of molecular solvophobicity vs. solvophilicity on device performances of dimeric perylene diimide based solution-processed non-fullerene organic solar cells. Physical Chemistry Chemical Physics : Pccp. 15: 11375-85. PMID 23739661 DOI: 10.1039/C3Cp51475G |
0.37 |
|
| 2013 |
Huang J, Zhan C, Zhang X, Zhao Y, Lu Z, Jia H, Jiang B, Ye J, Zhang S, Tang A, Liu Y, Pei Q, Yao J. Solution-processed DPP-based small molecule that gives high photovoltaic efficiency with judicious device optimization. Acs Applied Materials & Interfaces. 5: 2033-9. PMID 23427767 DOI: 10.1021/Am302896U |
0.343 |
|
| 2013 |
Tang A, Li L, Lu Z, Huang J, Jia H, Zhan C, Tan Z, Li Y, Yao J. Significant improvement of photovoltaic performance by embedding thiophene in solution-processed star-shaped TPA-DPP backbone Journal of Materials Chemistry. 1: 5747-5757. DOI: 10.1039/C3Ta10640C |
0.385 |
|
| 2013 |
Huang J, Wang X, Zhan C, Zhao Y, Sun Y, Pei Q, Liu Y, Yao J. Wide band gap copolymers based on phthalimide: synthesis, characterization, and photovoltaic properties with 3.70% efficiency Polymer Chemistry. 4: 2174. DOI: 10.1039/C3Py21134G |
0.358 |
|
| 2013 |
Jiang B, Zhang X, Zhan C, Lu Z, Huang J, Ding X, He S, Yao J. Benzodithiophene bridged dimeric perylene diimide amphiphiles as efficient solution-processed non-fullerene small molecules Polymer Chemistry. 4: 4631-4638. DOI: 10.1039/C3Py00457K |
0.391 |
|
| 2013 |
Zhang Z, Zhang X, Zhan C, Lu Z, Ding X, He S, Yao J. The leverage effect of the relative strength of molecular solvophobicity vs. solvophilicity on fine-tuning nanomorphologies of perylene diimide bolaamphiphiles Soft Matter. 9: 3089-3097. DOI: 10.1039/C2Sm27674G |
0.362 |
|
| 2012 |
Liu H, Jia H, Wang L, Wu Y, Zhan C, Fu H, Yao J. Intermolecular electron transfer promoted by directional donor-acceptor attractions in self-assembled diketopyrrolopyrrole-thiophene films. Physical Chemistry Chemical Physics : Pccp. 14: 14262-9. PMID 22951990 DOI: 10.1039/C2Cp41288H |
0.384 |
|
| 2012 |
Huang J, Jia H, Li L, Lu Z, Zhang W, He W, Jiang B, Tang A, Tan Z, Zhan C, Li Y, Yao J. Fine-tuning device performances of small molecule solar cells via the more polarized DPP-attached donor units. Physical Chemistry Chemical Physics : Pccp. 14: 14238-42. PMID 22847595 DOI: 10.1039/C2Cp42050C |
0.392 |
|
| 2012 |
Yu X, Zhang S, He W, Zhang Z, Guo F, Zhan C, Huang Y. Synthesis and Photovoltaic Performances of a Novel Phthalocyanine- perylene Molecular Heterojunction Chinese Journal of Organic Chemistry. 32: 1981. DOI: 10.6023/Cjoc201203015 |
0.386 |
|
| 2012 |
Huang J, Zhao Y, He W, Jia H, Lu Z, Jiang B, Zhan C, Pei Q, Liu Y, Yao J. Effects of structure-manipulated molecular stacking on solid-state optical properties and device performances Polymer Chemistry. 3: 2832. DOI: 10.1039/C2Py20406A |
0.364 |
|
| 2012 |
Huang J, Zhao Y, Ding X, Jia H, Jiang B, Zhang Z, Zhan C, He S, Pei Q, Li Y, Liu Y, Yao J. Synthesis and charge-transporting properties of electron-deficient CN2–fluorene based D–A copolymers Polymer Chemistry. 3: 2170. DOI: 10.1039/C2Py20184D |
0.322 |
|
| 2012 |
Lu Z, Zhan C, Yu X, He W, Jia H, Chen L, Tang A, Huang J, Yao J. Large-scale, ultra-dense and vertically standing zinc phthalocyanine π–π stacks as a hole-transporting layer on an ITO electrode Journal of Materials Chemistry. 22: 23492-23496. DOI: 10.1039/C2Jm35342C |
0.328 |
|
| 2011 |
Ke D, Zhan C, Xu S, Ding X, Peng A, Sun J, He S, Li AD, Yao J. Self-assembled hollow nanospheres strongly enhance photoluminescence. Journal of the American Chemical Society. 133: 11022-5. PMID 21699223 DOI: 10.1021/Ja202179T |
0.305 |
|
| 2011 |
Zhu H, He W, Zhan C, Li X, Guan Z, Guo F, Yao J. Synthesis, crystal structure, and different local conformations of pyridine–imide oligomers Tetrahedron. 67: 8458-8464. DOI: 10.1016/J.Tet.2011.09.006 |
0.311 |
|
| 2008 |
Li X, Zhan C, Wang Y, Yao J. Pyridine-imide oligomers. Chemical Communications (Cambridge, England). 2444-6. PMID 18491009 DOI: 10.1039/B800020D |
0.357 |
|
| 2008 |
Berni E, Dolain C, Kauffmann B, Léger JM, Zhan C, Huc I. Expanding the registry of aromatic amide foldamers: folding, photochemistry and assembly using diaza-anthracene units. The Journal of Organic Chemistry. 73: 2687-94. PMID 18331057 DOI: 10.1021/Jo702602W |
0.682 |
|
| 2006 |
Zhan C, Léger JM, Huc I. Cross-hybridization of pyridinedicarboxamide helical strands and their N-oxides. Angewandte Chemie (International Ed. in English). 45: 4625-8. PMID 16789035 DOI: 10.1002/Anie.200600785 |
0.514 |
|
| 2006 |
Zhan C, Li Y, Li D, Wang D, Nie Y. Multi-photon absorption and optical limiting from six stilbazolium derivatives: donor influences Optical Materials. 28: 289-293. DOI: 10.1016/J.Optmat.2005.01.002 |
0.32 |
|
| 2005 |
Chen P, Gao P, Zhan C, Liu M. Interfacial Langmuir-Blodgett assembly of straight and parallel aligned nanoribbons. Chemphyschem : a European Journal of Chemical Physics and Physical Chemistry. 6: 1108-13. PMID 15945044 DOI: 10.1002/Cphc.200400465 |
0.321 |
|
| 2005 |
Dolain C, Zhan C, Léger JM, Daniels L, Huc I. Folding directed N-oxidation of oligopyridine-dicarboxamide strands and hybridization of oxidized oligomers Journal of the American Chemical Society. 127: 2400-2401. PMID 15724988 DOI: 10.1021/Ja0424631 |
0.705 |
|
| 2003 |
Zhan C, Wang J, Yuan J, Gong H, Liu Y, Liu M. Synthesis of Right- and Left-Handed Silver Nanohelices with a Racemic Gelator Langmuir. 19: 9440-9445. DOI: 10.1021/La034958U |
0.312 |
|
| 2002 |
Zhan C, Zhang D, Zhu D, Wang D, Li Y, Li D, Lu Z, Zhao L, Nie Y. Third- and fifth-order optical nonlinearities in a new stilbazolium derivative Journal of the Optical Society of America B-Optical Physics. 19: 369-375. DOI: 10.1364/Josab.19.000369 |
0.315 |
|
| 2002 |
Zhan C, Xu W, Zhang D, Li D, Lu Z, Nie Y, Zhu D. Z-scan investigation of fifth-order optical nonlinearity induced by saturable-absorption from (TBA)2Ni(dmit)2: application for optical limiting Journal of Materials Chemistry. 12: 2945-2948. DOI: 10.1039/B203021G |
0.302 |
|
| 2002 |
Zhan C, Wang D. Nonlinear dependence of solvent polarity effects on twisted intramolecular charge-transfer states and linear relation for electronic spectra in a stilbazolium-like dye Journal of Photochemistry and Photobiology a-Chemistry. 147: 93-101. DOI: 10.1016/S1010-6030(01)00634-7 |
0.346 |
|
| 2001 |
Zhan C, Li D, Wang D, Zhang D, Li Y, Xu W, Lu Z, Zhao L, Nie Y, Zhu D. The high fifth-order nonlinearity in a new stilbazolium derivative: trans-1-[p-(p-dimethylaminobenzyl-azo)-benzyl]-2-(N-methyl-4-pyridinium)-ethene iodide Chemical Physics Letters. 347: 410-414. DOI: 10.1016/S0009-2614(01)01059-4 |
0.328 |
|
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