Tin-Lead Perovskite Solar Cells with Preferred Crystal Orientation by Buried Interface Approach.

Mixed tin-lead perovskite solar cells (PSCs) have garnered much attention for their ideal bandgap and high environmental research value. However, poly (3,4-ethylenedioxythiophene): poly (styrene sulfonate) (PEDOT: PSS), widely used as a hole transport layer (HTL) for Sn-Pb PSCs, results in unsatisfactory power conversion efficiency (PCE) and long-term stability of PSCs due to its acidity and moisture absorption. A synergistic strategy by incorporating histidine (HIS) into the PEDOT: PSS HTL is applied to simultaneously regulate the nucleation and crystallization of perovskite (PVK). HIS neutralizes the acidity of PEDOT: PSS and enhances conductivity. Especially, the coordination of the C═N and -COO- functional groups in the HIS molecule with Sn2+ and Pb2+ induces vertical growth of PVK film, resulting in the release of residual surface stress. Additionally, this strategy also optimizes the energy level alignment between the perovskite layer and the HTL, which improves charge extraction and transport. With these cooperative effects, the PCE of Sn-Pb PSCs reaches 21.46% (1 sun, AM1.5), maintaining excellent stability under a nitrogen atmosphere. Hence, the buried interface approach exhibits the potential for achieving high-performance and stable Sn-Pb PSCs.

Ternary-Metal Sn-Pb-Zn Perovskite to Reconstruct Top Surface for Efficient and Stable Less-Pb Perovskite Solar Cells.

Though Sn-Pb alloyed perovskite solar cells (PSCs) achieved great progress, there is a dilemma to further increase Sn for less-Pb requirement. High Sn ratio (>70%) perovskite exhibits nonstoichiometric Sn:Pb:I at film surface to aggravate Sn2+ oxidation and interface energy mismatch. Here, ternary metal alloyed (FASnI3 )0.7 (MAPb1- x Znx I3 )0.3 (x = 0-3%) is constructed for Pb% < 30% perovskite. Zn with smaller ionic size and stronger ionic interaction than Sn/Pb assists forming high-quality perovskite film with ZnI6 4- enriched at surface to balance Sn:Pb:I ratio. Differing from uniform bulk doping, surface-rich Zn with lower lying orbits pushes down the energy band of perovskite and adjusts the interface energy for efficient charge transfer. The alloyed PSC realizes efficiency of 19.4% at AM1.5 (one of the highest values reported for Pb% < 30% PSCs). Moreover, stronger bonding of Zn─I and Sn─I contributes to better durability of ternary perovskite than binary perovskite. This work highlights a novel alloy method for efficient and stable less-Pb PSCs.

Urea additive improves the performance of low bandgap tin-lead perovskite solar cells.

Recently, narrow bandgap tin-lead mixed perovskite solar cells (PSCs) have become a research hotspot because they can be applied in tandem cells to break the Shockley-Queisser radiative limit of the single junction PSCs. However, the introduction of tin, on the one hand, makes the crystal quality of perovskite thin film worse, leading to the increase of film defects; on the other hand, the easy oxidation of divalent tin also leads to the increase of defect states, which seriously affects the photoelectric conversion efficiency of tin-lead cell devices. Good crystallization and low defect density of perovskite layer are very important to ensure good light absorption and photogenerated carrier generation and transport. Here, we adjust the crystallization of tin-lead perovskite films by a Lewis base-urea (CO(NH2)2), which significantly increases the grain size and improves the film morphology. At the same time, because of the Lewis base property of urea, the uncoordinated Pb2+and Sn2+defects of Lewis acids in the tin-lead films are effectively passivated, and the occurrence of non-radiative recombination in the films is reduced. Under the dual effects of improving crystallization and passivating defects, the photoelectric performance of tin-lead perovskite solar cell devices is significantly improved to 18.1% compared with the original device of 15.4%.

[Analysis and Improvement Suggestions on Change of Medical Devices Licensing Items].

Based on the statistics of 350 technical evaluations of changes in licensing items of class Ⅱ passive and active medical devices completed in Henan province from July 2017 to November 2018, this paper summarized and analysed the common problems and requirements listed in the correction notifications of the technical evaluation, and put forward relevant countermeasures or suggestions, with a view to further speeding up the evaluation and approval of medical devices.

Polymer Lewis Base for Improving the Charge Transfer in Tin-Lead Mixed Perovskite Solar Cells.

The poor film stability of Sn-Pb mixed perovskite film and the mismatched interface energy levels pose significant challenges in enhancing the efficiency of tin-lead (Sn-Pb) mixed perovskite solar cells. In this study, polyvinylpyrrolidone (PVP) is introduced into the PVK perovskite precursor solution, effectively enhancing the overall stability of the film. This improvement is achieved through the formation of robust coordination bonds between the carbonyl (C=O) in the pyrrole ring and the undercoordinated SnII and PbII, thereby facilitating the passivation of defects. Furthermore, the introduction of PVP inhibits the oxidation of tin (Sn), thereby enhancing the n-type characteristics of the perovskite film. This adjustment in the energy level of the PVK perovskite film proves instrumental in reducing interface energy loss, subsequently improving interface charge transfer and mitigating device recombination. Consequently, perovskite solar cells incorporating PVP achieve an outstanding champion power conversion efficiency (PCE) of 21.31%.

Efficient Air-Processed MA-Free Perovskite Solar Cells by SH-Based Silane Interface Modification.

Air-processed perovskite solar cells (PSCs) with high photoelectric conversion efficiency (PCE) can not only further reduce the production cost but also promote its industrialization. During the preparation of the PSCs in ambient air, the contact of the buried interface not only affects the crystallization of the perovskite film but also affects the interface carrier transport, which is directly related to the performance of the device. Here, we optimize the buried interface by introducing 3-mercaptopropyltrimethoxysilane (MPTMS, (CH3O)3Si(CH2)3SH) on the nickel oxide (NiOx) surface. The crystallization of the perovskite film is improved by enhancing surface hydrophobicity; besides, the SH-based functional group of MPTMS passivates the uncoordinated lead at the interface, which effectively reduces the defects at the bottom interface of perovskite and inhibits the nonradiative recombination at the interface. Moreover, the energy level between the NiOx layer and the perovskite layer is better matched. Based on multiple functions of MPTMS modification, the open circuit voltage of the device is obviously improved, and efficient air-processed methylamine-free (MA-free) PSCs are realized with PCE reaching 21.0%. The device still maintains the initial PCE of 85% after 1000 h aging in the glovebox. This work highlights interface modification in air-processed MA-free PSCs to promote the industrialization of PSCs.

Reductive Sn2+ Compensator for Efficient and Stable Sn-Pb Mixed Perovskite Solar Cells.

Tin-lead (Sn-Pb) mixed perovskite with a narrow bandgap is an ideal candidate for single-junction solar cells approaching the Shockley-Queisser limit. However, due to the easy oxidation of Sn2+, the efficiency and stability of Sn-Pb mixed perovskite solar cells (PSCs) still lag far behind that of Pb-based solar cells. Herein, highly efficient and stable FA0.5MA0.5Pb0.5Sn0.5I0.47Br0.03 compositional PSCs are achieved by introducing an appropriate amount of multifunctional Tin (II) oxalate (SnC2O4). SnC2O4 with compensative Sn2+ and reductive oxalate group C2O4 2- effectively passivates the cation and anion defects simultaneously, thereby leading to more n-type perovskite films. Benefitting from the energy level alignment and the suppression of bulk nonradiative recombination, the Sn-Pb mixed perovskite solar cell treated with SnC2O4 achieves a power conversion efficiency of 21.43%. More importantly, chemically reductive C2O4 2- effectively suppresses the notorious oxidation of Sn2+, leading to significant enhancement in stability. Particularly, it dramatically improves light stability.

Photo-assisted degradation of Rhodamine B by a heterogeneous Fenton-like process: performance and kinetics.

This study presents the degradation of rhodamine B (RhB) by photo Fenton-like (PF-like) process under visible light irradiation (λ > 380 nm) using cobalt phosphate microparticles (CoP-MPs). The effects of the initial concentration of RhB, pH value, CoP-MPs dosage, hydrogen peroxide (H2O2) concentration, and salts found in textile wastewater (such as NaNO3, Na2SO4, and NaCl) were investigated in detail. It was found that CoP-MPs can maintain high catalytic activity with wide pH values varying from 4 to 8. This indicated that the use of CoP-MPs overcame the low efficiency of Fenton-like reaction at neutral and even weakly alkaline pH. The PF-like degradation of RhB followed pseudo-first order kinetics in various conditions. Moreover, a comparison of experimental results showed that the PF-like system has good degradation ability for RhB and methyl blue (MB) solution, but is poor for methyl orange (MO) solution. The repeat experiments indicated that the chemical structures of CoP-MPs were stable. Furthermore, the Co2+ ions leaching to the solutions were measured by an inductively coupled plasma mass spectrometer (ICP-MS). Analysis of UV-vis spectra suggested that RhB was degraded by the formation of a series of N-de-ethylated intermediates followed by cleavage of the whole conjugate chromophore structure.HighlightsRhB can be effectively degraded in the PF-like process under visible light irradiation by CoP-MPs.The PF-like process can maintain high catalytic activity at neutral and even weakly alkaline pH.Degradation kinetics exhibited pseudo-first-order kinetics and were influenced by the key parameters.The variation in the UV-vis spectra of RhB was analyzed in detail to infer a possible degradation pathway.

Thermoreversible and tunable supramolecular hydrogels based on chitosan and metal cations.

A new thermoreversible and tunable hydrogel CS-M with high water content prepared by metal cation (M = Cu2+, Zn2+, Cd2+ and Ni2+) and chitosan (CS) was reported. The influence of metal cations on the thermosensitive gelation of CS-M systems were studied. All prepared CS-M systems were in the transparent and stable sol state and could become the gel state at gelation temperature (Tg). These systems after gelation could recover to its original sol state at low temperature. CS-Cu hydrogel was mainly investigated and characterized due to its large Tg scale (32-80 °C), appropriate pH range (4.0-4.6) and low Cu2+ concentration. The result showed that the Tg range was influenced and could be tuned by adjusting Cu2+ concentration and system pH within an appropriate range. The influence of anions (Cl-, NO3- and Ac-) in cupric salts in the CS-Cu system was also investigated. Scale application as heat insulation window was investigated outdoors. The different supramolecular interactions of the -NH2 group in chitosan at different temperatures were proposed to dominate the thermoreversible process of CS-Cu hydrogel.

Alkali Metal Cations Modulate the Energy Level of SnO2 via Micro-agglomerating and Anchoring for Perovskite Solar Cells.

N-type tin oxide (SnO2) films are commonly used as an electron transport layer (ETL) in perovskite solar cells (PSCs). However, SnO2 films are of poor quality due to facile agglomeration under a low-temperature preparation method. In addition, energy level mismatch between the SnO2 and perovskite (PVK) layer as well as interfacial charge recombination would cause open-circuit voltage loss. In this work, alkali metal oxalates (M-Oxalate, M = Li, Na, and K) are doped into the SnO2 precursor to solve these problems. First, it is found that the hydrolyzed alkali metal cations tend to change colloid size distribution of SnO2, in which Na-Oxalate with suitable basicity leads to most uniform colloid size distribution and high-quality SnO2-Na films. Second, the electron conductivity is enhanced by slightly agglomerated SnO2-Na, which facilitates the transmission of electrons. Third, alkali metal cations increase the conduction band level of SnO2 in the sequence of K+, Na+, and Li+ to promote band alignment between ETLs and perovskite. Based on the optimized film quality and energy states of SnO2-Na, the best PSC efficiency of 20.78% is achieved with a significantly enhanced open-circuit voltage of 1.10 V. This work highlights the function of alkali metal salts on the colloid particle distribution and energy level modulation of SnO2.