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References from Recent advances in polymeric and small molecule donor materials for Y6 based organic solar cells. Local targets link to admitted publications; unresolved targets remain external evidence.
Organic bulk heterojunction photovoltaic structures: design, morphology and properties
10.1070/rc2014v083n07abeh004417 · 2014 · External reference
Efficiency of bulk-heterojunction organic solar cells
10.1016/j.progpolymsci.2013.05.001 · 2013 · External reference
Charge generation and transport in efficient organic bulk heterojunction solar cells with a perylene acceptor
10.1039/c3ee42484g · 2014 · External reference
Small molecule semiconductors for high-efficiency organic photovoltaics
10.1039/c2cs15313k · 2012 · External reference
“Plastic” solar cells: self-assembly of bulk heterojunction nanomaterials by spontaneous phase separation
10.1021/ar900065j · 2009 · External reference
Realizing 19.05% efficiency polymer solar cells by progressively improving charge extraction and suppressing charge recombination
10.1002/adma.202109516 · 2022 · External reference
Manipulating the D:a interfacial energetics and intermolecular packing for 19.2% efficiency organic photovoltaics
10.1039/d2ee00595f · 2022 · External reference
Single-junction organic solar cells with 19.17% efficiency enabled by introducing one asymmetric guest acceptor
10.1002/adma.202110147 · 2022 · External reference
Tandem organic solar cell with 20.2% efficiency
10.1016/j.joule.2021.12.017 · 2022 · External reference
Solar energy supply and storage for the legacy and nonlegacy worlds
10.1021/cr100246c · 2010 · External reference
Scaling Up ITO-Free Solar Cells
10.1002/aenm.201300498 · 2014 · External reference
Next-generation organic photovoltaics based on non-fullerene acceptors
10.1038/s41566-018-0104-9 · 2018 · External reference
Critical review of the molecular design progress in non-fullerene electron acceptors towards commercially viable organic solar cells
10.1039/c7cs00892a · 2019 · External reference
Achieving fast charge separation and low nonradiative recombination loss by rational fluorination for high-efficiency polymer solar cells
10.1002/adma.201905480 · 2019 · External reference
16.67% rigid and 14.06% flexible organic solar cells enabled by ternary heterojunction strategy
10.1002/adma.201902210 · 2019 · External reference
A monothiophene unit incorporating both fluoro and ester substitution enabling high-performance donor polymers for non-fullerene solar cells with 16.4% efficiency
10.1039/c9ee01890e · 2019 · External reference
New phase for organic solar cell research: emergence of y-series electron acceptors and their perspectives
10.1021/acsenergylett.0c00537 · 2020 · External reference
Graphdiyne derivative as multifunctional solid additive in binary organic solar cells with 17.3% efficiency and high reproductivity
10.1002/adma.201907604 · 2020 · External reference
18% efficiency organic solar cells
10.1016/j.scib.2020.01.001 · 2020 · External reference
A chlorinated copolymer donor demonstrates a 18.13% power conversion efficiency
10.1088/1674-4926/42/1/010501 · 2021 · External reference
Design rules for minimizing voltage losses in high-efficiency organic solar cells
2018 · External reference
Understanding energy loss in organic solar cells: toward a new efficiency regime
10.1016/j.joule.2017.09.020 · 2018 · External reference
Organic solar cells based on non-fullerene acceptors
2018 · External reference
High-efficiency polymer solar cells with small photon energy loss
2015 · External reference
Over 16% efficiency organic photovoltaic cells enabled by a chlorinated acceptor with increased open-circuit voltages
2019 · External reference
High-efficiency organic solar cells with low non-radiative recombination loss and low energetic disorder
10.1038/s41566-019-0573-5 · 2020 · External reference
Two‐layer organic photovoltaic cell
10.1063/1.96937 · 1986 · External reference
Polymer photovoltaic cells: enhanced efficiencies via a network of internal donor-acceptor heterojunctions
1995 · External reference
Efficient photodiodes from interpenetrating polymer networks
1995 · External reference
Fullerene derivative acceptors for high performance polymer solar cells
10.1039/c0cp01178a · 2011 · External reference
Organic solar cells based on non-fullerene acceptors
2018 · External reference
Non-fullerene acceptors for organic solar cells
2018 · External reference
Asymmetrical ladder-type donor-induced polar small molecule acceptor to promote fill factors approaching 77% for high-performance nonfullerene polymer solar cells
10.1002/adma.201800052 · 2018 · External reference
Enhancing performance of nonfullerene acceptors via side-chain conjugation strategy
10.1002/adma.201702125 · 2017 · External reference
Small-molecule acceptor based on the heptacyclic benzodi(cyclopentadithiophene) unit for highly efficient nonfullerene organic solar cells
10.1021/jacs.7b01170 · 2017 · External reference
Fullerene-free polymer solar cells with over 11% efficiency and excellent thermal stability
10.1002/adma.201600281 · 2016 · External reference
Critical review of the molecular design progress in non-fullerene electron acceptors towards commercially viable organic solar cells
10.1039/c7cs00892a · 2019 · External reference
Over 15% efficiency polymer solar cells enabled by conformation tuning of newly designed asymmetric small-molecule acceptors
10.1002/adfm.202000383 · 2020 · External reference
Single-junction organic solar cell with over 15% efficiency using fused-ring acceptor with electron-deficient core
10.1016/j.joule.2019.01.004 · 2019 · External reference
Subtle molecular tailoring induces significant morphology optimization enabling over 16% efficiency organic solar cells with efficient charge generation
10.1002/adma.201906324 · 2020 · External reference
High-efficiency organic solar cells with low non-radiative recombination loss and low energetic disorder
2020 · External reference
Alkyl chain tuning of small molecule acceptors for efficient organic solar cells
10.1016/j.joule.2019.09.010 · 2019 · External reference
Understanding energetic disorder in electron-deficient-core-based non-fullerene solar cells
10.1007/s11426-020-9747-9 · 2020 · External reference
Fine-tuning energy levels via asymmetric end groups enables polymer solar cells with efficiencies over 17%
10.1016/j.joule.2020.03.023 · 2020 · External reference
Over 16% efficiency organic photovoltaic cells enabled by a chlorinated acceptor with increased open-circuit voltages
2019 · External reference
Open circuit voltage of organic solar cells: an in-depth review
10.1039/c5ee02871j · 2016 · External reference
Thiolactone copolymer donor gifts organic solar cells a 16.72% efficiency
10.1016/j.scib.2019.10.002 · 2019 · External reference
Improving open-circuit voltage by a chlorinated polymer donor endows binary organic solar cells efficiencies over 17%
10.1007/s11426-019-9669-3 · 2020 · External reference
Thermodynamic properties and molecular packing explain performance and processing procedures of three D18:NFA organic solar cells
10.1002/adma.202005386 · 2020 · External reference
Introducing fluorine and sulfur atoms into quinoxaline-based p-type polymers to gradually improve the performance of fullerene-free organic solar cells
10.1021/acsmacrolett.9b00368 · 2019 · External reference
Molecular engineering of D-π-a copolymers based on 4,8-Bis(4-chlorothiophen-2-yl)benzo[1,2- b:4,5- b′]dithiophene (BDT-T-Cl) for high-performance fullerene-free organic solar cells
10.1021/acs.macromol.9b01233 · 2019 · External reference
Indacenodithieno[3,2- b]thiophene-based wide bandgap D-π-A copolymer for nonfullerene organic solar cells
10.1021/acsmacrolett.9b00704 · 2019 · External reference
Changing the π-bridge from thiophene to thieno[3,2-b]thiophene for the D–π–A type polymer enables high performance fullerene-free organic solar cells
10.1039/c9cc02904d · 2019 · External reference
New phase for organic solar cell research: emergence of y-series electron acceptors and their perspectives
10.1021/acsenergylett.0c00537 · 2020 · External reference
Constructing high-performance organic photovoltaics via emerging non-fullerene acceptors and tandem-junction structure
10.1002/aenm.202000746 · 2020 · External reference
The path to 20% power conversion efficiencies in nonfullerene acceptor organic solar cells
10.1002/aenm.202003441 · 2021 · External reference
Recent advances in non-fullerene organic solar cells: from lab to fab
10.1039/d0cc05528j · 2020 · External reference
Conjugated random terpolymer donors towards high-efficiency polymer solar cells
10.1002/cjoc.201900503 · 2020 · External reference
Recent advances in high-performance organic solar cells enabled by acceptor–donor–acceptor–donor–acceptor (A–DA′D–A) type acceptors
10.1039/d0qm00305k · 2020 · External reference
Benzodithiophenedione-based polymers: recent advances in organic photovoltaics
2020 · External reference
Conducting terpolymers and its hybrid nanocomposites variable trends. From synthesis to applications. A review
2020 · External reference
A-DA′D-A non-fullerene acceptors for high-performance organic solar cells
10.1007/s11426-020-9799-4 · 2020 · External reference
Small is powerful: recent progress in solution-processed small molecule solar cells
10.1002/aenm.201602242 · 2017 · External reference
A–π–D–π–a electron-donating small molecules for solution-processed organic solar cells: a review
10.1002/marc.201700470 · 2017 · External reference
Design, application, and morphology study of a new photovoltaic polymer with strong aggregation in solution state
10.1021/ma301900h · 2012 · External reference
Conjugated polymer for versatile photovoltaic applications with high performance
10.1002/adma.201502110 · 2015 · External reference
Over 14% efficiency in polymer solar cells enabled by a chlorinated polymer donor
10.1002/adma.201800868 · 2018 · External reference
From monomer to conjugated polymer: a perspective on best practices for synthesis
10.1021/acs.chemmater.1c01142 · 2021 · External reference
Renewed prospects for organic photovoltaics
10.1021/acs.chemrev.1c00955 · 2022 · External reference
Improving open-circuit voltage by a chlorinated polymer donor endows binary organic solar cells efficiencies over 17%
10.1007/s11426-019-9669-3 · 2020 · External reference
Fibril network strategy enables high-performance semitransparent organic solar cells
10.1002/adfm.202002181 · 2020 · External reference
Hot hydrocarbon-solvent slot-die coating enables high-efficiency organic solar cells with temperature-dependent aggregation behavior
10.1002/adma.202002302 · 2020 · External reference
Eco-compatible solvent-processed organic photovoltaic cells with over 16% efficiency
10.1002/adma.201903441 · 2019 · External reference
Toward green solvent processable photovoltaic materials for polymer solar cells: the role of highly polar pendant groups in charge carrier transport and photovoltaic behavior
10.1039/c3ee41838c · 2013 · External reference
Efficient organic solar cells processed from hydrocarbon solvents
2016 · External reference
2-b:4,5-c′]dithiophene-4,8-dione-based polymer donor achieving an efficiency over 16%
10.1002/adma.201907059 · 2020 · External reference
Tailoring regioisomeric structures of π-conjugated polymers containing monofluorinated π-bridges for highly efficient polymer solar cells
10.1021/acsenergylett.0c00939 · 2020 · External reference
Achieving fast charge separation and low nonradiative recombination loss by rational fluorination for high-efficiency polymer solar cells
10.1002/adma.201905480 · 2019 · External reference
Highly efficient fullerene-free organic solar cells operate at near zero highest occupied molecular orbital offsets
10.1021/jacs.8b12126 · 2019 · External reference
Optimizing microstructure morphology and reducing electronic losses in 1 cm2 polymer solar cells to achieve efficiency over 15%
10.1021/acsenergylett.9b01447 · 2019 · External reference
Tailoring regioisomeric structures of π-conjugated polymers containing monofluorinated π-bridges for highly efficient polymer solar cells
10.1021/acsenergylett.0c00939 · 2020 · External reference
Extension A unit in D-A polymer donor leads to higher JSC and FF for non-fullerene organic solar cells
10.1016/j.dyepig.2023.111498 · 2023 · External reference
Dithienobenzoselenadiazole-based polymer donors with tuned side chains for efficient polymer solar cells
10.1021/acsaem.3c00392 · 2023 · External reference
Side chain engineering of two-dimensional polymeric donors for high-efficiency organic solar cells
10.1021/acs.energyfuels.3c00526 · 2023 · External reference
A low cost and high performance polymer donor material for polymer solar cells
2018 · External reference
Designing simple conjugated polymers for scalable and efficient organic solar cells
10.1002/cssc.202100910 · 2021 · External reference
Achieving fast charge separation and low nonradiative recombination loss by rational fluorination for high‐efficiency polymer solar cells
10.1002/adma.201905480 · 2019 · External reference
Achieving efficient ternary organic solar cells using structurally similar non-fullerene acceptors with varying flanking side chains
10.1002/aenm.202100079 · 2021 · External reference
Fine-tuning of side-chain orientations on nonfullerene acceptors enables organic solar cells with 17.7% efficiency
10.1039/d0ee03506h · 2021 · External reference
High efficiency polymer solar cells with efficient hole transfer at zero highest occupied molecular orbital offset between methylated polymer donor and brominated
10.1021/jacs.9b09939 · 2020 · External reference
D–A copolymer donor based on bithienyl benzodithiophene D-unit and monoalkoxy bifluoroquinoxaline a-unit for high-performance polymer solar cells
10.1021/acs.chemmater.0c00459 · 2020 · External reference
Optimizing microstructure morphology and reducing electronic losses in 1 cm 2 polymer solar cells to achieve efficiency over 15%
10.1021/acsenergylett.9b01447 · 2019 · External reference
Achieving over 16% efficiency for single-junction organic solar cells
10.1007/s11426-019-9457-5 · 2019 · External reference
Flexible side-chain optimization in polymer donor enables improved photovoltaic performance
10.1016/j.orgel.2023.106765 · 2023 · External reference
18% Efficiency organic solar cells
10.1016/j.scib.2020.01.001 · 2020 · External reference
Dithieno[3′,2′:3,4;2′’,3′’:5,6]benzo[1,2-c][1,2,5]oxadiazole-based polymer donors with deep HOMO levels
10.1088/1674-4926/42/6/060501 · 2021 · External reference
Thiolactone copolymer donor gifts organic solar cells a 16.72% efficiency
10.1016/j.scib.2019.10.002 · 2019 · External reference
A chlorinated copolymer donor demonstrates a 18.13% power conversion efficiency
10.1088/1674-4926/42/1/010501 · 2021 · External reference
18.69% PCE from organic solar cells
2021 · External reference
Approaching 18% efficiency of ternary organic photovoltaics with wide bandgap polymer donor and well compatible Y6: Y6–1 O as acceptor
10.1093/nsr/nwaa305 · 2021 · External reference
Small-molecular donor guest achieves rigid 18.5% and flexible 15.9% efficiency organic photovoltaic via fine-tuning microstructure morphology
10.1016/j.joule.2021.06.017 · 2021 · External reference
Readily accessible benzo[d]thiazole polymers for nonfullerene solar cells with >16% efficiency and potential pitfalls
10.1021/acsenergylett.0c00691 · 2020 · External reference
Organic photovoltaics utilizing small‐molecule donors and Y‐series nonfullerene acceptors
2022 · External reference
Over 15% efficiency all-small-molecule organic solar cells enabled by a C-shaped small molecule donor with tailorable asymmetric backbone
2020 · External reference
15.71% efficiency all-small-molecule organic solar cells based on low-cost synthesized donor molecules
10.1002/adfm.202110159 · 2022 · External reference
Influence of altering chlorine substitution positions on the photovoltaic properties of small molecule donors in all-small-molecule organic solar cells
10.1039/d1tc05486d · 2022 · External reference
All-small-molecule organic solar cells with an ordered liquid crystalline donor
10.1016/j.joule.2019.09.009 · 2019 · External reference
13.4% efficiency from all-small-molecule organic solar cells based on a crystalline donor with chlorine and trialkylsilyl substitutions
10.1002/cssc.202100860 · 2021 · External reference
Highly efficient all-small-molecule organic solar cells with appropriate active layer morphology by side chain engineering of donor molecules and thermal annealing
10.1002/adma.201908373 · 2020 · External reference
13.34% efficiency non-fullerene all-small-molecule organic solar cells enabled by modulating the crystallinity of donors via a fluorination strategy
10.1002/anie.201910297 · 2020 · External reference
Effects of alkyl side chains of small molecule donors on morphology and the photovoltaic property of all-small-molecule solar cells
10.1021/acsami.1c15377 · 2021 · External reference
Over 14% efficiency nonfullerene all-small-molecule organic solar cells enabled by improving the ordering of molecular donors: via side-chain engineering
10.1039/d0ta01893g · 2020 · External reference
Improving molecular planarity by changing alky chain position enables 12.3% efficiency all-small-molecule organic solar cells with enhanced carrier lifetime and reduced recombination
10.1002/solr.201900326 · 2020 · External reference
Efficient small-molecule donor with improved structural order and molecular aggregation enabled by side-chain modification
2021 · External reference
Modulating crystallinity and miscibility via side-chain variation enable high performance all-small-molecule organic solar cells
10.1002/cjoc.202100216 · 2021 · External reference
Introducing siloxane-terminated side chains in small molecular donors for all-small-molecule organic solar cells: modulated molecular orientation and enhanced efficiency
10.1021/acsami.1c07863 · 2021 · External reference
Modulation of molecular stacking via tuning 2-ethylhexyl alkyl chain enables improved efficiency for all-small-molecule organic solar cells
10.1021/acsami.3c00167 · 2023 · External reference
Over 17% efficiency all-small-molecule organic solar cells based on an organic molecular donor employing a 2d side chain symmetry breaking strategy
10.1039/d2ee02107b · 2022 · External reference
Asymmetric substitution of end-groups triggers 16.34% efficiency for all-small-molecule organic solar cells
10.1002/adma.202202752 · 2022 · External reference
High-efficiency all-small-molecule organic solar cells based on an organic molecule donor with an asymmetric thieno[2,3-f] benzofuran unit
10.1007/s11426-020-9753-x · 2020 · External reference
Backbone engineering with asymmetric core to finely tune phase separation for high-performance all-small-molecule organic solar cells
10.1021/acsami.0c21986 · 2021 · External reference
Achieving 10% efficiency in non-fullerene all-small-molecule organic solar cells without extra treatments
10.1039/d1ta01680f · 2021 · External reference
Moving alkyl-chain branching point induced a hierarchical morphology for efficient all-small-molecule organic solar cells
10.1002/adfm.202005426 · 2020 · External reference
Renewed prospects for organic photovoltaics
10.1021/acs.chemrev.1c00955 · 2022 · External reference
Evaluation of acceptor strength in thiophene coupled donor-acceptor chromophores for optimal design of organic photovoltaic materials
10.1021/jp309950f · 2012 · External reference
