Operation Of Photovoltaic Devices Research Articles

An n‐n Heterojunction Configuration for Efficient Electron Transport in Organic Photovoltaic Devices

AbstractSelective electron transport and extraction are essential to the operation of photovoltaic devices. Electron transport layer (ETL) is therefore critical to organic photovoltaics (OPV). Herein, an ETL configuration is presented comprising a solution‐processed n‐n organic heterojunction to enhance electron transport and hole blocking, and boost power conversion efficiency (PCE) in OPV. Specifically, the n‐n heterojunction is constructed by stacking a narrow‐band n‐type conjugated polymer layer (PNDIT‐F3N) and a wide‐band n‐type conjugated molecule layer (Phen‐NaDPO). Based on the ultraviolet photoelectron spectroscopy measurement and numerical simulation of current density‐voltage characteristics, the formation of the built‐in potential is investigated. In three OPVs with different active layers, substantial improvements are observed in performance following the introduction of this ETL configuration. The performance enhancement arises from the combination of selective carrier transport properties and reduced recombination. Another contributing factor is the good film‐forming quality of the new ETL configuration, where the surface energies of the related materials are well‐matched. The n‐n organic heterojunction represents a viable and promising ETL construction strategy for efficient OPV devices.

Computational Design of Crescent Shaped Promising Nonfullerene Acceptors with 1,4-Dihydro-2,3-quinoxalinedione Core and Different Electron-withdrawing Terminal Units for Photovoltaic Applications.

This study aims to design a series of nonfullerene acceptors (NFAs) for photovoltaic applications having 1,4-dihydro-2,3-quinoxalinedione fused thiophene derivative as the core unit and 1,1-dicyanomethylene-3-indanone (IC) derivatives and different π-conjugated molecules other than IC as terminal acceptor units. All the investigated NFAs are found air-stable as the computed highest occupied molecular orbitals (HOMOs) are below the air oxidation threshold (ca. -5.27 eV vs saturated calomel electrode). The studied NFAs can act as potential nonfullerene acceptor candidates as they are found to have sufficient open-circuit voltage (Voc) and fill factor (FF) ranging from 0.62 to 1.41 V and 83%-91%, respectively. From the anisotropic mobility analysis, it is noticed that the studied NFAs except dicyano-rhodanine terminal unit containing NFA, exhibit better electron mobility than the hole mobility, and therefore, they can be more promising electron transporting acceptor materials in the active layer of an organic photovoltaic cell. From the optical absorption analysis, it is noted that all the designed NFAs have the maximum absorption spectra ranging from 597 nm-730 nm, which lies in the visible region and near-infrared (IR) region of the solar spectrum. The computed light-harvesting efficiencies for the PM6 (thiophene derivative donor selected in our study):NFA blends are found to lie in the range of 0.96-0.99, which indicates efficient light-harvesting by the PM6:NFA blends during photovoltaic device operation.

Improving the efficiency of organic sensitizers with various anchoring groups for solar energy applications

Acceptor electron groups play a key role in sensitizer proficiency in the DSSCs. To study this effect, a variety of acceptor electron groups were placed on a common scaffold. In this way, various intermediates and dyes were engineered, synthesized, purified and identified. Titanium dioxide and Na-doped TiO2 were employed to prepare of nanocrystalline layer of the photovoltaic devices. The blue movement was beholden in the UV–Visible test the coated photosensitizers on nanoparticle due to the J-type aggregation. To predict the usability of dyes in the structure of the solar cells, two methods, DFT and CV were employed. Finally, the DSSCs devices were prepared based on synthesized dyes and Na-doped TiO2 or TiO2. The photovoltaic device, which contains Dye 2, has the highest Jsc. The operation of photovoltaic device based on titanium dioxide is lower than that of Na-doped TiO2.

High stability photosensitizers for dye-sensitized solar cells: Synthesis, characterization and optical performance

Abstract The output of various donating substituents on the optical behavior of new photosensitizers in the solar cells was investigated. The pure intermediates and dyes were identified via an analytical procedure and confirmed the chemical structure. Zinc oxide and titanium dioxide were operated to fabricate the nanocrystalline layer of the solar cells. The UV–Visible spectra of all synthesized dyes on ZnO and TiO2 illustrated blue shift due to the J-aggregation of organic dyes on the semiconductor substrate. To predict the usability of dyes in the structure of the solar cells, two methods, DFT and CV were employed. Finally, the DSSCs devices were prepared based on synthesized dyes and ZnO or TiO2. The highest photocurrent was achieved for individual device-TiO2 sensitized with Dye 2 containing thioindigo and cyanoacrylic acid. The operation of photovoltaic device based on zinc oxide was lower than that of titanium dioxide.

Quantum-kinetic perspective on photovoltaic device operation in nanostructure-based solar cells

Abstract

Revealing the recombination dynamics in squaraine-based bulk heterojunction solar cells

We combine steady-state with transient optoelectronic characterization methods to understand the operation of photovoltaic devices based on a benchmark model squaraine blended with a fullerene acceptor. These devices suffer from a gradual decrease in the fill factor when increasing the active layer thickness and incident light intensity. Using transient photocurrent, transient photovoltage, and bias-assisted charge extraction measurements, we show that the fill factor deteriorates due to slow charge carrier collection competing with bimolecular recombination. Under normal operating conditions, we find a bimolecular recombination rate constant of ∼10–17 m3 s−1, which corresponds to a reduction of one to two orders of magnitude compared to the Langevin model.

The nonequilibrium Green’s function picture of inelastic processes in nanostructure photovoltaics

We discuss within the nonequilibrium Green's function formalism the self-consistent Born approximation of the electronic self-energy for concurrent coupling of charge carriers to photons and phonons. The expansion of the charge carrier Green's function is shown to provide a description for a range of physical processes with relevance for the photovoltaic device operation, such as indirect optical transitions, thermally assisted photocarrier escape from quantum wells or phonon-mediated interband transfer in tunnel junctions. The nonequilibrium Green's function picture of these processes is reviewed with focus on the evolution of the system towards the steady state in the convergence of the self-consistency iteration process and on the impact of inelastic scattering on device operation.

Tuning of undoped ZnO thin film via plasma enhanced atomic layer deposition and its application for an inverted polymer solar cell

We studied the tuning of structural and optical properties of ZnO thin film and its correlation to the efficiency of inverted solar cell using plasma-enhanced atomic layer deposition (PEALD). The sequential injection of DEZn and O2 plasma was employed for the plasma-enhanced atomic layer deposition of ZnO thin film. As the growth temperature of ZnO film was increased from 100 °C to 300 °C, the crystallinity of ZnO film was improved from amorphous to highly ordered (002) direction ploy-crystal due to self crystallization. Increasing oxygen plasma time in PEALD process also introduces growing of hexagonal wurtzite phase of ZnO nanocrystal. Excess of oxygen plasma time induces enhanced deep level emission band (500 ∼ 700 nm) in photoluminescence due to Zn vacancies and other defects. The evolution of structural and optical properties of PEALD ZnO films also involves in change of electrical conductivity by 3 orders of magnitude. The highly tunable PEALD ZnO thin films were employed as the electron conductive layers in inverted polymer solar cells. Our study indicates that both structural and optical properties rather than electrical conductivities of ZnO films play more important role for the effective charge collection in photovoltaic device operation. The ability to tune the materials properties of undoped ZnO films via PEALD should extend their functionality over the wide range of advanced electronic applications.

Simulation of Nanostructure-Based High-Efficiency Solar Cells: Challenges, Existing Approaches, and Future Directions

Many advanced concepts for high-efficiency photovoltaic devices exploit the peculiar optoelectronic properties of semiconductor nanostructures such as quantum wells, wires and dots. While the optics of such devices is only modestly affected due to the small size of the structures, the optical transitions and electronic transport can strongly deviate from the simple bulk picture known from conventional solar cell devices. This review article discusses the challenges for an adequate theoretical description of the photovoltaic device operation arising from the introduction of nanostructure absorber and/or conductor components and gives an overview of existing device simulation approaches.

Theory and simulation of quantum photovoltaic devices based on the non-equilibrium Green’s function formalism

This article reviews the application of the non-equilibrium Green’s function formalism to the simulation of novel photovoltaic devices utilizing quantum confinement effects in low dimensional absorber structures. It covers well-known aspects of the fundamental NEGF theory for a system of interacting electrons, photons and phonons with relevance for the simulation of optoelectronic devices and introduces at the same time new approaches to the theoretical description of the elementary processes of photovoltaic device operation, such as photogeneration via coherent excitonic absorption, phonon-mediated indirect optical transitions or non-radiative recombination via defect states. While the description of the theoretical framework is kept as general as possible, two specific prototypical quantum photovoltaic devices, a single quantum well photodiode and a silicon-oxide based superlattice absorber, are used to illustrated the kind of unique insight that numerical simulations based on the theory are able to provide.

Self‐Assembly of Thiophene‐ and Furan‐Appended Methanofullerenes with Poly(3‐Hexylthiophene) in Organic Solar Cells

Novel fullerene derivatives bearing thiophene and furan residues were synthesized and studied as electron acceptor materials in bulk heterojunction organic solar cells, together with poly(3-hexylthiophene) (P3HT) as the donor polymer. Some compounds showed large nanomorphological inhomogenities in blends with P3HT; in particular, clusters with dimensions in the range of 100-1000 nm were formed. However, some blends that showed such large clusters yielded at the same time high power conversion efficiencies in photovoltaic devices, approaching 3.7 %. This is in sharp contrast with previously studied systems, in which a substantial phase separation always resulted in a poor photovoltaic performance. We assume that the attachment of thienyl or furyl groups to the fullerene cage results in a certain ordering of the designed fullerene derivatives I-IX with P3HT in photoactive blends. Both the fullerene derivative and P3HT might assemble via pi-pi stacking of the thiophene units to form the nanostructures observed in the films by optical and atomic force microscopy. The presence of ordered donor and acceptor counterparts in these nanostructures results in superior photovoltaic device operation.