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1.
近年来,基于ABX3结构的有机无机杂化钙钛矿材料因其具有优良的光电特性和廉价的制作成本得到了全世界的广泛关注,但体系中的有机组分容易受到光、热、湿等外界条件的影响而分解,导致器件的PCE发生严重的下降,极大地限制了PSCs(Perovskite solar cells,PSCs)的产业化进程.利用纯无机阳离子完全取代A...  相似文献   

2.
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Poly(3-hexylthiophene) (P3HT) has been used in CsPbI3 perovskite solar cells (PSCs) as the hole transport layer (HTL), due to its excellent hydrophobic property and cheap cost. However, the inevitable defects in perovskite lead to the limited photovoltaic performance of CsPbI3 PSCs. In this study, diethylammonium iodide (DEAI) was doped as an additive to passivate the defects in P3HT based CsPbI3 perovskite. Considering the diethylamine cations can effectively form hydrogen bonds with halide ion, the DEAI doping method could not only reduce the defect density but also facilitate the extraction and transport of carriers in the device. The optimal power conversion efficiency of the device prepared with DEAI doping method increases from 14.68% to 16.75%. In addition, the stability of the device is also significantly upgraded due to the improvement of CsPbI3 perovskite film. This work can provide reliable theoretical and experimental evidence for further PSCs research.  相似文献   

3.
    
In the literature, lead halide perovskites are very notable for their degradation in the presence of polar solvents, such as water. In contrast, in this research, it is observed that adding a minor amount of water into the precursor solution can improve the stability and photoluminescence quantum yield of CsPbBr3 nanocrystals through a ligand-assisted reprecipitation (LARP) method. In this way, the shape and phase transformation from CsPbBr3 nanoplates to CsPbBr3/Cs4PbBr6 nanorods and Cs4PbBr6 nanowires can be controlled with increasing water content in the precursor solution. Upon adding water up to an ideal amount, CsPbBr3 maintains its phase and nanoplate morphology. The key role of water amount for tuning the crystallinity, stability, morphology, optical properties, and phase transformation of cesium lead halide perovskite nanocrystals will be beneficial in the future commercialization of optoelectronics.  相似文献   

4.
    
Encapsulation methods have shown to be effective in imparting improved stability to metal-halide perovskite nanocrystals (NCs). Atomic layer deposition (ALD) of metal oxides is one of the promising approaches for such encapsulation, yet better control on the process parameters are required to achieve viable lifetimes for several optoelectronic and photocatalytic applications. Herein, we optimize the ALD process of amorphous aluminum oxide (AlOx) as an encapsulating layer for CsPbBr3 NC thin films by using oxygen (O2) as a molecular diffusion probe to assess the uniformity of the deposited AlOx layer. When O2 reaches the NC surface, it extracts the photogenerated electrons, thus quenching the PL of the CsPbBr3 NCs. As the quality of the ALD layer improves, less quenching is expected. We compare three different ALD deposition modes. We find that the low temperature/high temperature and the exposure modes improve the quality of the alumina as a gas barrier when compared with the low temperature mode. We attribute this result to a better diffusion of the ALD precursor throughout the NC film. We propose the low temperature/high temperature as the most suitable mode for future implementation of multilayered coatings.  相似文献   

5.
    
As a result of their attractive optoelectronic properties, metal halide APbI3 perovskites employing formamidinium (FA+) as the A cation are the focus of research. The superior chemical and thermal stability of FA+ cations makes α‐FAPbI3 more suitable for solar‐cell applications than methylammonium lead iodide (MAPbI3). However, its spontaneous conversion into the yellow non‐perovskite phase (δ‐FAPbI3) under ambient conditions poses a serious challenge for practical applications. Herein, we report on the stabilization of the desired α‐FAPbI3 perovskite phase by protecting it with a two‐dimensional (2D) IBA2FAPb2I7 (IBA=iso‐butylammonium overlayer, formed via stepwise annealing. The α‐FAPbI3/IBA2FAPb2I7 based perovskite solar cell (PSC) reached a high power conversion efficiency (PCE) of close to 23 %. In addition, it showed excellent operational stability, retaining around 85 % of its initial efficiency under severe combined heat and light stress, that is, simultaneous exposure with maximum power tracking to full simulated sunlight at 80 °C over 500 h.  相似文献   

6.
    
As a result of their attractive optoelectronic properties, metal halide APbI3 perovskites employing formamidinium (FA+) as the A cation are the focus of research. The superior chemical and thermal stability of FA+ cations makes α-FAPbI3 more suitable for solar-cell applications than methylammonium lead iodide (MAPbI3). However, its spontaneous conversion into the yellow non-perovskite phase (δ-FAPbI3) under ambient conditions poses a serious challenge for practical applications. Herein, we report on the stabilization of the desired α-FAPbI3 perovskite phase by protecting it with a two-dimensional (2D) IBA2FAPb2I7 (IBA=iso-butylammonium overlayer, formed via stepwise annealing. The α-FAPbI3/IBA2FAPb2I7 based perovskite solar cell (PSC) reached a high power conversion efficiency (PCE) of close to 23 %. In addition, it showed excellent operational stability, retaining around 85 % of its initial efficiency under severe combined heat and light stress, that is, simultaneous exposure with maximum power tracking to full simulated sunlight at 80 °C over 500 h.  相似文献   

7.
    
The primary challenge facing perovskite nanocrystals (PNCs) is their stability, which hinders their potential impact on the industry. This study focuses on new organic–inorganic metal halide perovskites (OIMHPs) with stable deep blue emission using the beneficial encapsulation aspects of metal–organic frameworks (MOFs). Novel (Et)3NHPbBr3 PNCs with deep blue emission were synthesized via the facile ligand-assisted reprecipitation (LARP) technique. To address both stability issues and low emission efficiency, the (Et)3NHPbBr3 PNCs were effectively embedded within zinc-based mesoporous MOF-5 structures. The pore structure of MOF-5 microporous (with pores size of 1.68 nm) was initially modified to mesoporous (M3 with pores size of 36.88 nm) to facilitate the localization of PNCs inside MOF pores. Then, a full series of experimental parameters were optimized, which resulted in about 10-fold enhancement in photoluminescence quantum efficiency (PLQE) from 6% for the bare (Et)3NHPbBr3 PNCs to 58% for the (Et)3NHPbBr3@MOF-5 composite with emission signal located at around 394 nm. The emission stability of the fabricated composite was also investigated against external conditions and showed that the optimized composite has an excellent emission after 180 days of storage in environmental conditions, along with a preserved PL emission at elevated temperatures up to 100 °C. This study presents a straightforward and cost-effective method for producing novel deep-blue emissive (Et)3NHPbBr3 PNCs encapsulated within MOFs, showcasing substantial improvements in PLQE and stability that are crucial for the development of efficient optoelectronic devices.  相似文献   

8.
    
Perovskite nanocrystals (PNCs) are emerging luminescent materials due to their fascinating physic‐optical properties. However, their sensitive surface chemistry with organic polar solvents, oxygen, and moisture greatly hinders their developments towards practical applications. Herein we promote silica‐passivated PNCs (SP‐PNCs) by in situ hydrolyzing the surface ligands of (3‐aminopropyl) triethoxysilane. The resultant SP‐PNCs possesses a high quantum yield (QY) of 80 % and are precipitable by polar solvents, such as ethanol and acetone, without destroying their surface chemistry or losing QY, which offers an eco‐friendly and efficient method for separation, purification, and phase transfer of PNCs. Moreover, we further promoted a swelling–deswelling encapsulation process to incorporate the as‐made SP‐PNCs into non‐crosslinked polystyrene microspheres (PMs), which can largely increase the stability of the SP‐PNCs against moisture for long‐term storage.  相似文献   

9.
    
Rare earth (RE) ions, with abundant 4f energy level and unique electronic arrangement, are considered as substitutes for Pb2+ in perovskite nanocrystals (PNCs), allowing for partial or complete replacement of lead and minimizing environmental impact. This review provides a comprehensive overview of the characteristics of RE-doped PNCs, including up-conversion luminescence, down-conversion luminescence, and quantum confinement effects, etc. Additionally, RE doping has been found to effectively suppress defect formation, reduce nonradiative recombination, enhance photoluminescence quantum yield (PLQY), and even allow for controlling over the morphology of the nanocrystals. The review also highlights the recent advancements in lead-free RE-based perovskites, especially in the case of Eu-based perovskites (CsEuBr3 and CsEuCl3). Furthermore, it briefly introduces the applications of PNCs in various fields, such as perovskite solar cells (PSCs), luminescent solar concentrators (LSCs), photodetectors (PDs), and light-emitting diodes (LEDs). A systematic discussion on the luminescence mechanisms of RE-doped PNCs and lead-free RE-based perovskites is provided, along with an outlook on future research directions. The ultimate goal of this review is to provide guidance for the development of RE-based perovskite optoelectronic devices.  相似文献   

10.
钙钛矿量子点发光二极管(QLEDs)因其色纯度高、颜色控制精准、色域广以及溶液可加工等特点,在显示和照明等领域有着极大的应用前景.针对红光钙钛矿CsPbI3量子点纯化过程中相变和表面配体损失造成的荧光退化问题,本工作发展了一种甲苯和乙酸乙酯协同的混合溶剂纯化策略,能够避免纯化过程中的相变问题,获得了纯立方相的CsPbI...  相似文献   

11.
The stability of a solution of charged polystyrene particles in the presence of nonadsorbing polyelectrolyte macromolecules is measured using optical light scattering. The particles were negatively charged polystyrene latex spheres (0.5–1 μm diameter) while the macromolecules were simulated using negatively charged colloidal silica spheres (5–7 nm diameter). Because of the electrostatic repulsion between the particles, the solution is found to be stable against primary flocculation (irreversible flocculation into a primary energy minima). However, because of long-range attractive depletion forces, reversible secondary flocculation of the particles occurs into a local potential energy minimum. As observed with uncharged macromolecules, the polyelectrolyte first induces flocculation at a critical flocculation concentration (v*), but later restabilizes the system at a critical restabilization concentration (v**). These critical concentrations are found to decrease with decreasing macromolecule size and increasing particle size. The restabilized solutions are found to remain suspended for periods greater than 20 days. Comparison of the measured flocculation and restabilization results to predictions made using a recently developed force-balance model show qualitative agreement.  相似文献   

12.
    
Double perovskites (DPs) with a generic formula A2M′(I)MIIIX6 (A and M are metal ions, and X=Cl, Br, I) are now being explored as potential alternatives to Pb‐halide perovskites for solar cells and other optoelectronic applications. However, these DPs typically suffer from wide (≈3 eV) and/or indirect band gaps. In 2017, a new structural variety, namely layered halide DP Cs4CuSb2Cl12 (CCSC) with bivalent CuII ion in the place of M′(I) was reported, which exhibit a band gap of approximately 1 eV. Here, we report a mechanochemical synthesis of CCSC, its thermal and chemical stability, and magnetic response of CuII d9 electrons controlling the optoelectronic properties. A simple grinding of precursor salts at ambient conditions provides a stable and scalable product. CCSC is stable in water/acetone solvent mixtures (≈30 % water) and many other polar solvents unlike Pb‐halide perovskites. It decomposes to Cs3Sb2Cl9, Cs2CuCl4, and SbCl3 at 210 °C, but the reaction can be reversed back to produce CCSC at lower temperatures and high humidity. A long‐range magnetic ordering is observed in CCSC even at room temperature. The role of such magnetic ordering in controlling the dispersion of the conduction band, and therefore, controlling the electronic and optoelectronic properties of CCSC has been discussed.  相似文献   

13.
全无机钙钛矿太阳电池因其热稳定性好、载流子迁移率高,可用于制备叠层电池等优点备受关注.随着人们对全无机钙钛矿太阳电池的深入研究和制备工艺的持续优化,全无机钙钛矿太阳电池的光电转换效率已经突破19％.然而,全无机钙钛矿材料相稳定性较差,这使得实现全无机钙钛矿太阳电池在空气环境下制备和长期使用面临巨大挑战.众多科研工作者通...  相似文献   

14.
以N-异丙基丙烯酰胺(NIPAM)、甲基丙烯酸(MAA)为单体,N,N-亚甲基双丙烯酰胺(MBA)为交联剂,制备了温敏性聚(N-异丙基丙烯酰胺)(PNIPAM)和具有温度、pH敏感性的聚(N-异丙基丙烯酰胺-co-甲基丙烯酸)(PNIPAM-MAA)微凝胶。通过测定不同温度和pH条件下微凝胶浊度变化,表征微凝胶的温度及pH敏感性,描述了NaCl浓度和pH对微凝胶体积相转变温度的影响。同时,测定了微凝胶的临界聚沉浓度及临界絮凝温度,表征了微凝胶的稳定性,讨论了影响微凝胶的稳定性因素。  相似文献   

15.
    
Traditional CdSe‐based colloidal quantum dots (cQDs) have interesting photoluminescence (PL) properties. Herein we highlight the advantages in both ensemble and single‐nanocrystal PL of colloidal CsPbBr3 nanocrystals (NCs) over the traditional cQDs. An ensemble of colloidal CsPbBr3 NCs (11 nm) exhibits ca. 90 % PL quantum yield with narrow (FWHM=86 meV) spectral width. Interestingly, the spectral width of a single‐NC and an ensemble are almost identical, ruling out the problem of size‐distribution in PL broadening. Eliminating this problem leads to a negligible influence of self‐absorption and Förster resonance energy transfer, along with batch‐to‐batch reproducibility of NCs exhibiting PL peaks within ±1 nm. Also, PL peak positions do not alter with measurement temperature in the range of 25 to 100 °C. Importantly, CsPbBr3 NCs exhibit suppressed PL blinking with ca. 90 % of the individual NCs remain mostly emissive (on‐time >85 %), without much influence of excitation power.  相似文献   

16.
    
The growing demand for perovskite nanocrystals (NCs) for various applications has stimulated the development of facile synthetic methods. Perovskite NCs have often been synthesized by either ligand‐assisted reprecipitation (LARP) at room temperature or by hot‐injection at high temperatures and inert atmosphere. However, the use of polar solvents in LARP affects their stability. Herein, we report on the spontaneous crystallization of perovskite NCs in nonpolar organic media at ambient conditions by simple mixing of precursor–ligand complexes without application of any external stimuli. The shape of the NCs can be controlled from nanocubes to nanoplatelets by varying the ratio of monovalent (e.g. formamidinium+ (FA+) and Cs+) to divalent (Pb2+) cation–ligand complexes. The precursor–ligand complexes are stable for months, and thus perovskite NCs can be readily prepared prior to use. Moreover, we show that this versatile synthetic process is scalable and generally applicable for perovskite NCs of different compositions.  相似文献   

17.
    
We developed a microwave‐assisted slowed‐down synthesis of CsPbBr3 perovskite nanocrystals, which retards the reaction and allows us to gather useful insights into the formation mechanism of these nanoparticles, by examining the intermediate stages of their growth. The trends in the decay of the emission intensity of CsPbBr3 nanocrystals under light exposure are well correlated with their stability against decomposition in TEM under electron beam. The results show the change of the crystal structure of CsPbBr3 nanocrystals from a deficient and easier to be destroyed lattice to a well crystallized one. Conversely the shift in the ease of degradation sheds light on the formation mechanism, indicating first the formation of a bromoplumbate ionic scaffold, with Cs‐ion infilling lagging a little behind. Increasing the cation to halide ratio towards the stoichiometric level may account for the improved radiative recombination rates observed in the longer reaction time materials.  相似文献   

18.
Ba0.9R0.1Co0.7Fe0.225Ta0.075O3-δ(BRCFT, R = Ca, La or Sr) membranes were synthesized by a solid-state reaction. Metal cation Ca2+,La3+or Sr2+doping on A-site partially substituted Ba2+in BaCo0.7Fe0.225Ta0.075O3-δoxides, and its subsequent effects on phase structure stability, oxygen permeability and oxygen desorption were systematically investigated by XRD, TG-DSC, H2-TPR, O2-TPD techniques and oxygen permeation experiments. The partial substitution with Ca2+, La3+or Sr2+, whose ionic radii are smaller than that of Ba2+, succeeded in stabilizing the cubic perovskite structure without formation of impurity phases, as revealed by XRD analysis. Oxygen-involving experiments showed that BRCFT with A-site fully occupied by Ba2+exhibited good oxygen permeation flux under He flow, reaching about 2.3mL min-1 cm-2at 900 ℃ with 1 mm thickness. Of all the membranes, BLCFT membrane showed better chemical stability in CO2, owing to the reduction in alkalinity of the mixed conductor oxide by La doping. In addition, we also found the stability of the perovskite structure under reducing atmospheres was strengthened by increasing the size of A-site cation(Ba2+La3+Sr2+Ca2+).  相似文献   

19.
    
Lead‐halide perovskites are well known to decompose rapidly when exposed to polar solvents, such as water. Contrary to this common‐place observation, we have found that through introducing a suitable minor amount of water into the reaction mixture, we can synthesize stable CsPbBr3 nanocrystals. The size and the crystallinity, and as a result the band gap tunability of the strongly emitting CsPbBr3 nanocrystals correlate with the water content. Suitable amounts of water change the crystallization environment, inducing the formation of differently shaped perovskites, namely spherical NCs, rectangular nanoplatelets, or nanowires. Bright CsPbBr3 nanocrystals with the photoluminescence quantum yield reaching 90 % were employed for fabrication of inverted hybrid inorganic/organic light‐emitting devices, with the peak luminance of 4428 cd m?2 and external quantum yield of 1.7 %.  相似文献   

20.
张恒  王婷婷  林维明 《应用化学》2009,26(11):1328-1331
利用柠檬酸络合法制备了SrFe(Cu,Ti)O3-δ混合导体透氧材料。 采用XRD、O2-TPD、H2-TPR、SEM等测试技术考察了材料的稳定性。 结果表明,SrFe0.7Cu0.3O3-δ在低氧压下会发生相分解,产生SrCuO2杂相,而掺杂Ti后的SrFe0.6Cu0.3Ti0.1O3-δ在低氧压下保持单一的钙钛矿结构。 H2-TPR和O2-TPD的测试表明,Ti4+的掺杂提高了材料的氧脱附起始温度和其它金属离子的还原温度。 SrFe0.6Cu0.3Ti0.1O3-δ膜在透氧过程中,会有Cu2+和Sr2+从钙钛矿结构中析出,在原晶粒边界形成新的小晶粒,但这种轻微的组分偏析没有影响到材料的透氧量,此透氧膜在66 h的操作过程中显示了良好的稳定性。  相似文献   

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