摘要：Polycaprolactone(PCL)scaffolds that are produced through additive manufacturing are one of the most researched bone tissue engineering structures in the *** to the intrinsic limitations of PCL,carbon nanomaterials are often investigated to reinforce the PCL *** several studies that have been conducted on carbon nanomaterials,such as graphene(G)and graphene oxide(GO),certain challenges remain in terms of the precise design of the biological and nonbiological properties of the *** paper addresses this limitation by investigating both the nonbiological(element composition,surface,degradation,and thermal and mechanical properties)and biological characteristics of carbon nanomaterial-reinforced PCL scaffolds for bone tissue engineering *** showed that the incorporation of G and GO increased surface properties(reduced modulus and wettability),material crystallinity,crystallization temperature,and degradation ***,the variations in compressive modulus,strength,surface hardness,and cell metabolic activity strongly depended on the type of ***,a series of phenomenological models were developed based on experimental results to describe the variations of scaffold’s weight,fiber diameter,porosity,and mechanical properties as functions of degradation time and carbon nanomaterial *** results presented in this paper enable the design of three-dimensional(3D)bone scaffolds with tuned properties by adjusting the type and concentration of different functional fillers.

摘要：Here, we report a study of ion transport across graphene oxide （GO） membranes of various thicknesses, made by vacuum filtration of GO aqueous solutions. The diffusive transport rates of two charge-equivalent ruthenium complex ions Ru（bpy）3^2＋ and Ru（phen）32% with a sub-angstrom size difference, are distinguishable through GO membranes and their ratio can be a unique tool for probing the transport-relevant pore structures. Pore and slit-dominant hindered diffusion models are presented and correlated to experimental results. Our analysis suggests that ion transport is mostly facilitated by large pores （larger than 1.75 nm in diameter） in the relatively thin GO membranes, while slits formed by GO stacking （less than 1.42 nm in width） become dominant only in thick membranes. By grafting PEG molecules to the lateral plane of GO sheets, membranes with enlarged interlayer spacing were engineered, which showed drastically increased ion transport rates and lower distinction among the two ruthenium complex ions, consistent with the prediction by the slit-dominant steric hindered diffusion model.

摘要：The high surface energy of nanomaterials endows them a metastable nature,which greatly limits their ***,in some cases,the degradation process derived from the poor stability of nanomaterials offers an unconventional approach to design and obtain functional ***,based on the poor stability of ZnSe-[DETA]0.5 hybrid nanobelts,we developed a new strategy to chemically graphitize and functionalize graphene oxide(GO).When ZnSe[DETA]0.5 hybrid nanobelts encountered a strong acid,they were attacked by H^+cations and could release highly reactive Se^2−anions into the reaction *** other common reductants(such as N2H4·H2O),these Se^2−anions exhibited an excellent ability to restore the structure of *** structural restoration of GO was greatly affected by the reaction time,the volume of HCl,and the mass ratio between GO and ZnSe[DETA]0.5 *** carefully controlling the reaction process and the post-processing process,we finally obtained several Se-based reduced GO(RGO)nanocomposites(such as ZnSe/Se-RGO,ZnSe-RGO,and Se-RGO)and various selenide/metal-RGO nanocomposites(such as Ag2Se-RGO,Cu2Se-RGO,and Pt-RGO).Although the original structure and composition of ZnSe[DETA]0.5 nanobelts are destroyed,the procedure presents an unconventional way to chemically graphitize and functionalize GO and thus provides a new material synthesis platform for nanocomposites.

摘要：Hierarchical microspheres of a graphene oxide（GO） coupled to N‐doped（BiO）2CO3 composite（N‐BOC‐GO） was synthesized by a simple hydrothermal approach. The N‐BOC‐GO composite gave enhancement in photocatalytic activity compared to the pure BOC and N‐BOC samples. With 1.0wt% GO, 62% NO removal was obtained with N‐BOC‐GO. The factors enhancing the photocatalytic performance were the high electron‐withdrawing ability and high conductivity of GO and improved visible light‐harvesting ability of N‐BOC‐GO with a 3D hierarchical architecture due to the surface scattering and reflecting（SSR） effect. An effective charge transfer from N‐BOC to GO was demonstrated by the much weakened photoluminescene intensity of the N‐BOC‐GO composite. This work highlights the potential application of GO‐based photocatalysts in air purification.

摘要：Vibrio parahaemolyticus is the leading causal agent of human acute gas- troenteritis. Real-time accurate detection means is the key to prevention and control of its spread. This study provided a novel detection strategy for realizing rapid and specific determination of V. parahaemolyticus by labeling its monoclonal antibody （Ab） with quantum dots （QDs）. The results showed that the fluorescence of these QDs-Ab bioconjugates was quenched by graphene oxide （GO） to produce a bacteri- um capture probe. And the optimal quenched concentration of GO was 60 ng/ml. When the bacterium capture probe was exposed to the target, green color fluores- cence was turned on by releasing the QDs-Ab due to the antibody antigen combi- nation. The detection limit of V. parahaemolyticus was 104 CFU/ml based on 3 times signal-to-noise ratio. The specificity of the FRET sensor towards V. para- haemolyticus was examined by comparing with controls such as V. splendidus, V. alginolyticus, Edwardsiella tarda and Aeromonas hydrophila with the same condition. The controls couldn＇t cause obvious fluorescence alteration, while the target resulted in significant fluorescence enhancement. This strategy could be further used as a universal method for any bacterial determination by changing the conjugated antibod- ies in early disease diagnosis. Therefore, the sensor has good potential to expand its application to the early diagnosis and determination of bacteria.

摘要：Natural enzymes have been praised highly as ideal catalysts, presumably owing to their remarkable advantages of high efficiency,high selectivity, and mild reaction conditions. The reports of chemical simulation and systematic synthesis of natural enzymes such as peroxidase(POD) are rare because of their complex biological structures. POD represents a large family of oxidoreductases and offers a wide range of applications in many fields of science. Recent advance in the fusion of nanomaterial, catalysis, and biochemistry has inspired the development of artificial enzymes implemented with desired catalytic features of natural ***, we review the redox chemistry of POD and compare its catalytic performance to graphene-based nanomaterials(G-NMs)as POD mimetic nanoenzymes bases on catalytic center, binding site, and carrier function. Based on the viewpoints of stereo chemistry and molecular kinetic and dynamics in heterogeneous system, we evaluate and compare the suitability of different NMs as artificial enzyme constituent. We propose that reevaluates design strategies of graphene-based peroxidase(G-POD) mimetic materials and emphasizes on their selectivity(role as catalytic center, binding site, or carrier) is of uttermost.

摘要：A one-pot method for the preparation of g-C3N4/reduced graphene oxide（rGO） composite photocatalysts with controllable band structures is *** photocatalysts are characterized by Fouirer transform infrared spectroscopy,X-ray diffraction,scanning electron microscope,transmission electron microscope,and Mott-Schottky *** valance band（VB） of g-C3N4 exhibits a noticeable positive shift upon hybridizing with rGO,and thus results in a strong photo-oxidation *** g-C3N4/rGO composites show a higher photodegradation activity for 2,4-dichlorophenol（2,4-DCP） and rhodamine B（RhB） under visible light irradiation（λ≥420 ran）.The g-C3N4/rGO-1sample exhibits the highest photocatalytic activity,which is 1.49 and 1.52 times higher than that of bulk g-C3N4 for 2,4-DCP and 1.52 times degradation,*** enhanced photocatalytic activity for g-C3N4 originates from the improved visible light usage,enhanced electronic conductivity and photo-oxidation ability by the formed strong π-π stacking interactions with rGO.