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Dithienoquinoxalineimide‐Based Polymer Donor Enables All‐Polymer Solar Cells Over 19 % Efficiency

https://doi.org/10.1002/ange.202319755
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The 48 checked references that resolve
resolves10.1002/adfm.202201828
Quasiplanar Heterojunction All‐Polymer Solar Cells: A Dual Approach to Stability
resolves10.1002/adma.202211296
Manipulating Polymer Backbone Configuration via Halogenated Asymmetric End‐Groups Enables Over 18% Efficiency All‐Polymer Solar Cells
resolves10.1038/s41467-022-32964-z
High performance polymerized small molecule acceptor by synergistic optimization on π-bridge linker and side chain
resolves10.1016/j.matt.2021.12.002
Achieving high efficiency and well-kept ductility in ternary all-polymer organic photovoltaic blends thanks to two well miscible donors
resolves10.1002/anie.201707678
Constructing a Strongly Absorbing Low‐Bandgap Polymer Acceptor for High‐Performance All‐Polymer Solar Cells
resolves10.1016/j.joule.2020.03.019
Controlling Molecular Mass of Low-Band-Gap Polymer Acceptors for High-Performance All-Polymer Solar Cells
resolves10.1002/adma.202005942
Precisely Controlling the Position of Bromine on the End Group Enables Well‐Regular Polymer Acceptors for All‐Polymer Solar Cells with Efficiencies over 15%
resolves10.1002/adma.202200361
A Vinylene‐Linker‐Based Polymer Acceptor Featuring a Coplanar and Rigid Molecular Conformation Enables High‐Performance All‐Polymer Solar Cells with Over 17% Efficiency
resolves10.1002/adma.202301906
Over 18% Efficiency of All‐Polymer Solar Cells with Long‐Term Stability Enabled by Y6 as a Solid Additive
resolves10.1002/adma.202307398
Central Core Substitutions and Film‐Formation Process Optimization Enable Approaching 19% Efficiency All‐Polymer Solar Cells
resolves10.1002/anie.202308306
Biselenophene Imide: Enabling Polymer Acceptor with High Electron Mobility for High‐Performance All‐Polymer Solar Cells
resolves10.1038/s41467-023-37738-9
Improved photovoltaic performance and robustness of all-polymer solar cells enabled by a polyfullerene guest acceptor
resolves10.1002/adma.202304632
Tunable Donor Aggregation Dominance in a Ternary Matrix of All‐Polymer Blends with Improved Efficiency and Stability
resolves10.1002/adma.202308334
Isomerized Green Solid Additive Engineering for Thermally Stable and Eco‐Friendly All‐Polymer Solar Cells with Approaching 19% Efficiency
resolves10.1002/marc.202200753
Linear Regulating of Polymer Acceptor Aggregation with Short Alkyl Chain Units Enhances All‐Polymer Solar Cells’ Efficiency
resolves10.1021/acs.chemmater.2c02299
Constructing a Double-Cable Polymer Acceptor for Efficient All-Polymer Solar Cells with a Non-Radiative Recombination Energy Loss of 0.16 eV
resolves10.1002/adma.202202608
A Top‐Down Strategy to Engineer ActiveLayer Morphology for Highly Efficient and Stable All‐Polymer Solar Cells
resolves10.1002/adma.202212275
Unveiling the Morphological and Physical Mechanism of Burn‐in Loss Alleviation by Ternary Matrix Toward Stable and Efficient All‐Polymer Solar Cells
resolves10.1039/D2EE03535A
Suppressing the energetic disorder of all-polymer solar cells enables over 18% efficiency
resolves10.1039/D3EE02700G
Suppression of energy disorder by incorporating a small-molecule acceptor into binary all-polymer solar cells
resolves10.1002/adma.202306990
18.6% Efficiency All‐Polymer Solar Cells Enabled by a Wide Bandgap Polymer Donor Based on Benzo[1,2‐d:4,5‐d′]bisthiazole
resolves10.1038/s41467-023-39832-4
All-polymer organic solar cells with nano-to-micron hierarchical morphology and large light receiving angle
resolves10.1002/smll.202206607
Halogen‐Free Donor Polymers Based on Dicyanobenzotriazole with Low Energy Loss and High Efficiency in Organic Solar Cells
resolves10.1016/j.cej.2022.136068
Halogen-free donor polymers based on dicyanobenzotriazole for additive-free organic solar cells
resolves10.1002/adma.202105803
A Universal Nonhalogenated Polymer Donor for High‐Performance Organic Photovoltaic Cells
resolves10.1016/j.cej.2021.133575
Synchronously regulating the alkyl side-chain and regioisomer of polymerized small molecule acceptor enabling highly efficient all-polymer solar cells processed with non-halogenated solvent
resolves10.1021/ma301900h
Design, Application, and Morphology Study of a New Photovoltaic Polymer with Strong Aggregation in Solution State
resolves10.1039/D1TA00838B
All-polymer solar cells with efficiency approaching 16% enabled using a dithieno[3′,2′:3,4;2′′,3′′:5,6]benzo[1,2- <i>c</i> ][1,2,5]thiadiazole (fDTBT)-based polymer donor
resolves10.1021/cm3017006
Conjugated Side-Chain-Isolated D–A Copolymers Based on Benzo[1,2-<i>b</i>:4,5-<i>b</i>′]dithiophene-<i>alt</i>-dithienylbenzotriazole: Synthesis and Photovoltaic Properties
resolves10.1002/anie.202101577
Multi‐Selenophene‐Containing Narrow Bandgap Polymer Acceptors for All‐Polymer Solar Cells with over 15 % Efficiency and High Reproducibility
resolves10.1002/aenm.202102559
π‐Extended Conjugated Polymer Acceptor Containing Thienylene–Vinylene–Thienylene Unit for High‐Performance Thick‐Film All‐Polymer Solar Cells with Superior Long‐Term Stability
resolves10.1039/D2EE01996E
Random copolymerization strategy for non-halogenated solvent-processed all-polymer solar cells with a high efficiency of over 17%
resolves10.1016/j.chempr.2023.04.021
Morphology control by tuning electrostatic interactions for efficient polythiophene-based all-polymer solar cells
resolves10.1039/D3EE00186E
Achieving 17.94% efficiency all-polymer solar cells by independently induced D/A orderly stacking
resolves10.1002/adma.201502110
A Large‐Bandgap Conjugated Polymer for Versatile Photovoltaic Applications with High Performance
resolves10.1038/s41467-020-18378-9
Random terpolymer based on thiophene-thiazolothiazole unit enabling efficient non-fullerene organic solar cells
resolves10.1016/j.scib.2020.01.001
18% Efficiency organic solar cells
resolves10.1002/adma.202101090
A New Conjugated Polymer that Enables the Integration of Photovoltaic and Light‐Emitting Functions in One Device
resolves10.1016/j.joule.2021.02.003
Naphthalenothiophene imide-based polymer exhibiting over 17% efficiency
resolves10.1039/D0CC00896F
Design and synthesis of non-fullerene acceptors based on a quinoxalineimide moiety as the central building block for organic solar cells
resolves10.1039/D1SE01748A
New wide-bandgap D–A polymer based on pyrrolo[3,4- <i>b</i> ] dithieno[2,3- <i>f</i> :3′,2′- <i>h</i> ]quinoxalindione and thiazole functionalized benzo[1,2- <i>b</i> :4,5- <i>b</i> ′]dithiophene units for high-performance ternary organic solar cells with over 16% efficiency
resolves10.1002/aenm.202104050
The Renaissance of Oligothiophene‐Based Donor–Acceptor Polymers in Organic Solar Cells
resolves10.1016/j.nanoen.2022.107463
Low-cost and high-performance poly(thienylene vinylene) derivative donor for efficient versatile organic photovoltaic cells
resolves10.1002/anie.202219245
Harnessing the Structure‐Performance Relationships in Designing Non‐Fused Ring Acceptors for Organic Solar Cells
resolves10.1063/1.1736034
Detailed Balance Limit of Efficiency of<i>p-n</i>Junction Solar Cells
resolves10.1016/j.cej.2022.139080
Organic photovoltaic cells offer ultrahigh VOC of ∼ 1.2 V under AM 1.5G light and a high efficiency of 21.2 % under indoor light
resolves10.1002/adma.202102420
Single‐Junction Organic Photovoltaic Cell with 19% Efficiency
resolves10.1021/acsenergylett.2c01438
High-Performance Ternary Organic Solar Cells through Incorporation of a Series of A<sub>2</sub>-A<sub>1</sub>-D-A<sub>1</sub>-A<sub>2</sub> Type Nonfullerene Acceptors with Different Terminal Groups
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