Robust nonfullerene solar cells approaching unity external quantum efficiency enabled by suppression of geminate recombination
暂无分享,去创建一个
C. Brabec | J. Durrant | T. Kirchartz | Marios Neophytou | D. Baran | N. Gasparini | Z. Hamid | I. McCulloch | A. Wadsworth | Weimin Zhang | Xin Song | N. Wehbe | Ching-Hong Tan
[1] James H. Bannock,et al. Burn‐in Free Nonfullerene‐Based Organic Solar Cells , 2017 .
[2] Zhe Li,et al. An Efficient, “Burn in” Free Organic Solar Cell Employing a Nonfullerene Electron Acceptor , 2017, Advanced materials.
[3] H. Ade,et al. Achieving Highly Efficient Nonfullerene Organic Solar Cells with Improved Intermolecular Interaction and Open‐Circuit Voltage , 2017, Advanced materials.
[4] Feng Liu,et al. Efficient Semitransparent Solar Cells with High NIR Responsiveness Enabled by a Small‐Bandgap Electron Acceptor , 2017, Advanced materials.
[5] Wenjun Zhang,et al. Fullerene-Free Organic Solar Cells with Efficiency Over 12% Based on EDTA-ZnO Hybrid Cathode Interlayer , 2017 .
[6] Joo-Hyun Kim,et al. Efficient Nonfullerene Polymer Solar Cells Enabled by a Novel Wide Bandgap Small Molecular Acceptor , 2017, Advanced materials.
[7] Wei You,et al. Single‐Junction Binary‐Blend Nonfullerene Polymer Solar Cells with 12.1% Efficiency , 2017, Advanced materials.
[8] Runnan Yu,et al. Design, Synthesis, and Photovoltaic Characterization of a Small Molecular Acceptor with an Ultra-Narrow Band Gap. , 2017, Angewandte Chemie.
[9] C. J. M. Emmott,et al. Reducing the efficiency-stability-cost gap of organic photovoltaics with highly efficient and stable small molecule acceptor ternary solar cells. , 2017, Nature materials.
[10] Christoph J. Brabec,et al. Abnormal strong burn-in degradation of highly efficient polymer solar cells caused by spinodal donor-acceptor demixing , 2017, Nature Communications.
[11] C. McNeill,et al. Critical Role of Pendant Group Substitution on the Performance of Efficient All-Polymer Solar Cells , 2017 .
[12] David G Lidzey,et al. Light‐Soaking‐Free Inverted Polymer Solar Cells with an Efficiency of 10.5% by Compositional and Surface Modifications to a Low‐Temperature‐Processed TiO2 Electron‐Transport Layer , 2017, Advanced materials.
[13] I. McCulloch,et al. Reduced voltage losses yield 10% efficient fullerene free organic solar cells with >1 V open circuit voltages† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c6ee02598f Click here for additional data file. , 2016, Energy & environmental science.
[14] Long Ye,et al. Energy‐Level Modulation of Small‐Molecule Electron Acceptors to Achieve over 12% Efficiency in Polymer Solar Cells , 2016, Advanced materials.
[15] Jean-Luc Brédas,et al. Thieno[3,4-c]pyrrole-4,6-dione-3,4-difluorothiophene Polymer Acceptors for Efficient All-Polymer Bulk Heterojunction Solar Cells. , 2016, Angewandte Chemie.
[16] R. Friend,et al. What Controls the Rate of Ultrafast Charge Transfer and Charge Separation Efficiency in Organic Photovoltaic Blends. , 2016, Journal of the American Chemical Society.
[17] Fujun Zhang,et al. Alloy Acceptor: Superior Alternative to PCBM toward Efficient and Stable Organic Solar Cells , 2016, Advanced materials.
[18] C. Brabec,et al. Designing ternary blend bulk heterojunction solar cells with reduced carrier recombination and a fill factor of 77% , 2016, Nature Energy.
[19] X. Zhan,et al. Molecular Lock: A Versatile Key to Enhance Efficiency and Stability of Organic Solar Cells , 2016, Advanced materials.
[20] H. Ade,et al. Fast charge separation in a non-fullerene organic solar cell with a small driving force , 2016, Nature Energy.
[21] Alberto Salleo,et al. High-efficiency and air-stable P3HT-based polymer solar cells with a new non-fullerene acceptor , 2016, Nature Communications.
[22] J. Yao,et al. High-Efficiency Nonfullerene Polymer Solar Cell Enabling by Integration of Film-Morphology Optimization, Donor Selection, and Interfacial Engineering. , 2016, ACS applied materials & interfaces.
[23] Manas R. Parida,et al. Remarkably High Conversion Efficiency of Inverted Bulk Heterojunction Solar Cells: From Ultrafast Laser Spectroscopy and Electron Microscopy to Device Fabrication and Optimization , 2016 .
[24] Jianhui Hou,et al. Breaking the 10% Efficiency Barrier in Organic Photovoltaics: Morphology and Device Optimization of Well‐Known PBDTTT Polymers , 2016 .
[25] Luping Yu,et al. Covalently Bound Clusters of Alpha-Substituted PDI-Rival Electron Acceptors to Fullerene for Organic Solar Cells. , 2016, Journal of the American Chemical Society.
[26] Raja Shahid Ashraf,et al. Exploring the origin of high optical absorption in conjugated polymers. , 2016, Nature materials.
[27] Yongfang Li,et al. Non-Fullerene Polymer Solar Cells Based on Alkylthio and Fluorine Substituted 2D-Conjugated Polymers Reach 9.5% Efficiency. , 2016, Journal of the American Chemical Society.
[28] Andrew J Pearson,et al. Critical light instability in CB/DIO processed PBDTTT-EFT:PC71BM organic photovoltaic devices , 2016 .
[29] Bertrand J. Tremolet de Villers,et al. Removal of Residual Diiodooctane Improves Photostability of High-Performance Organic Solar Cell Polymers , 2016 .
[30] J. Durrant,et al. Singlet Exciton Lifetimes in Conjugated Polymer Films for Organic Solar Cells , 2016, Polymers.
[31] C. Brabec,et al. An Alternative Strategy to Adjust the Recombination Mechanism of Organic Photovoltaics by Implementing Ternary Compounds , 2015 .
[32] C. B. Nielsen,et al. Non-Fullerene Electron Acceptors for Use in Organic Solar Cells , 2015, Accounts of chemical research.
[33] Matthew Y. Sfeir,et al. Molecular helices as electron acceptors in high-performance bulk heterojunction solar cells , 2015, Nature Communications.
[34] J. Jung,et al. Low-Bandgap Small Molecules as Non-Fullerene Electron Acceptors Composed of Benzothiadiazole and Diketopyrrolopyrrole for All Organic Solar Cells , 2015 .
[36] Jianqi Zhang,et al. Conjugated Polymer-Small Molecule Alloy Leads to High Efficient Ternary Organic Solar Cells. , 2015, Journal of the American Chemical Society.
[37] F. Krebs,et al. Comparative Indoor and Outdoor Degradation of Organic Photovoltaic Cells via Inter-laboratory Collaboration , 2015, 2015 IEEE 42nd Photovoltaic Specialist Conference (PVSC).
[38] Feng Liu,et al. Fluoro‐Substituted n‐Type Conjugated Polymers for Additive‐Free All‐Polymer Bulk Heterojunction Solar Cells with High Power Conversion Efficiency of 6.71% , 2015, Advanced materials.
[39] Dieter Neher,et al. Competition between recombination and extraction of free charges determines the fill factor of organic solar cells , 2015, Nature Communications.
[40] Bumjoon J. Kim,et al. High‐Performance All‐Polymer Solar Cells Via Side‐Chain Engineering of the Polymer Acceptor: The Importance of the Polymer Packing Structure and the Nanoscale Blend Morphology , 2015, Advanced materials.
[41] Feng Liu,et al. Single-junction polymer solar cells with high efficiency and photovoltage , 2015, Nature Photonics.
[42] C. B. Nielsen,et al. A rhodanine flanked nonfullerene acceptor for solution-processed organic photovoltaics. , 2015, Journal of the American Chemical Society.
[43] S. Jenekhe,et al. Beyond fullerenes: design of nonfullerene acceptors for efficient organic photovoltaics. , 2014, Journal of the American Chemical Society.
[44] Daisuke Mori,et al. Highly efficient charge-carrier generation and collection in polymer/polymer blend solar cells with a power conversion efficiency of 5.7% , 2014 .
[45] J. Behrends,et al. Correlated Donor/Acceptor Crystal Orientation Controls Photocurrent Generation in All‐Polymer Solar Cells , 2014 .
[46] Juliane Kniepert,et al. Nongeminate and Geminate Recombination in PTB7:PCBM Solar Cells , 2014, 2106.10101.
[47] C. Brabec,et al. Two similar near-infrared (IR) absorbing benzannulated aza-BODIPY dyes as near-IR sensitizers for ternary solar cells. , 2013, ACS applied materials & interfaces.
[48] J. Nelson,et al. Meaning of reaction orders in polymer:fullerene solar cells , 2012 .
[49] Paul L. Burn,et al. A Narrow Optical Gap Small Molecule Acceptor for Organic Solar Cells , 2012 .
[50] B. Collins,et al. Molecular Miscibility of Polymer-Fullerene Blends , 2010 .