Improving Photovoltaic Performance of All-Polymer Solar Cells by Adding an Amorphous B←N Embedded Polymer as the Third Component.

Currently, most of the disclosed ternary strategies to improve photovoltaic performance of all-polymer solar cells (all-PSCs) commonly focus on the guest polymers having similar structures with the host polymer donors or acceptors. Herein, this work develops a distinctive ternary method that adding an amorphous B←N embedded polymer named BN-Cl-2fT to a crystallized host polymer blend of PM6 (a commercialized polymer donor) and PY-TT (a copolymer of Y6 and thieno[3,2-b]thiophene). Although the structures between BN-Cl-2fT and PM6 and PY-TT are completely different, excellent miscibility is found between BN-Cl-2fT and both of the host PM6 and PY-TT, which can be interpreted by the crowded phenyl groups anchoring along the backbone of BN-Cl-2fT, leading to weak self-aggregation. Glazing incidence wide-angle X-ray diffraction (GIWAXS) measurements explicitly confirm the crystallization of PM6 and PY-TT and amorphous feature of BN-Cl-2fT. Furthermore, adding 10 wt% BN-Cl-2fT to PM6:PY-TT can significantly enhance the crystallization of the host polymers. Thus the ternary devices based on PM6:PY-TT:BN-Cl-2fT afford promote short-circuit current density (JSC , 23.29 vs. 21.80 mA cm-2 ), fill factor (FF, 62.4% vs. 60.0%), and power conversion efficiency (PCE, 13.70% vs. 12.23%) in contrast to these parameters of binary devices based on PM6:PY-TT. This work provides a unique and enlightening avenue to design high performance all-PSCs by adding amorphous B←N embedded polymers as guest component to enhance host-crystallization.

A Study on the Electro-Optical Properties of Thiol-Ene Polymer Dispersed Cholesteric Liquid Crystal (PDChLC) Films.

In this study, a polymer dispersed cholesteric liquid crystal (PDChLC) film obtained via a one-step fabrication technique based on photopolymerization of a thiol-acrylate reaction system was prepared and characterized for the first time. The effects of the chiral dopant, the influence of thiol monomer functionality and content on the morphology and subsequent performance of the PDChLC films were systematically investigated. It was demonstrated that the addition of a small amount of chiral dopant slightly increased the driving voltage, but decreased the off-state transmittance significantly. Furthermore, scanning electron micrographs (SEM) shown that the liquid crystal (LC) droplet size decreased at first and then increased with the increasing amount of thiol monomer functionality, while increasing the thiol content increased the LC droplet size. Correspondingly, the electro-optical switching behavior was directly dependent on LC droplet size. By tuning the raw material composition, PDChLC film with optimized electro-optical performance was prepared.

Effect of a Polymercaptan Material on the Electro-Optical Properties of Polymer-Dispersed Liquid Crystal Films.

Polymer-dispersed liquid crystal (PDLC) films were prepared by the ultraviolet-light-induced polymerization of photopolymerizable monomers in nematic liquid crystal/chiral dopant/thiol-acrylate reaction monomer composites. The effects of the chiral dopant and crosslinking agents on the electro-optical properties of the PDLC films were systematically investigate. While added the chiral dopant S811 into the PDLC films, the initial off-state transmittance of the films was decreased. It was found that the weight ratio among acrylate monomers, thiol monomer PETMP and the polymercaptan Capcure 3-800 showed great influence on the properties of the fabricated PDLC films because of the existence of competition between thiol-acrylate reaction and acrylate monomer polymerization reaction. While adding polymercaptans curing agent Capcure 3-800 with appropriate concentration into the PDLC system, lower driven voltage and higher contrast ratio were achieved. This made the polymer network and electro-optical properties of the PDLC films easily tunable by the introduction of the thiol monomers.

A simulation study on the self-assembly of rod-coil-rod triblock copolymers within nanoslits.

Self-assembly of rod-coil-rod R4C12R4 triblock copolymers within a nanoslit is investigated by using dissipative particle dynamics simulations. Perpendicular lamellae (L⊥) in nonselective or weak selective slits and parallel lamellae (L∥) in coil-selective slits are observed, and both are almost independent of the slit thickness. However, in the rod-selective slits, the assembled structures are strongly dependent on the slit thickness. With an increase in the slit thickness, we sequentially observe hexagonally packed cylinders (HC) of rod blocks perpendicular to surfaces in thin slits, parallel wavy lamellae, orderly packed alternating cylinders in moderate slits, a mixture structure of HC near surfaces and L⊥ in the interior region, and finally L∥ in wide slits. Our simulation results reveal that the rod block and surface properties play an important role in the assembly of confined rod-coil-rod triblock copolymers. Results also illustrate the competition between the slit thickness and the length scale of lamellae in bulk for the confined copolymers in nanoslits.

Toxic effects of microplastics and nitrite exposure on intestinal histology, digestion, immunity, and microbial community of shrimp Litopenaeus vannamei.

Nitrite and microplastics (MPs) are environmental pollutants that threaten intestinal integrity and affect immune function of shrimp. In this study, the shrimp Litopenaeus vannamei were exposed to the individual and combined stress of nitrite and microplastics for 14 days, and the changes of intestinal histology and physiological functions were investigated. After single and combined stress, affectations occurred in intestinal tissue; the antioxidant enzyme activities (MDA, H2O2, CAT increased) and gene expression levels (CAT, SOD, GPx, HSP70 up-regulated) changed. The expression levels of detoxification genes (CYP450, UGT down-regulated, GST up-regulated), apoptosis genes (CASP-3 up-regulated) and endoplasmic reticulum stress genes (Bip, GRP94 down-regulated) changed. Furthermore, the stress also increased intestinal microbial diversity, causing bacterial composition variation, especially beneficial bacteria and pathogenic bacteria. These results suggested that nitrite and microplastics stress had adverse effects on the intestinal health of L. vannamei by affecting intestinal tissue morphology, immune response and microbial community.

Solvent-free synthesis of high-performance polyurethane elastomer based on low-molecular-weight alkali lignin.

Using cheap and green lignin as a partial substitute for petroleum-based polyols is highly attractive for sustainable development of polyurethane elastomers (LPUes). However, the traditional synthesis process of LPUes inevitably uses toxic solvents that are difficult to remove or carcinogenic. Here, we reported a solvent-free synthesis method to prepare lignin-containing polyurethane elastomers (SF-LPUes) with high strength, high toughness and high elasticity. Most of the hydroxyl groups of lignin reacted with isocyanates to form a strong chemical cross-linking network, while the unreacted ones formed a dynamic hydrogen bond network with polyurethane matrix, contributing to the in-situ formation of lignin nanoparticles to build a nano-micro phase separation structure. Consequently, a dual-crosslinking network structure was formed and endowed SF-LPUes with excellent mechanical properties. Especially, the SF-LPUes prepared from low molecular alkali lignin possessed a tensile strength as high as 38.2 MPa, a maximum elongation at break of 1108 %, and an elastic recovery ratio of up to 98.7 %. Moreover, SF-LPUes showed impressing reprocessing performance and aging resistance. This work provides an industrial application prospect for the synthesis of lignin-containing polyurethane elastomers via a solvent-free synthesis process.

Preparation and characterization of catalase-loaded solid lipid nanoparticles based on soybean phosphatidylcholine.

BACKGROUND: High-purity soybean phosphatidylcholine (SPC) (94%) were prepared using macroporous resin adsorption chromatography previously. Catalase is a food enzyme for promoting health and protecting against many age-related disease. Solid lipid nanoparticles (SLN) are safe immobilizing systems for efficient protein transportation to biomembranes while avoiding adverse degradation of protein. This study was aimed at developing and characterizing catalase-loaded SLN using SPC as solubilizers and stabilizing agents, to protect catalase from proteolysis. RESULTS: Catalase-loaded SLN were prepared by the double emulsification method and solvent evaporation techniques, using acetone-methylene chloride (1:1, v/v) as an organic solvent, SPC-tripalmitin as oil phase and Poloxamer 188 as a surfactant. The optimized SLN were prepared using an SPC:tripalmitin ratio of 5% (w/w), 20 s plus 30 s sonication, 20 g L⁻¹ Poloxamer 188 and 1:2 (v/v) of oily phase:outer aqueous phase ratio. The mean particle size of SLN was 296.0 ± 7.0 nm, polydispersity index range and zeta potential were 0.322-0.354 and -36.4 ± 0.6, respectively, and encapsulation efficiency reached its maximum of 77.9 ± 1.56%. Catalase, which was found to distribute between the solid lipid and inner aqueous phase, was gradually released from SLN up to 20% within 20 h. Catalase-loaded SLN had stably retained 30% of H2O2-degrading activity for at least 24 h in a proteolytic environment, while free catalase lost its activity within 1 h. CONCLUSION: Catalase can indeed be loaded in tripalmitin-based SLN using SPC as solubilizers and stabilizing agents, which protected it against proteolysis, suggesting the potential application of SPC in delivery and protection of functional food enzyme.

Synergistic poly(lactic acid) photoreforming and H2 generation over ternary NixCo1-xP/reduced graphene oxide/g-C3N4 composite.

Effective utilization of photoexcited electrons and holes is always a challenge in photocatalytic reactions. Herein, we reported ternary NixCo1-xP/reduced graphene oxide/g-C3N4 (NixCo1-xP/rGO/CN) composite as a photocatalyst for synergistic poly(lactic acid) photoreforming and H2 generation in alkaline aqueous solution. The rate of H2 production over the optimal 15Ni0·1Co0·9P/rGO/CN reached 576.7 µmol h-1 g-1, which is 3.6 times as high as binary 15Ni0·1Co0·9P/CN composite. The apparent quantum efficiency of the optimal 15Ni0·1Co0·9P/rGO/CN was 1.7% at λ = 420 nm monochromatic light. Mott-Schottky analysis suggested that the photogenerated electrons transfer along the pathway of CN→rGO→Ni0·1Co0·9P, where rGO and Ni0·1Co0·9P functioned as the medium for electron transporting and reaction site for H2 generation, respectively. Meanwhile, poly(lactic acid) was photoreformed into formate and acetate by the photogenerated holes and hydroxyl radical. This work demonstrates that ternary NixCo1-xP/rGO/CN composite can be applied as a cheap and promising photocatalyst for synergistic plastic photoreforming and H2 generation.

The Feasibility of Robot-Assisted Chin Osteotomy on Skull Models: Comparison with Surgical Guides Technique.

Surgical robotic technology is characterized by its high accuracy, good stability, and repeatability. The accuracy of mandibular osteotomy is important in tumor resection, function reconstruction, and abnormality correction. This study is designed to compare the operative accuracy between robot-assisted osteotomy and surgical guide technique in the skull model trials which simulated the genioplasty. In an experimental group, robot-assisted chin osteotomy was automatically performed in 12 models of 12 patients according to the preoperative virtual surgical planning (VSP). In a control group, with the assistance of a surgical guide, a surgeon performed the chin osteotomy in another 12 models of the same patients. All the mandibular osteotomies were successfully completed, and then the distance error and direction error of the osteotomy plane were measured and analyzed. The overall distance errors of the osteotomy plane were 1.57 ± 0.26 mm in the experimental group and 1.55 ± 0.23 mm in the control group, and the direction errors were 7.99 ± 1.10° in the experimental group and 8.61 ± 1.05° in the control group. The Bland-Altman analysis results revealed that the distance error of 91.7% (11/12) and the direction error of 100% (12/12) of the osteotomy plane were within the 95% limits of agreement, suggesting the consistency of differences in the osteotomy planes between the two groups. Robot-assisted chin osteotomy is a feasible auxiliary technology and achieves the accuracy level of surgical guide-assisted manual operation.

Entropy-Enhanced Mechanochemical Activation for Thermal Degrafting of Surface-Tethered Dry Polystyrene Brushes.

Dry polymer brushes have attracted great attention because of their potential utility in regulating interface properties. However, it is still unknown whether dry polymer brushes will exhibit degrafting behavior as a result of thermal annealing. Herein, a study of the conformational entropy effect on thermal degrafting of dry polystyrene (PS) brushes is presented. For PS brushes with an initial grafting density (σpini) of 0.61 nm-2, degrafting behavior was observed at 393 K, and the equilibrium σp was approximately 0.14 nm-2 at 413 K. However, for brushes with σpini ≤ 0.14 nm-2, thermal degrafting was not observed even if the temperature was increased to 453 K. Furthermore, we found that the degrafting rate was faster for PS brushes with higher σpini and higher molecular weights when σpini > 0.14 nm-2. Our findings confirmed that degrafting is a mechanochemical activation process driven by tension imposed on bonds that anchor the chains to the surface, and the process is amplified by conformational entropy.

Biomass-based indole derived composited with cotton cellulose fiber integrated as sensitive fluorescence platform for NH3 detection and monitoring of seafood spoilage.

Herein, an indole-derived water-soluble fluorescence nanomaterial and biomass-based cellulose filter paper integrated as solid-state fluorescence platform (H2-FP) for seafood spoilage detection was prepared. H2 exhibits high fluorescence stability and good biocompatibility with green beans, onion tissues, blood and zebrafish, which proving that H2 has a wide range of application scenarios. Further, H2-FP with effective, solid-state fluorescence, portable, and reusable characteristics is nanoengineered for NH3 quantitative and qualitative detection (DOL = 2.6 ppm). Then, H2-FP has been successfully used to monitor NH3 release in the seafood spoilage process at various storage time (4 °C and 25 °C). More importantly, fluorescence color of H2-FP is integrated smartphone are converted to digital values through RGB channels and successfully used to visualize semi-quantitative recognition of NH3. This sensing fluorescence platform integrated with smartphone furnishes an effective fabrication strategy and broad prospects for explore various biomass-based materials for sensing NH3 change in biological and environmental samples.

Co-benefits of nonpharmaceutical intervention against COVID-19 on infectious diseases in China: A large population-based observational study.

Background: Nonpharmaceutical interventions (NPIs) are public health measures that aim to suppress the transmission of infectious diseases, including border restrictions, quarantine and isolation, community management, social distancing, face mask usage, and personal hygiene. This research aimed to assess the co-benefits of NPIs against COVID-19 on notifiable infectious diseases (NIDs) in Guangdong Province, China. Methods: Based on NID data from the Notifiable Infectious Diseases Surveillance System in Guangdong, we first compared the incidence of NIDs during the emergency response period (weeks 4-53 of 2020) with those in the same period of 2015-2019 and then compared that with the expected incidence during the synchronous period of 2020 for each city by using a Bayesian structural time series model. Findings: A total of 514,341 cases of 39 types of NIDs were reported in Guangdong during the emergency response period in 2020, which decreased by 50·7% compared with the synchronous period during 2015-2019. It was estimated that the number of 39 NIDs during the emergency response in 2020 was 65·6% (95% credible interval [CI]: 64·0% - 68·2%) lower than expected, which means that 982,356 (95% CI: 913,443 - 1,105,170) cases were averted. The largest reduction (82·1%) was found for children aged 0-14 years. For different categories of NIDs, natural focal diseases and insect-borne infectious diseases had the greatest reduction (89·4%), followed by respiratory infectious diseases (87·4%), intestinal infectious diseases (59·4%), and blood-borne and sexually transmitted infections (18·2%). Dengue, influenza, and hand-foot-and-mouth disease were reduced by 99·3%, 95·1%, and 76·2%, respectively. Larger reductions were found in the regions with developed economies and a higher number of COVID-19 cases. Interpretation: NPIs against COVID-19 may have a large co-benefit on the prevention of other infectious diseases in Guangdong, China, and the effects have heterogeneity in populations, diseases, time and space. Funding: Key-Area Research and Development Program of Guangdong Province.

Phylogeny and species delimitation of the genus Longgenacris and Fruhstorferiola viridifemorata species group (Orthoptera: Acrididae: Melanoplinae) based on molecular evidence.

Phylogenetic positions of the genus Longgenacris and one of its members, i.e. L. rufiantennus are controversial. The species boundaries within both of L. rufiantennus+Fruhstorferiola tonkinensis and F. viridifemorata species groups are unclear. In this study, we explored the phylogenetic positions of the genus Longgenacris and the species L. rufiantennus and the relationships among F. viridifemorata group based on the 658-base fragment of the mitochondrial gene cytochrome c oxidase subunit I (COI) barcode and the complete sequences of the internal transcribed spacer regions (ITS1 and ITS2) of the nuclear ribosomal DNA. The phylogenies were reconstructed in maximum likelihood framework using IQ-TREE. K2P distances were used to assess the overlap range between intraspecific variation and interspecific divergence. Phylogenetic species concept and NJ tree, K2P distance, the statistical parsimony network as well as the generalized mixed Yule coalescent model (GMYC) were employed to delimitate the species boundaries in L. rufiantennus+F. tonkinensis and F. viridifemorata species groups. The results demonstrated that the genus Longgenacris should be placed in the subfamily Melanoplinae but not Catantopinae, and L. rufiantennus should be a member of the genus Fruhstorferiola but not Longgenacris. Species boundary delimitation confirmed the presence of oversplitting in L. rufiantennus+F. tonkinensis and F. viridifemorata species groups and suggested that each group should be treated as a single species.

Dissipative particle dynamics simulation on a ternary system with nanoparticles, double-hydrophilic block copolymers, and solvent.

Dissipative particle dynamics (DPD) simulations are performed to study the aggregation of hydrophobic nanoparticles in the presence of double-hydrophilic block copolymer (DHBC). A single compact spherical nanoparticle aggregate is formed in the absence of DHBC. The response of the aggregate to a continuous increase in the concentration of DHBC has been investigated in detail. We observe the evolvement from single spherical aggregate, through single ellipsoidal aggregate, single platelike aggregate, single long and curly rod, dispersed aggregates, then to hexagonally packed cylinders, and ultimately to ordered lamellar structures upon slow addition of DHBC chains. However, when nanoparticles and DHBCs are added into the system simultaneously at the beginning of simulation, we only obtain single spherical aggregate, dispersed aggregates, hexagonally packed cylinders, and ordered lamellar structures at different concentrations of DHBC. Phase diagrams of structures against concentration of DHBC are presented for these two methods, and the stabilities of structures obtained with the two methods are compared.

Control of aggregation of nanoparticles by double-hydrophilic block copolymers: a dissipative particle dynamics study.

Double-hydrophilic block copolymer (DHBC)-directed mineralization is investigated by dissipative particle dynamics (DPD) simulation. By mineralization, we refer to the formation of inorganic crystals from the solution. In the current study, the DHBCs are modeled as chains of A and B blocks with repulsion between unlike blocks, while the mineralization is approximated by aggregation of hydrophobic nanoparticles from the solution. Depending on the relative concentrations of nanoparticles and DHBC, dispersed spherical aggregates, hexagonally packed cylinders, and ordered lamellae structures are obtained. The structures formed are seen to be controlled by competing forces between aggregation of nanoparticles, the interaction of DHBC with nanoparticles, and the self-assembly of DHBC in the solution. The time evolutions of hexagonally packed cylinders and ordered lamellae are studied. For the development of cylinders, nanoparticles first aggregate into orientationally disordered small cylinders, then these cylinders slowly grow into hexagonally packed long cylinders. For the development of ordered lamellae, nanoparticles first form a disordered structure, then grow into disordered lamellae, and at last evolve into ordered lamellae. The simulation demonstrates that addition of DHBC can effectively control the aggregation of inorganic particles and lead to formation of a variety of nanostructures.

Dynamic Monte Carlo simulation of aggregation of nanoparticles in the presence of diblock copolymer.

The aggregation of hydrophobic nanoparticles in the presence of diblock copolymers is investigated using dynamic Monte Carlo simulation on a simple cubic lattice. One nanoparticle occupies one lattice site, one block copolymer (A(m)B(m)) occupies 2m sequentially linked sites with m segments of A and m segments of B, and solvents are represented by any unoccupied sites. All of them are self-avoiding and nearest-neighbor interactions are considered. A compact big aggregate, dispersed aggregates wrapped by polymer chains, and an ordered lamellar structure are obtained by varying the concentration of copolymer. The structures are seen to be controlled by competing forces between the interaction of copolymer with nanoparticles and the self-assembly of copolymer in solution. The critical concentration of copolymer needed to form the lamellar structure, C(p,L), decreases with the chain length. It is also found that C(p,L) decreases roughly linearly with the concentration of nanoparticles C(n), which can be approximately expressed as C(p,L)=0.764-0.857C(n) when m=2. The simulation demonstrates that addition of diblock copolymer can effectively control the aggregation of nanoparticles and lead to the formation of a variety of nanostructures.

Enrichment and purification process of astragalosides and their anti-human gastric cancer MKN-74 cell proliferation effect.

BACKGROUND: Radix astragali mainly contains saponins, polysaccharides, flavonoids, amino acids and other chemical constituents of which total astragalosides have immunomodulatory, anti-viral, hepatoprotective, and gastric mucosa protective effects. OBJECTIVE: To investigate the process conditions for extraction, purification and enrichment of total astragalosides by macroporous adsorption resin, and to study the inhibitory effect of total astragalosides on growth of human gastric cancer cell line MKN-74. METHODS: UV spectrophotometry was applied to determine the adsorption and desorption capacity of macroporous adsorption resin on total astragaloside content, MTT assay was used to determine the inhibition of MKN-74 cell growth by total astragalosides. RESULTS: The dynamic adsorption performance of DA201 adsorption resin was examined, and the dynamic adsorption curve of total astragalosides on DA201 resin column was plotted. Meanwhile, eluent and elution flow rate were investigated, the results showed that the choice of eluent of 80% ethanol, and a flow rate of 5 BV/h could maximize the yield of total astragalosides. MTT assay found that astragalosides could relatively pronouncedly inhibit the proliferation of MKN-74 cells, and the inhibitory effect was enhanced with the increase of astragaloside dose and the extension of processing time, which showed a dose-and time-dependence. CONCLUSION: DA201 resin can effectively enrich total astragalosides, total astragalosides have an inhibitory effect on growth of MKN-74 cells.

A potential perylene diimide dimer-based acceptor material for highly efficient solution-processed non-fullerene organic solar cells with 4.03% efficiency.

A highly efficient acceptor material for organic solar cells (OSCs)--based on perylene diimide (PDI) dimers--shows significantly reduced aggregation compared to monomeric PDI. The dimeric PDI shows a best power conversion efficiency (PCE) approximately 300 times that of the monomeric PDI when blended with a conjugate polymer (BDTTTT-C-T) and with 1,8-diiodooctane as co-solvent (5%). This shows that non-fullerene materials also hold promise for efficient OSCs.

Hydrodynamic interaction in polymer solutions simulated with dissipative particle dynamics.

The authors analyzed extensively the dynamics of polymer chains in solutions simulated with dissipative particle dynamics (DPD), with a special focus on the potential influence of a low Schmidt number of a typical DPD fluid on the simulated polymer dynamics. It has been argued that a low Schmidt number in a DPD fluid can lead to underdevelopment of the hydrodynamic interaction in polymer solutions. The authors' analyses reveal that equilibrium polymer dynamics in dilute solution, under typical DPD simulation conditions, obey the Zimm [J. Chem. Phys. 24, 269 (1956)] model very well. With a further reduction in the Schmidt number, a deviation from the Zimm model to the Rouse model is observed. This implies that the hydrodynamic interaction between monomers is reasonably developed under typical conditions of a DPD simulation. Only when the Schmidt number is further reduced, the hydrodynamic interaction within the chains becomes underdeveloped. The screening of the hydrodynamic interaction and the excluded volume interaction as the polymer volume fraction is increased are well reproduced by the DPD simulations. The use of soft interaction between polymer beads and a low Schmidt number do not produce noticeable problems for the simulated dynamics at high concentrations, except for the entanglement effect which is not captured in the simulations.

[Clinical value of cast post-core porcelain fused to metal crown in restorating residual root and crown of molars].

OBJECTIVE: To investigate the effect of cast post-core porcelain fused to metal crown on the restoration of residual root and crown of molars. METHODS: One hundred and sixty-four residual roots and crowns of molars were treated with root canal therapy and restored by cast core porcelain fused to metal crown. The restoration effect was assessed at the 3rd, 6th, 12th and 24th month. RESULTS: The strength of dental prosthesis retention, marginal fitness, and strength of crowns were satisfactory. The effective rate reached 95.12% during the 2 year follow-up. CONCLUSION: The cast post-core porcelain fused to metal crown is a better method in treating the residual root and crown of molars.