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References from In Silico Modeling of New “Y-Series”-Based Near-Infrared Sensitive Non-Fullerene Acceptors for Efficient Organic Solar Cells. Local targets link to admitted publications; unresolved targets remain external evidence.
Reduced voltage losses yield 10% efficient fullerene free organic solar cells with> 1 V open circuit voltages
10.1039/c6ee02598f · 2016 · External reference
Highly Efficient Organic Solar Cells with Improved Vertical Donor–Acceptor Compositional Gradient Via an Inverted Off-Center Spinning Method
10.1002/adma.201504014 · 2016 · External reference
Organic solar cells: An overview
10.1557/jmr.2004.0252 · 2004 · External reference
Progress in Poly (3-Hexylthiophene) Organic Solar Cells and the Influence of Its Molecular Weight on Device Performance
10.1002/aenm.201801001 · 2018 · External reference
P3HT:PCBM, best seller in polymer photovoltaic research
10.1002/adma.201100792 · 2011 · External reference
Novel mussel-inspired injectable self-healing hydrogel with anti-biofouling property
10.1002/adma.201405166 · 2015 · External reference
Dihydronaphthyl-based [60] fullerene bisadducts for efficient and stable polymer solar cells
10.1039/c1cc15508c · 2012 · External reference
Polymer photovoltaic cells: enhanced efficiencies via a network of internal donor-acceptor heterojunctions
10.1126/science.270.5243.1789 · 1995 · External reference
A new dialkylthio-substituted naphtho [2,3-c] thiophene-4,9-dione based polymer donor for high-performance polymer solar cells
10.1039/c8ee03608j · 2019 · External reference
Evaporation-Free Nonfullerene Flexible Organic Solar Cell Modules Manufactured by An All-Solution Process
10.1002/aenm.201902065 · 2019 · External reference
Solution-Processable Conjugated Polymers as Anode Interfacial Layer Materials for Organic Solar Cells
10.1002/aenm.201800022 · 2018 · 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
Achieving over 16% efficiency for single-junction organic solar cells
10.1007/s11426-019-9457-5 · 2019 · External reference
17% Efficient Organic Solar Cells Based on Liquid Exfoliated WS2 as a Replacement for PEDOT:PSS
10.1002/adma.201902965 · 2019 · External reference
Monolayer hexagonal boron nitride films with large domain size and clean interface for enhancing the mobility of graphene-based field-effect transistors
10.1002/adma.201304937 · 2014 · 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
16.67% rigid and 14.06% flexible organic solar cells enabled by ternary heterojunction strategy
10.1002/adma.201902210 · 2019 · External reference
Reliability of charge carrier recombination data determined with charge extraction methods
10.1063/1.5129037 · 2019 · External reference
Rational Tuning of Molecular Interaction and Energy Level Alignment Enables High-Performance Organic Photovoltaics
10.1002/adma.201904215 · 2019 · External reference
Terthiophene-based D–A polymer with an asymmetric arrangement of alkyl chains that enables efficient polymer solar cells
10.1021/jacs.5b08556 · 2015 · External reference
Fused-ring acceptors with asymmetric side chains for high-performance thick-film organic solar cells
10.1002/adma.201703527 · 2017 · 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
Efficient organic solar cells based on a new “Y-series” non-fullerene acceptor with an asymmetric electron-deficient-core
10.1039/c9cc10076h · 2020 · External reference
Unresolved reference
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Unresolved reference
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Long-range corrected hybrid density functionals with damped atom–atom dispersion corrections
10.1039/b810189b · 2008 · External reference
Exchange functionals with improved long-range behavior and adiabatic connection methods without adjustable parameters: The m PW and m PW1PW models
10.1063/1.475428 · 1998 · External reference
A new hybrid exchange–correlation functional using the Coulomb-attenuating method (CAM-B3LYP)
10.1016/j.cplett.2004.06.011 · 2004 · External reference
A long-range correction scheme for generalized-gradient-approximation exchange functionals
10.1063/1.1383587 · 2001 · External reference
The M06 suite of density functionals for main group thermochemistry, thermochemical kinetics, noncovalent interactions, excited states, and transition elements: two new functionals and systematic testing of four M06-class functionals and 12 other functionals
10.1007/s00214-007-0310-x · 2008 · External reference
B3LYP augmented with an empirical dispersion term (B3LYP-D*) as applied to molecular crystals
10.1039/b715018k · 2008 · External reference
Designing triazatruxene-based donor materials with promising photovoltaic parameters for organic solar cells
10.1039/c9ra03856f · 2019 · External reference
Enhancement in Photovoltaic Properties of N, N-diethylaniline based Donor Materials by Bridging Core Modifications for Efficient Solar Cells
10.1002/slct.202000096 · 2020 · External reference
Designing indenothiophene-based acceptor materials with efficient photovoltaic parameters for fullerene-free organic solar cells
10.1007/s00894-020-04386-5 · 2020 · External reference
Design of donors with broad absorption regions and suitable frontier molecular orbitals to match typical acceptors via substitution on oligo (thienylenevinylene) toward solar cells
10.1002/jcc.22966 · 2012 · External reference
Theoretical and Conceptual Framework to Design Efficient Dye-Sensitized Solar Cells (DSSCs): Molecular Engineering by DFT Method
10.1007/s10876-020-01783-x · 2020 · External reference
First Theoretical Framework of Triphenylamine–Dicyanovinylene-Based Nonlinear Optical Dyes: Structural Modification of π-Linkers
10.1021/acs.jpcc.7b12293 · 2018 · External reference
Effect of π-conjugation spacer (C C) on the first hyperpolarizabilities of polymeric chain containing polyoxometalate cluster as a side-chain pendant: A DFT study
10.1016/j.comptc.2012.06.011 · 2012 · External reference
A DFT Study on The Two-Dimensional Second-Order Nonlinear Optical (NLO) Response of Terpyridine-Substituted Hexamolybdates: Physical Insight on 2D Inorganic–Organic Hybrid Functional Materials
10.1002/ejic.201101092 · 2012 · External reference
First theoretical probe for efficient enhancement of nonlinear optical properties of quinacridone based compounds through various modifications
10.1016/j.cplett.2018.11.051 · 2019 · External reference
Prediction of Second-Order Nonlinear Optical Properties of D–p–A Compounds Containing Novel Fluorene Derivatives: A Promising Route to Giant Hyperpolarizabilities
10.1007/s10876-018-01489-1 · 2019 · External reference
Quantum Chemical Designing of Indolo [3,2,1-jk] carbazole-based Dyes for Highly Efficient Nonlinear Optical Properties
10.1016/j.cplett.2019.01.043 · 2019 · External reference
Fluorooxoborates: beryllium-free deep-ultraviolet nonlinear optical materials without layered growth
10.1002/anie.201700540 · 2017 · External reference
Finding the next deep-ultraviolet nonlinear optical material: NH4B4O6F
10.1021/jacs.7b05943 · 2017 · External reference
Designing a deep-ultraviolet nonlinear optical material with a large second harmonic generation response
10.1021/ja400500m · 2013 · External reference
K3B6O10Cl: a new structure analogous to perovskite with a large second harmonic generation response and deep UV absorption edge
10.1021/ja111083x · 2011 · External reference
CsB4O6F: A Congruent-Melting Deep-Ultraviolet Nonlinear Optical Material by Combining Superior Functional Units
10.1002/anie.201708231 · 2017 · External reference
SrB5O7F3 Functionalized with [B5O9F3]6– Chromophores: Accelerating the Rational Design of Deep-Ultraviolet Nonlinear Optical Materials
10.1002/anie.201802058 · 2018 · External reference
Cation-Tuned Synthesis of Fluorooxoborates: Towards Optimal Deep-Ultraviolet Nonlinear Optical Materials
10.1002/anie.201712168 · 2018 · External reference
Designing an excellent deep-ultraviolet birefringent material for light polarization
10.1021/jacs.8b10009 · 2018 · External reference
Chemical cosubstitution-oriented design of rare-earth borates as potential ultraviolet nonlinear optical materials
10.1021/jacs.7b11263 · 2017 · External reference
Zinc-Doped Boron Phosphide Nanocluster as Efficient Sensor for SO2
10.1155/2020/2629596 · 2020 · External reference
Adsorption of Phosgene Gas on Pristine and Copper-Decorated B12N12 Nanocages: A Comparative DFT Study
10.1021/acsomega.0c00507 · 2020 · External reference
Design rules for donors in bulk-heterojunction solar cells─Towards 10% energy-conversion efficiency
10.1002/adma.200501717 · 2006 · 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
Excitons in organic semiconductors
10.1016/j.synthmet.2011.04.003 · 2011 · External reference
Why is exciton dissociation so efficient at the interface between a conjugated polymer and an electron acceptor?
10.1063/1.1586456 · 2003 · External reference
Dipole assisted exciton dissociation at conjugated polymer/fullerene photovoltaic interfaces: A molecular study using density functional theory calculations
10.1016/j.synthmet.2009.12.026 · 2010 · External reference
Positional disorder enhancement of exciton dissociation at donor/acceptor interface
10.1063/1.2174118 · 2006 · External reference
