Project description:The long-term stability of perovskite solar cells (PSCs) remains an issue impeding their commercialization. Generally, polycrystalline perovskite thin films have many defects on the grain boundaries, which affect the optoelectronic performance and stability of the devices under moisture, heat, illumination, and the presence of an electric field condition. The O-donor Lewis base is often employed to regulate the performance of PSCs such as carbonyl and carboxyl compounds. Herein, we have developed a concept of radical molecular modulation using the O-donor group for high-performance perovskite photovoltaic devices. The judiciously designed radical modulators 2,2,6,6-tetramethyl-1-piperidinyloxy (TEMPO), which located at the perovskite grain boundary through interaction with the perovskite surface sites, effectively passivated the surface defects while templating the formation of large grain crystal and high-quality perovskite thin films. Accordingly, the optimized TEMPO-modulated PSCs achieved a power conversion efficiency of 20.73% with superior stability. This work makes an important contribution for exploring the effect of radical in perovskites to improve the performance of PSCs and other optoelectronic devices.
Project description:The comprehensive design approach is established with coupled optical-electrical simulation for perovskite-based solar cell, which emerged as one of the most promising competitors to silicon solar cell for its low-cost fabrication and high PCE. The selection of structured surface, effect of geometry parameters, incident angle-dependence and polarization-sensitivity are considered in the simulation. The optical modeling is performed via the finite-difference time-domain method whilst the electrical properties are obtained by solving the coupled nonlinear equations of Poisson, continuity, and drift-diffusion equations. The optical and electrical performances of five different structured surfaces are compared to select a best structured surface for perovskite solar cell. The effects of the geometry parameters on the optical and electrical properties of the perovskite cell are analyzed. The results indicate that the light harvesting is obviously enhanced by the structured surface. The electrical performance can be remarkably improved due to the enhanced light harvesting of the designed best structured surface. The angle-dependence for s- and p-polarizations is investigated. The structured surface exhibits omnidirectional behavior and favorable polarization-insensitive feature within a wide incident angle range. Such a comprehensive design approach can highlight the potential of perovskite cell for power conversion in the full daylight.
Project description:In this work, we report an easy, efficient method to synthesize high quality lithium-based upconversion nanoparticles (UCNPs) which combine two promising materials (UCNPs and lithium ions) known to enhance the photovoltaic performance of perovskite solar cells (PSCs). Incorporating the synthesized YLiF4:Yb,Er nanoparticles into the mesoporous layer of the PSCs cells, at a certain doping level, demonstrated a higher power conversion efficiency (PCE) of 19%, additional photocurrent, and a better fill factor (FF) of 82% in comparison to undoped PSCs (PCE = ~16.5%; FF = 71%). The reported results open a new avenue toward efficient PSCs for renewable energy applications.
Project description:The performance of organometallic perovskite solar cells has rapidly surpassed that of both conventional dye-sensitized and organic photovoltaics. High-power conversion efficiency can be realized in both mesoporous and thin-film device architectures. We address the origin of this success in the context of the materials chemistry and physics of the bulk perovskite as described by electronic structure calculations. In addition to the basic optoelectronic properties essential for an efficient photovoltaic device (spectrally suitable band gap, high optical absorption, low carrier effective masses), the materials are structurally and compositionally flexible. As we show, hybrid perovskites exhibit spontaneous electric polarization; we also suggest ways in which this can be tuned through judicious choice of the organic cation. The presence of ferroelectric domains will result in internal junctions that may aid separation of photoexcited electron and hole pairs, and reduction of recombination through segregation of charge carriers. The combination of high dielectric constant and low effective mass promotes both Wannier-Mott exciton separation and effective ionization of donor and acceptor defects. The photoferroic effect could be exploited in nanostructured films to generate a higher open circuit voltage and may contribute to the current-voltage hysteresis observed in perovskite solar cells.
Project description:In several photovoltaic (PV) technologies, the presence of electronic defects within the semiconductor band gap limit the efficiency, reproducibility, as well as lifetime. Metal halide perovskites (MHPs) have drawn great attention because of their excellent photovoltaic properties that can be achieved even without a very strict film-growth control processing. Much has been done theoretically in describing the different point defects in MHPs. Herein, we discuss the experimental challenges in thoroughly characterizing the defects in MHPs such as, experimental assignment of the type of defects, defects densities, and the energy positions within the band gap induced by these defects. The second topic of this Review is passivation strategies. Based on a literature survey, the different types of defects that are important to consider and need to be minimized are examined. A complete fundamental understanding of defect nature in MHPs is needed to further improve their optoelectronic functionalities.
Project description:Perovskite solar cells (PSCs) suffer from significant nonradiative recombination at perovskite/charge transport layer heterojunction, seriously limiting their power conversion efficiencies. Herein, solution-processed chromium multioxide (CrOx ) is judiciously selected to construct a MAPbI3 /CrOx /Spiro-OMeTAD hole-selective heterojunction. It is demonstrated that the inserted CrOx not only effectively reduces defect sites via redox shuttle at perovskite contact, but also decreases valence band maximum (VBM)-HOMO offset between perovskite and Spiro-OMeTAD. This will diminish thermionic losses for collecting holes and thus promote charge transport across the heterojunction, suppressing both defect-assisted recombination and interface carrier recombination. As a result, a remarkable improvement of 21.21% efficiency with excellent device stability is achieved compared to 18.46% of the control device, which is among the highest efficiencies for polycrystalline MAPbI3 based n-i-p planar PSCs reported to date. These findings of this work provide new insights into novel charge-selective heterojunctions for further enhancing efficiency and stability of PSCs.
Project description:Planar perovskite solar cells (PSCs) with perovskite and [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) heterojunction have attracted much interest because they can be fabricated by a low-temperature process and exhibit high power conversion efficiency (PCE). Various compositional engineering and interface engineering approaches have been applied to produce high-performance PSC devices. In this study, we found that high-quality lead halide crystal precursor has a significant effect on the perovskite film quality and it could enhance perovskite film light absorption, reduce crystal defects, and suppress charge recombination, resulting in enhanced device performance (from 8.9 to 15.0% for CH3NH3PbI3 and from 14.2 to 18.0% for MA0.7FA0.3PbI3-x Cl x ). Moreover, electron and hole interlayer free devices were achieved by using high-quality PbI2 crystals and the devices exhibited a high PCE of 13.6 and 10.4% for glass and flexible substrates, respectively. This is important for simplifying the perovskite solar cell fabrication process without complex interface engineering involved, especially for printed PSCs.
Project description:Fabricating inorganic-organic hybrid perovskite solar cells (PSCs) on plastic substrates broadens their scope for implementation in real systems by imparting portability, conformability and allowing high-throughput production, which is necessary for lowering costs. Here we report a new route to prepare highly dispersed Zn2SnO4 (ZSO) nanoparticles at low-temperature (<100 °C) for the development of high-performance flexible PSCs. The introduction of the ZSO film significantly improves transmittance of flexible polyethylene naphthalate/indium-doped tin oxide (PEN/ITO)-coated substrate from ∼75 to ∼90% over the entire range of wavelengths. The best performing flexible PSC, based on the ZSO and CH3NH3PbI3 layer, exhibits steady-state power conversion efficiency (PCE) of 14.85% under AM 1.5G 100 mW·cm(-2) illumination. This renders ZSO a promising candidate as electron-conducting electrode for the highly efficient flexible PSC applications.
Project description:Charged defects at the surface of the organic-inorganic perovskite active layer are detrimental to solar cells due to exacerbated charge carrier recombination. Here we show that charged surface defects can be benign after passivation and further exploited for reconfiguration of interfacial energy band structure. Based on the electrostatic interaction between oppositely charged ions, Lewis-acid-featured fullerene skeleton after iodide ionization (PCBB-3N-3I) not only efficiently passivates positively charged surface defects but also assembles on top of the perovskite active layer with preferred orientation. Consequently, PCBB-3N-3I with a strong molecular electric dipole forms a dipole interlayer to reconfigure interfacial energy band structure, leading to enhanced built-in potential and charge collection. As a result, inverted structure planar heterojunction perovskite solar cells exhibit the promising power conversion efficiency of 21.1% and robust ambient stability. This work opens up a new window to boost perovskite solar cells via rational exploitation of charged defects beyond passivation.
Project description:A promising route to widespread deployment of photovoltaics is to harness inexpensive, highly-efficient tandems. We perform holistic life cycle assessments on the energy payback time, carbon footprint, and environmental impact scores for perovskite-silicon and perovskite-perovskite tandems benchmarked against state-of-the-art commercial silicon cells. The scalability of processing steps and materials in the manufacture and operation of tandems is considered. The resulting energy payback time and greenhouse gas emission factor of the all-perovskite tandem configuration are 0.35 years and 10.7 g CO2-eq/kWh, respectively, compared to 1.52 years and 24.6 g CO2-eq/kWh for the silicon benchmark. Prolonging the lifetime provides a strong technological lever for reducing the carbon footprint such that the perovskite-silicon tandem can outcompete the current benchmark on energy and environmental performance. Perovskite-perovskite tandems with flexible and lightweight form factors further improve the energy and environmental performance by around 6% and thus enhance the potential for large-scale, sustainable deployment.