Large area monolithic organic solar cells

Although efficiencies of > 10% have recently been achieved in laboratory-scale organic solar cells, these competitive performance figures are yet to be translated to large active areas and geometries relevant for viable manufacturing. One of the factors hindering scale-up is a lack of knowledge of device physics at the sub-module level, particularly cell architecture, electrode geometry and current collection pathways. A more in depth understanding of how photocurrent and photovoltage extraction can be optimised over large active areas is urgently needed. Another key factor suppressing conversion efficiencies in large area cells is the relatively high sheet resistance of the transparent conducting anode typically indium tin oxide. Hence, to replace ITO with alternative transparent conducting anodes is also a high priority on the pathway to viable module-level organic solar cells. In our paper we will focus on large area devices relevant to sub-module scales - 5 cm x 5 cm monolithic geometry. We have applied a range of experimental techniques to create a more comprehensive understanding of the true device physics that could help make large area, monolithic organic solar cells more viable. By employing this knowledge, a novel transparent anode consisting of molybdenum oxide (MoOx) and silver (Ag) is developed to replace ITO and PEDOT-free large area solar cell sub-modules, acting as both a transparent window and hole-collecting electrode. The proposed architecture and anode materials are well suited to high throughput, low cost all-solution processing

The nature and role of trap states in a dendrimer-based organic field-effect transistor explosive sensor

We report the fabrication and charge transport characterization of carbazole dendrimer-based organic field-effect transistors (OFETs) for the sensing of explosive vapors. After exposure to para-nitrotoluene (pNT) vapor, the OFET channel carrier mobility decreases due to trapping induced by the absorbed pNT. The influence of trap states on transport in devices before and after exposure to pNT vapor has been determined using temperature-dependent measurements of the field-effect mobility. These data clearly show that the absorption of pNT vapor into the dendrimer active layer results in the formation of additional trap states. Such states inhibit charge transport by decreasing the density of conducting states. (C) 2013 AIP Publishing LLC

Charge transport in an organic light emitting diode material measured using metal-insulator-semiconductor charge extraction by linearly increasing voltage with parameter variation

Charge transport measurement using the Metal-Insulator-Semiconductor Charge Extraction by Linearly Increasing Voltage (MIS-CELIV) technique is a promising method for determining charge mobility in organic semiconductors because of its ability to study electron and hole mobilities independently. However, MIS-CELIV measurements have a number of parameters that can potentially affect the calculated mobility. There are only a few reports on MIS-CELIV being used to determine the charge mobility for materials typically used in organic light-emitting diodes (OLEDs), and the impact of each of the MIS-CELIV experimental parameters on the mobility is presently unknown. We find that the pulse duration, injection time, maximum voltage, offset voltage, and external load resistance have different levels of influence on the calculated mobility. Using the hole transporting OLED host material, tris(4-carbazoyl-9-ylphenyl)amine (TCTA), we show that having an injection time sufficient to fully charge the insulator layer, a pulse duration comparable to the transit time, and an external circuit time constant much smaller than the transit time is required to give a mobility relevant to an OLED. The optimized MIS-CELIV parameters led to the measurement having a similar current density and electric field to that of an operational OLED. Under these conditions, the hole mobility of TCTA was determined to be 2.90 ± 0.07 × 10 cm V s, which is similar to that measured using time-of-flight techniques. Using inappropriate experimental parameters could lead to an underestimation of the mobility by an order of magnitude. Simulations of the MIS-CELIV measurements verified the effect the different parameters played in determining the charge mobility

Influence of processing additives to nano-morphology and efficiency of bulk-heterojunction solar cells: A comparative review

Research and development towards high efficiency plastic solar cells have been accelerating in recent years. Polymer-based bulk heterojunction solar cells are offering an attractive and inexpensive concept for large scale production by solution processing as well as advantageous flexible and aesthetic form factors. The thin film nano-morphology of bulk-heterojunction solar cells has been shown to dramatically influence the photovoltaic performance of the devices. This article reviews the different methods used to control the film nano-morphology of bulk-heterojunction solar cells focussing on the chemical additives during solution processing. All power conversion efficiency limiting mechanisms of bulk-heterojunction solar cells are discussed in detail. It is shown, how the formation of optimal percolation pathways between donor and acceptor influences the photovoltaic device performance. It is explained how the film nano-morphology relates to light absorption, free charge carrier generation as well as charge transport to the electrodes

Photocarrier lifetime and recombination losses in photovoltaic systems

[Extract] To the Editor — The photocarrier lifetime is commonly employed to describe the performance of photovoltaic and photodetecting devices fabricated from crystalline or non-crystalline materials. Numerous studies have obtained photocarrier lifetimes from transient decay signals in a multitude of non-crystalline systems, such as dye-sensitized solar cells, organic donor–acceptor blends, perovskites, nanoparticles, quantum dots and nanowires

Advanced Monitoring and Control System for Virtual Power Plants for Enabling Customer Engagement and Market Participation

To integrate large-scale renewable energy into energy systems, an effective participation from private investors and active customer engagement are essential. Virtual power plants (VPPs) are a very promising approach. To realize this engagement, an efficient monitoring and control system needs to be implemented for the VPP to be flexible, scalable, secure, and cost-effective. In this paper, a realistic VPP in Western Australia is studied, comprising 67 dwellings, including a 810 kW rooftop solar photovoltaic (PV) system, a 700 kWh vanadium redox flow battery (VRFB), a heat pump hot water system (HWS), an electric vehicle (EV) charging station, and demand management mechanisms. The practical and detailed concept design of the monitoring and control system for EEBUS-enabled appliances, and also for the PV and VRFB system, with smart inverters, is proposed. In addition, a practical fog-based storage and computing system is developed to enable the VPP owner to manage the PV, VRFB, and EV charging station for maximizing the benefit to the customers and the VPP owner. Further, the proposed cloud-based applications enable customers to participate in gamified demand response programs for increasing the level of their engagement while satisfying their comfort level. All proposed systems and architecture in this paper have the capability of being implemented fully and relevant references for practical devices are given where necessary

Thin film properties of triphenylamine-cored dendrimers: A molecular approach to control aggregation

The solid-state photophysical and charge transport properties of two first-generation dendrimers are presented. The dendrimers are comprised of a triphenylamine core, dendrons containing a phenyl branching unit with thiophene (Dendrimer 1) or bithiophene (Dendrimer 2) moieties, and dodecyl surface groups. For Dendrimer 1, the excited state is located within the center of the dendrimer giving rise to a moderate solid-state photoluminescence quantum yield (Φpl) (0.13) and significant charge trapping, with both observations due to the degree of overlap of the main electroactive chromophores on adjacent dendrimers. For Dendrimer 2, the excited state is located within the dendron and in the solid-state this leads to a strongly red-shifted and weakened emission (Φpl ~ 0.02) due to strong intermolecular chromophore interactions. For films of Dendrimer 2 the charge mobility was higher than Dendrimer 1 but was still limited by a low density of strongly interacting electroactive chromophores. The pronounced difference between the solid-state properties of the two dendrimers is simply engineered by the addition of an extra thiophene in each of the dendrons