About: Isomer-free: Precise Positioning of Chlorine-Induced Interpenetrating Charge Transfer for Elevated Solar Conversion

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About: Isomer-free: Precise Positioning of Chlorine-Induced Interpenetrating Charge Transfer for Elevated Solar Conversion Goto Sponge NotDistinct Permalink

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scientific article published on 28 June 2019

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rdf:type	Item
description	wetenschappelijk artikel (nl) artículu científicu espublizáu en xunu de 2019 (ast) scientific article published on 28 June 2019 (en) наукова стаття, опублікована 28 червня 2019 (uk) գիտական հոդված հրատարակված 2019 թվականի հունիսի 28-ին (hy)
publication date	wds:Q92024292-BA71D822-C34E-489A-905B-F2343106264D
publication date	2019-06-28 00:00:00Z (xsd:dateTime)
cites work	wds:Q92024292-10B2F691-8D5D-40D0-87DB-0142E13770D8 wds:Q92024292-167CCACA-B7F3-4203-B260-2E843CE24AC1 wds:Q92024292-19197DCC-71BC-44C1-8561-E855A5959E5B wds:Q92024292-1C0A2C29-3C53-4654-9E14-5C73F49EC2C1 wds:Q92024292-23548385-BD5F-41B8-85DB-F5ADA9EC7379 wds:Q92024292-25745AEC-B6E2-4F84-8958-C514C838E478 wds:Q92024292-29F6E59D-E74C-46C3-9114-4F12F8AADC43 wds:Q92024292-38447B4F-FFB6-4668-8FB9-DF39DD67103B wds:Q92024292-3B766545-905C-45FC-B08A-16F469155C2A wds:Q92024292-4815B334-BFBD-4C78-B12A-CDE8BFB7D18F wds:Q92024292-54C57244-23D8-4C7B-AAAA-8C8CFBE2AA4B wds:Q92024292-5C6C017E-CFC4-441F-A902-68EC06C02952 wds:Q92024292-6919B3F5-0255-4C44-BF73-AD2F402ECEA4 wds:Q92024292-793B7FF3-3174-48C6-A115-E5B9E09C29D5 wds:Q92024292-908D84BD-A622-475E-996C-57C7B8F95123 wds:Q92024292-9B369D4D-CE36-4383-B936-F8EDEF905376 wds:Q92024292-9D392860-6BB9-447A-A494-100CA7782A3D wds:Q92024292-A5024F5D-02EF-40F2-AAF7-AD751449AB8C wds:Q92024292-A5775852-B0D1-46BC-A5FA-DDE3CCA84FDF wds:Q92024292-B0E20DBA-ED34-4F45-9A6F-6C44DBBFD470 wds:Q92024292-B971DA7F-FEB1-49CF-BA4F-B77FB9A1ABC7 wds:Q92024292-BF3220AA-7BFA-4C81-876A-33E62D05EEFD wds:Q92024292-C1D6F09F-CD2B-472C-84AF-1B4731D3CD4C wds:Q92024292-C67C91C7-45CE-433A-824A-0DF64D20DBD2 wds:Q92024292-CF2E4A80-79EF-47C0-9112-8B228AA066B0 wds:Q92024292-DBE0FA22-525F-4F1F-877A-30FB0AFF17F6 wds:Q92024292-DD00001C-6304-4315-87AE-7F18EB848433 wds:Q92024292-E1C5655A-4BA1-411A-9D97-53C4E88AA9E8 wds:Q92024292-F1418C69-B671-4F26-B170-08D37F846D98 wds:Q92024292-F90FE9A8-B6F0-46CB-9B30-D196FCB03C83 wds:Q92024292-FA3ACB55-F9A7-4B7F-BEDC-4D16B6A4704C wds:Q92024292-FB80B2A4-CE85-486D-98EA-C1F469CA69B1 wds:Q92024292-FBE49240-A39A-4779-B31F-4CF164C5C53B wds:Q92024292-FE355B86-7F28-483D-8820-A0682912C9D5 wds:Q92024292-FFD3B9A4-4A9F-4999-8A2B-E603FABD3DD5
cites work	Aggregation and morphology control enables multiple cases of high-efficiency polymer solar cells Non-fullerene electron acceptors for use in organic solar cells High-efficiency and air-stable P3HT-based polymer solar cells with a new non-fullerene acceptor An electron acceptor challenging fullerenes for efficient polymer solar cells Beyond fullerenes: design of nonfullerene acceptors for efficient organic photovoltaics. An Efficient, "Burn in" Free Organic Solar Cell Employing a Nonfullerene Electron Acceptor Side-Chain Isomerization on an n-type Organic Semiconductor ITIC Acceptor Makes 11.77% High Efficiency Polymer Solar Cells. Enhancing Performance of Nonfullerene Acceptors via Side-Chain Conjugation Strategy. Small-Molecule Acceptor Based on the Heptacyclic Benzodi(cyclopentadithiophene) Unit for Highly Efficient Nonfullerene Organic Solar Cells. Single-Junction Binary-Blend Nonfullerene Polymer Solar Cells with 12.1% Efficiency. A Facile Planar Fused-Ring Electron Acceptor for As-Cast Polymer Solar Cells with 8.71% Efficiency. Dithienopicenocarbazole-Based Acceptors for Efficient Organic Solar Cells with Optoelectronic Response Over 1000 nm and an Extremely Low Energy Loss. Fine-Tuned Photoactive and Interconnection Layers for Achieving over 13% Efficiency in a Fullerene-Free Tandem Organic Solar Cell. Organic solar cells based on non-fullerene acceptors. Molecular Aggregate Photophysics beyond the Kasha Model: Novel Design Principles for Organic Materials. A Wide Band Gap Polymer with a Deep Highest Occupied Molecular Orbital Level Enables 14.2% Efficiency in Polymer Solar Cells Over 14% Efficiency in Polymer Solar Cells Enabled by a Chlorinated Polymer Donor. Morphology Control Enables Efficient Ternary Organic Solar Cells Dithieno[3,2-b:2',3'-d]pyrrol Fused Nonfullerene Acceptors Enabling Over 13% Efficiency for Organic Solar Cells. Over 14% Efficiency in Organic Solar Cells Enabled by Chlorinated Nonfullerene Small-Molecule Acceptors Effect of Isomerization on High-Performance Nonfullerene Electron Acceptors High Efficiency Near-Infrared and Semitransparent Non-Fullerene Acceptor Organic Photovoltaic Cells. Critical review of the molecular design progress in non-fullerene electron acceptors towards commercially viable organic solar cells. An Alkylated Indacenodithieno[3,2-b]thiophene-Based Nonfullerene Acceptor with High Crystallinity Exhibiting Single Junction Solar Cell Efficiencies Greater than 13% with Low Voltage Losses Concurrent Cooperative J-Aggregates and Anticooperative H-Aggregates. Chlorine Atoms Induced Molecular Interlocked Network in a Non-Fullerene Acceptor Fluorination Effects on Indacenodithienothiophene Acceptor Packing and Electronic Structure, End-Group Redistribution, and Solar Cell Photovoltaic Response Fused-Ring Acceptors with Asymmetric Side Chains for High-Performance Thick-Film Organic Solar Cells. A High-Efficiency Organic Solar Cell Enabled by the Strong Intramolecular Electron Push-Pull Effect of the Nonfullerene Acceptor Fine-Tuning the Energy Levels of a Nonfullerene Small-Molecule Acceptor to Achieve a High Short-Circuit Current and a Power Conversion Efficiency over 12% in Organic Solar Cells. Nonfullerene Tandem Organic Solar Cells with High Performance of 14.11 Asymmetrical Ladder-Type Donor-Induced Polar Small Molecule Acceptor to Promote Fill Factors Approaching 77% for High-Performance Nonfullerene Polymer Solar Cells Closely packed, low reorganization energy π-extended postfullerene acceptors for efficient polymer solar cells Realizing Over 13% Efficiency in Green-Solvent-Processed Nonfullerene Organic Solar Cells Enabled by 1,3,4-Thiadiazole-Based Wide-Bandgap Copolymers. Efficient Semitransparent Organic Solar Cells with Tunable Color enabled by an Ultralow-Bandgap Nonfullerene Acceptor.
author name string	wds:Q92024292-0B337DE7-98CB-42D5-834E-B9872E89DDBF wds:Q92024292-106127DA-F625-4C48-823E-3D564372279C wds:Q92024292-3ABA012E-8052-41CF-B6D4-BA038DB72F50 wds:Q92024292-5E31016A-E53B-4255-A1DA-AB505C8EFCFD wds:Q92024292-60CFC328-304C-4EDA-BBE4-DDEFC0AD2203 wds:Q92024292-902990A1-DE5C-43C9-A294-FFACD4C25793 wds:Q92024292-96E5A357-0641-42D6-946F-0E5AFC15165C wds:Q92024292-BC64F4A9-C106-49DC-93D5-F91668D15AD9 wds:Q92024292-D532574E-6193-408D-822F-6A2053D92109
author name string	Tao Liu Hui Chen Nan Zheng Jiadong Zhou Zengqi Xie Xiaoyong Chang Hanjian Lai Pengjie Chao Jianfei Qu
rdfs:label	Isomer-free: Precise Positioning of Chlorine-Induced Interpenetrating Charge Transfer for Elevated Solar Conversion (en) Isomer-free: Precise Positioning of Chlorine-Induced Interpenetrating Charge Transfer for Elevated Solar Conversion (nl)
skos:prefLabel	Isomer-free: Precise Positioning of Chlorine-Induced Interpenetrating Charge Transfer for Elevated Solar Conversion (en) Isomer-free: Precise Positioning of Chlorine-Induced Interpenetrating Charge Transfer for Elevated Solar Conversion (nl)

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