Deploying a Dipole Electric Field at the CsPbI3 Perovskite/Carbon Interface for Enhancing Hole Extraction and Photovoltaic Performance.

Carbon-based CsPbI3 perovskite solar cells without hole transporter (C-PSCs) have achieved intense attention due to its simple device structure and high chemical stability. However, the severe interface energy loss at the CsPbI3/carbon interface, attributed to the lower hole selectivity for inefficient charge separation, greatly limits device performance. Hence, dipole electric field (DEF) is deployed at the above interface to address the above issue by using a pole molecule, 4-trifluoromethyl-Phenylammonium iodide (CF3-PAI), in which the ─NH3 group anchors on the perovskite surface and the ─CF3 group extends away from it and connects with carbon electrode. The DEF is proven to align with the built-in electric field, that is pointing toward carbon electrode, which well enhances hole selectivity and charge separation at the interface. Besides, CF3-PAI molecules also serve as defect passivator for reducing trap state density, which further suppresses defect-induced non-radiative recombination. Consequently, the CsPbI3 C-PSCs achieve an excellent efficiency of 18.33% with a high VOC of 1.144 V for inorganic C-PSCs without hole transporter.

Nanofibrous Porous Organic Polymers and Their Derivatives: From Synthesis to Applications.

Engineering porous organic polymers (POPs) into 1D morphology holds significant promise for diverse applications due to their exceptional processability and increased surface contact for enhanced interactions with guest molecules. This article reviews the latest developments in nanofibrous POPs and their derivatives, encompassing porous organic polymer nanofibers, their composites, and POPs-derived carbon nanofibers. The review delves into the design and fabrication strategies, elucidates the formation mechanisms, explores their functional attributes, and highlights promising applications. The first section systematically outlines two primary fabrication approaches of nanofibrous POPs, i.e., direct bulk synthesis and electrospinning technology. Both routes are discussed and compared in terms of template utilization and post-treatments. Next, performance of nanofibrous POPs and their derivatives are reviewed for applications including water treatment, water/oil separation, gas adsorption, energy storage, heterogeneous catalysis, microwave absorption, and biomedical systems. Finally, highlighting existent challenges and offering future prospects of nanofibrous POPs and their derivatives are concluded.

Spatially selective defect management of CsPbI3 films for high-performance carbon-based inorganic perovskite solar cells.

Defects formed at the surface, buried interface and grain boundaries (GB) of CsPbI3 perovskite films considerably limit photovoltaic performance. Such defects could be passivated effectively by the most prevalent post modification strategy without compromising the photoelectric properties of perovskite films, but it is still a great challenge to make this strategy comprehensive to different defects spatially distributed throughout the films. Herein, a spatially selective defect management (SSDM) strategy is developed to roundly passivate various defects at different locations within the perovskite film by a facile one-step treatment procedure using a piperazine-1,4-diium tetrafluoroborate (PZD(BF4)2) solution. The small-size PZD2+ cations could penetrate into the film interior and even make it all the way to the buried interface of CsPbI3 perovskite films, while the BF4- anions, with largely different properties from I- anions, mainly anchor on the film surface. Consequently, virtually all the defects at the surface, buried interface and grain boundaries of CsPbI3 perovskite films are effectively healed, leading to significantly improved film quality, enhanced phase stability, optimized energy level alignment and promoted carrier transport. With these films, the fabricated CsPbI3 PSCs based on carbon electrode (C-PSCs) achieve an efficiency of 18.27%, which is among the highest-reported values for inorganic C-PSCs, and stability of 500 h at 85 °C with 65% efficiency maintenance.

Synchronous Modulation of Energy Level Gradient and Defects for High-Efficiency HTL-Free Carbon-Based All-Inorganic Perovskite Solar Cells.

In order to improve the thermal stability of perovskite solar cells (PSCs) and reduce production costs, hole transport layer (HTL)-free carbon-based CsPbI3 PSCs (C-PSCs) have attracted the attention of researchers. However, the power conversion efficiency (PCE) of HTL-free CsPbI3 C-PSCs is still lower than that of PSCs with HTL/ metal electrodes. This is because the direct contact between the carbon electrode and the perovskite layer has a higher requirement on the crystal quality of perovskite layer and matched energy level at perovskite/carbon interface. Herein, the acyl chloride group and its derivative trichloroacetyl chloride are used to passivate CsPbI3 C-PSCs for the first time. The results show that the carbonyl group of trichloroacetyl chloride can effectively passivate the uncoordinated Pb2+ ions in perovskite. At the same time, leaving group Cl- ions can increase the grain size of perovskite and improve the crystallization quality of perovskite layer. In addition, the trichloroacetyl chloride tends to generate cesium chloride acetate, which acts as an electron blocking layer, reduces charge recombination, promotes gradient energy level arrangement, and effectively improves the separation and extraction ability of carriers. The PCE of CsPbI3 HTL-free C-PSCs is successfully increased from 13.40% to 14.82%.

Preparation of High-Efficiency (>14%) HTL-Free Carbon-Based All-Inorganic Perovskite Solar Cells by Passivation with PABr Derivatives.

Due to the advantages of low cost and good thermal stability, all-inorganic CsPbI2Br carbon-based perovskite solar cells (C-PSCs) without a hole transport layer have been rapidly developed in recent years. While the carbon electrode is in direct contact with the CsPbI2Br film, higher requirements are placed on the defects and energy level arrangement of the CsPbI2Br layer, which leads to the relatively low photoelectric conversion efficiency (PCE) of C-PSCs. Herein, propylamine hydrobromide (PABr) and its derivative 3-bromopropylamine hydrobromide (3Br-PABr) were used to passivate the surface defects of CsPbI2Br C-PSCs for the first time. The results show that passivation molecules are modulated by the substituent effect, leading to a stronger interaction between amino groups and uncoordinated Pb2+ ions, which facilitates a better passivation effect of 3Br-PABr. In addition, 3Br-PABr promotes the gradient arrangement of energy levels while passivating surface defects, which accelerates the rapid extraction of holes. After the passivation by PABr and 3Br-PABr, the PCE of HTL-free CsPbI2Br C-PSCs increased from 12.15% for the control device to 13.15 and 14.04%, respectively, which are among the highest reported values of CsPbI2Br C-PSCs.

Absorption of Carbon-13 Labelled Fullerene (C60) on Rice Seedlings and Effect of Phytohormones on Growth.

This study explores the effects of nanomaterials in rice seedlings using carbon 13 (13C)-labelled fullerene (C60). The experiment consisted of three groups, one CK and two nano particle groups with C60: 100 mg L-1 and 20 mg L-1. Mass spectrometry indicated higher 13C abundances in the nano particle groups compared with the CK. The 13C abundances of the 20 mg L-1 group, 100 mg L-1 group and CK were 1.0718%, 1.0715% and 1.0704%, respectively. We analyzed phytohormone concentrations in the rice at harvest time. Decreases in the concentrations of dihydrozeatin riboside (23% and 18% for the 20 mg L-1 and 100 mg L-1 group, respectively), zeatin riboside (23% and 18%, respectively), abscisic acid (11.1% and 12.7%, respectively), brassinolide (12.9% and 13.1%, respectively) and gibberellic acid 4 (12.9% and 13.1%, respectively) were observed compared with the CK. The gibberellic acid 3 concentrations in the 20 mg L-1 and 100 mg L-1 group increased by 12% and 7% compared with the CK, respectively. The methyl jasmonate concentration in the 100 mg L-1 group increased by 19.4% compared with the CK. The concentration of indole-3-acetic acid in the 100 mg L-1 group decreased by 13.5% compared with the CK. There was no change on isopentenyl adenosine concentration. This study indicates that C60 can be absorbed by rice and its effect on the growth of rice via phytohormones, including ABA, IAA, IPA, BR, GA3, GA4, DHZR, ZR and JA-ME. The results showed that, under the treatments of C60 NMs, the contents of some phytohormone in rice were decreased in comparison with CK.

Effects of spraying nano-materials on the absorption of metal(loid)s in cucumber.

This report investigates the spraying of nano-silica and fullerene on cucumber leaves to expose their ability to reduce the toxicity and uptake of metal(loid)s. Cucumber seedlings were randomly divided into six treatment groups: 10 mg/L nano-SiO2, 20 mg/L nano-SiO2, 10 mg/L Fullerene, 20 mg/L Fullerene, 5 mg/L Fullerene + 5 mg/L nano-SiO2, and 10 mg/L Fullerene + 10 mg/L nano-SiO2. Nano-silica-treated plants exhibited evidence of the potential mitigation of metal(loid)s poisoning. Specifically, results showed that 20 mg/L of nano-silica promoted Cd uptake by plants; comparatively, 10 mg/L of nano-silica did not significantly increase the silicon content in plants. Both low-concentration combined treatment and low-concentration fullerene groups inhibited metal(loid)s uptake by plants. Scanning electron microscopy (SEM) was then used to observe the surface morphology of cucumber leaves. Significant differences were observed on disease resistance in plants across the different nano-material conditions. Collectively, these findings suggest that both nano-silica materials and fullerene have the potential to control metal(loid)s toxicity in plants.

Effects of cerium oxide on rice seedlings as affected by co-exposure of cadmium and salt.

Effects of CeO2 NPs (200 mg.L-1) on rice (Oryza sativa L.) alone or co-exposure with cadmium (Cd) and salt (sodium chloride, NaCl) were investigated in hydroponic systems for two weeks. Physiological results show that rice biomass was significantly inhibited when NaCl or CdCl2 added alone or in co-exposure treatment. CeO2 NPs significantly relieve the chlorophyll damage under CdCl2 environmental stress. The presence of CeO2 NPs alleviated both stressors induced damages to rice as indicated by the reduced proline level. Additionally, CeO2 NPs triggered the antioxidant defense systems to counteract the oxidative stress caused by NaCl and CdCl2. The level of 8-OHdG, one of the most important indicators for genotoxicity, in rice suggest that the presence of CeO2 NPs reduced the DNA damage in NaCl treated rice. Elemental analysis indicated that co-exposure to NaCl and CdCl2 slightly decreased the Cd content as compared to the one in the CdCl2 alone treatment, and this co-exposure also significantly reduced the Na content when comparing with the NaCl alone treatment. Taken together, our findings suggest that CeO2 NPs could alleviate the CdCl2 and NaCl stresses, but could not completely change the phenotype of both contaminants treated rice.

Highly Efficient Red and White Organic Light-Emitting Diodes with External Quantum Efficiency beyond 20% by Employing Pyridylimidazole-Based Metallophosphors.

Two highly efficient red neutral iridium(III) complexes, Ir1 and Ir2, were rationally designed and synthesized by selecting two pyridylimidazole derivatives as the ancillary ligands. Both Ir1 and Ir2 show nearly the same photoluminescence emission with the maximum peak at 595 nm (shoulder band at about 638 nm) and achieve high solution quantum yields of up to 0.47 for Ir1 and 0.57 for Ir2. Employing Ir1 and Ir2 as emitters, the fabricated red organic light-emitting diodes (OLEDs) show outstanding performance with the maximum external quantum efficiency (EQE), current efficiency (CE), and power efficiency (PE) of 20.98%, 33.04 cd/A, and 33.08 lm/W for the Ir1-based device and 22.15%, 36.89 cd/A, and 35.85 lm/W for the Ir2-based device, respectively. Furthermore, using Ir2 as red emitter, a trichromatic hybrid white OLED, showing good warm white emission with low correlated color temperature of <2200 K under the voltage of 4-6 V, was fabricated successfully. The white device also realizes excellent device efficiencies with the maximum EQE, CE, and PE reaching 22.74%, 44.77 cd/A, and 46.89 lm/W, respectively. Such high electroluminescence performance for red and white OLEDs indicates that Ir1 and Ir2 as efficient red phosphors have great potential for future OLED displays and lightings applications.

[Elevated expression of lymphocyte activation gene-3 on peripheral blood CD8(+) T lymphocytes in patients with chronic hepatitis B virus infection].

OBJECTIVE: To evaluate the relationships between lymphocyte activation gene-3 (LAG-3) expression levels on peripheral blood T lymphocytes and other hepatitis related laboratory indexes (ALT, HBeAg and HBV DNA) in the different phases of the natural course of chronic hepatitis B virus (HBV) infection. METHODS: The study enrolled 24 chronic HBV-infected patients in the immune-tolerant (IT) phase, 32 in the immune clearance (IC) phase, 31 in the inactive or low replication (LR) phase and 30 healthy control individuals (HC). The LAG-3 expression levels on peripheral blood T lymphocytes were measured by flow cytometry. Biochemical analyses, immunoassay and polymerase chain reaction (PCR) were used to detect the liver function, serological markers of HBV and HBV DNA viral copies, respectively. Mann-Whitney U test was used to compare the expression levels of LAG-3 in groups. Spearman correlation analysis was performed to analyze the relationships between the serum levels of ALT, HBeAg, HBV DNA and the positive expression rate of LAG-3. RESULTS: A statistically higher ratio of LAG-3+CD8+ T cells was confirmed in chronic HBV-infected patients than in healthy controls. Patients in the IT phase of chronic HBV infection had even higher ratio of LAG-3+CD8+ T cells than those in the IC phase or the LR phase. The ratios of peripheral blood LAG-3+CD8+ T cells and LAG-3+CD4+ T cells in the IC phase of chronic HBV-infection were negatively correlated with the serum ALT level. The ratios of peripheral blood LAG-3+CD8+ T cells and LAG-3+CD4+ T cells in the IT phase of chronic HBV-infection were positively correlated with the serum HBeAg level. There was no correlation between the ratio of peripheral blood LAG-3+CD4+ T cells or LAG-3+CD8+ T cells and HBV DNA viral copies in chronic HBV-infected patients. CONCLUSION: LAG-3, an immunoinhibitory receptor, is highly expressed in peripheral blood CD8+ T cells in chronic HBV-infected patients, especially in the patients experiencing IT phase. The high expression level of LAG-3 on CD8+T cells might be one of the vital immune factors leading to the dysfunction of CD8+T cells and the continuous replication of HBV in the patients with chronic HBV infection.

Surface mesh to volumetric spline conversion with generalized polycubes.

This paper develops a novel volumetric parameterization and spline construction framework, which is an effective modeling tool for converting surface meshes to volumetric splines. Our new splines are defined upon a novel parametric domain called generalized polycubes (GPCs). A GPC comprises a set of regular cube domains topologically glued together. Compared with conventional polycubes (CPCs), the GPC is much more powerful and flexible and has improved numerical accuracy and computational efficiency when serving as a parametric domain. We design an automatic algorithm to construct the GPC domain while also permitting the user to improve shape abstraction via interactive intervention. We then parameterize the input model on the GPC domain. Finally, we devise a new volumetric spline scheme based on this seamless volumetric parameterization. With a hierarchical fitting scheme, the proposed splines can fit data accurately using reduced number of superfluous control points. Our volumetric modeling scheme has great potential in shape modeling, engineering analysis, and reverse engineering applications.

Restricted trivariate polycube splines for volumetric data modeling.

This paper presents a volumetric modeling framework to construct a novel spline scheme called restricted trivariate polycube splines (RTP-splines). The RTP-spline aims to generalize both trivariate T-splines and tensor-product B-splines; it uses solid polycube structure as underlying parametric domains and strictly bounds blending functions within such domains. We construct volumetric RTP-splines in a top-down fashion in four steps: 1) Extending the polycube domain to its bounding volume via space filling; 2) building the B-spline volume over the extended domain with restricted boundaries; 3) inserting duplicate knots by adding anchor points and performing local refinement; and 4) removing exterior cells and anchors. Besides local refinement inherited from general T-splines, the RTP-splines have a few attractive properties as follows: 1) They naturally model solid objects with complicated topologies/bifurcations using a one-piece continuous representation without domain trimming/patching/merging. 2) They have guaranteed semistandardness so that the functions and derivatives evaluation is very efficient. 3) Their restricted support regions of blending functions prevent control points from influencing other nearby domain regions that stay opposite to the immediate boundaries. These features are highly desirable for certain applications such as isogeometric analysis. We conduct extensive experiments on converting complicated solid models into RTP-splines, and demonstrate the proposed spline to be a powerful and promising tool for volumetric modeling and other scientific/engineering applications where data sets with multiattributes are prevalent.