Browse
Submit Data
Databases
API
Help

Dataset Information

16 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Inverted organic photovoltaic device with a new electron transport layer.

ABSTRACT: We demonstrate that there is a new solution-processed electron transport layer, lithium-doped zinc oxide (LZO), with high-performance inverted organic photovoltaic device. The device exhibits a fill factor of 68.58%, an open circuit voltage of 0.86 V, a short-circuit current density of -9.35 cm/mA2 along with 5.49% power conversion efficiency. In addition, we studied the performance of blend ratio dependence on inverted organic photovoltaics. Our device also demonstrates a long stability shelf life over 4 weeks in air.

SUBMITTER: Kim HP

PROVIDER: S-EPMC3986668 | biostudies-literature | 2014 Mar

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Publications

Inverted organic photovoltaic device with a new electron transport layer.

Kim Hyeong Pil HP Yusoff Abd Rashid Bin Mohd AR Kim Hyo Min HM Lee Hee Jae HJ Seo Gi Jun GJ Jang Jin J

Nanoscale research letters 20140327 1

We demonstrate that there is a new solution-processed electron transport layer, lithium-doped zinc oxide (LZO), with high-performance inverted organic photovoltaic device. The device exhibits a fill factor of 68.58%, an open circuit voltage of 0.86 V, a short-circuit current density of -9.35 cm/mA2 along with 5.49% power conversion efficiency. In addition, we studied the performance of blend ratio dependence on inverted organic photovoltaics. Our device also demonstrates a long stability shelf l ...[more]

PMID: 24674457

Similar Datasets

Zwitterion Nondetergent Sulfobetaine-Modified SnO2 as an Efficient Electron Transport Layer for Inverted Organic Solar Cells.

Project description:Tin oxide (SnO2) has been widely accepted as an effective electron transport layer (ETL) for optoelectronic devices because of its outstanding electro-optical properties such as its suitable band energy levels, high electron mobility, and high transparency. Here, we report a simple but effective interfacial engineering strategy to achieve highly efficient and stable inverted organic solar cells (iOSCs) via a low-temperature solution process and an SnO2 ETL modified by zwitterion nondetergent sulfobetaine 3-(4-tert-butyl-1-pyridinio)-1-propanesulfonate (NDSB-256-4T). We found that NDSB-256-4T helps reduce the work function of SnO2, resulting in more efficient electron extraction and transport to the cathode of iOSCs. NDSB-256-4T also passivates the defects in SnO2, which serves as recombination centers that greatly reduce the device performance of iOSCs. In addition, NDSB-256-4T provides the better interfacial contact between SnO2 and the active layer. Thus, a higher power conversion efficiency (PCE) and longer device stability of iOSCs are expected for a combination of SnO2 and NDSB-256-4T than for devices based on SnO2 only. With these enhanced interfacial properties, P3HT:PC60BM-based iOSCs using SnO2/NDSB-256-4T (0.2 mg/mL) as an ETL showed both a higher average PCE of 3.72%, which is 33% higher than devices using SnO2 only (2.79%) and excellent device stability (over 90% of the initial PCE remained after storing 5 weeks in ambient air without encapsulation). In an extended application of the PTB7-Th:PC70BM systems, we achieved an impressive average PCE of 8.22% with SnO2/NDSB-256-4T (0.2 mg/mL) as the ETL, while devices based on SnO2 exhibited an average PCE of only 4.45%. Thus, the use of zwitterion to modify SnO2 ETL is a promising way to obtain both highly efficient and stable iOSCs.

| S-EPMC6868909 | biostudies-literature

Dual Role of Graphene Quantum Dots in Active Layer of Inverted Bulk Heterojunction Organic Photovoltaic Devices.

Project description:Graphene quantum dots (GQDs) have shown broad application prospects in the field of photovoltaic devices due to their unique quantum confinement and edge effects. Here, we prepared GQDs by a photon-Fenton reaction as reported in our previous work, which has great advantage in the preparation scale. The photoelectric properties of the inverted hybrid solar cells based on poly(3-hexylthiophene) (P3HT):(6,6)-phenyl-C61 butyric acid methylester (PCBM):GQDs and P3HT:GQDs with different contents of GQDs as the active layers are demonstrated, as well as their morphology and structure by atomic force microscopy images. Then, the different roles of GQDs played in the ternary (P3HT:PCBM:GQDs) and binary (P3HT:GQDs) hybrid solar cells are studied systematically. The results indicate that the GQDs provide an efficient excition separation interface and charge transport channel for the improvement of hybrid solar cells. The preliminary exploration and elaboration of the role of GQDs in hybrid solar cells will be beneficial to understand the interfacial procedure and improve device performance in the future.

| S-EPMC6777089 | biostudies-literature

Preparation of Transparent Conductive Electrode via Layer-By-Layer Deposition of Silver Nanowires and Its Application in Organic Photovoltaic Device.

Project description:Solution processed transparent conductive electrodes (TCEs) were fabricated via layer-by-layer (LBL) deposition of silver nanowires (AgNWs). First, the AgNWs were coated on (3-Mercaptopropyl)trimethoxysilane modified glass substrates. Then, multilayer AgNW films were obtained by using 1,3-propanedithiol as a linker via LBL deposition, which made it possible to control the optical transmittance and sheet resistance of multilayer thin films. Next, thermal annealing of AgNW films was performed in order to agent their electrical conductivity. AgNW monolayer films were characterized by UV-Vis spectrometer, field emission scanning electron microscopy, optical microscopy, atomic force microscopy and sheet resistance measurement by four-point probe method. The high performances were achieved with multilayer films, which provided sheet resistances of 9 ?/sq, 11 ?/sq with optical transmittances of 71%, 70% at 550 nm, which are comparable to commercial indium tin oxide (ITO) electrodes. Finally, an organic photovoltaic device was fabricated on the AgNW multilayer electrodes for demonstration purpose, which exhibited power conversion efficiency of 1.1%.

| S-EPMC7022465 | biostudies-literature

Urea-Doped ZnO Films as the Electron Transport Layer for High Efficiency Inverted Polymer Solar Cells.

Project description:In this paper, urea-doped ZnO (U-ZnO) is investigated as a modified electron transport layer (ETL) in inverted polymer solar cells (PSCs). Using a blend of Poly{4,8-bis[(2-ethylhexyl)oxy] benzo [1,2-b:4,5-b'] dithiophene-2,6-diyl-alt-3-fluoro-2-[(2-ethylhexyl)carbonyl] thieno [3,4-b] thiophene-4,6-diyl}(PTB7), and [6,6]-phenyl-C71-butyric acid methyl ester (PC71BM) as light absorber, a champion power conversion efficiency (PCE) of 9.15% for U-ZnO ETL based PSCs was obtained, which is 15% higher than that of the pure ZnO ETL based PSCs (7.76%). It was demonstrated that urea helps to passivate defects in ZnO ETL, resulting in enhanced exciton dissociation, suppressed charge recombination and efficient charge extraction efficiency. This work suggests that the utilization of the U-ZnO ETL offer promising potential for achieving highly efficient PSCs.

| S-EPMC6138008 | biostudies-literature

Effects of ZnMgO Electron Transport Layer on the Performance of InP-Based Inverted Quantum Dot Light-Emitting Diodes.

Project description:An environment-friendly inverted indium phosphide red quantum dot light-emitting diode (InP QLED) was fabricated using Mg-doped zinc oxide (ZnMgO) as the electron transport layer (ETL). The effects of ZnMgO ETL on the performance of InP QLED were investigated. X-ray diffraction (XRD) analysis indicated that ZnMgO film has an amorphous structure, which is similar to zinc oxide (ZnO) film. Comparison of morphology between ZnO film and ZnMgO film demonstrated that Mg-doped ZnO film remains a high-quality surface (root mean square roughness: 0.86 nm) as smooth as ZnO film. The optical band gap and ultraviolet photoelectron spectroscopy (UPS) analysis revealed that the conduction band of ZnO shifts to a more matched position with InP quantum dot after Mg-doping, resulting in the decrease in turn-on voltage from 2.51 to 2.32 V. In addition, the ratio of irradiation recombination of QLED increases from 7% to 25% using ZnMgO ETL, which can be attributed to reduction in trap state by introducing Mg ions into ZnO lattices. As a result, ZnMgO is a promising material to enhance the performance of inverted InP QLED. This work suggests that ZnMgO has the potential to improve the performance of QLED, which consists of the ITO/ETL/InP QDs/TCTA/MoO3/Al, and Mg-doping strategy is an efficient route to directionally regulate ZnO conduction bands.

| S-EPMC8151885 | biostudies-literature

Color-Stable White Organic Light-Emitting Diodes Utilizing a Blue-Emitting Electron-Transport Layer.

Project description:We have fabricated efficient and color-stable white organic light-emitting diodes (WOLEDs) based on a simple double-layer device structure consisting of a blue-emitting oligoquinoline electron-transport layer and a poly(N-vinyl carbazole) layer doped with phosphorescent green and red iridium emitters. Pure white color with the CIE coordinates from (0.30, 0.31) to (0.34, 0.37) in the whole operating bias voltage range and luminous efficiency higher than 7 cd/A at a brightness up to 12?000 cd/m2 was achieved. These results demonstrate a new strategy to realizing easily processable, highly efficient, and color-stable WOLEDs with a simple structure.

| S-EPMC6645075 | biostudies-literature

Modified SnO<sub>2</sub> with Alkali Carbonates as Robust Electron-Transport Layers for Inverted Organic Solar Cells.

Project description:We report for the first time that alkali carbonates (Li2CO3, K2CO3, and Rb2CO3) based on a low-temperature solution process can be used as interfacial modifiers for SnO2 as robust electron-transport layers (ETL) for inverted organic solar cells (iOSCs). The room-temperature photoluminescence, the electron-only devices, and the impedance studies altogether suggested the interfacial properties of the alkali carbonates-modified SnO2 ETLs, which were much better than those based on the SnO2 only, provided efficient charge transport, and reduced the charge recombination rates for iOSCs. The iOSCs using the polymer donor poly[4,8-bis(5-(2-ethylhexyl)thiophen-2-yl)benzo[1,2-b;4,5-b']dithiophene-2,6-diyl-alt-(4-(2-ethylhexyl)-3-fluorothieno[3,4-b]thiophene-)-2-carboxylate-2-6-diyl] and the fullerene acceptor phenyl-C70-butyric acid methyl ester as the active layer showed the average power-conversion efficiencies (PCEs) based on ten devices of 6.70, 6.85, and 7.35% with Li2CO3-, K2CO3-, and Rb2CO3-modified SnO2 as ETLs, respectively; these are more than 22, 24, and 33% higher than those based on the SnO2 only (5.49%). Moreover, these iOSC devices exhibited long-term stabilities, with over 90% PCEs remaining after the devices were stored in ambient air for 6 weeks without encapsulations. We believe that alkali carbonates-modified SnO2 approaches are an effective way to achieve stable and highly efficient iOSCs and might also be suitable for other optoelectronic devices where an ETL is needed, such as perovskite solar cells or organic light-emitting diodes.

| S-EPMC6643860 | biostudies-literature

Conjugated polyelectrolyte hole transport layer for inverted-type perovskite solar cells.

Project description:Organic-inorganic hybrid perovskite materials offer the potential for realization of low-cost and flexible next-generation solar cells fabricated by low-temperature solution processing. Although efficiencies of perovskite solar cells have dramatically improved up to 19% within the past 5 years, there is still considerable room for further improvement in device efficiency and stability through development of novel materials and device architectures. Here we demonstrate that inverted-type perovskite solar cells with pH-neutral and low-temperature solution-processable conjugated polyelectrolyte as the hole transport layer (instead of acidicPedotPSS) exhibit a device efficiency of over 12% and improved device stability in air. As an alternative toPedotPSS, this work is the first report on the use of an organic hole transport material that enables the formation of uniform perovskite films with complete surface coverage and the demonstration of efficient, stable perovskite/fullerene planar heterojunction solar cells.

| S-EPMC4557298 | biostudies-literature

Device Modeling and Design of Inverted Solar Cell Based on Comparative Experimental Analysis between Effect of Organic and Inorganic Hole Transport Layer on Morphology and Photo-Physical Property of Perovskite Thin Film.

Project description:It is crucial to find a good material as a hole transport layer (HTL) to improve the performance of perovskite solar cells (PSCs), devices with an inverted structure. Polyethylene dioxythiophene-poly (styrene sulfonate) (PEDOT:PSS) and inorganic nickel oxide (NiOx) have become hotspots in the study of hole transport materials in PSCs on account of their excellent properties. In our research, NiOx and PEDOT: PSS, two kinds of hole transport materials, were prepared and compared to study the impact of the bottom layer on the light absorption and morphology of perovskite layer. By the way, some experimental parameters are simulated by wx Analysis of Microelectronic and Photonic Structures (wxAMPS). In addition, thin interfacial layers with deep capture levels and high capture cross sections were inserted to simulate the degradation of the interface between light absorption layer and PEDOT:PSS. This work realizes the combination of experiment and simulation. Exploring the mechanism of the influence of functional layer parameters plays a vital part in the performance of devices by establishing the system design. It can be found that the perovskite film growing on NiOx has a stronger light absorption capacity, which makes the best open-circuit voltage of 0.98 V, short-circuit current density of 24.55 mA/cm2, and power conversion efficiency of 20.01%.

| S-EPMC8123108 | biostudies-literature

The Halogenation Effects of Electron Acceptor ITIC for Organic Photovoltaic Nano-Heterojunctions.

Project description:Molecular engineering plays a critical role in the development of electron donor and acceptor materials for improving power conversion efficiency (PCE) of organic photovoltaics (OPVs). The halogenated acceptor materials in OPVs have shown high PCE. Here, to investigate the halogenation mechanism and the effects on OPV performances, based on the density functional theory calculations with the optimally tuned screened range-separated hybrid functional and the consideration of solid polarization effects, we addressed the halogenation effects of acceptor ITIC, which were modeled by bis-substituted ITIC with halogen and coded as IT-2X (X = F, Cl, Br), and PBDB-T:ITIC, PBDB-T:IT-2X (X = F, Cl, Br) complexes on their geometries, electronic structures, excitations, electrostatic potentials, and the rate constants of charge transfer, exciton dissociation (ED), and charge recombination processes at the heterojunction interface. The results indicated that halogenation of ITIC slightly affects molecular geometric structures, energy levels, optical absorption spectra, exciton binding energies, and excitation properties. However, the halogenation of ITIC significantly enlarges the electrostatic potential difference between the electron acceptor and donor PBDB-T with the order from fluorination and chlorination to bromination. The halogenation also increases the transferred charges of CT states for the complexes. Meanwhile, the halogenation effects on CT energies and electron process rates depend on different haloid elements. No matter which kinds of haloid elements were introduced in the halogenation of acceptors, the ED is always efficient in these OPV devices. This work provides an understanding of the halogenation mechanism, and is also conducive to the designing of novel materials with the aid of the halogenation strategy.

| S-EPMC8708652 | biostudies-literature

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

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