Efficient modulation of end groups for the asymmetric small molecule acceptors enabling organic solar cells with over 15% efficiency
暂无分享,去创建一个
Gang Li | M. Zhang | B. Tang | Feng Liu | H. Yan | Ruijie Ma | Tao Liu | Zhenghui Luo | Guanwei Cui | Liang Xu | Zaiyu Wang | Li-li Tong | Dandan Li | Dandan Li
[1] C. Zhong,et al. Altering alkyl-chains branching positions for boosting the performance of small-molecule acceptors for highly efficient nonfullerene organic solar cells , 2020, Science China Chemistry.
[2] Yongfang Li,et al. Improving open-circuit voltage by a chlorinated polymer donor endows binary organic solar cells efficiencies over 17% , 2020, Science China Chemistry.
[3] B. Liu,et al. A monothiophene unit incorporating both fluoro and ester substitution enabling high-performance donor polymers for non-fullerene solar cells with 16.4% efficiency , 2019, Energy & Environmental Science.
[4] C. Zhong,et al. Significantly improving the performance of polymer solar cells by the isomeric ending-group based small molecular acceptors: Insight into the isomerization , 2019 .
[5] Weihua Tang,et al. Nonacyclic carbazole-based non-fullerene acceptors enable over 12% efficiency with enhanced stability for organic solar cells , 2019, Journal of Materials Chemistry A.
[6] P. Hao,et al. Methane-perylene diimide-based small molecule acceptors for high efficiency non-fullerene organic solar cells , 2019, Journal of Materials Chemistry C.
[7] X. Gu,et al. Aggregation‐Induced Multilength Scaled Morphology Enabling 11.76% Efficiency in All‐Polymer Solar Cells Using Printing Fabrication , 2019, Advanced materials.
[8] Yanming Sun,et al. Asymmetric A–D–π–A-type nonfullerene small molecule acceptors for efficient organic solar cells , 2019, Journal of Materials Chemistry A.
[9] Yong Cui,et al. Eco‐Compatible Solvent‐Processed Organic Photovoltaic Cells with Over 16% Efficiency , 2019, Advanced materials.
[10] J. Yao,et al. A nonfullerene acceptor with a 1000 nm absorption edge enables ternary organic solar cells with improved optical and morphological properties and efficiencies over 15% , 2019, Energy & Environmental Science.
[11] A. Jen,et al. Fused selenophene-thieno[3,2-b]thiophene-selenophene (ST)-based narrow-bandgap electron acceptor for efficient organic solar cells with small voltage loss. , 2019, Chemical communications.
[12] Q. Zheng,et al. Enhancing the Photovoltaic Performance of Ladder-Type Dithienocyclopentacarbazole-Based Nonfullerene Acceptors through Fluorination and Side-Chain Engineering , 2019, Chemistry of Materials.
[13] Wei Ma,et al. Single‐Junction Polymer Solar Cells with 16.35% Efficiency Enabled by a Platinum(II) Complexation Strategy , 2019, Advanced materials.
[14] F. Gao,et al. Over 16% efficiency organic photovoltaic cells enabled by a chlorinated acceptor with increased open-circuit voltages , 2019, Nature Communications.
[15] C. Zhong,et al. Unconjugated Side‐Chain Engineering Enables Small Molecular Acceptors for Highly Efficient Non‐Fullerene Organic Solar Cells: Insights into the Fine‐Tuning of Acceptor Properties and Micromorphology , 2019, Advanced Functional Materials.
[16] W. Gao,et al. A High‐Performance Non‐Fullerene Acceptor Compatible with Polymers with Different Bandgaps for Efficient Organic Solar Cells , 2019, Solar RRL.
[17] Jacek Ulanski,et al. Single-Junction Organic Solar Cell with over 15% Efficiency Using Fused-Ring Acceptor with Electron-Deficient Core , 2019, Joule.
[18] Jianqi Zhang,et al. Tuning the dipole moments of nonfullerene acceptors with an asymmetric terminal strategy for highly efficient organic solar cells , 2019, Journal of Materials Chemistry A.
[19] He Yan,et al. Reduced Energy Loss Enabled by a Chlorinated Thiophene‐Fused Ending‐Group Small Molecular Acceptor for Efficient Nonfullerene Organic Solar Cells with 13.6% Efficiency , 2019, Advanced Energy Materials.
[20] Christoph J. Brabec,et al. Critical review of the molecular design progress in non-fullerene electron acceptors towards commercially viable organic solar cells. , 2019, Chemical Society reviews.
[21] Wenkai Zhong,et al. Achieving over 16% efficiency for single-junction organic solar cells , 2019, Science China Chemistry.
[22] Weihua Tang,et al. Nonfullerene Acceptor for Organic Solar Cells with Chlorination on Dithieno[3,2-b:2′,3′-d]pyrrol Fused-Ring , 2019, ACS Energy Letters.
[23] G. Schatz,et al. Fluorination Effects on Indacenodithienothiophene Acceptor Packing and Electronic Structure, End-Group Redistribution, and Solar Cell Photovoltaic Response. , 2019, Journal of the American Chemical Society.
[24] B. Tang,et al. Non-fullerene acceptor engineering with three-dimensional thiophene/selenophene-annulated perylene diimides for high performance polymer solar cells , 2018 .
[25] Changduk Yang,et al. One-pot synthesis of electron-acceptor composite enables efficient fullerene-free ternary organic solar cells , 2018 .
[26] Ling Hong,et al. Selenopheno[3,2-b]thiophene-Based Narrow-Bandgap Nonfullerene Acceptor Enabling 13.3% Efficiency for Organic Solar Cells with Thickness-Insensitive Feature , 2018, ACS Energy Letters.
[27] Yongfang Li,et al. Use of two structurally similar small molecular acceptors enabling ternary organic solar cells with high efficiencies and fill factors , 2018 .
[28] Yanming Sun,et al. High-Performance Eight-Membered Indacenodithiophene-Based Asymmetric A-D-A Type Non-Fullerene Acceptors , 2018, Solar RRL.
[29] B. Tang,et al. Pyran-annulated perylene diimide derivatives as non-fullerene acceptors for high performance organic solar cells , 2018 .
[30] Yanming Sun,et al. Extension of indacenodithiophene backbone conjugation enables efficient asymmetric A–D–A type non-fullerene acceptors , 2018 .
[31] Yong Cao,et al. Organic and solution-processed tandem solar cells with 17.3% efficiency , 2018, Science.
[32] Feng Liu,et al. High-efficiency small-molecule ternary solar cells with a hierarchical morphology enabled by synergizing fullerene and non-fullerene acceptors , 2018, Nature Energy.
[33] Xuemei Li,et al. Nonfullerene small-molecule acceptors with perpendicular side-chains for fullerene-free solar cells , 2018 .
[34] H. Ade,et al. Modulation of End Groups for Low‐Bandgap Nonfullerene Acceptors Enabling High‐Performance Organic Solar Cells , 2018, Advanced Energy Materials.
[35] A. Jen,et al. Highly Efficient Organic Solar Cells Based on S,N-Heteroacene Non-Fullerene Acceptors , 2018, Chemistry of Materials.
[36] S. Forrest,et al. Donor–Acceptor–Acceptor's Molecules for Vacuum‐Deposited Organic Photovoltaics with Efficiency Exceeding 9% , 2018 .
[37] C. Zhong,et al. Asymmetrical Small Molecule Acceptor Enabling Nonfullerene Polymer Solar Cell with Fill Factor Approaching 79 , 2018 .
[38] A. Jen,et al. Mapping Nonfullerene Acceptors with a Novel Wide Bandgap Polymer for High Performance Polymer Solar Cells , 2018, Advanced Energy Materials.
[39] C. Zhong,et al. Asymmetrical Ladder‐Type Donor‐Induced Polar Small Molecule Acceptor to Promote Fill Factors Approaching 77% for High‐Performance Nonfullerene Polymer Solar Cells , 2018, Advanced materials.
[40] Ling Zhou,et al. π-π stacking induced high current density and improved efficiency in ternary organic solar cells. , 2018, Nanoscale.
[41] Jie Zhu,et al. Over 14% Efficiency in Polymer Solar Cells Enabled by a Chlorinated Polymer Donor , 2018, Advanced materials.
[42] Fujun Zhang,et al. Dithieno[3,2‐b:2′,3′‐d]pyrrol Fused Nonfullerene Acceptors Enabling Over 13% Efficiency for Organic Solar Cells , 2018, Advanced materials.
[43] Seth R. Marder,et al. Non-fullerene acceptors for organic solar cells , 2018 .
[44] Ke Gao,et al. Dithienopicenocarbazole-Based Acceptors for Efficient Organic Solar Cells with Optoelectronic Response Over 1000 nm and an Extremely Low Energy Loss. , 2018, Journal of the American Chemical Society.
[45] R. Friend,et al. Organic solar cells based on non-fullerene acceptors. , 2018, Nature materials.
[46] Feng Gao,et al. Organic solar cells based on non-fullerene acceptors. , 2018, Nature materials.
[47] Fan Yang,et al. "Double-Cable" Conjugated Polymers with Linear Backbone toward High Quantum Efficiencies in Single-Component Polymer Solar Cells. , 2017, Journal of the American Chemical Society.
[48] S. Forrest,et al. High Efficiency Near-Infrared and Semitransparent Non-Fullerene Acceptor Organic Photovoltaic Cells. , 2017, Journal of the American Chemical Society.
[49] Fujun Zhang,et al. Ternary small molecule solar cells exhibiting power conversion efficiency of 10.3 , 2017 .
[50] Maksim Y. Livshits,et al. "Roller-Wheel"-Type Pt-Containing Small Molecules and the Impact of "Rollers" on Material Crystallinity, Electronic Properties, and Solar Cell Performance. , 2017, Journal of the American Chemical Society.
[51] Yun Zhang,et al. Molecular Optimization Enables over 13% Efficiency in Organic Solar Cells. , 2017, Journal of the American Chemical Society.
[52] Fujun Zhang,et al. Highly Efficient Parallel-Like Ternary Organic Solar Cells , 2017 .
[53] Zhishan Bo,et al. Exploiting Noncovalently Conformational Locking as a Design Strategy for High Performance Fused-Ring Electron Acceptor Used in Polymer Solar Cells. , 2017, Journal of the American Chemical Society.
[54] Ke Gao,et al. Solution-processed organic tandem solar cells with power conversion efficiencies >12% , 2016, Nature Photonics.
[55] Chunru Wang,et al. Fused Nonacyclic Electron Acceptors for Efficient Polymer Solar Cells. , 2017, Journal of the American Chemical Society.
[56] Jianqi Zhang,et al. Fluorination-enabled optimal morphology leads to over 11% efficiency for inverted small-molecule organic solar cells , 2016, Nature Communications.
[57] Feng Liu,et al. A Thieno[3,4-b]thiophene-Based Non-fullerene Electron Acceptor for High-Performance Bulk-Heterojunction Organic Solar Cells. , 2016, Journal of the American Chemical Society.
[58] Yanming Sun,et al. A Facile Planar Fused-Ring Electron Acceptor for As-Cast Polymer Solar Cells with 8.71% Efficiency. , 2016, Journal of the American Chemical Society.
[59] H. Ade,et al. Efficient organic solar cells processed from hydrocarbon solvents , 2016, Nature Energy.
[60] Xiaojing Long,et al. An Electron-Deficient Building Block Based on the B←N Unit: An Electron Acceptor for All-Polymer Solar Cells. , 2016, Angewandte Chemie.
[61] Luping Yu,et al. Recent Advances in Bulk Heterojunction Polymer Solar Cells. , 2015, Chemical reviews.
[62] Yongsheng Chen,et al. A series of simple oligomer-like small molecules based on oligothiophenes for solution-processed solar cells with high efficiency. , 2015, Journal of the American Chemical Society.
[63] Feng Liu,et al. Single-junction polymer solar cells with high efficiency and photovoltage , 2015, Nature Photonics.
[64] Huiqiong Zhou,et al. Polymer Homo‐Tandem Solar Cells with Best Efficiency of 11.3% , 2015, Advanced materials.
[65] Daoben Zhu,et al. An Electron Acceptor Challenging Fullerenes for Efficient Polymer Solar Cells , 2015, Advanced materials.
[66] Guillermo C Bazan,et al. Bulk heterojunction solar cells: morphology and performance relationships. , 2014, Chemical reviews.
[67] Yang Yang,et al. Polymer solar cells , 2012, Nature Photonics.
[68] O. Inganäs,et al. An Easily Synthesized Blue Polymer for High‐Performance Polymer Solar Cells , 2010, Advanced materials.