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It Takes Two to TangoDouble-Layer Selective Contacts in Perovskite Solar Cells for Improved Device Performance and Reduced Hysteresis
Multifunctional Materials for High-Performance Double-Layer Organic Light-Emitting Diodes: Comparison of Isomers with and without Thermally Activated Delayed Fluorescence
Reduction of Charge-Carrier Recombination at ZnO–Polymer Blend Interfaces in PTB7-Based Bulk Heterojunction Solar Cells Using Regular Device Structure: Impact of ZnO Nanoparticle Size and Surfactant
Layer-by-Layer-Processed Ternary Organic Solar Cells Using Perylene Bisimide as a Morphology-Inducing Component
Normal and Inverted Hysteresis in Perovskite Solar Cells
Molecular Optimization Enables over 13% Efficiency in Organic Solar Cells
Solar Cells: Dual Interfacial Modifications Enable High Performance Semitransparent Perovskite Solar Cells with Large Open Circuit Voltage and Fill Factor (Adv. Energy Mater. 9/2017)
In article number 1602333, Shihe Yang, Yutaka Matsuo, Hin-Lap Yip, and co-workers simultaneously optimize both the power conversion efficiency (>12.5%) and average visible transmittance (>20%) of semitransparent perovskite solar cells (ST-PVSCs) through dual interfacial modifications. The success demonstration of high performance ST-PVSCs paves the way for using them as power generating windows, as illustrated in the image.
Dry-Stamping-Transferred PC71BM Charge Transport Layer via an Interface-Controlled Polyurethane Acrylate Mold Film for Efficient Planar-Type Perovskite Solar Cells
Enhancing the Performance of Quantum Dot Light-Emitting Diodes Using Room-Temperature-Processed Ga-Doped ZnO Nanoparticles as the Electron Transport Layer
Charge Transport in Intermixed Regions of All-Polymer Solar Cells Studied by Conductive Atomic Force Microscopy
Enhanced Performance and Stability of Polymer Solar Cells by In Situ Formed AlOx Passivation and Doping
Recombination in Perovskite Solar Cells: Significance of Grain Boundaries, Interface Traps, and Defect Ions
Wide bandgap BaSnO3 films with room temperature conductivity exceeding 104 S cm−1
Wide bandgap BaSnO3 films with room temperature conductivity exceeding 104 S cm−1
Nature Communications, Published online: 5 May 2017; doi:10.1038/ncomms15167
With impressive electronic transport properties, wide bandgap perovskite oxides are promising transparent conductors. Prakash et al. report n-type BaSnO3 films with room temperature conductivity exceeding 104 S cm−1 and investigate factors limiting carrier mobility.
Non-Conjugated Polymer as an Efficient Dopant-Free Hole-Transporting Material for Perovskite Solar Cells
Abstract
A new non-conjugated polymer (PVCz-OMeDAD) with good solution processability was developed to serve as an efficient dopant-free hole-transporting material (HTM) for perovskite solar cells (PSCs). PVCz-OMeDAD was simply prepared by the free-radical polymerization of vinyl monomers, which were synthesized from low-cost raw materials through three high-yield synthesis steps. The combination of the flexible non-conjugated polyvinyl main chain and hole-transporting methoxydiphenylamine-substituted carbazole side chains endowed PVCz-OMeDAD with excellent film-forming ability, a suitable energy level, and high hole mobility. As a result, by using an ultra-thin (≈30 nm) PVCz-OMeDAD film as cost-effective dopant-free polymer HTM, the conventional n–i–p-type PSCs demonstrated a power conversion efficiency (PCE) up to 16.09 %, suggesting the great potential of the polymer film for future low-cost, large-scale, flexible PSCs applications.
Be flexible: By integrating a flexible polyvinyl main chain with carbazole-based hole-transporting side chains, a new non-conjugated polymer (PVCz-OMeDAD) with excellent film-forming ability and good hole mobility is designed and synthesized in high yield through a three-step reaction. By employing the ultra-thin PVCz-OMeDAD film (≈30 nm) as dopant-free hole-transporting layer, perovskite solar cells (PSCs) can realize a power conversion efficiency up to 16.09 %, suggesting the great potential of this non-conjugated polymer for future low-cost, large-scale, flexible PSCs applications.
Increased Efficiency for Perovskite Photovoltaics Based on Aluminum-Doped Zinc Oxide Transparent Electrodes via Surface Modification
Hole Trapping by Iodine Interstitial Defects Decreases Free Carrier Losses in Perovskite Solar Cells: A Time-Domain Ab Initio Study
Charge Generation and Mobility-Limited Performance of Bulk Heterojunction Solar Cells with a Higher Adduct Fullerene
Efficient Bulk Heterojunction CH3NH3PbI3–TiO2 Solar Cells with TiO2 Nanoparticles at Grain Boundaries of Perovskite by Multi-Cycle-Coating Strategy
Comparison of Ag(In,Ga)Se2/Mo and Cu(In,Ga)Se2/Mo Interfaces in Solar Cells
Photocurrent Enhancement of Perovskite Solar Cells at the Absorption Edge by Electrode-Coupled Plasmons of Silver Nanocubes
Perovskite CH3NH3PbI3–xBrx Single Crystals with Charge-Carrier Lifetimes Exceeding 260 μs
One-Pot Large-Scale Synthesis of Carbon Quantum Dots: Efficient Cathode Interlayers for Polymer Solar Cells
Effects of Small Polar Molecules (MA+ and H2O) on Degradation Processes of Perovskite Solar Cells
Origin and Whereabouts of Recombination in Perovskite Solar Cells
Highly Oriented Low-Dimensional Tin Halide Perovskites with Enhanced Stability and Photovoltaic Performance
Abnormal Oxidation of Ag Films and Its Application to Fabrication of Photocatalytic Films with a-TiO2/h-Ag2O Heterostructure
Organic Halides and Nanocone Plastic Structures Enhance the Energy Conversion Efficiency and Self-Cleaning Ability of Colloidal Quantum Dot Photovoltaic Devices
Enhanced planar perovskite solar cells with efficiency exceeding 16% via reducing the oxygen vacancy defect state in titanium oxide electrode
DOI: 10.1039/C7CP01936J, Paper
In this work, the influence of oxygen vacancy defect (OVD) in compact titanium oxide (c-TiO2) on the performance of planar perovskite solar cells (p-PSCs) is investigated, and the possible mechanisms are also proposed.
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