Gradient‑Layered MXene/Hollow Lignin Nanospheres Architecture Design for Flexible and Stretchable Supercapacitors

With the rapid development of flexible wearable electronics,the demand for stretchable energy storage devices has surged.In this work,a novel gradient-layered architecture was design based on single-pore hollow lignin nanospheres(HLNPs)-intercalated two-dimensional transition metal carbide(Ti_(3)C_(2)T_(x) MXene)for fabricating highly stretchable and durable supercapacitors.By depositing and inserting HLNPs in the MXene layers with a bottom-up decreasing gradient,a multilayered porous MXene structure with smooth ion channels was constructed by reducing the overstacking of MXene lamella.Moreover,the micro-chamber architecture of thin-walled lignin nanospheres effectively extended the contact area between lignin and MXene to improve ion and electron accessibility,thus better utilizing the pseudocapacitive property of lignin.All these strategies effectively enhanced the capacitive performance of the electrodes.In addition,HLNPs,which acted as a protective phase for MXene layer,enhanced mechanical properties of the wrinkled stretchable electrodes by releasing stress through slip and deformation during the stretch-release cycling and greatly improved the structural integrity and capacitive stability of the electrodes.Flexible electrodes and symmetric flexible all-solid-state supercapacitors capable of enduring 600%uniaxial tensile strain were developed with high specific capacitances of 1273 mF cm^(−2)(241 F g^(−1))and 514 mF cm^(−2)(95 F g^(−1)),respectively.Moreover,their capacitances were well preserved after 1000 times of 600%stretch-release cycling.This study showcased new possibilities of incorporating biobased lignin nanospheres in energy storage devices to fabricate stretchable devices leveraging synergies among various two-dimensional nanomaterials.

Efficacy and safety of transhepatic arterial chemoembolization with drug-loaded microspheres in unresectable primary liver cancer

BACKGROUND Transhepatic arterial chemoembolization(TACE),as a local treatment,has been widely used in the treatment of unresectable liver cancer.The introduction of drug carrier microspheres has brought new hope for the therapeutic effect of TACE.Microspheres can realize the slow release and directional delivery of drugs,reduce systemic toxicity and improve local curative effect.AIM To compare the effectiveness of traditional transcatheter arterial chemoembolization against microsphere-assisted transcatheter arterial chemoembolization in the treatment of hepatocellular carcinoma that is incurable.METHODS We searched the PubMed,Embase,Cochrane Library,and CNKI databases for clinical trials of drug-luting beads TACE(DEB-TACE)vs conventional TACE(cTACE)for the treatment of unresectable liver cancer.We screened references based on inclusion and exclusion criteria and then selected valid data for meta-analysis using RevMan 53 software.The complete response(CR)rate,partial response(PR)rate,postoperative stable disease(SD)rate,and 6-month and 12-month survival rates were compared.RESULTS A total of 12 articles were included,including 1177 patients,519 of whom received DEB-TACE and 658 of whom received cTACE.The CR rate in the DEB-TACE group was much greater than that in the cTACE group[relative risk(RR)=1.42,95%CI:1.18-1.72,P=0.0002].The 12-month survival rate significantly increased(RR=1.09;95%CI:1.01-1.17,P=0.03);the PR rate(RR=1.13;95%CI:0.97-1.30,P=0.12);the SD rate(RR=0.82;95%CI:0.64-1.05,P=0.12);and the 6-month survival rate(RR=1.05;95%CI:1.00-1.10,P=0.07).There was no significant difference(P<0.05).CONCLUSION Compared with those of iodized oil TACE,the drug-loaded microspheres tended to have therapeutic advantages.

Controllable synthesis of CdS nanospheres photoelectrode for photoelectrochemical water splitting

CdS nanospheres were grown on indium tin oxide(ITO)substrate using a hydrothermal method.The crystal structure,morphology and electronic structure of the samples synthesized were characterized in detail.The results confirm that the crystallinity,size,crystal defects of the CdS nanospheres and the film thickness of CdS photoelectrodes can be tuned by varying the precursor Cd2+concentration.Combined with charge transfer dynamics analysis,it can be found that proper particle size and film thickness,as well as fewer defects,will result in better charge separation efficiency of the prepared CdS/ITO photoelectrodes,thereby exhibiting better photoelectrochemical performance for water splitting.The optimized CdS/ITO photoelectrode synthesized with a Cd2+concentration of 0.14 mol⋅L1 gave a photocurrent density of 5.10 mA⋅cm^(-2)at potential of 1.23 V versus the reversible hydrogen electrode(RHE),under a simulated solar illumination of 100 mW⋅cm^(-2).

Targeting Effect Study of ￣(3) H-Mitoxantrone Nanosphereson Hepatocellular Carcinoma(HCC) Model in Nude Mice

The distribution of ￣(3)H-mitoxantrone polybutyl cyanoacrylate nanospheres(￣(3)H-DHAQ-PBCA-NS)in the viscera,muscle and tumors of human hepatocellular carcinoma (HCC)model in nude mice was studied with liquid scintillation counting techniique. The results showed that the ￣(3)H-DHAQ-PBCA-NS had remarkable liver targeting effect. The content of ￣(3)H-DHAQ-PBCA-NSin liver and heterotopic liver tumor was found to be 71.31±10. 49% of total amount of drug in animal body. It was also found that the content of ￣(3)H-DHAQ-PBCA-NS in liver was higher than that in liver tissue, and the content of ￣(3)H-DHAQ-PBCA-NS in annpit tumor was higher than that in armpit muscle tissue,but had no significant difference;It provides an ideal preparation for the DHAQ admini-stration.

SnS_2@C Hollow Nanospheres with Robust Structural Stability as High?Performance Anodes for Sodium Ion Batteries

Constructing unique and highly stable structures with plenty of electroactive sites in sodium storage materials is a key factor for achieving improved electrochemical properties through favorable sodium ion di usion kinetics. An SnS_2@carbon hollow nanospheres(SnS_2@C) has been designed and fabricated via a facile solvothermal route, followed by an annealing treatment. The SnS_2@C hybrid possesses an ideal hollow structure, rich active sites, a large electrode/electrolyte interface, a shortened ion transport pathway, and, importantly, a bu er space for volume change, generated from the repeated insertion/extraction of sodium ions. These merits lead to the significant reinforcement of structural integrity during electrochemical reactions and the improvement in sodium storage properties, with a high specific reversible capacity of 626.8 mAh g^(-1) after 200 cycles at a current density of 0.2 A g^(-1) and superior high-rate performance(304.4 mAh g^(-1) at 5 A g^(-1)).

Continued sustained release of VEGF by PLGA nanospheres modified BAMG stent for the anterior urethral reconstruction of rabbit

Objective:To study the biocompatibility and neovascularization of the PLGA nanospheres wrapped with vascular endothelial growth factor(VEGF).which can improve bladder acellular matrix graft(BAMG) with local continuous release of VEGF.Methods:A total of 18 rabbit model (length of stenosis:3cm) with anterior urethral stricture were used as experimental animals and divided into three groups.Group A as the control group:Simple BAMG scaffold materials for urethral reconstruction.Group B as the blank group:PLGA microspheres modified BAMG for urethral reconstruction.Group C:PLGA conjugated with VEGF and modified BAMG for the urethral reconstruction.All rabbits underwent urethral angiography after 7 days,15 days,1 month and 3 months after the operation,and one rabbit in each group was sacrificed to be prepared for the organization histologic examination,HE staining,masson staining,CD31,34 and a-SAM immunohistochemical detection in the repaired sites.Results:In group A,significant urethral restenosis occurred in two rabbits after 15 days of the operation,HE and masson staining showed a lot of collagen arranged in the repaired sites,and there were a large number of inflammatory cell infiltration,and there were also CD31,34 in the repaired sites.a-SAM microvascular tag count showed a small amount of microvascular;Croup B showed anastomotic restenosis,HE and masoon staining showed inflammatory cell infiltration and collagen deposition;Group C:urethrography showed lumen patency.There were a small amount of inflammatory cell infiltration after 7 and 15 days after the operation,and there were also CD31,34 in the repaired sites.The a-SAM microvascular tag count showed many microvascular.And the difference was significant.Conclusions:Anterior urethral reconstruction with sustained-release of VEGF by PLGA nanospheres modified BAMG stents can reduce postoperative restenosis.It can also reduce collagen deposition and scar formation,promote angiogenesis of the repair tissue;therefore it in valuable in the tissue-engineered urethral reconstruction.

Facile synthesis of nanoporous CuS nanospheres for high-performance supercapacitor electrodes

In recent years, development of high-performance supercapacitor electrode materials has stimulated a great deal of scientific research. The electrochemical performance of a supercapacitor strongly depends on its material structures. Herein, we report a simple strategy for high-performance supercapacitors by building pseudocapacitive CuS nanospheres with nanoporous structures, nanosized walls（<10 nm） and relatively large specific surface area of 65 m;/g. This electrode demonstrates excellent electrochemical performance including a maximum specific capacitance of 814 F/g at 1 A/g, significant rate capability of 42% capacitance retention at an ultrafast rate of 50 A/g, and outstanding long-term cycling stability at various current densities. The remarkable electrochemical performance of as-prepared nanoporous CuS nanospheres electrode has been attributed to its unique structures that plays a key role in providing short ion and electron diffusion pathways, facilitated ion transport and more active sites for electrochemical reactions. This work sheds a new light on the metal sulfides design philosophy, and demonstrates that nanoporous CuS nanospheres electrode is a promising candidate for application in high-performance supercapacitors.

Structure and Magnetic Properties of Monodisperse Fe^(3+)-doped CeO_2 Nanospheres

This work reports the study concerning the structure and magnetic properties of undoped CeO_2 and Fe-doped CeO_2(Ce_(1-x) Fe_xO_2, 0.01 ≤ x ≤ 0.07) nanospheres with diameters of 100~200 nm prepared by hydrothermal method using polyvinylpyrrolidone(PVP) as surfactant. The prepared samples were studied by using X-ray diffraction(XRD), Raman spectroscopy, transmission electron microscopy(TEM), high-resolution transmission electron microscopy(HRTEM), X-ray absorption near-edge structure(XANES), and vibrating sample magnetometry(VSM). The XRD results showed that Fe-doped CeO_2 was single-phased with a cubic structure, and with Fe^(3+)successfully substituting in Ce^(4+) sites. Raman spectra showed a redshift of F_(2g) mode that caused by the Fe doping. The samples of both undoped CeO_2 and Fe-doped CeO_2 exhibited room temperature ferromagnetism, and the saturated magnetization(Ms) increased with increasing Fe content until x = 0.05, and then the samples displayed ferromagnetic loops as well as paramagnetic behavior. The roles of Ce^(3+) and Fe^(3+)spin electrons are discussed for the ferromagnetism in the Fe-doped CeO_2.

Highly sensitive room-temperature gas sensors based on hydrothermal synthesis of Cr_2O_3 hollow nanospheres

This paper reports that Cr2O3 hollow nanospheres （HNs） were synthesized via a hydrothermal approach and characterized by scanning electron microscopy, x-ray powder diffraction, transmission electron microscopy （TEM）, selective area electron diffraction and high resolution TEM, respectively. In addition, the room-temperature （RT） gas sensing properties of Cr2O3 HNs and conventional powders （CPs） were investigated by means of the surface photovoltage technique. The experimental data demonstrate that the RT gas sensor of the as-fabricated HNs reaches below 5 ppm whereas that of the CPs is about 40 ppm, which results from there being much more adsorbed and desorbed oxygen in HNs than in CPs at RT. The as-prepared Cr2O3 HNs could have potential applications as RT nanosensors.

Preparation of phosphorus-doped carbon nanospheres and their electrocatalytic performance for O_2 reduction

Phosphorus-doped carbon nanospheres without any metal residues were synthesized and characterized. The results revealed that the doping phosphorus atoms could significantly improve the electrocatalytic activity of graphitic carbon for the oxygen-reduction reaction （ORR） both in acidic and alkaline media, and the materials exhibited high electrocatalytic activity, long-term stability, and excellent tolerance to crossover effects especially in alkaline media. Quantum mechanics calculations with the density functional theory demonstrated that the changes in charge density and energetic characteristics of frontier orbitals for the P-doped graphene sheet could facilitate the ORR.

Atomic Layer Deposition-Assisted Construction of Binder-Free Ni@N-Doped Carbon Nanospheres Films as Advanced Host for Sulfur Cathode

Rational design of hybrid carbon host with high electrical conductivity and strong adsorption toward soluble lithium polysulfides is the main challenge for achieving high-performance lithium-sulfur batteries(LSBs).Herein,novel binder-free Ni@N-doped carbon nanospheres(N-CNSs)films as sulfur host are firstly synthesized via a facile combined hydrothermal-atomic layer deposition method.The cross-linked multilayer N-CNSs films can effectively enhance the electrical conductivity of electrode and provide physical blocking“dams”toward the soluble long-chain polysulfides.Moreover,the doped N heteroatoms and superficial NiO layer on Ni layer can work synergistically to suppress the shuttle of lithium polysulfides by effective chemical interaction/adsorption.In virtue of the unique composite architecture and reinforced dual physical and chemical adsorption to the soluble polysulfides,the obtained Ni@N-CNSs/S electrode is demonstrated with enhanced rate performance(816 mAh g?1 at 2 C)and excellent long cycling life(87%after 200 cycles at 0.1 C),much better than N-CNSs/S electrode and other carbon/S counterparts.Our proposed design strategy offers a promising prospect for construction of advanced sulfur cathodes for applications in LSBs and other energy storage systems.

Construction of highly-stable graphene hollow nanospheres and their application in supporting Pt as effective catalysts for oxygen reduction reaction

The construction and surface modification of three-dimensional(3D) graphene structures have been recognized as effective ways to prepare high-performance graphene-based composites in energy-related applications. Herein, on the basis of well-defined morphology and efficient electron conduction, the 3D highly-stable graphene hollow nanospheres have been synthesized by using sacrificial template method. The asprepared 3D graphene nanospheres exhibit superior mechanical stability, electrochemical stability, and strong hydrophobicity, which may accelerate the emission of H2O in acidic medium-based ORR. Accordingly, the 3D highly-stable graphene nanospheres are used to confine tiny Pt nanoparticles(3Dr-GO@Pt HNSs) for ORR in acidic medium, exhibiting superior activity with 4-electron-transfered pathway. Meanwhile,dramatically improved durability are achieved in terms of both ORR mass activity and electrochemically surface area compared to those of commercial Pt/C.

Effective Organochlorine Pesticides Removal from Aqueous Systems by Magnetic Nanospheres Coated with Polystyrene

In this paper, magnetic nanospheres coated with polystyrene （Fe3O4@PS） were prepared for the removal of organochlorine pesticides from aqueous solutions. The obtained Fe3O4@PS was round shape with diameter of 55±11 nm. The VSM results illustrated that its higher saturated magnetization was 36.76 emu g^-1 and it could be easily separated from aqueous solutions with a permanent magnet. The adsorption results showed that pesticides could be effectively adsorbed and the adsorption equilibrium time was less than 20 mins. The pseudo-second-order model was suitable to describe the adsorption kinetics. Compared with the Freundlich adsorption model, the adsorption data fitted well with Langmuir model. The effect of salinity and humic acid was also studied and the results illustrated that they could be neglected under optimized conditions. The asobtained sorbent showed a good performance with more than 93.3% pesticides removal in treating actual water samples.

Fabrication of Fluorescent Porphyrin/Polystyrene Composite Nanospheres by Electrospinning

Fluorescent polystyrene（PS）/porphyrin（TPPA） composite nanospheres were successfully fabricated by electrospinning. The SEM images clearly show that owing to adding TPPA in PS, the averaged diameter of the composite nanospheres became smaller, from 1500 to 580 nm. Fourier-transform infrared（FTIR） spectra determined the chemical composition of the resulting PS/TPPA composite nanospheres. The photoluminescent（PL） spectral analysis indicates that the peak position of the composite nanospheres in either solid state or water is identical to that of pure TPPA, at about 652 nm, and is still unchangeable when they are left for at least 20 d, indicating the stable photoluminescent property of the fluorescent composite nanospheres.

Integrated carbon nanospheres arrays as anode materials for boosted sodium ion storage

Developing cost-effective advanced carbon anode is critical for innovation of sodium ion batteries. Herein, we develop a powerful combined method for rational synthesis of free-standing binder-free carbon nanospheres arrays via chemical bath plus hydrothermal process. Impressively,carbon spheres with diameters of 150-250 nm are randomly interconnected with each other forming highly porous arrays. Positive advantages including large porosity, high surface and strong mechanical stability are combined in the carbon nanospheres arrays. The obtained carbon nanospheres arrays are tested as anode material for sodium ion batteries(SIBs) and deliver a high reversible capacity of 102 mAh g^(-1) and keep a capacity retention of 95% after 100 cycles at a current density of 0.25 A g^(-1) and good rate performance(65 mAh g^(-1) at a high current density of 2 A g^(-1)). The good electrochemical performance is attributed to the stable porous nanosphere structure with fast ion/electron transfer characteristics.

Pyraclostrobin-loaded poly(lactic-co-glycolic acid) nanospheres: Preparation and characteristics

We used poly(lactic-co-glycolic acid)(PLGA) as a carrier polymer for pyraclostrobin-loaded nanospheres. Using the ultrasound emulsification-solvent evaporation method, the physicochemical characteristics and release properties of the pyraclostrobin-loaded nanospheres were studied by dialysis. The optimal nanospheres prepared had a diameter of 0.6 μm, an active ingredient loading of 17.2%, and a loading rate of 89.7%. Infrared spectroscopy data and differential scanning calorimetry revealed that pyraclostrobin was successfully embedded in the carrier PLGA, and photostability tests indicated enhanced ultraviolet resistance of pyraclostrobin-loaded PLGA nanospheres nanospheres. Release property testing indicated that smaller particles had a faster release rate. Nanospheres also had a faster release rate in slightly acidic and slightly basic environments than in a neutral condition. Agitated nanospheres had a faster release rate than immobile nanospheres. The cumulative release kinetics of pyraclostrobin-loaded nanospheres was consistent with the first order kinetic equation and the Weibull equation.

Template-free synthesis of hollow TiO2 nanospheres supported Pt for selective photocatalytic oxidation of benzyl alcohol to benzaldehyde

Heterogeneous photocatalytic system are widely applied to degrade organic pollutants or converse into high value-added chemicals. Both environmental and energy aspects should be considered to improve these chemical processes, favoring reaction conditions that involve room temperature and ambient O2 pressure. In the present work, hollow titanium dioxide nanospheres were fabricated via template-free method. The prepared samples were characterized by X-ray diffraction, N2 adsorption–desorption isotherms, transmission electron microscopy, and X-ray photoelectron spectroscopy. The photocatalytic activity was evaluated by photocatalytic oxidation of benzyl alcohol to benzaldehyde with visible light under atmospheric pressure at room temperature. The designed hollow structure(2%Pt–TiO2–5) not only exhibited a very high surface area,but also promoted photonic behavior and multiple light scattering, which as an efficient photocatalyst performed moderate conversion(about 20%) and high selectivity(> 99%) for oxidation of benzyl alcohol to benzaldehyde at room temperature with visible light in solvent of toluene.This work suggests that both hollow structure and Pt nanoparticles have great potential for execution of oxidative transformations under visible light.

Design of pyrite/carbon nanospheres as high-capacity cathode for lithium-ion batteries

Transition metal sulfides are emerging as promising electrode materials for energy storage and conversion.In this work,hierarchical FeS2/C nanospheres are synthesized through a controllable solvothermal method followed by the annealing process.Spherical FeS2 core is homogeneously coated by thin carbon shell.The hierarchical nanostructure and carbon coating can enhance electron transfer and accommodate the stress originated from the volume change as well as suppress the shuttle effect of polysulfide.Consequently,as the cathode material of lithium ion batteries(LIBs),the FeS2/C nanospheres exhibit high reversible capacity of 676 m Ahg^-1 and excellent cycling life with the capacity retention of 97.1%after100 cycles.In addition,even at the high current density of 1.8 C,a reversible capacity of 437 m Ahg^-1 is obtained for the FeS2/C nanospheres,demonstrating its great prospect for practical applications in highperformance LIBs.

Synthesis and Characterization of Core-shell Hydroxyapatite/chitosan Biocomposite Nanospheres

Novel core-shell hydroxyapatite/chitosan biocomposite nanospheres were synthesized in a multiple emulsion. The multiple emulsion was a w/o/w emulsion, made of diammonium phosphate solution as an inner aqueous phase, cyclohexane as an oil phase, and calcium nitrate solution and chitosan solution as an outer aqueous. The forming mechanism of core-shell spheres and the influence of temperature on the morphology of the nanospheres were investigated. The diameter of the resulting core-shell nanospheres was 100-200 nm and the thickness of the chitosan shell was about 10 nm. And it concluded that at different reaction temperature the morphologies of the products would be changed. The core-shell nanospheres have potential applications for the development of new biomedical materials.

A NOVEL METHOD TO PREPARE CROSSLINKED POLYETHYLENEIMINE HOLLOW NANOSPHERES

A novel method to prepare crosslinked polyethyleneimine （CPEI） hollow nanospheres was reported. Uniform silica nanospheres were used as templates, 3-aminopropyl trimethoxysilane （APS） was immobilized on the surface of silica nanospheres as couple agent. Aziridine was initiated ring-opening polymerization with the amino groups in APS to form polyethyleneimine （PEI） shell layer. 1,4-Butanediol diacrylate was utilized to crosslink PEI polymeric shell. The silica nanospheres in core were etched by hydrofluoric acid to obtain hollow CPEI nanospheres. The hollow nanospheres were characterized by X-ray photoelectron spectroscopy （XPS）, transmission electron microscopy （TEM）, and thermogravimetric analysis （TGA）.