Browse
Submit Data
Databases
API
Help

Dataset Information

24 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

15.3% Efficiency All-Small-Molecule Organic Solar Cells Achieved by a Locally Asymmetric F, Cl Disubstitution Strategy.

ABSTRACT: Single junction binary all-small-molecule (ASM) organic solar cells (OSCs) with power conversion efficiency (PCE) beyond 14% are achieved by using non-fullerene acceptor Y6 as the electron acceptor, but still lag behind that of polymer OSCs. Herein, an asymmetric Y6-like acceptor, BTP-FCl-FCl, is designed and synthesized to match the recently reported high performance small molecule donor BTR-Cl, and a record efficiency of 15.3% for single-junction binary ASM OSCs is achieved. BTP-FCl-FCl features a F,Cl disubstitution on the same end group affording locally asymmetric structures, and so has a lower total dipole moment, larger average electronic static potential, and lower distribution disorder than those of the globally asymmetric isomer BTP-2F-2Cl, resulting in improved charge generation and extraction. In addition, BTP-FCl-FCl based active layer presents more favorable domain size and finer phase separation contributing to the faster charge extraction, longer charge carrier lifetime, and much lower recombination rate. Therefore, compared with BTP-2F-2Cl, BTP-FCl-FCl based devices provide better performance with FF enhanced from 71.41% to 75.36% and J _sc increased from 22.35 to 24.58 mA cm^-2, leading to a higher PCE of 15.3%. The locally asymmetric F, Cl disubstitution on the same end group is a new strategy to achieve high performance ASM OSCs.

SUBMITTER: Hu D

PROVIDER: S-EPMC8061398 | biostudies-literature |

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Similar Datasets

Asymmetric Non-Fullerene Small Molecule Acceptor with Unidirectional Non-Fused π-Bridge and Extended Terminal Group for High-Efficiency Organic Solar Cells.

Project description:We designed and synthesized an asymmetric non-fullerene small molecule acceptor (NF-SMA) IDT-TNIC with an A-D-π-A structure, based on an indacenodithiophene (IDT) central core, with a unidirectional non-fused alkylthio-thiophene (T) π-bridge, and 2-(3-oxo-2,3-dihydro-1H-cyclopenta[b]naphthalen-1-ylidene)malononitrile (NIC) extended terminal groups. IDT-TNIC molecules still maintain a good coplanar structure, which benefits from the non-covalent conformational locks (NCL) between O···S and S···S. The asymmetric structure increases the molecular dipole moment, and the extended terminal group broadens the absorption of the material, resulting in an excellent photovoltaic performance of IDT-TNIC. The photovoltaic device, based on PBDB-T:IDT-TNIC, exhibits an energetic PCE of 11.32% with a high Voc of 0.87 V, high Jsc of 19.85 mA cm-2, and a low energy loss of 0.57 eV. More importantly, IDT-TNICs with asymmetric structures show a superior property compared to symmetric IDT-Ns. The results demonstrate that it is an effectual strategy to enhance the properties of asymmetric A-D-π-A-based NF-SMAs with non-fused NCL π-bridges and extended terminal groups.

| S-EPMC9456090 | biostudies-literature

Asymmetric electron acceptor enables highly luminescent organic solar cells with certified efficiency over 18.

Project description:Enhancing the luminescence property without sacrificing the charge collection is one key to high-performance organic solar cells (OSCs), while limited by the severe non-radiative charge recombination. Here, we demonstrate efficient OSCs with high luminescence via the design and synthesis of an asymmetric non-fullerene acceptor, BO-5Cl. Blending BO-5Cl with the PM6 donor leads to a record-high electroluminescence external quantum efficiency of 0.1%, which results in a low non-radiative voltage loss of 0.178 eV and a power conversion efficiency (PCE) over 15%. Importantly, incorporating BO-5Cl as the third component into a widely-studied donor:acceptor (D:A) blend, PM6:BO-4Cl, allows device displaying a high certified PCE of 18.2%. Our joint experimental and theoretical studies unveil that more diverse D:A interfacial conformations formed by asymmetric acceptor induce optimized blend interfacial energetics, which contributes to the improved device performance via balancing charge generation and recombination.

| S-EPMC9095617 | biostudies-literature

All-small-molecule organic solar cells with over 14% efficiency by optimizing hierarchical morphologies.

Project description:The high efficiency all-small-molecule organic solar cells (OSCs) normally require optimized morphology in their bulk heterojunction active layers. Herein, a small-molecule donor is designed and synthesized, and single-crystal structural analyses reveal its explicit molecular planarity and compact intermolecular packing. A promising narrow bandgap small-molecule with absorption edge of more than 930?nm along with our home-designed small molecule is selected as electron acceptors. To the best of our knowledge, the binary all-small-molecule OSCs achieve the highest efficiency of 14.34% by optimizing their hierarchical morphologies, in which the donor or acceptor rich domains with size up to ca. 70?nm, and the donor crystals of tens of nanometers, together with the donor-acceptor blending, are proved coexisting in the hierarchical large domain. All-small-molecule photovoltaic system shows its promising for high performance OSCs, and our study is likely to lead to insights in relations between bulk heterojunction structure and photovoltaic performance.

| S-EPMC6879588 | biostudies-literature

A rare case of brominated small molecule acceptors for high-efficiency organic solar cells.

Project description:Given that bromine possesses similar properties but extra merits of easily synthesizing and polarizing comparing to homomorphic fluorine and chlorine, it is quite surprising very rare high-performance brominated small molecule acceptors have been reported. This may be caused by undesirable film morphologies stemming from relatively larger steric hindrance and excessive crystallinity of bromides. To maximize the advantages of bromides while circumventing weaknesses, three acceptors (CH20, CH21 and CH22) are constructed with stepwise brominating on central units rather than conventional end groups, thus enhancing intermolecular packing, crystallinity and dielectric constant of them without damaging the favorable intermolecular packing through end groups. Consequently, PM6:CH22-based binary organic solar cells render the highest efficiency of 19.06% for brominated acceptors, more excitingly, a record-breaking efficiency of 15.70% when further thickening active layers to ~500 nm. By exhibiting such a rare high-performance brominated acceptor, our work highlights the great potential for achieving record-breaking organic solar cells through delicately brominating.

| S-EPMC10404295 | biostudies-literature

Fluorination-enabled optimal morphology leads to over 11% efficiency for inverted small-molecule organic solar cells.

Project description:Solution-processable small molecules for organic solar cells have attracted intense attention for their advantages of definite molecular structures compared with their polymer counterparts. However, the device efficiencies based on small molecules are still lower than those of polymers, especially for inverted devices, the highest efficiency of which is <9%. Here we report three novel solution-processable small molecules, which contain ?-bridges with gradient-decreased electron density and end acceptors substituted with various fluorine atoms (0F, 1F and 2F, respectively). Fluorination leads to an optimal active layer morphology, including an enhanced domain purity, the formation of hierarchical domain size and a directional vertical phase gradation. The optimal morphology balances charge separation and transfer, and facilitates charge collection. As a consequence, fluorinated molecules exhibit excellent inverted device performance, and an average power conversion efficiency of 11.08% is achieved for a two-fluorine atom substituted molecule.

| S-EPMC5187412 | biostudies-literature

Donor Derivative Incorporation: An Effective Strategy toward High Performance All-Small-Molecule Ternary Organic Solar Cells.

Project description:Thick-film all-small-molecule (ASM) organic solar cells (OSCs) are preferred for large-scale fabrication with printing techniques due to the distinct advantages of monodispersion, easy purification, and negligible batch-to-batch variation. However, ASM OSCs are typically constrained by the morphology aspect to achieve high efficiency and maintain thick film simultaneously. Specifically, synchronously manipulating crystallinity, domain size, and phase segregation to a suitable level are extremely challenging. Herein, a derivative of benzodithiophene terthiophene rhodanine (BTR) (a successful small molecule donor for thick-film OSCs), namely, BTR-OH, is synthesized with similar chemical structure and absorption but less crystallinity relative to BTR, and is employed as a third component to construct BTR:BTR-OH:PC71BM ternary devices. The power conversion efficiency (PCE) of 10.14% and fill factor (FF) of 74.2% are successfully obtained in ?300 nm OSC, which outperforms BTR:PC71BM (9.05% and 69.6%) and BTR-OH:PC71BM (8.00% and 65.3%) counterparts, and stands among the top values for thick-film ASM OSCs. The performance enhancement results from the enhanced absorption, suppressed bimolecular/trap-assisted recombination, improved charge extraction, optimized domain size, and suitable crystallinity. These findings demonstrate that the donor derivative featuring similar chemical structure but different crystallinity provides a promising third component guideline for high-performance ternary ASM OSCs.

| S-EPMC6839630 | biostudies-literature

Design and Application of an Asymmetric Naphthalimide-based Molecule with Improved Hydrophobicity for Highly Stable Organic Solar Cells.

Project description:With the photovoltaic efficiency of organic solar cells (OSCs) exceeding 17%, improving the stability of these systems has become the most important issue for their practical applications. In particular, moisture in the environment may erode the interlayer molecules, which has been proved to be the main reason for the efficiency decay. At present, the development of moisture-resistant interlayer molecules remains a great challenge to the field. Herein, we designed two naphthalene diimide (NDI)-based organic compounds, namely, NDI-M and NDI-S, exhibiting suitable energy level and excellent electron extraction property. In addition to this, NDI-S has extremely low hygroscopicity. An efficiency of 17.27% was achieved for the NDI-S inverted cells, and the long-term stability under continuous illumination conditions was significantly improved with a T80 lifetime (the time required to reach 80% of initial performance) of over 28 000 h. More importantly, we demonstrated that, by using a covalent bond to link the counter ions with the host molecular structure in the zwitterion, the asymmetric molecule NDI-S can transform from amorphous to crystalline hydrate at high humidity and exhibited outstanding non-hygroscopic nature; this could decrease the interaction between the cell and the moisture, obviously improving the device stability under high humidity.

| S-EPMC9400047 | biostudies-literature

High efficiency silicon solar cell based on asymmetric nanowire.

Project description:Improving the efficiency of solar cells through novel materials and devices is critical to realize the full potential of solar energy to meet the growing worldwide energy demands. We present here a highly efficient radial p-n junction silicon solar cell using an asymmetric nanowire structure with a shorter bottom core diameter than at the top. A maximum short circuit current density of 27.5 mA/cm(2) and an efficiency of 7.53% were realized without anti-reflection coating. Changing the silicon nanowire (SiNW) structure from conventional symmetric to asymmetric nature improves the efficiency due to increased short circuit current density. From numerical simulation and measurement of the optical characteristics, the total reflection on the sidewalls is seen to increase the light trapping path and charge carrier generation in the radial junction of the asymmetric SiNW, yielding high external quantum efficiency and short circuit current density. The proposed asymmetric structure has great potential to effectively improve the efficiency of the SiNW solar cells.

| S-EPMC4495391 | biostudies-other

Water-Processed Organic Solar Cell with Efficiency Exceeding 11.

Project description:Water processing is an ideal strategy for the ecofriendly fabrication of organic photovoltaics (OPVs) and exhibits a strong market-driven demand. Here, we report a state-of-the-art active material, namely PM6:BTP-eC9, for the synthesis of water-borne nanoparticle (NP) dispersion towards ecofriendly OPV fabrication. The surfactant-stripping technique, combined with a poloxamer, facilitates purification and eliminates excess surfactant in water-dispersed organic semiconducting NPs. The introduction of 1,8-diiodooctane (DIO) for the synthesis of surfactant-stripped NP (ssNP) further promotes a percolated microstructure of the polymer and NFA in each ssNP, yielding water-processed OPVs with a record efficiency of over 11%. The use of an additive during water-borne ssNP synthesis is a promising strategy for morphology optimization in NP OPVs. It is believed that the findings in this work will engender more research interest and effort relating to water-processing in preparation of the industrial production of OPVs.

| S-EPMC9573733 | biostudies-literature

Increased efficiency in small molecule organic solar cells through the use of a 56-? electron acceptor--methano indene fullerene.

Project description:Organic solar cells (OSCs) offer the possibility of harnessing the sun's ubiquitous energy in a low-cost, environmentally friendly and renewable manner. OSCs based on small molecule semiconductors (SMOSCs)--have made a substantial improvement in recent years and are now achieving power conversion efficiencies (PCEs) that match those achieved for polymer:fullerene OSCs. To date, all efficient SMOSCs have relied on the same fullerene acceptor, PCBM, in order to achieve high performance. The use of PCBM however, is unfavourable due to its low lying LUMO level, which limits the open-circuit voltage (VOC). Alternative fullerene derivatives with higher lying LUMOs are thus required to improve the VOC. The challenge, however, is to prevent the typical concomitant decrease in the short circuit current density (JSC) when using a higher LUMO fullerene. In this communication, we address the issue by applying methano indene fullerene, MIF, a bis-functionalised C60 fullerene that has a LUMO level 140?mV higher than PCBM, in solution processed SMOSCs with a well known small molecule donor, DPP(TBFu)2. MIF-based devices show an improved VOC of 140?mV over PC61BM and only a small decrease in the JSC, with the PCE increasing to 5.1% (vs. 4.5% for PC61BM).

| S-EPMC4321161 | biostudies-other

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data