Wallace C. H. Choy

Dual Plasmonic Nanostructures for High Performance Inverted Organic Solar Cells

Polymer-fullerene-based bulk heterojunction (BHJ) solar cells have many advantages, including low-cost, low-temperature fabrication, semi-transparency, and mechanical fl exibility. [ 1 , 2 ] However, there is a mismatch between optical absorption length and charge transport scale. [ 3 , 4 ] These factors lead to recombination losses, higher series resistances, and lower fi ll factors. Attempts to optimize both the optical and electrical properties of the photoactive layer in organic solar cells (OSCs) inevitably result in a demand to develop a device architecture that can enable effi cient optical absorption in fi lms thinner than the optical absorption length. [ 5 , 6 ] Here, we report the use of two metallic nanostructures to achieve broad light absorption enhancement, increased shortcircuit current ( J sc ), and improved fi ll factor ( FF ) simultaneously based on the new small-bandgap polymer donor poly{[4,8-bis(2-ethyl-hexyl-thiophene-5-yl)-benzo[1,2-b:4,5-b ′ ]dithiophene2,6-diyl]alt -[2-(2 ′ -ethyl-hexanoyl)-thieno[3,4-b]thiophen-4,6-diyl]} (PBDTTT-C-T) in BHJ cells. [ 7 ] The dual metallic nanostructure consists of a metallic nanograting electrode as the back refl ector and metallic nanoparticles (NPs) embedded in the active layer. Consequently, we achieve the high power conversion effi ciency (PCE) of 8.79% for a single-junction BHJ OSC. Recently, plasmonic nanostructures have been introduced into solar cells for highly effi cient light harvesting. [ 5 , 8–17 ] Two types of plasmonic resonances, surface plasmonic resonances (SPRs) [ 18–22 ] and localized plasmonic resonances (LPRs), [ 11–14 ] can be used for enhancing light absorption. Metallic gratingbased light-trapping schemes have been investigated in traditional inorganic photovoltaic cells. [ 18–20 ] For metallic nanogratings, which can support SPRs, it is still challenging to experimentally demonstrate the enhancement of PCE in OSCs owing to the obvious issue of solution processing of

Enhancing the Brightness of Cesium Lead Halide Perovskite Nanocrystal Based Green Light-Emitting Devices through the Interface Engineering with Perfluorinated Ionomer

High photoluminescence quantum yield, easily tuned emission colors, and high color purity of perovskite nanocrystals make this class of material attractive for light source or display applications. Here, green light-emitting devices (LEDs) were fabricated using inorganic cesium lead halide perovskite nanocrystals as emitters. By introducing a thin film of perfluorinated ionomer (PFI) sandwiched between the hole transporting layer and perovskite emissive layer, the device hole injection efficiency has been significantly enhanced. At the same time, PFI layer suppressed charging of the perovskite nanocrystal emitters thus preserving their superior emissive properties, which led to the three-fold increase in peak brightness reaching 1377 cd m(-2). The full width at half-maximum of the symmetric emission peak with color coordinates of (0.09, 0.76) was 18 nm, the narrowest value among perovskite based green LEDs.

Vacuum-Assisted Thermal Annealing of CH3NH3PbI3 for Highly Stable and Efficient Perovskite Solar Cells

Solar cells incorporating lead halide-based perovskite absorbers can exhibit impressive power conversion efficiencies (PCEs), recently surpassing 15%. Despite rapid developments, achieving precise control over the morphologies of the perovskite films (minimizing pore formation) and enhanced stability and reproducibility of the devices remain challenging, both of which are necessary for further advancements. Here we demonstrate vacuum-assisted thermal annealing as an effective means for controlling the composition and morphology of the CH(3)NH(3)PbI(3) films formed from the precursors of PbCl(2) and CH(3)NH(3)I. We identify the critical role played by the byproduct of CH(3)NH(3)Cl on the formation and the photovoltaic performance of the perovskite film. By completely removing the byproduct through our vacuum-assisted thermal annealing approach, we are able to produce pure, pore-free planar CH(3)NH(3)PbI(3) films with high PCE reaching 14.5% in solar cell device. Importantly, the removal of CH(3)NH(3)Cl significantly improves the device stability and reproducibility with a standard deviation of only 0.92% in PCE as well as strongly reducing the photocurrent hysteresis.

Simultaneous optimization of charge-carrier balance and luminous efficacy in highly efficient white polymer light-emitting devices.

The use of white organic light-emitting devices (WOLEDs) for solid-state lighting applications is becoming increasingly attractive, [ 1 − 5 ] given that legislation in more countries is banning the use of ineffi cient incandescent lamps. Moreover, since fl uorescent lamps involve the use of mercury and its disposal represents a great challenge, many scientists have been working aggressively to make the replacement of the fl uorescent light sources by WOLEDs a reality. Indeed, the effi ciency of multilayer vacuum-evaporated WOLEDs based on small molecules has been greatly improved in the past several years [ 6 − 10 ] and has already exceeded that of fl uorescent lamps. [ 11 ] In contrast, despite many unique advantages, such as low-cost manufacturing using solution-processing techniques, easy processability over large-areas by spin-coating or ink-jet printing, compatibility with fl exible substrates, a relatively small amount of wasted material, and precise control of the doping level, the application of white polymer light-emitting diodes (WPLEDs) is still severely hindered by the relatively low device effi ciency. [ 3 , 12 − 16 ]

Optical and electrical properties of efficiency enhanced polymer solar cells with Au nanoparticles in a PEDOT–PSS layer

We unveil new device physics and provide details of device mechanisms by investigating polymer solar cells (PSCs) incorporating Au nanoparticles (NPs) into the hole collection poly(3,4-ethylenedioxythiophene) poly(styrenesulfonate) (PEDOT:PSS) layer. Theoretical and experimental results show that the very strong near field around Au NPs due to Localized Surface Plasmonic Resonance (LSPR) mainly distributes laterally along the PEDOT:PSS layer rather than vertically into the adjacent active layer, leading to minimal enhancement of light absorption in the active layer. This finding can be extended to a typical class of solar cells incorporating metallic NPs in spacing layers adjacent to the active layer. With optical effects proven to be minor contributors to device performance improvements, we investigate the electrical properties of the PSCs and obtain insights into the detailed device mechanisms. Improvements in power conversion efficiency (PCE) of solar cells are found to originate from the enlarged active layer/PEDOT:PSS interfacial area and improved PEDOT:PSS conductivity. At high NP concentrations, reduced exciton quenching at donor/acceptor junctions is found to cause PCE deterioration. Our findings indicate that it is highly important to investigate both optical and electrical effects for understanding and optimizing PSC performances.

Optical and electrical effects of gold nanoparticles in the active layer of polymer solar cells

The effects of Au nanoparticles (NPs) incorporated into the active layer of polymer solar cells (PSCs) with a newly synthesized donor polymer are investigated in detail. Our work shows that localized surface plasmon resonance (LSPR) introduced by the metallic NPs can experimentally and theoretically enhance the light absorption in the active layer of PSCs because the strong LSPR near field mainly distributes laterally along the active layer. The understanding can be applied to other metallic NP incorporated organic solar cells. Meanwhile, our results show that electrical properties can counter-diminish the optical enhancement from LSPR and thus reduce the overall performance improvement. It is important that both optical and electrical properties need to be studied and optimized simultaneously for achieving improved power conversion efficiency. The study contributes to better understanding the uses of Au NPs for enhancing PSC performances.

Poly(3-hexylthiophene):TiO2 nanocomposites for solar cell applications

The properties of organic/inorganic poly(3-hexylthiophene) (P3HT):TiO2 nanocomposite films and nanocomposite based solar cells as a function of TiO2 concentration and the solvent used for the film fabrication were studied. For low nanoparticle concentration (20?30%) the device performance was worse compared to pure P3HT, while for nanoparticle concentration of 50% and 60% significant improvements were obtained. P3HT photoluminescence quenching in 600?800?nm spectral region changes by a factor of two for the increase in TiO2 concentration from 20% to 60%, while the AM1 power conversion efficiency increases times. Photoluminescence quenching and solar cell efficiency were found to be strongly dependent not only on nanoparticle concentration but also on the solvent used for spin-coating. The changes in the film and device properties were explained by the change in the film morphology. For optimal fabrication conditions, external quantum efficiency up to 15% and AM1 power conversion efficiency of 0.42% were obtained.

Pinhole-Free and Surface-Nanostructured NiOx Film by Room-Temperature Solution Process for High-Performance Flexible Perovskite Solar Cells with Good Stability and Reproducibility

Recently, researchers have focused on the design of highly efficient flexible perovskite solar cells (PVSCs), which enables the implementation of portable and roll-to-roll fabrication in large scale. While NiOx is a promising material for hole transport layer (HTL) candidate for fabricating efficient PVSCs on a rigid substrate, the reported NiOx HTLs are formed using different multistep treatments (such as 300-500 °C annealing, O2-plasma, UVO, etc.), which hinders the development of flexible PVSCs based on NiOx. Meanwhile, the features of nanostructured morphology and flawless film quality are very important for the film to function as highly effective HTL of PVSCs. However, it is difficult to have the two features coexist natively, particularly in a solution process that flawless film will usually come with smooth morphology. Here, we demonstrate the flawless and surface-nanostructured NiOx film from a simple and controllable room-temperature solution process for achieving high performance flexible PVSCs with good stability and reproducibility. The power conversion efficiency (PCE) can reaches a promising value of 14.53% with no obvious hysteresis (and a high PCE of 17.60% for PVSC on ITO glass). Furthermore, the NiOx-based PVSCs show markedly improved air stability. Regarding the performance improvement, the flawless and surface-nanostructured NiOx film can make the interfacial recombination and monomolecular Shockley-Read-Hall recombination of PVSC reduce. In addition, the formation of an intimate junction of large interfacial area at NiOx film/the perovskite layer improve the hole extraction and thus PVSC performances. This work contributes to the evolution of flexible PVSCs with simple fabrication process and high device performances.

Recent Advances in Transition Metal Complexes and Light‐Management Engineering in Organic Optoelectronic Devices

Two of the recent major research topics in optoelectronic devices are discussed: the development of new organic materials (both molecular and polymeric) for the active layer of organic optoelectronic devices (particularly organic light-emitting diodes (OLEDs)), and light management, including light extraction for OLEDs and light trapping for organic solar cells (OSCs). In the first section, recent developments of phosphorescent transition metal complexes for OLEDs in the past 3-4 years are reviewed. The discussion is focused on the development of metal complexes based on iridium, platinum, and a few other transition metals. In the second part, different light-management strategies in the design of OLEDs with improved light extraction, and of OSCs with improved light trapping is discussed.

Low-temperature solution-processed hydrogen molybdenum and vanadium bronzes for an efficient hole-transport layer in organic electronics.

A simple one-step method is reported to synthesize low-temperature solution-processed transition metal oxides (TMOs) of molybdenum oxide and vanadium oxide with oxygen vacancies for a good hole-transport layer (HTL). The oxygen vacancy plays an essential role for TMOs when they are employed as HTLs: TMO films with excess oxygen are highly undesirable for their application in organic electronics.