Showing papers on "Solar cell published in 2019"

Halide Perovskite Photovoltaics: Background, Status, and Future Prospects

Abstract: The photovoltaics of organic–inorganic lead halide perovskite materials have shown rapid improvements in solar cell performance, surpassing the top efficiency of semiconductor compounds such as CdTe and CIGS (copper indium gallium selenide) used in solar cells in just about a decade. Perovskite preparation via simple and inexpensive solution processes demonstrates the immense potential of this thin-film solar cell technology to become a low-cost alternative to the presently commercially available photovoltaic technologies. Significant developments in almost all aspects of perovskite solar cells and discoveries of some fascinating properties of such hybrid perovskites have been made recently. This Review describes the fundamentals, recent research progress, present status, and our views on future prospects of perovskite-based photovoltaics, with discussions focused on strategies to improve both intrinsic and extrinsic (environmental) stabilities of high-efficiency devices. Strategies and challenges regardi...

Stabilizing halide perovskite surfaces for solar cell operation with wide-bandgap lead oxysalts.

Abstract: We show that converting the surfaces of lead halide perovskite to water-insoluble lead (II) oxysalt through reaction with sulfate or phosphate ions can effectively stabilize the perovskite surface and bulk material. These capping lead oxysalt thin layers enhance the water resistance of the perovskite films by forming strong chemical bonds. The wide-bandgap lead oxysalt layers also reduce the defect density on the perovskite surfaces by passivating undercoordinated surface lead centers, which are defect-nucleating sites. Formation of the lead oxysalt layer increases the carrier recombination lifetime and boosts the efficiency of the solar cells to 21.1%. Encapsulated devices stabilized by the lead oxysalt layers maintain 96.8% of their initial efficiency after operation at maximum power point under simulated air mass (AM) 1.5 G irradiation for 1200 hours at 65°C.

Strain engineering in perovskite solar cells and its impacts on carrier dynamics.

Abstract: The mixed halide perovskites have emerged as outstanding light absorbers for efficient solar cells. Unfortunately, it reveals inhomogeneity in these polycrystalline films due to composition separation, which leads to local lattice mismatches and emergent residual strains consequently. Thus far, the understanding of these residual strains and their effects on photovoltaic device performance is absent. Herein we study the evolution of residual strain over the films by depth-dependent grazing incident X-ray diffraction measurements. We identify the gradient distribution of in-plane strain component perpendicular to the substrate. Moreover, we reveal its impacts on the carrier dynamics over corresponding solar cells, which is stemmed from the strain induced energy bands bending of the perovskite absorber as indicated by first-principles calculations. Eventually, we modulate the status of residual strains in a controllable manner, which leads to enhanced PCEs up to 20.7% (certified) in devices via rational strain engineering. The residual strains in the mixed halide perovskite thin films and their effects on the solar cell devices are less understood. Here Zhu et al. study the impact of the gradient in-plane strain on the carrier dynamics of the strained perovskite films and optimize the device efficiency.

Passivating contacts for crystalline silicon solar cells

Abstract: The global photovoltaic (PV) market is dominated by crystalline silicon (c-Si) based technologies with heavily doped, directly metallized contacts. Recombination of photo-generated electrons and holes at the contact regions is increasingly constraining the power conversion efficiencies of these devices as other performance-limiting energy losses are overcome. To move forward, c-Si PV technologies must implement alternative contacting approaches. Passivating contacts, which incorporate thin films within the contact structure that simultaneously supress recombination and promote charge-carrier selectivity, are a promising next step for the mainstream c-Si PV industry. In this work, we review the fundamental physical processes governing contact formation in c-Si. In doing so we identify the role passivating contacts play in increasing c-Si solar cell efficiencies beyond the limitations imposed by heavy doping and direct metallization. Strategies towards the implementation of passivating contacts in industrial environments are discussed. The development of passivating contacts holds great potential for enhancing the power conversion efficiency of silicon photovoltaics. Here, De Wolf et al. review recent advances in material design and device architecture, and discuss technical challenges to industrial fabrication.

Reduction of lead leakage from damaged lead halide perovskite solar modules using self-healing polymer-based encapsulation

Abstract: In recent years, the major factors that determine commercialization of perovskite photovoltaic technology have been shifting from solar cell performance to stability, reproducibility, device upscaling and the prevention of lead (Pb) leakage from the module over the device service life. Here we simulate a realistic scenario in which perovskite modules with different encapsulation methods are mechanically damaged by a hail impact (modified FM 44787 standard) and quantitatively measure the Pb leakage rates under a variety of weather conditions. We demonstrate that the encapsulation method based on an epoxy resin reduces the Pb leakage rate by a factor of 375 compared with the encapsulation method based on a glass cover with an ultraviolet-cured resin at the module edges. The greater Pb leakage reduction of the epoxy resin encapsulation is associated with its optimal self-healing characteristics under the operating conditions and with its increased mechanical strength. These findings strongly suggest that perovskite photovoltaic products can be deployed with minimal Pb leakage if appropriate encapsulation is employed. Lead leakage from damaged perovskite solar cells poses a challenge to the deployment of such technology. Here, Jiang, Qiu and co-workers quantify lead leakage caused by a simulated hail impact under a number of weather conditions and show that self-healing encapsulations can effectively reduce it.

Interface and Defect Engineering for Metal Halide Perovskite Optoelectronic Devices.

Abstract: Metal halide perovskites have been in the limelight in recent years due to their enormous potential for use in optoelectronic devices, owing to their unique combination of properties, such as high absorption coefficient, long charge-carrier diffusion lengths, and high defect tolerance. Perovskite-based solar cells and light-emitting diodes (LEDs) have achieved remarkable breakthroughs in a comparatively short amount of time. As of writing, a certified power conversion efficiency of 22.7% and an external quantum efficiency of over 10% have been achieved for perovskite solar cells and LEDs, respectively. Interfaces and defects have a critical influence on the properties and operational stability of metal halide perovskite optoelectronic devices. Therefore, interface and defect engineering are crucial to control the behavior of the charge carriers and to grow high quality, defect-free perovskite crystals. Herein, a comprehensive review of various strategies that attempt to modify the interfacial characteristics, control the crystal growth, and understand the defect physics in metal halide perovskites, for both solar cell and LED applications, is presented. Lastly, based on the latest advances and breakthroughs, perspectives and possible directions forward in a bid to transcend what has already been achieved in this vast field of metal halide perovskite optoelectronic devices are discussed.

Record Efficiency for Thin-Film Polycrystalline Solar Cells Up to 22.9% Achieved by Cs-Treated Cu(In,Ga)(Se,S) 2

Abstract: An efficiency of 22.9% for 1-cm2-sized Cu(In,Ga)(Se,S)2 solar cells has been independently verified, establishing a record device efficiency for thin-film polycrystalline solar cells. The main improvement in the solar cell device is due to a reduction in the deficit of the open-circuit voltage ( V oc), which is notably suppressed by modifying the absorber formation. This is presumably due to reduced defect density, as suggested by the enhanced photoluminescence performance. Such improvement in the absorber quality allowed for an opportunity to benefit from the effects of a wider absorber bandgap. The reverse saturation current density and V oc were significantly improved. Meanwhile, heavier alkali treatment on the absorber surface using cesium was adopted to further boost the device performance. As a result, the significant enhancements in V oc and fill factor led to the achievement of this record-breaking efficiency. These findings have been systematically reproduced and will be leveraged to improve the module performance of Solar Frontier's production in the near future.

Harnessing MOF materials in photovoltaic devices: recent advances, challenges, and perspectives

Abstract: Metal–organic framework (MOF) materials have achieved significant research interest in the fields of gas storage and separation over the last two decades because of the need for hydrogen utilization and carbon dioxide reduction. Besides, recently numerous functional MOFs have been exploited and applied in the optoelectronic field owing to some unique properties of MOF materials in those photovoltaic devices with enhanced performance and stability. This review focuses on the comprehensive summary of recent representative progress in the applications of MOFs in solar cell devices, including dye-sensitized solar cells, organic–inorganic hybrid perovskite solar cells, and organic solar cells, aiming to portray their prospects in the future.

Effect of solid-H2S gas reactions on CZTSSe thin film growth and photovoltaic properties of a 12.62% efficiency device

Abstract: We fabricated CZTSSe thin films using optimized SLG-Mo/Zn/Cu/Sn (MZCT) as a stacked structure and described the phenomenon of Zn elemental volatilization using the MZCT stacked structure. We introduced H2S gas to effectively control the S/(S + Se) ratio of the film in the sulfo-selenization process and to suppress Zn volatilization. Unlike during the selenization process, a stable ZnSSe thin film was formed on the precursor surface during the sulfo-selenization process. The formation of the ZnSSe thin film inhibited Zn volatilization, which facilitated control of the thin film stoichiometry and played an important role in crystal growth. In addition, the sulfo-selenization process using H2S forms a grading of the S/(S + Se) ratio in the depth direction in the ZnSSe layer. The ZnSSe layer with this property causes the band gap grading in the CZTSSe absorption layer. Finally, through our optimized annealing process, we realized a world record CZTSSe solar cell with a certified power conversion efficiency of 12.62% and a centimetre-scale (1.1761 cm2) efficiency of 11.28%.

Exceeding 20% efficiency with in situ group V doping in polycrystalline CdTe solar cells

Abstract: CdTe-based solar technology has achieved one of the lowest levelized costs of electricity among all energy sources as well as state-of-the-art field stability. Yet, there is still ample headroom to improve. For decades, mainstream technology has combined fast CdTe deposition with a CdCl2 anneal and Cu doping. The resulting defect chemistry is strongly compensated and limits the useful hole density to ~1014 cm−3, creating a ceiling for fill factor, photovoltage and efficiency. In addition, Cu easily changes energy states and diffuses spatially, creating a risk of instabilities that must be managed with care. Here, we demonstrate a significant shift by doping polycrystalline CdSexTe1 − x and CdTe films with As while removing Cu entirely from the solar cell. The absorber majority-carrier density is increased by orders of magnitude to 1016–1017 cm−3 without compromising the lifetime, and is coupled with a high photocurrent greater than 30 mA cm−2. We demonstrate pathways for fast dopant incorporation in polycrystalline thin films, improved stability and 20.8% solar cell efficiency. CdTe solar cells have relied for decades on copper, which creates limited hole density, stability issues and a ceiling for voltage and efficiency. Now, Metzger et al. demonstrate As-doped Cu-free polycrystalline CdTe cells with enhanced hole density and dopant stability, achieving 20.8% efficiency.

Sensitization of silicon by singlet exciton fission in tetracene

Abstract: Silicon dominates contemporary solar cell technologies1. But when absorbing photons, silicon (like other semiconductors) wastes energy in excess of its bandgap2. Reducing these thermalization losses and enabling better sensitivity to light is possible by sensitizing the silicon solar cell using singlet exciton fission, in which two excited states with triplet spin character (triplet excitons) are generated from a photoexcited state of higher energy with singlet spin character (a singlet exciton)3–5. Singlet exciton fission in the molecular semiconductor tetracene is known to generate triplet excitons that are energetically matched to the silicon bandgap6–8. When the triplet excitons are transferred to silicon they create additional electron–hole pairs, promising to increase cell efficiencies from the single-junction limit of 29 per cent to as high as 35 per cent9. Here we reduce the thickness of the protective hafnium oxynitride layer at the surface of a silicon solar cell to just eight angstroms, using electric-field-effect passivation to enable the efficient energy transfer of the triplet excitons formed in the tetracene. The maximum combined yield of the fission in tetracene and the energy transfer to silicon is around 133 per cent, establishing the potential of singlet exciton fission to increase the efficiencies of silicon solar cells and reduce the cost of the energy that they generate. A silicon and tetracene solar cell employing singlet fission uses an eight-angstrom-thick hafnium oxynitride interlayer to promote efficient triplet transfer, increasing the efficiency of the cell.

Encapsulation of Organic and Perovskite Solar Cells: A Review

Abstract: Photovoltaic is one of the promising renewable sources of power to meet the future challenge of energy need. Organic and perovskite thin film solar cells are an emerging cost-effective photovoltaic technology because of low-cost manufacturing processing and their light weight. The main barrier of commercial use of organic and perovskite solar cells is the poor stability of devices. Encapsulation of these photovoltaic devices is one of the best ways to address this stability issue and enhance the device lifetime by employing materials and structures that possess high barrier performance for oxygen and moisture. The aim of this review paper is to find different encapsulation materials and techniques for perovskite and organic solar cells according to the present understanding of reliability issues. It discusses the available encapsulate materials and their utility in limiting chemicals, such as water vapour and oxygen penetration. It also covers the mechanisms of mechanical degradation within the individual layers and solar cell as a whole, and possible obstacles to their application in both organic and perovskite solar cells. The contemporary understanding of these degradation mechanisms, their interplay, and their initiating factors (both internal and external) are also discussed.

Slow Hot‐Carrier Cooling in Halide Perovskites: Prospects for Hot‐Carrier Solar Cells

Abstract: Rapid hot-carrier cooling is a major loss channel in solar cells. Thermodynamic calculations reveal a 66% solar conversion efficiency for single junction cells (under 1 sun illumination) if these hot carriers are harvested before cooling to the lattice temperature. A reduced hot-carrier cooling rate for efficient extraction is a key enabler to this disruptive technology. Recently, halide perovskites emerge as promising candidates with favorable hot-carrier properties: slow hot-carrier cooling lifetimes several orders of magnitude longer than conventional solar cell absorbers, long-range hot-carrier transport (up to ≈600 nm), and highly efficient hot-carrier extraction (up to ≈83%). This review presents the developmental milestones, distills the complex photophysical findings, and highlights the challenges and opportunities in this emerging field. A developmental toolbox for engineering the slow hot-carrier cooling properties in halide perovskites and prospects for perovskite hot-carrier solar cells are also discussed.

Dynamical Transformation of Two-Dimensional Perovskites with Alternating Cations in the Interlayer Space for High-Performance Photovoltaics

Abstract: The two-dimensional (2D) perovskites stabilized by alternating cations in the interlayer space (ACI) define a new type of structure with different physical properties than the more common Ruddlesden-Popper counterparts. However, there is a lack of understanding of material crystallization in films and its influence on the morphological/optoelectronic properties and the final photovoltaic devices. Herein, we undertake in situ studies of the solidification process for ACI 2D perovskite (GA)(MA) nPb nI3 n+1 (⟨ n⟩ = 3) from ink to solid-state semiconductor, using solvent mixture of DMSO:DMF (1:10 v/v) as the solvent and link this behavior to solar cell devices. The in situ grazing-incidence X-ray scattering (GIWAXS) analysis reveals a complex journey through disordered sol-gel precursors, intermediate phases, and ultimately to ACI perovskites. The intermediate phases, including a crystalline solvate compound and the 2D GA2PbI4 perovskite, provide a scaffold for the growth of the ACI perovskites during thermal annealing. We identify 2D GA2PbI4 to be the key intermediate phase, which is strongly influenced by the deposition technique and determines the formation of the 1D GAPbI3 byproducts and the distribution of various n phases of ACI perovskites in the final films. We also confirm the presence of internal charge transfer between different n phases through transient absorption spectroscopy. The high quality ACI perovskite films deposited from solvent mixture of DMSO:DMF (1:10 v/v) deliver a record power conversion efficiency of 14.7% in planar solar cells and significantly enhanced long-term stability of devices in contrast to the 3D MAPbI3 counterpart.

Performance of perovskite solar cells under simulated temperature-illumination real-world operating conditions

Abstract: Since reaching 20% efficiency, research in perovskite photovoltaics has shifted from a race for efficiency to a race for stability. For efficiency, the standard test conditions set the rules for the race. However, the term ‘stability’ is used very broadly and assessed in various ways, meaning different groups are running different races. For the application, only energy yields that can be achieved under real-world, long-term operation matter. Here, we characterize and analyse the performance of an efficient perovskite solar cell (PSC) under simulated ambient conditions based on real temperature and irradiance data from selected days over one year at a location in central Europe. We find that the PSC shows only a low decrease of efficiency with elevated temperature and low light intensity, maintaining almost optimum values for ambient conditions, under which most of the solar energy is incident on the solar cell. The overall energy yield differs from what is expected from standard test condition measurements and is influenced by reversible degradation (delivering the highest performance in the morning) and by a slight permanent degradation that is observable during the year. With reference to tandem cells, we compare the PSC with a silicon device. Real-world conditions under which solar cells operate can be different from standard testing conditions. Tress et al. investigate the effects of temperature and irradiation on the performance of a perovskite cell and a reference silicon cell, reproducing real weather conditions in the laboratory.

Two-Dimensional Halide Perovskites in Solar Cells: 2D or not 2D?

Abstract: Two-dimensional (2D) halide perovskites have recently emerged as a more stable and more versatile family of materials than three-dimensional (3D) perovskite solar cell absorbers. Although solar cells made with 2D perovskites have yet to improve their power conversion efficiencies to compete with 3D perovskite solar cells, their immense diversity offers great opportunities and avenues for research that will likely close the gap between these two. Further, 2D perovskites can have various roles within a solar cell, either as the primary light absorber, as a capping layer, passivating layer, or within a mixed 2D/3D perovskite solar cell absorber. In this Minireview, we will review the history of 2D perovskites in solar cells, the relevant properties of such materials, the different roles that they can play in a solar cell, as well as current trends and challenges.

A Review: Thermal Stability of Methylammonium Lead Halide Based Perovskite Solar Cells

Abstract: Perovskite solar cells have achieved photo-conversion efficiencies greater than 20%, making them a promising candidate as an emerging solar cell technology. While perovskite solar cells are expected to eventually compete with existing silicon-based solar cells on the market, their long-term stability has become a major bottleneck. In particular, perovskite films are found to be very sensitive to external factors such as air, UV light, light soaking, thermal stress and others. Among these stressors, light, oxygen and moisture-induced degradation can be slowed by integrating barrier or interface layers within the device architecture. However, the most representative perovskite absorber material, CH3NH3PbI3 (MAPbI3), appears to be thermally unstable even in an inert environment. This poses a substantial challenge for solar cell applications because device temperatures can be over 45 °C higher than ambient temperatures when operating under direct sunlight. Herein, recent advances in resolving thermal stability problems are highlighted through literature review. Moreover, the most recent and promising strategies for overcoming thermal degradation are also summarized.

Fine Multi-Phase Alignments in 2D Perovskite Solar Cells with Efficiency over 17% via Slow Post-Annealing.

Abstract: Layered Ruddlesden-Popper (RP) phase (2D) halide perovskites have attracted tremendous attention due to the wide tunability on their optoelectronic properties and excellent robustness in photovoltaic devices. However, charge extraction/transport and ultimate power conversion efficiency (PCE) in 2D perovskite solar cells (PSCs) are still limited by the non-eliminable quantum well effect. Here, a slow post-annealing (SPA) process is proposed for BA2 MA3 Pb4 I13 (n = 4) 2D PSCs by which a champion PCE of 17.26% is achieved with simultaneously enhanced open-circuit voltage, short-circuit current, and fill factor. Investigation with optical spectroscopy coupled with structural analyses indicates that enhanced crystal orientation and favorable alignment on the multiple perovskite phases (from the 2D phase near bottom to quasi-3D phase near top regions) is obtained with SPA treatment, which promotes carrier transport/extraction and suppresses Shockley-Read-Hall charge recombination in the solar cell. As far as it is known, the reported PCE is so far the highest efficiency in RP phase 2D PSCs based on butylamine (BA) spacers (n = 4). The SPA-processed devices exhibit a satisfactory stability with <4.5% degradation after 2000 h under N2 environment without encapsulation. The demonstrated process strategy offers a promising route to push forward the performance in 2D PSCs toward realistic photovoltaic applications.

Ultraefficient thermophotovoltaic power conversion by band-edge spectral filtering.

Abstract: Thermophotovoltaic power conversion utilizes thermal radiation from a local heat source to generate electricity in a photovoltaic cell It was shown in recent years that the addition of a highly reflective rear mirror to a solar cell maximizes the extraction of luminescence This, in turn, boosts the voltage, enabling the creation of record-breaking solar efficiency Now we report that the rear mirror can be used to create thermophotovoltaic systems with unprecedented high thermophotovoltaic efficiency This mirror reflects low-energy infrared photons back into the heat source, recovering their energy Therefore, the rear mirror serves a dual function; boosting the voltage and reusing infrared thermal photons This allows the possibility of a practical >50% efficient thermophotovoltaic system Based on this reflective rear mirror concept, we report a thermophotovoltaic efficiency of 291 ± 04% at an emitter temperature of 1,207 °C

Dion–Jacobson Two-Dimensional Perovskite Solar Cells Based on Benzene Dimethanammonium Cation

Abstract: Organic–inorganic perovskite structured compounds have recently emerged as attractive materials in the fields of photovoltaic due to their exciting optical properties and easy syntheses, as well as exceptional structural and optical tunability. This work presents a Dion–Jacobson two-dimensional (2D) perovskite using diammonium as the barrier molecule. We show that the diammonium barrier molecule is responsible for the perovskite layers’ orientation supported by Hall Effect measurements, which results in a high efficiency solar cell for 2D perovskite without the need for additives or any additional treatment. The 2D perovskite cells achieved an efficiency of 15.6%, which was one of the highest reported for low-dimensional perovskite. Charge extraction, voltage decay, and charge collection efficiency measurements show the beneficial alignment of the 2D perovskites related to the selective contacts. Stability characterization shows that the stability for the 2D perovskite was enhanced compared with their 3D ...