Synergy Between Surface Confinement and Heterointerfacial Regulations with Fast Electron/Ion Migration in InSe-PPy for Sodium-Ion Storage.

Layered indium selenide (InSe) is a new 2D semiconductor material with high carrier mobility, widely adjustable bandgap, and high ductility. However, its ion storage behavior and related electrochemical reaction mechanism are rarely reported. In this study, InSe nanoflakes encapsulated in conductive polypyrrole (InSe@PPy) are designed in consideration of restraining the severe volume change in the electrochemical reaction and increasing conductivity via in situ chemical oxidation polymerization. Density functional theory calculations demonstrate that the construction of heterostructure can generate an internal electric field to accelerate electron transfer via additional driving forces, offering synergistically enhanced structural stability, electrical conductivity, and Na+ diffusion process. The resulting InSe@PPy composite shows outstanding electrochemical performance in the sodium ion batteries system, achieving a high reversible capacity of 336.4 mA h g-1 after 500 cycles at 1 A g-1 and a long-term cyclic stability with capacity of 274.4 mA h g-1 after 2800 cycles at 5 A g-1 . In particular, the investigation of capacity fluctuation within the first cycling reveals the alternating significance of intercalation and conversion reactions and evanescent alloying reaction. The combined reaction mechanism of insertion, conversion, and alloying of InSe@PPy is revealed by in situ X-ray diffraction, ex situ electrochemical impedance spectroscopy, and transmission electron microscopy.

Regulation of Notch Signaling Pathway to Innate Lymphoid Cells in Patients with Acute Myocardial Infarction.

The Notch signaling pathway is an important regulator in fate decisions and immune responses of innate lymphoid cells (ILCs). However, the function of Notch signaling in ILCs in acute coronary syndrome is still not fully elucidated. Thirty-one unstable angina pectoris (UAP) patients, 21 acute myocardial infarction (AMI) patients, and 20 controls were included in this study. Peripheral blood mononuclear cells (PBMCs) were isolated. The mRNA expression levels of Notch receptors and ligands were measured by real-time PCR, while ILC subsets were measured by flow cytometry. Lin- cells were purified and stimulated with γ-secretase inhibitor (GSI). ILC subsets, transcription factors, and secreted cytokines were assessed. Notch receptor and ligand mRNA levels were elevated in PBMCs and peripheral lin- cells from AMI patients. There was no significant difference in total lin-CD45+CD161+CD127+ ILC frequency among three groups. The CRTH2-CD117- ILC1 subset was down-regulated, while the CRTH2+ ILC2 subset was up-regulated in AMI patients. The CRTH2-CD117+ ILC3 subpopulation was comparable among the three groups. ILC1% was negatively correlated with Notch1 and Notch2 in AMI patients. Inhibition of Notch signaling pathway by GSI induced elevations in ILC1 frequency, T-bet mRNA expression, and interferon-γ secretion and reduced ILC2 frequency, GATA3 mRNA levels, and interleukin-5/interleukin-13 production by lin- cells from AMI patients. The current data indicated that activation of Notch signaling pathway might contribute to ILC1-to-ILC2 shift in peripheral blood in AMI patients.

Fluoroscopy-guided direct anterior approach total hip arthroplasty provides more accurate component positions in the supine position than in the lateral position.

PURPOSE: The position of the acetabular and femoral components is critical for stability and wear resistance. The aim of this study is to investigate whether the fluoroscopy-guided direct anterior approach in the supine position (S-DAA) is more helpful in improving the position of acetabular and femoral components than the fluoroscopy-guided direct anterior approach in the lateral decubitus position (L-DAA). METHODS: A retrospective analysis of 76 cases of fluoroscopy-guided direct anterior approach total hip arthroplasty (38 cases in the S-DAA and 38 cases in the L-DAA group) was performed in one hospital from 2019 to 2021. The differences in inclination, anteversion, femoral offset (FO), global offset (GO), and leg length discrepancy (LLD) measurements during and after surgery were analyzed. The postoperative femoral offset (FO), global offset (GO), leg length discrepancy (LLD), and preoperative and postoperative Harris hip score were compared between the two groups. RESULTS: In the S-DAA group, there were no significant differences in the mean intraoperative inclination angle anteversion angle, FO, GO, and LLD compared to the postoperative values, whereas in the L-DAA group, there were significant differences between the intraoperative and postoperative measurements (P < 0.001, P = 0.009, P＜0.001, P＜0.001 and P = 0.008, respectively). Additionally, there were significant differences in the accuracy of LLD, FO, and GO between the two groups (P < 0.001). Compared with the L-DAA group, the average differences of inclination, anteversion, LLD, FO, and GO during and after operation in the S-DAA group were smaller, and the consistency was higher. There was a significant difference in Harris hip score between the two groups at 1 week after surgery (P = 0.033). There was no significant difference in Harris hip score between 1 month and 3 months after surgery (P = 0.482 and P = 0.797, respectively). CONCLUSIONS: In the supine group, the direct anterior approach (DAA) provides more accurate positioning of the acetabular and femoral components. However, there was no significant difference in hip joint function and activity between the two groups at follow-up.

High-performance natural-sunlight-driven Ag/AgCl photocatalysts with a cube-like morphology and blunt edges via a bola-type surfactant-assisted synthesis.

Ag/AgCl-based structures have recently been receiving considerable attention as visible-light-driven plasmonic photocatalysts, wherein the fabrication of Ag/AgCl species shaped with an anisotropic morphology is considered to be an efficient way to enhance their performances. While the past decade has witnessed great progress in this direction, it is still strongly desired to initiate a green and low-cost protocol for the synthesis of Ag/AgCl based structures with high catalytic activity. Using a surfactant-assisted synthesis protocol, wherein a cationic bola-type surfactant of chloride counteranions serves both as a reactant (namely, source of chlorine) for the generation of AgCl structures and as a directing template to assist the formation of anisotropic structures, we herein report that cube-like Ag/AgCl with blunt edges could be fabricated simply by dropping an aqueous solution of silver nitrate into an ethanol solution of the hexane-1,6-bis(trimethylammonium chloride) surfactant. Importantly, compared to the sphere-like counterparts manufactured using a conventional tadpole surfactant, the as-fabricated cube-like structures exhibit substantially improved catalytic performances under visible-light or natural-sunlight irradiation. It has been revealed that photogenerated holes might serve as the main active species during the catalytic process. Meanwhile, our results have disclosed that in contrast to the sphere-like Ag/AgCl structures, the as-constructed cube-like structures are relatively enriched with high-index AgCl facets of smaller hole effective mass, which promote a faster carrier transfer, facilitate the migration of the photogenerated holes to the surface to be involved in photocatalytic reactions, and suppress carrier recombination, leading to their enhanced photocatalytic performances. Considering the tremendous diversity of surfactants (bola-, gemini-, polymeric surfactants etc.) with various halide counteranions and their sophisticated template effects, our new strategy might open up new opportunities for silver/silver halide (Ag/AgX, X = Cl, Br, and I)-based plasmonic structures with various morphologies and with superior light-to-chemical energy conversion capability.

Sub-10 nm Ag Nanoparticles/Graphene Oxide: Controllable Synthesis, Size-Dependent and Extremely Ultrahigh Catalytic Activity.

While tremendous advancements in Ag nanoparticle (AgNP)-based materials have been made, the development of a facile protocol for preparing sub-10 nm AgNPs with controllable size and ultrahigh performance remains a formidable challenge. It is shown that AgNPs/graphene oxide (AgNPs/GO) bearing 2.5, 4.3, and 6.2 nm AgNPs (2.5-AgNPs/GO, 4.3-AgNPs/GO, and 6.2-AgNPs/GO, respectively) could be fabricated via light-induced synthesis. Their catalytic activity toward 4-nitrophenol (4-NP) reduction, which is a "gold standard" for evaluating the performance of noble metal-based catalysts, is studied. When normalized by mole and area, the activity exhibits an order of 4.3-AgNPs/GO > 6.2-AgNPs/GO > 2.5-AgNPs/GO and 6.2-AgNPs/GO > 4.3-AgNPs/GO > 2.5-AgNPs/GO, respectively. This trend is a result of GO-induced electron concentration reduction with decreasing AgNP size. Significantly, under similar conditions, the activity of 4.3-AgNPs/GO is substantially superior to that of numerous state-of-the-art noble metal-based catalysts. The ultrafine size of the AgNPs and their surface accommodation on the unobstructed 2D GO scaffolds without capping reagents/covers, which make the abundantly exposed catalytically active sites highly accessible to substrate molecules, play an important role in their extremely ultrahigh performance. This work paves a new avenue for high-performance AgNP-based materials, and by taking 4-NP reduction as a proof-of-concept, provides new scientific insights into the rational design of surface-based advanced materials.

Spreading Films of Anthracene-Containing Gelator Molecules at the Air/Water Interface: Nanorod and Circularly Polarized Luminescence.

Two enantiomeric gelator molecules containing anthracene moiety were assembled at the air/water interface and several new insights into the films of the gelator molecules were revealed. When these molecules were spread at the air/water interface, they formed the nanorod structured monolayers and could be subsequently transferred to the solid substrate. The formed Langmuir-Blodgett (LB) films showed both optical activity and circularly polarized luminescence (CPL) due to the chirality transfer upon assembling. The dissymmetric factors of the CPL in the LB films were enhanced nearly 5 times than those in gel systems. Through the formation of the organized nanofilms, the arrangement of the molecules become compact and the film showed enantioselectivity to chiral species, whereas the molecular solution could not.

Platinized spherical supramolecular nanoassemblies of a porphyrin: facile synthesis and excellent catalytic recyclability.

Porphyrin-based supramolecular nanoassemblies of a spherical morphology have been attracting broad interest owing to their wide application possibilities in numerous fields of paramount significance. Most of the existing assembly protocols, however, either suffer from the requirement of elaborately-designed yet tediously-synthesized ad hoc porphyrins, the use of surfactant templates, or accurate consideration of the experimental parameters etc. The initiation of a facile surfactant-free fabrication protocol performable under ambient conditions using commercial porphyrins as building blocks is strongly desired. We herein report that a commercial metal-free porphyrins, 5,10,15,20-tetrakis(4-aminophenyl)porphyrin (TPPNH2), could be facilely organized to form well-defined discrete spherical nanoassemblies at room temperature by means of a simple reprecipitation method. We further find that the as-manufactured TPPNH2 nanospheres could work as photocatalysts towards the reduction of potassium tetrachloroplatinate(ii), leading to their self-platinization and the production of platinum/porphyrin nanosphere nanocomposites, wherein ultrathin Pt nanoparticles of a size of ca. 3 nm are immobilized on the porphyrin nanospheres. Significantly, by taking the advantage of their easy sedimentation from aqueous suspensions, we show that the as-produced composites could serve as qualified heterogeneous nanocatalysts in terms of their excellent catalytic stability and recyclability towards the reduction of 4-nitrophenol, where the catalytic reactivity exhibits only trivial changes even after the reactions have been repeated 8 times continuously. Taking into account the general concerns of porphyrins- and Pt-based nanostructures, this might provide a facile method for the construction of spherical porphyrin nanostructures with self-platinization capability. Meanwhile, considering the high cost and scarcity of Pt, our nanocomposites with excellent stability and recyclability likely have a bright future of potential uses.

Organic Light-Emitting Transistors: Materials, Device Configurations, and Operations.

Organic light-emitting transistors (OLETs) represent an emerging class of organic optoelectronic devices, wherein the electrical switching capability of organic field-effect transistors (OFETs) and the light-generation capability of organic light-emitting diodes (OLEDs) are inherently incorporated in a single device. In contrast to conventional OFETs and OLEDs, the planar device geometry and the versatile multifunctional nature of OLETs not only endow them with numerous technological opportunities in the frontier fields of highly integrated organic electronics, but also render them ideal scientific scaffolds to address the fundamental physical events of organic semiconductors and devices. This review article summarizes the recent advancements on OLETs in light of materials, device configurations, operation conditions, etc. Diverse state-of-the-art protocols, including bulk heterojunction, layered heterojunction and laterally arranged heterojunction structures, as well as asymmetric source-drain electrodes, and innovative dielectric layers, which have been developed for the construction of qualified OLETs and for shedding new and deep light on the working principles of OLETs, are highlighted by addressing representative paradigms. This review intends to provide readers with a deeper understanding of the design of future OLETs.

Interfacial organization of achiral porphyrins via unidirectional compression: a general method for chiroptical porphyrin assemblies of selected chirality.

Porphyrins are considered to be important scaffolds bridging supramolecular chemistry and chiral chemistry, where chirality selection via physical effects such as directional stirring and spin-coating has aroused particular interest. Nevertheless, these protocols could only work on a limited number of achiral porphyrins. It still remains a formidable challenge to pave a general avenue for the construction of chiral assemblies using achiral porphyrins. By means of a unique Langmuir-Schaefer (LS) technique of a unidirectional compression configuration, we herein have demonstrated that a series of achiral porphyrins could be facilely organized to form chiral interfacial assemblies of controlled supramolecular chirality. It has been disclosed that such a fascinating chirality selection scenario is intimately related to the direction of the compression-generated vortex-like flow, while the compression speed, one of the most significant parameters of the Langmuir technique, contributes less to this issue. With regard to a surface-pressure-dependent chirality selection phenomenon, it is suggested that the directional vortex-like flow generated by lateral compression might play a role in promoting the preferential growth of chiral assemblies showing an enhanced yet controlled CD signal. Our protocol might be, to some extent, a general method for achieving chiral porphyrin assemblies of controlled chirality.

Sheet-like and truncated-dodecahedron-like AgI structures via a surfactant-assisted protocol and their morphology-dependent photocatalytic performance.

Silver halide-based structures have been attracting great interest as efficient visible-light-driven photocatalysts towards the photodegradation of organic pollutants, and those studies focusing on their morphology-dependent catalytic performances have received particular attention. While great advancements in this regard have been witnessed in the past few years with respect to AgCl- and AgBr-based photocatalysts, relevant explorations concerning AgI-based species are relatively rare, even though the excellent durability of AgI-based structures renders them attractive candidates for potential photocatalytic uses. By means of chemical reactions between AgNO3 and tetramethylammonium iodide (TMAI), and AgNO3 and tetrabutylammonium iodide (TBAI), we herein report that AgI structures with a sheet-like and a truncated-dodecahedron-like morphology, respectively, could be controllably synthesized via a surfactant-assisted fabrication protocol. In our synthesis systems, AgNO3 works as the silver source, while the TMAI and TBAI surfactants serve not only as an iodine source but also as a directing reagent for controllable fabrication. It has been demonstrated that our AgI structures could work as visible-light-energized photocatalysts towards the photodegradation of methyl orange. We find that compared to their sheet-like counterparts, the truncated-dodecahedron-like AgI architectures exhibit substantially boosted catalytic performances. Moreover, we disclose that our truncated-dodecahedron-like AgI-based species could display excellent photocatalytic stability, wherein their catalytic reactivity displays only trivial fluctuations under visible-light irradiation even after the photoreactions have been repeated 22 times continuously. Our work might not only introduce a facile protocol for the controllable synthesis of AgI structures but also pave an avenue for facile enhancement of their catalytic performances via morphology alterations.

Organic field-effect transistor-based gas sensors.

Organic field-effect transistors (OFETs) are one of the key components of modern organic electronics. While the past several decades have witnessed huge successes in high-performance OFETs, their sophisticated functionalization with regard to the responses towards external stimulations has also aroused increasing attention and become an important field of general concern. This is promoted by the inherent merits of organic semiconductors, including considerable variety in molecular design, low cost, light weight, mechanical flexibility, and solution processability, as well as by the intrinsic advantages of OFETs including multiparameter accessibility and ease of large-scale manufacturing, which provide OFETs with great potential as portable yet reliable sensors offering high sensitivity, selectivity, and expeditious responses. With special emphases on the works achieved since 2009, this tutorial review focuses on OFET-based gas sensors. The working principles of this type of gas sensors are discussed in detail, the state-of-the-art protocols developed for high-performance gas sensing are highlighted, and the advanced gas discrimination systems in terms of sensory arrays of OFETs are also introduced. This tutorial review intends to provide readers with a deep understanding for the future design of high-quality OFET gas sensors for potential uses.

Spherical and sheetlike Ag/AgCl nanostructures: interesting photocatalysts with unusual facet-dependent yet substrate-sensitive reactivity.

We herein report that spherical and sheetlike Ag/AgCl nanostructures could be controllably synthesized by means of chemical reactions between AgNO3 and cetyltrimethylammonium chloride (CTAC) surfactant. In this synthesis system, AgNO3 works as the silver source, while CTAC serves not only as the chlorine source but also as the directing reagent for a controllable nanofabrication. We show that compared to the spherical Ag/AgCl nanostructures, the sheetlike counterparts, wherein the AgCl nanospecies are predominantly enriched with {111} facets, could exhibit superior catalytic performances toward the photodegradation of methyl orange. Interestingly, we further demonstrate that when 4-chlorophenol or phenol is used as the substrate, the sheetlike Ag/AgCl nanostructures exhibit inferior catalytic reactivity, whereas the spherical counterparts display superior catalytic performances comparatively. Our results disclose new insights on the facet-dependent catalytic performances with regard to a facet-selective but substrate-sensitive photoinduced electron-hole separation.

Visible-light-driven Ag/AgCl plasmonic photocatalysts via a surfactant-assisted protocol: enhanced catalytic performance by morphology evolution from near-spherical to 1D structures.

Ag/AgCl-based plasmonic photocatalysts have received much attention as emerging visible-light-driven photocatalysts, wherein those characterized by 1D morphology have aroused great expectations. Most of the current existing protocols for the fabrication of 1D materials, however, suffer from either multistep tedious synthesis processes or the requirement of rigorous experimental conditions. A one-pot fabrication method feasible under ambient conditions is strongly desired. By means of a surfactant-assisted protocol, we report herein that Ag/AgCl structures of near-spherical and 1D morphology could be controllably produced. We show that near-spherical Ag/AgCl species could be produced immediately after dropping an AgNO3 aqueous solution into an aqueous solution of cetyltrimethylammonium chloride (CTAC) surfactant under stirring. Interestingly, we show that these initially formed near-spherical species could automatically evolve into 1D Ag/AgCl fibers simply by extending the stirring time under ambient conditions. In our new protocol, CTAC works not only as a chlorine source but also as a directing reagent to assist the formation of 1D Ag/AgCl structures. Moreover, we demonstrate that compared to near-spherical structures, our Ag/AgCl fibers could display boosted catalytic performances towards the photodegradation of the methyl orange pollutant under visible light irradiation. Our work might launch an easy method for the construction of fibrous Ag/AgCl architectures of superior photocatalytic reactivity, and it also provides deep insights into the surfactant-assisted synthesis.

Pristine graphdiyne-hybridized photocatalysts using graphene oxide as a dual-functional coupling reagent.

Advanced functional hybrids based on carbon materials (CMs) represent one of the main achievements of scientific communities. To achieve the hybridization, pristine CMs have to be chemically modified, or surfactants, which are nonfunctional for the performances of the hybrids, have to be employed as a cross-linkage. The construction of pristine CM-based hybrids using dual-functional coupling reagents, which work not only as a glue for hybridization but also as a functional component for enhanced performance, is strongly desired. Here, we report that pristine graphdiyne (GD), a recently synthesized new carbon allotrope, can be facilely hybridized with Ag/AgBr using graphene oxide (GO) as a cross-linkage. We demonstrate that compared to Ag/AgBr, Ag/AgBr/GO, and Ag/AgBr/GD, our Ag/AgBr/GO/GD exhibits an enhanced photocatalytic performance toward the degradation of methyl orange (MO) pollutant under visible light irradiation. In our Ag/AgBr/GO/GD, GO serves not only as a glue for a successful hybridization, but also as a functional component for enhanced catalytic performance. Beyond GD, our work likely paves a new avenue for the fabrication of advanced functional hybrids based on pristine carbon allotropes, wherein desired functions or properties might be achieved by choosing desired CMs and desired hybridized components.

Cost-Utility Analysis of Vericiguat in Heart Failure with Reduced Ejection Fraction After Worsening Heart Failure Events in China.

OBJECTIVE: Vericiguat is a new medication to demonstrate clinical efficacy in heart failure with reduced ejection fraction (HFrEF) after worsening heart failure (WHF) events, but its cost-utility was unknown. We aimed to assess the cost-utility of combining the application of vericiguat with standard treatment in HFrEF patients who had WHF events. METHODS: A multistate Markov model was implemented to mimic the economic results of HFrEF patients who had WHF events in China after receiving vericiguat or placebo. An analysis of cost-utility was conducted; most parameters were set according to the published studies and related databases. All the utilities and costs were decreased at a rate of 5% annually. The incremental cost-effectiveness ratios (ICERs) were the primary outcome measure. We also conducted sensitivity analyses. RESULTS: Over a 20 year lifetime horizon, additional use of vericiguat led to an elevated cost from US$9725.03 to US$20,660.76 at the current vericiguat costs. This was related to increased quality-adjusted life years (QALYs) from 2.50 to 2.66, along with an ICER of US$65,057.24 per QALY, which was over the willingness-to-pay (WTP) threshold of US$36,096.30 per QALY. If the vericiguat costs were discounted at 80%, it contributed to an ICER of US$12,226.77 per QALY. Additional use of vericiguat for patients with plasma N-terminal pro-B-type natriuretic peptide (NT-proBNP) of ≤ 5314 pg per ml produced an ICER of US$23,688.46 per QALY. The outcomes of the one-way sensitivity analysis showed the risk of death from cardiovascular disease in both groups was variable with the highest sensitivity. The probabilistic sensitivity analysis showed that 41.6% of the mimicked population receiving vericiguat combined with standard therapy was cost-effective at the WTP threshold of US$36,096.30 per QALY. CONCLUSIONS: From the perspective of Chinese public healthcare system, the combined use of vericiguat and standard treatment in patients with HFrEF following WHF events did not generate advantages in cost-utility in China but was a cost-effective therapeutic strategy for those who with plasma NT-proBNP of ≤ 5314 pg per ml.

High-performance visible-light-driven plasmonic photocatalysts Ag/AgCl with controlled size and shape using graphene oxide as capping agent and catalyst promoter.

We report herein that Ag/AgCl-based plasmonic photocatalysts with controlled size and shape could be easily formulated by a one-pot approach via a precipitation reaction between AgNO3 or Ag(NH3)2NO3 and NaCl. It is found that near-spherical and cube-like Ag/AgCl nanoarchitectures of 500 nm could be fabricated at lower and higher temperature, respectively. Fascinatingly, when graphene oxide (GO) nanosheets are introduced into the synthesis medium, the size of the formulated near-spherical and cube-like nanostructures, Ag/AgCl/GO, could be 2.5 and 5 times reduced to ca. 200 and 100 nm, respectively, when AgNO3 and Ag(NH3)2NO3 are employed as the silver source. The series of our Ag/AgCl-based nanostructures could be used as visible-light-driven plasmonic photocatalysts for the photodegradation of methyl orange pollutants, wherein the cube-like Ag/AgCl/GO nanoarchitectures of 100 nm display the highest catalytic activity. It is disclosed that the synergistic effect of size, shape, and GO nanosheets plays an important role for their boosted photocatalytic performances. The investigation reveals that GO nanosheets work not only as a capping agent for a controllable fabrication of Ag/AgCl nanostructures, but also as catalyst promoter during the photocatalytic performances, leading to an enhanced catalytic activity. Our unique GO-assisted method likely paves a facile avenue and initiates new opportunities for the exploration of GO-hybridized high-performance catalysts.

Sunlight-driven Ag-AgCl(1-x)Br(x) photocatalysts: enhanced catalytic performances via continuous bandgap-tuning and morphology selection.

The solid solution (SS) method is an effective way to design impactful photocatalysts, owing to its merit of continuous bandgap-tuning. A calcination, usually breaking the morphology of a material, has to be used to synthesize such catalysts, although the morphology is a critical issue affecting its catalytic behavior. It thus is strongly desired to construct SS-based catalysts with a shaped morphology. Here, we report that AgCl(1-x)Br(x) SS-based photocatalysts, Ag-AgCl(1-x)Br(x), with a shaped morphology, can be produced via an ion-exchange between nanostructured Ag-AgCl and KBr. It is found that when sphere-like Ag-AgCl is employed as a precursor, the Ag-AgCl(1-x)Br(x), maintains its morphology when x is in the range of 0-1. The bandgap, and the catalytic activities of these Ag-AgCl(1-x)Br(x) for the degradation of methyl orange, display a monotonic narrowing and a continuous enhancement, respectively, with the increase of x. In contrast, when cube-like Ag-AgCl is used as a precursor, the Ag-AgCl(1-x)Br(x) preserves its morphological features when x ≤ 0.5, while a morphology distortion is observed when x ≥ 0.75. Fascinatingly, although the bandgap of thus-constructed Ag-AgCl(1-x)Br(x) also exhibits a monotonic narrowing with the increase of x, they (x ≠ 0, 1) display enhanced catalytic activity compared with the two terminal materials, Ag-AgCl and Ag-AgBr, wherein Ag-AgCl0.5Br0.5, with a cube-like morphology, shows the highest catalytic performance. The synergistic effect of morphology selection and bandgap narrowing plays an important role for these intriguing new findings. Our work provides a unique forum for an optimized selection of SS-based photocatalysts in terms of morphology selection and bandgap-tuning.

Fluorographene nanosheets with broad solvent dispersibility and their applications as a modified layer in organic field-effect transistors.

As the youngest in the graphene family, fluorographene has received numerous expectations from the scientific community. Investigation of fluorographene is similar to graphene and graphene oxide, wherein fabrication is an importance subject in the infancy stage. Fluorographene produced by the currently existing protocols, however, could only disperse in a limited number of solvents, and the dispersions generally exhibit short-term stability, restricting its manipulation and processing. To address this formidable challenge, we herein report that fluorographene nanosheets, most of which have a single-layered structure, could be easily formulated from commercially available graphite fluoride via a one-pot chloroform-mediated sonochemical exfoliation under ambient conditions without any pretreatment, special protection or stabilizers. Significantly, owing to the exceptional volatility of chloroform, our fluorographene originally dispersed in chloroform, could be facilely transferred into other 24 kinds of solvents via a volatilization-redispersion process, wherein dispersions of extremely long-term stability (more than six months) could be obtained. As an example to demonstrate the merit of the as-formulated fluorographene and its potential application possibilities, we further show that our fluorographene could be easily assembled as a modified layer in pentacene-based organic field-effect transistors simply by a spin-coating method, wherein distinctly increased mobility and positively shifted threshold voltage could be achieved. Considering the excellent popularity of chloroform in the scientific community, the remarkable volatility of chloroform, the broad solvent dispersibility of our fluorographene, and together with the long-term stability of the dispersions, our chloroform-mediated sonochemical exfoliation protocol likely endow fluorographene with new and broad opportunities for fabrication of graphene-based advanced functional films and nanocomposites via liquid-phase manipulation or solution-processing strategies.

Why does such a cyst appear after unilateral biportal endoscopy surgery: A case report and literature review.

BACKGROUND: Unilateral biportal endoscopy (UBE) has been widely and skillfully used in the treatment of lumbar disc herniation and spinal canal stenosis. UBE surgery also brings some complications, such as dural tear, epidural hematoma, residual nucleus pulposus, etc. And we found a rare case of arachnoid cyst after UBE. CASE PRESENTATION: A 48 years old female who had a history of cholecystectomy, nephrolithiasis, hyperthyroidism, chronic atrophic gastritis, and colonic polyps with several years of low back pain and numbness in both lower limbs was found have arachnoid cyst 3 years after UBE operation. We hope that we can give a new aspect of complication after the UBE treatment in the future. CONCLUSION: We believe that the postoperative hypertension and the lack of postoperative back muscle strength training and some personal factors are the possible reasons for the arachnoid cyst in this case.

Porphyrin assemblies through the air/water interface: effect of hydrogen bond, thermal annealing, and amplification of supramolecular chirality.

Molecular assemblies of two achiral porphyrins with different substituents, 5-(4-methoxycarbonylphenyl)-10,15,20-triphenyl-21H,23H-porphine (TPPCOOMe) and 5-(4-carboxyphenyl)-10,15,20-triphenyl-21H,23H-porphine (TPPCOOH), have been fabricated by the Langmuir-Blodgett (LB) technique. It is disclosed that although only slight differences exist in the molecular skeleton of these two compounds, their interfacial assemblies display distinct chiroptical properties. It is found that weak circular dichroism (CD) signals are observed from the TPPCOOH assemblies, while in the case of the TPPCOOMe assemblies, only negligible CD signals could be detected. Interestingly, after the assemblies are subjected to a thermal annealing treatment, TPPCOOH assemblies show a distinct amplification of CD signals, while those of TPPCOOMe do not. An explanation in terms of the effect of substituents on the spreading properties of the compounds and the effect of intermolecular hydrogen bonds on the cooperative stacking of the building blocks is proposed to explain these new findings. The investigation suggests that in the present porphyrin systems, besides a nice spreading property, the cooperative interaction of various noncovalent interactions, including hydrogen bonding, π-π stacking, and hydrophobic interactions, is essentially required for the occurrence of symmetry breaking at the air/water interface.