Research graph
References from Novel Dyes Design Based on First Principles and the Prediction of Energy Conversion Efficiencies of Dye-Sensitized Solar Cells. Local targets link to admitted publications; unresolved targets remain external evidence.
SolEn for a Sustainable Future: Developing and Teaching a Multidisciplinary Course on Solar Energy To Further Sustainable Education in Chemistry
10.1021/ed400345m · 2014 · External reference
Solution-Processed Organic Solar Cells with High Open-Circuit Voltage of 1.3 V and Low Non-Radiative Voltage Loss of 0.16 V
10.1002/adma.202002122 · 2020 · External reference
Benzotriazole-Based Acceptor and Donors, Coupled with Chlorination, Achieve a High VOC of 1.24 V and an Efficiency of 10.5% in Fullerene-Free Organic Solar Cells
10.1021/acs.chemmater.8b05316 · 2019 · External reference
Low-Bandgap n-Type Polymer Based on a Fused-DAD-Type Heptacyclic Ring for All-Polymer Solar Cell Application with a Power Conversion Efficiency of 10.7%
10.1021/acsmacrolett.0c00234 · 2020 · External reference
Data mining with molecular design rules identifies new class of dyes for dye-sensitised solar cells
10.1039/c4cp02645d · 2014 · External reference
Sn- and Pd-Free Synthesis of D−π–A Organic Sensitizers for Dye-Sensitized Solar Cells by Cu-Catalyzed Direct Arylation
10.1002/cssc.201700421 · 2017 · External reference
Effects of meta or para connected organic dyes for dye-sensitized solar cell
10.1016/j.dyepig.2018.05.037 · 2018 · External reference
Performance evaluation of natural native dyes as photosensitizer in dye-sensitized solar cells
10.1016/j.optmat.2020.110441 · 2020 · External reference
Dithienopyrrolobenzothiadiazole-based metal-free organic dyes with double anchors and thiophene spacers for efficient dye-sensitized solar cells
10.1016/j.solener.2020.08.064 · 2020 · External reference
A Blue Photosensitizer Realizing Efficient and Stable Green Solar Cells via Color Tuning by the Electrolyte
10.1002/adma.202000193 · 2020 · External reference
Thienochrysenocarbazole based organic dyes for transparent solar cells with over 10% efficiency
10.1039/c9ta03115d · 2019 · External reference
Tuning the Color Palette of Semi-Transparent Solar Cells via Lateral π-Extension of Polycyclic Heteroaromatics of Donor–Acceptor Dyes
10.1021/acsaem.0c00216 · 2020 · External reference
Synthesise of nanocrystalline titanium dioxide dye sensitised solar cell
10.1038/353737a0 · 1991 · External reference
Dithienopicenocarbazole as the kernel module of low-energy-gap organic dyes for efficient conversion of sunlight to electricity
10.1039/c5ee02822a · 2015 · External reference
Sensitizer molecular structure-device efficiency relationship in dye sensitized solar cells
10.1039/b920664g · 2011 · External reference
Dihydrophenanthrene-based metal-free dyes for highly efficient cosensitized solar cells
10.1021/ol301374c · 2012 · External reference
Improvement of Light Harvesting by Addition of a Long-Wavelength Absorber in Dye-Sensitized Solar Cells Based on ZnO and Indoline Dyes
10.1021/jp511122u · 2015 · External reference
Transient states and the role of excited state self-quenching of indoline dyes in complete dye-sensitized solar cells
10.1016/j.dyepig.2014.10.008 · 2015 · External reference
Revealing the Photophysical Mechanism of N,N′-Diphenyl-aniline Based Sensitizers with the D–D−π–A Framework: Theoretical Insights
10.1021/acssuschemeng.0c04061 · 2020 · External reference
Effect of solvents in the extraction and stability of anthocyanin from the petals of Caesalpinia pulcherrima for natural dye sensitized solar cell applications
10.1007/s10854-017-6743-7 · 2017 · External reference
Optical absorption study of anthoxanthin based natural dyes for dye sensitized solar cells: Experimental and theoretical investigations
10.1016/j.matlet.2020.128089 · 2020 · External reference
Synthesis and density functional theory study of novel coumarin-type dyes for dye sensitized solar cells
10.1016/j.jphotochem.2014.06.001 · 2014 · External reference
Novel Polyene Dyes for Highly Efficient Dye-Sensitized Solar Cells
10.1039/b210384b · 2003 · External reference
Novel organic dyes based on diarylmethylene-bridged triphenylamine for dye-sensitized solar cells
10.1016/j.synthmet.2015.03.033 · 2015 · External reference
Novel D-π-A organic sensitizers containing diarylmethylene-bridged triphenylamine and different spacers for solar cell application
10.1016/j.tetlet.2015.01.156 · 2015 · External reference
Enhancement of quantum efficiency by co-adsorbing small julolidine dye and bulky triphenylamine dye in dye-sensitized solar cells
10.1016/j.jphotochem.2018.01.021 · 2018 · External reference
Tuning the electron donating ability in the triphenylamine-based D-π-A architecture for highly efficient dye-sensitized solar cells
10.1016/j.jphotochem.2013.09.002 · 2014 · External reference
Theoretical Study of Acene-Bridged Dyes for Dye-Sensitized Solar Cells
10.1021/acs.jpca.5b00798 · 2015 · External reference
Benzo[a]carbazole-Based Donor-π-Acceptor Type Organic Dyes for Highly Efficient Dye-Sensitized Solar Cells
10.1021/am508400a · 2015 · External reference
Effect of Electron-Withdrawing/-Donating Groups on the Sensitizing Action of the Novel Organic Dye “3-(5-(4-(Diphenylamino)styryl)thiophen-2-yl)-2-cyanoacrylic Acid” for N-Type Dye-Sensitized Solar Cells: A Theoretical Study
10.1021/acs.jpcc.0c00369 · 2020 · External reference
New carbazole based metal-free organic dyes with D-π-A-π-A architecture for DSSCs: Synthesis, theoretical and cell performance studies
10.1016/j.solener.2017.05.088 · 2017 · External reference
Organic D-A-π-A Solar Cell Sensitizers with Improved Stability and Spectral Response
10.1002/adfm.201001801 · 2011 · External reference
Comparison between Benzothiadizole–Thiophene- and Benzothiadizole–Furan-Based D–A−π–A Dyes Applied in Dye-Sensitized Solar Cells: Experimental and Theoretical Insights
10.1021/acsomega.0c02060 · 2020 · External reference
Comparison of second-order nonlinear optical chromophores with D−π–A, D–A−π–A and D–D−π–A architectures: diverse NLO effects and interesting optical behavior
10.1039/c4ra08951k · 2014 · External reference
Efficient triarylamine-perylene dye-sensitized solar cells: influence of triple-bond insertion on charge recombination
10.1021/am507261j · 2015 · External reference
Porphyrins bearing a consolidated anthryl donor with dual functions for efficient dye-sensitized solar cells
10.1039/c5ee02505b · 2016 · External reference
The impact of adjusting auxiliary donors on the performance of dye-sensitized solar cells based on phenothiazine D-D-π-A sensitizers
10.1016/j.dyepig.2017.06.068 · 2017 · External reference
The effect of twisted D-D-π-A configuration on electron transfer and photo-physics characteristics
10.1080/00268976.2017.1414968 · 2018 · External reference
Novel D-D-π-A indoline-linked coumarin sensitizers for dye-sensitized solar cells
10.1016/j.jphotochem.2019.112031 · 2019 · External reference
Design of Dye Acceptors for Photovoltaics from First-Principles Calculations
10.1021/jp201646q · 2011 · External reference
Molecular Engineering of Indoline-Based D–A−π–A Organic Sensitizers toward High Efficiency Performance from First-Principles Calculations
10.1021/jp402645h · 2013 · External reference
Benchmarking the Conductor-like Polarizable Continuum Model (CPCM) for Aqueous Solvation Free Energies of Neutral and Ionic Organic Molecules
10.1021/ct049977a · 2005 · External reference
Aromaticity–Photovoltaic Property Relationship of Triphenylamine-Based D-π-A Dyes: Leads from DFT Calculations
10.1021/acs.jpca.9b10245 · 2020 · External reference
Excited State Geometries and Vertical Emission Energies of Solvated Dyes for DSSC: A PCM/TD-DFT Benchmark Study
10.1021/ct500328t · 2014 · External reference
Ab initio molecular-dynamics simulation of the liquid-metal-amorphous-semiconductor transition in germanium
10.1103/physrevb.49.14251 · 1994 · External reference
Effect of on-site Coulomb repulsion term U on the band-gap states of the reduced rutile (110) Ti O 2 surface
10.1103/physrevb.77.045118 · 2008 · External reference
The DFT + U method in the linear combination of Gaussian-type orbitals framework: Role of 4 f orbitals in the bonding of LuF 3
10.1016/j.cplett.2008.12.021 · 2009 · External reference
Simple and efficient way of speeding up transmission calculations with k-point sampling
10.3762/bjnano.6.164 · 2015 · External reference
How to design proper π-spacer order of the D-π-A dyes for DSSCs? A density functional response
10.1016/j.dyepig.2012.05.020 · 2012 · External reference
High efficiency and stable dye-sensitized solar cells with an organic chromophore featuring a binary pi-conjugated spacer
10.1039/b822325d · 2009 · External reference
Opto-electronic and interfacial charge transfer properties of azobenzene dyes on anatase TiO 2 (001) surface – The effect of anchoring group
10.1016/j.jphotochem.2017.06.013 · 2017 · External reference
Dye-Anchoring Modes at the Dye···TiO2 Interface of N3- and N749-Sensitized Solar Cells Revealed by Glancing-Angle Pair Distribution Function Analysis
10.1021/acs.jpcc.0c02314 · 2020 · External reference
Predicting Device Parameters for Dye-Sensitized Solar Cells from Electronic Structure Calculations to Reproduce Experiment
10.1021/acsaem.0c00060 · 2020 · External reference
Unveiling iodine-based electrolytes chemistry in aqueous dye-sensitized solar cells
10.1039/c6sc01145d · 2016 · External reference
Size of the emission source and collectivity in ultra-relativistic p-Pb collisions
10.1016/j.physletb.2013.02.014 · 2013 · External reference
Kinetics of Iodine-Free Redox Shuttles in Dye-Sensitized Solar Cells: Interfacial Recombination and Dye Regeneration
10.1021/ar500337g · 2015 · External reference
