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[IEEE 2019 IEEE 46th Photovoltaic Specialists Conference (PVSC) - Chicago, IL, USA (2019.6.16-2019.6.21)] 2019 IEEE 46th Photovoltaic Specialists Conference (PVSC) - Aqueous Solution Processed Copper Iodide as Hole Transport Material For Planar Inverted Perovskite Solar Cells
摘要： The inorganic carrier transport layers are robust and stable to the environment compared to the organic hole transport layer (HTL). Here, we report on the fabrication of the halide perovskite devices employing CuI as HTL and explored material properties and optoelectronic characterizations. The CuI device demonstrated the device efficiency of 14.1%. The film morphology of CuI is found to have the influence on the perovskite film growth and hence affected on the device parameters. The interface activation energy (EA) ~Eg suggests the recombination activities in the perovskite bulk is dominant. The capacitance analysis revealed the two trap centers of 0.527 eV and 0.332 eV in the perovskite bulk.
关键词： capacitance spectra,interface recombination,defect,copper iodide,halide perovskite
更新于2025-09-23 15:21:01
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Ultrafast Interfacial Charge Transfer of Cesium Lead Halide Perovskite Films CsPbX3 (X = Cl, Br, I) with Different Halogen Mixing
摘要： Understanding the interfacial charge transfer of the photoinduced transients of all-inorganic cesium lead halide perovskites (CsPbX3; X = Cl, Br, I) is critical for their photovoltaic applications. Ultrafast dynamics can provide comprehensive information about the transient behavior of the carriers and their transfer mechanism in the materials. In this work, the interfacial charge transfer of CsPbX3 films assembled with TiO2 with different halogen doping ratios was studied using femtosecond transient absorption (TA) spectroscopy combined with global analysis. Four subsequent decay processes after photoexcitation were obtained, including hot carrier cooling, free exciton forming, electron transfer, and charge recombination. The results indicate that the time constant of the interfacial electron transfer varies with the location of the trap state of these perovskites and the relative energy of CBs in the perovskite and TiO2 and that the time constant of the charge recombination can be attributed to the electron–hole interactions. These interpretations are supported by calculations based on first-principles density functional theory (DFT). Greater iodine doping in such perovskite CsPbX3/TiO2 systems increases the time constants of the electron transfer and charge recombination, which suggests that all-inorganic perovskite CsPbX3 with a high iodine content is favorable for improving the power conversion efficiency of solar cells.
关键词： cesium lead halide perovskite,transient absorption,global analysis,interfacial charge transfer
更新于2025-09-23 15:21:01
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One-step Co-evaporation of All-Inorganic Perovskite Thin Films with Room Temperature Ultralow Amplified Spontaneous Emission Threshold and Air-stability
摘要： Inorganic cesium lead halide perovskite has been successfully applied in optoelectronic field due to its remarkable optical gain properties. Unfortunately, conventional solution-processed CsPbX3 films suffer unavoidable pinhole defects and poor surface morphology, severely limiting their performance on amplified spontaneous emission (ASE) and lasing application. Herein, a dual-source thermal evaporation approach is explored in our work to achieve a uniform and high-coverage CsPbX3 polycrystalline thin film. It is found that the one-step co-evaporated CsPbBr3 (OC-CsPbBr3) thin films without post-annealing exhibit an ultralow ASE threshold of ~ 3.3 μJ/cm2 and gain coefficient above 300 cm-1. The coexistence of cubic and orthorhombic phases in this materials naturally form an energy cascade for the exciton transfer process, which enables rapid accumulation of excitons. Stable ASE intensity without degradation for at least 7 hours is also realized from OC-CsPbBr3 thin films under continuous excitation, which is superior to that in the solution-processed CsPbBr3 thin film. Notably, a Fabry-Perot (F-P) cavity laser based on the OC-CsPbBr3 thin film is first achieved, featuring an ultralow lasing threshold (1.7 μJ/cm2) and directional output (beam divergence of ~ 3.8°). This work highlights the noteworthy optical properties of OC-CsPbBr3 thin films, leading to potential available applications in the integrated optoelectronic chips.
关键词： amplified spontaneous emission,Cesium lead halide perovskite,vapor deposition,long-term stability,thin films
更新于2025-09-23 15:21:01
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Intrinsic anion diffusivity in lead halide perovskites is facilitated by a soft lattice
摘要： Facile ionic transport in lead halide perovskites plays a critical role in device performance. Understanding the microscopic origins of high ionic conductivities has been complicated by indirect measurements and sample microstructural heterogeneities. Here, we report the direct visualization of halide anion interdiffusion in CsPbCl3–CsPbBr3 single crystalline perovskite nanowire heterojunctions using wide-field and confocal photoluminescence measurements. The combination of nanoscale imaging techniques with these single crystalline materials allows us to measure intrinsic anionic lattice diffusivities, free from complications of microscale inhomogeneity. Halide diffusivities were found to be between 10?13 and ～10?12 cm2/second at about 100 °C, which are several orders of magnitudes lower than those reported in polycrystalline thin films. Spatially resolved photoluminescence lifetimes and surface potential measurements provide evidence of the central role of halide vacancies in facilitating ionic diffusion. Vacancy formation free energies computed from molecular simulation are small due to the easily deformable perovskite lattice, accounting for the high equilibrium vacancy concentration. Furthermore, molecular simulations suggest that ionic motion is facilitated by low-frequency lattice modes, resulting in low activation barriers for vacancy-mediated transport. This work elucidates the intrinsic solid-state ion diffusion mechanisms in this class of semisoft materials and offers guidelines for engineering materials with long-term stability in functional devices.
关键词： anion diffusivity,nanoscale imaging,molecular simulation,halide perovskite nanowire,soft lattice
更新于2025-09-23 15:21:01
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Recent Progress of Strong Exciton-Photon Coupling in Lead Halide Perovskites
摘要： The semiconductor exciton–polariton, arising from the strong coupling between excitons and confined cavity photon modes, is not only of fundamental importance in macroscopic quantum effects but also has wide application prospects in ultralow-threshold polariton lasers, slowing-light devices, and quantum light sources. Very recently, metallic halide perovskites have been considered as a great candidate for exciton–polariton devices owing to their low-cost fabrication, large exciton oscillator strength, and binding energy. Herein, the latest progress in exciton–polaritons and polariton lasers of perovskites are reviewed. Polaritons in planar and nanowires Fabry–Pérot microcavities are discussed with particular reference to material and photophysics. Finally, a perspective on the remaining challenges in perovskite polaritons research is given.
关键词： exciton–polariton,low threshold laser,lead halide perovskite,optical microcavity,strong light–matter interaction
更新于2025-09-23 15:21:01
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On the determination of absorption cross section of colloidal lead halide perovskite quantum dots
摘要： The absorption cross section of lead halide perovskite nanocrystals is important for understanding their photophysical properties, especially those depending on the density of photoexcited charge carriers. Despite its importance, there are large discrepancies among the reported absorption cross section values determined employing different methods. Here, we measured the absorption cross section of CsPbBr3 quantum dots (QDs) of varying sizes using elemental analysis and transient absorption (TA) saturation methods and compared with the previously reported values determined from elemental analysis and transient photoluminescence (PL) saturation methods. A careful comparison indicates that the reliable absorption cross section of lead halide perovskite QDs is obtained from both elemental analysis and TA saturation methods, while many previously reported values determined from the PL saturation method underestimate the absorption cross section.
关键词： quantum dots,absorption cross section,photoluminescence,transient absorption,lead halide perovskite
更新于2025-09-23 15:19:57
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The influence of electrode for electroluminescence devices based on all-inorganic halide perovskite CsPbBr<sub>3</sub>
摘要： Electroluminescence devices based all-inorganic halide perovskite material with the excellent luminescence performance have been studied extensively in recent years. However, the important role for the electrodes of electroluminescence devices is payed few attention by theoretical and experimental studies. Appropriate electrodes can reduce the Schottky barrier height to decrease the energy loss, and prevent the metal impurities from diffusing into the perovskite material to generate deep traps levels, which improves the luminous efficiency and lifetime of devices. In this paper, not only the interface effects between CsPbBr3 and common metal electrode (Ag, Au, Ni, Cu and Pt) are studied by first-principle calculations, but also the diffusion effects of metal electrode atom into the CsPbBr3 layer are also explored by nudged elastic band calculations. The calculated results show the metal Ag is more suitable for the cathode for CsPbBr3 electroluminescence devices, while the metal Pt is more applicable for the anode. Based on the overall consideration about the interface effects and diffusion effects of the CsPbBr3-metal electrode junctions, the essential principle provide a valuable reference how to select the suitable electrodes for other electroluminescence devices.
关键词： electroluminescence devices,diffusion effects,Schottky barrier height,CsPbBr3,all-inorganic halide perovskite,metal electrodes
更新于2025-09-23 15:19:57
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In situ observation of ?′ phase suppression by lattice strain in all-inorganic perovskite solar cells
摘要： The phase control and ordered crystal growth play a crucial role in the efficiency and stability of all-inorganic perovskite solar cells (PSCs). However, the innate dynamics of crystal growth driving the stable phase and high performance are unknown. Here, we for the first time unraveled that the degree of lattice strain is responsible for the suppression of the δ phase growth by in situ Grazing-Incidence Wide-Angle X-ray Scattering (GIWAXS) technique. We shadow the internal crystal structural changes in real time and successfully decoupled crystal growth dynamics under different substrate temperatures. The symmetrical crystal lattice and vertical substrate growth were finally achieved. This finding provides insights on the inorganic perovskite crystal growth and has significant benefit for high performing all-inorganic PSCs.
关键词： GIWAXS,CsPbI2Br,Inorganic halide perovskite,Lattice strain
更新于2025-09-23 15:19:57
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Thermodynamics of Multicomponent Perovskites: A Guide to Highly Efficient and Stable Solar Cell Materials
摘要： With their dramatic improvement of photoconversion efficiency, metal-halide perovskite (MHP) solar cells are receiving great attention. For successful deployment of these materials as next-generation solar cells, many research efforts are being undertaken to develop highly efficient and stable perovskite solar cells. Because compositional engineering in particular has provided a powerful route to optimize the material properties, MHPs with high efficiency and stability often include a number of different components. In this study, using ab-initio thermodynamics for ternary mixtures at the A-site (FA, MA, and Cs) and varying Br/I content at the X-site, we provide thermodynamic modeling on how mixtures of different cations and halides at A- and X-sites can modify the stability of MHPs. Our in-depth calculation reveals that Br mixing is inevitable to stabilize the corner-shared perovskite structure of highly efficient FAPbI3 with low bandgap. To maintain the minimal content of Br, which widens the bandgap, MA co-mixing is required, while Cs mixing contributes to prevent the decomposition of MHPs into precursors. We anticipate that the present study will provide thermodynamic insight into the distinctive roles of different components of MHPs and offer a design guideline for future compositional engineering of MHPs.
关键词： efficiency,thermodynamics,metal-halide perovskite,compositional engineering,stability,solar cells
更新于2025-09-23 15:19:57
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Strong Spin-Selective Optical Stark Effect in Lead Halide Perovskite Quantum Dots
摘要： The optical Stark effect (OSE) stems from a coherent, nonlinear interaction between a transition and a non-resonant light field, which usually causes a blue-shift of the transition energy. This shift can be understood using the picture of so-called photon-dressed states or Floquet states. The perturbation induced by a light filed which is periodical in time results in a series of quasi-static Floquet eigenstates periodically spaced in units of the photon energy. The repulsion (hybridization) between the Floquet and equilibrium states causes a blueshift of the transition between the equilibrium states, as schematically shown in Fig. 1a. The OSE effect is intrinsically helicity-selective, that is, a left circularly polarized light couples only to the |0> to |+1> but not the |0> to |-1> transition and vice versa (the number in the ket is the azimuthal quantum number of the total angular momentum). Experimentally, the OSE can be conveniently observed using circularly polarized transient absorption (TA) spectroscopy. With a co-circularly polarized pump-probe configuration, the probe pulse measures a blue-shifted transition in the duration of the pump pulse and a derivative-like difference spectrum (with respect to the unpumped spectrum) can be detected (Fig. 1b), whereas with a counter-circularly polarized configuration nothing can be detected if multi-photon absorption is negligible.
关键词： transient absorption spectroscopy,optical Stark effect,spin-selective,lead halide perovskite,quantum dots
更新于2025-09-23 15:19:57