Preparation and Characterization of Polyaniline Nanofibers by Template-free Method

In the presence of p-toluene sulfonic acid (TSA) as a dopant, polyaniline (PAni) nanofibers, (about 80^-65 nm in diameter) were successfully synthesized with a chemical template-free method. It was found that the formation probability, morphology, and diameter of the resulting PAni-TSA nanofibers were sensitive to the synthetic conditions, such as reaction temperature, the molar ratio of TSA to aniline, and the concentration of TSA in the polymerization media. The molecular structure was characterized by using the FT-IR, Raman spectra and X-ray diffraction, which shows that the main chain structure of PAni-TSA nanofibers was in agreement with that of granular PAni.

Template-free Synthesis of a Novel 3D Cage-like Nanostructured α-Fe_2O_3

Synthesis of inorganic nanostructures with specific size and well defined morphologies has attracted considerable attention due to their superior electrical, optical, magnetic, and chemical properties. Up to now, various kinds of metal oxide, sulfide, and hydrate with controlled hierarchical and complex morphologies have been successfully synthesized.

Template-Free Bipotentiostatic Deposition of Thermoelectric BixTey Nano Arrays

Monodispersed Bi-Tenano arrays are achieved via template-free bipotentiostatic deposition. The diameter and length of individual nanorod is ~80 nm and ~250 nm respectively. The electrodeposition process is demonstrated to follow a two-step mechanism: an instantaneous reductive potential is applied to form dispersive nuclei, then a reverse oxidative potential strips partial Bi atoms to prevent further cross-growth. Repeatedly, the nano arrays film is obtained eventually. The thermoelectric properties of the obtained Bi-Tenano arrays such as electrical resistance, carrier density, Seebeck coefficient and power factor are measured to be 2.438 × 10-4?Ω·m, 4.251 × 1020 cm-3, -25.892 μV·K-1, 2.750 × 10-6 W·m-1·K2, respectively.

Template-Free Hydrothermal Synthesis of β-FeOOH Nanorods and Their Catalytic Activity in the Degradation of Methyl Orange by a Photo-Fenton-Like Process

The rod-shaped form of crystalline β-FeOOH (akaganeite) was prepared by the template-free hydrothermal method with urea as the homogeneous precipitant. X-ray diffraction, field-emission scanning electron microscope and Fourier transform infrared spectrum were used to characterize the resulting products. The degradation of methyl orange (MO) was studied using the prepared nanostructure materials in a photo-Fenton-like process. MO degradation was effectively achieved by hydroxyl radicals that were generated in the heterogeneous catalysis process. Specific surface area of the prepared β-FeOOH was an important factor affecting the efficiency of MO degradation, which depended on the synthesis conditions such as the reaction temperature, the initial concentration of urea and FeCl3.6H2O as well as the n(urea)/n(Fe3+) ratio. The photodegradation efficiencies slightly decreased with the increase of initial pH in the range of 4.5 - 9.5, which indicated the prepared β-FeOOH catalyst can well overcome the drawback of a narrow pH range of homogeneous Fenton reaction. β-FeOOH catalysts loading and H2O2 concentration also play important effect on the degradation efficiency of MO. The prepared β-FeOOH showed good ability of reuse for multiple trials.

Design of Cadmium Hydroxyapatite Hierarchical Structures with Adjustable Morphology by a Template-free Hydrothermal Route

Cadmium hydroxyapatite（Cd-Hap） hierarchical structures with novel morphologies were successfully synthesized via a simple template-free and mild hydrothermal method. By properly monitoring the initial pH value of the reaction solutions, the morphology of the Cd-Hap crystals could be tuned to be bunch-like（consist of nanosized cuboids）, quasi peanut-like（consist of nanoparticles） and flower-like（consist of assembled bundles units）. On the basis of a series of contrast experiments over time, the probable growth mechanism and fabrication process of the products were proposed. The optical and photocatalytic properties of the obtained Cd-Hap hierarchical structures were firstly investigated. The results showed that pure Cd-Hap could only absorb UV light with wavelength shorter than -350 nm while hydroxyapatite supported Ag3PO4 composites showed a pronounced photocatalytic activity upon decomposition of methyl orange dye in aqueous solution under visible light irradiation. The support of hydroxyapatite can also greatly reduce the cost of expensive Ag3PO4 photocatalysts in practical applications.

Template-Free Synthesis of Aligned Polyaniline Nanorods/Tubes and Copper/Copper Hydroxide Nanowires for Application as Fillers in Polymer Nanocomposites

Aligned polyaniline nanorods were synthesized in the presence of salicylic acid. Nanorods and nanotubes were also formed in the presence of camphorsulfonic acid (CSA) and para-toluenesulfonic acid (pTSA). Electrical conductivity measurements showed that the aligned nanorods had better electrical conductivity than the non-aligned nanostructures. Nanospheres were also observed in some cases. The formation of elongated nanostructures or spheres depended on the aniline monomer to surfactant molar ratio. This method in which nanostructures are formed using soft templates is often referred to as the template-free approach. Our success motivated us to explore the feasibility of obtaining similar metallic nanostructures without the use of a template. We successfully synthesized copper and copper hydroxide nanowires. While the copper nanowires formed as a mesh, the copper hydroxide nanowires formed as winding bundles. Upon switching the order in which the reactants were added, copper hydroxide nanoribbons were formed instead of bundles. Characterization of these nanostructures was done using Scanning Electron Microscopy (SEM), Atomic Force Microscopy (AFM), Transmission Electron Microscopy (TEM), Fourier Transform Infrared Spectroscopy (FTIR) and the Four-point probe to measure electrical conductivity. Both metallic and organic nanowires that are fabricated by template-free methods are potential candidates for use as fillers in polymer nanocomposites. Polymer nanocomposites are found to be used in many advanced modern applications such as thermal interface materials in electronic devices which continue to be miniaturized, aerospace engineering where lightweight and robustness are important, sensors, medicine and catalytic activity.

Coupling WO_(3-x) dots-encapsulated metal-organic frameworks and template-free branched polymerization for dual signal-amplified electrochemiluminescence biosensing

Developing accurate and sensitive DNA methyltransferase(MTase) analysis methods is essential for early clinical diagnosis and development of antimicrobial drug targets. In this work, by coupling WO_(3-x) dotsencapsulated metal-organic frameworks(MOFs) as co-reactants and terminal deoxynucleotidyl transferase(Td T)-mediated template-free branched polymerization, a dual signal-amplified electrochemiluminescent(ECL) biosensor was constructed to detect DNA adenine methylation(Dam) MTase. The employment of WO_(3-x) dots-encapsulated MOFs(i.e., NH_(2)-UIO66@WO_(3-x) ) was not only beneficial for biomolecule conjugation because of the abundant amino groups but also led to a 7-fold enhanced ECL response due to the increased loading of WO_(3-x). Moreover, Td T-mediated template-free branched polymerization promoted the capture of ECL emitters on the electrode surface, achieving 20-fold enhanced signal amplification. The presented ECL biosensor demonstrated a low detection limit of 2.4 × 10^(-4)U/m L, and displayed high reliability for the detection of Dam MTase in both spiked human serum and E. coli cell samples, and for the screening of potential inhibitors. This study opens a new avenue for designing a dual signal amplificationbased ECL bioassay for Dam MTase and screening inhibitors in the fields of clinical diagnosis and drug development.

Template-free synthesis of hollow carbon-based nanostructures from MOFs for rechargeable battery applications

Hollow carbon-based nanostructures(HCNs)have found broad applications in various fields,particularly rechargeable batteries.However,the syntheses of HCNs usually rely on template methods,which are time-consuming,low-yield,and environmentally detrimental.Metal-organic frameworks(MOFs),constructed by organic ligands and inorganic metal nodes,have been identified as effective platforms for preparing HCNs without adding extra templates.This review summarized the recent progress in template-free synthesis of HCNs enabled by MOFs and their applications in rechargeable batteries.Different template-free strategies were introduced first with mechanistic insights into the hollowing mechanism.Then the electrochemical performances of the HCNs were discussed with highlight on the structure-function correlation.It is found that the built-in cavities and nonporous for HCNs is of critical importance to increase the storage sites for high capacity,to enhance charge and mass transport kinetics for high-rate capability,and to ensure the resilient electrode structure for stable cycling.Finally,the challenges and opportunities regarding MOFs-derived HCNs and their applications in rechargeable batteries were discussed.

Template-free preparation of non-metal(B,P,S)doped g-C_(3)N_(4)tubes with enhanced photocatalytic H_(2)O_(2)generation

Developing environmentally friendly methods to produce hydrogen peroxide(H_(2)O_(2))has received increasing attention.Photocatalysis has been proved to be a sustainable technology for H_(2)O_(2)production.Herein,the novel non-metal elements(B,P,and S)doped g-C_(3)N_(4)tubes(B-CNT,P-CNT,and S-CNT)photocatalysts were obtained via a hydrothermal synthesis followed by thermal polymerization.By adjusting the precursor,the yield of g-C_(3)N_(4)tubes(CNT)materials has been greatly improved.The as-prepared B-CNT,P-CNT,and S-CNT photocatalysts show an enhanced photocatalytic H_(2)O_(2)production with the formation rate constants values of 42.31μM min^(-1),24.95μM min^(-1),and 24.22μM min^(-1),respectively,which is higher than that of bulk CN(16.40μM min^(-1)).The doped B,P,S elements significantly enhanced the photocatalytic activity by adjusting their electronic structures and promoting the separation of electronhole carriers.The results have shown great potential for the practical application of CNT photocatalysts.

Preparation and characterization of hollow carambola-shaped silver sulfide microspheres using a microwave-assisted template-free method

A simple and convenient method, free of template, has been proposed to synthesize hollow carambolashaped Ag2 S microspheres with Ag NO3, thiourea（TU）, Na Cl and diethanolamine as reagents using a microwave-assisted method, at low temperatures of below 100 ℃. Powder X-ray diffraction（XRD）,scanning electron microscopy（FESEM） and high resolution transmission electron microscopy（HRTEM）were employed to characterize the morphology and composition of those microspheres. The results indicated that the hollow carambola-shaped silver sulfide microspheres（with high purity and homogeneous morphology） were prepared by an Ostwald ripening process. A possible formation mechanism of hollow carambola-shaped Ag2 S microspheres was proposed.

Facile Template-free Synthesis of Carbonated Hydroxyapatite Spheres in Aqueous Solution

Prickly carbonated hydroxyapatite（CHAp） spheres were obtained via a facile template-free self-assembly method with Na2HPO4 and self-made cubic CaCO3 as reactants. X-ray diffraction results of the product revealed CHAp with high crystallinity could be successfully prepared in a short reaction time. A nucleation mechanism was proposed according to the results of characterizing the resultant powders and analyzing the growth process. It shows that the self-made CaCO3 particles play an important role in the template-free synthesis of prickly spheres.

Template-Free Synthesis of Ordered Mesoporous NiO/Poly (Sodium-4-Styrene Sulfonate) Functionalized Carbon Nanotubes Composite for Electrochemical Capacitors

We report the first example of a practical and efficient template-free strategy for synthesizing ordered mesoporous NiO/poly(sodium-4-styrene sulfonate)(PSS)functionalized carbon nanotubes(FCNTs)composites by calcining a Ni(OH)_(2)/FCNTs precursor prepared by refl uxing an alkaline solution of Ni(NH_(3))x^(2)+and FCNTs at 97 oC for 1 h.The morphology and structure were characterized by X-ray diffraction,scanning electron microscopy,and transmission electron microscopy.Thermal decomposition of the precursor results in the formation of ordered mesoporous NiO/FCNTs composite(ca.48 wt%NiO)with large specifi c surface area.Due to its enhanced electronic conductivity and hierarchical(meso-and macro-)porosity,composite simultaneously meets the three requirements for energy storage in electrochemical capacitors at high rate,namely,good electron conductivity,highly accessibleelectrochemical surface areas owing to the existence of mesopores,and efficient mass transport from the macropores.Electrochemical data demonstrated that the ordered mesoporous NiO/FCNTs composite is capable of delivering a specifi c capacitance(SC)of 526 F/g at 1 A/g and a SC of 439 F/g even at 6 A/g,and show a degradation of only ca.6%in SC after 2000 continuous charge/discharge cycles.

Template-free synthesis and characterization of K-phillipsite for use in potassium extraction from seawater

Kbphillipsite was prepared using a hydrothermal method. Soluble glass and sodium aluminate were used as raw materials in the absence of an organic template. Investigations regarding the K＋ ions were con- ducted at room temperature to determine the ion-exchange capacity in the seawater sample and the selectivity coefficient of the mixed K＋-Na~ solution. The sample was characterized by X-ray diffraction （XRD）, scanning electron microscopy （SEM）, and energy dispersion spectroscopy （EDS）. The K＋ ion- exchange capacity is 51 mg/g in seawater and the selectivity coefficient is 75.1 in the mixed K＋-Na＋ solution. The sample has a selectivity preference for K＋, and therefore can be used to selectively extract potassium from seawater. The sample composed of Si, Al, K, Na, and O exhibits a cross-like shape and is a typical K-phillipsite structure.

Simplification of Template-free Method to Prepare Polyaniline Nanotubes

1 Introduction Conducting polymer nanostructures (e.g.nanotubes or nanofibers) have received considerable attention owing their unique properties and promising applications in technology and nano-devices[1]. Conducting polymer nanostructures can be generally synthesized through "hard" and "soft" template method.Usually an external hard template in a "hard-template" method is required and the post-treatment of removing template is rather tedious."Soft-template" method is advantageous of omitting external...

Facile synthesis of hierarchical NaX zeolite from natural kaolinite for efficient Knoevenagel condensation

Zeolite catalysts have found extensive applications in the synthesis of various fine chemicals.However,the micropores of zeolites impose diffusion limitations on bulky molecules,greatly reducing the catalytic efficiency.Herein,we explore an economic and environmentally friendly method for synthesizing hierarchical NaX zeolite that exhibits improved catalytic performance in the Knoevenagel condensation reaction for producing the useful fine chemical 2-cyano-3-phenylacrylate.The synthesis was achieved via a low-temperature activation of kaolinite and subsequent in-situ transformation strategy without any template or seed.Systematic characterizations reveal that the synthesized NaX zeolite has both intercrystalline and intra-crystalline mesopores,smaller crystal size,and larger external specific surface area compared to commercial NaX zeolite.Detailed mechanism investigations show that the inter-crystalline mesopores are generated by stacking smaller crystals formed from in-situ crystallization of the depolymerized kaolinite,and the intra-crystalline mesopores are inherited from the pores in the depolymerized kaolinite.This synthesis strategy provides an energy-saving and effective way to construct hierarchical zeolites,which may gain wide applications in fine chemical manufacturing.

Two dimensional nanocarbons from biomass and biological molecules:Synthetic strategies and energy related applications

Two-dimensional(2D)carbon materials with ultrathin thickness,large lateral size,large surface area,accessible active sites and unique physical-chemical properties have been proven to be attractive electrode materials or catalysts for high-efficient energy storage and conversion materials.However,the conventional synthesis method for 2D carbon materials heavily depends on fossil-based feedstocks and goes through harsh conditions(e.g.,chemical vapor deposition),which are unsustainable and costly.Besides,the top-down method needs to use massive strong acids/oxidants,which is environmentallyunfriendly.Therefore,it is necessary to commit to seek green,sustainable and cost-effective approach for the synthesis of 2D carbon materials.As of now,biomass or biological molecules as carbon-rich resources have been viewed as a promising candidate for the 2D carbon material preparation owing to its abundance,renewability,nontoxicity and low-cost.Especially for nucleobases,as an emerging molecule have been shown great advantages for the construction of 2D materials guided by its multiple hydrogen-bonding interaction.Recently,our group have proposed a rather innovative strategy to produce 2D carbon materials by carbonization of nucleobases which has relatively high electrode potentials.These nucleobases can form planar network structure through hydrogen bonding interaction.Such hydrogenbonding can be stable at relatively high temperature,which confines C-C or C-N polymerization in a 2D plane.As a result,direct carbonization of nucleobases enables the formation of 2D carbon with highly sp2-conjugated and feature of heteroatom doping.This review systematically summarizes the recent development of the strategies to synthesize 2D sustainable carbon materials from biomass and biological molecules.The corresponding electrochemical applications such as lithium ion batteries,supercapacitors and fuel cell are selectively presented.At the end,the summary and future perspectives in this important field are provided to inspire further exploration.

Synthesis of ZSM-5 zeolite membranes without organic templates using a varying-concentration technique

Template-free nanosized ZSM-5 seeds with an average size of 15 nm were prepared from a synthesis solution with the composition 12Na2O∶100SiO2∶2Al2O3∶2500H2O. By the use of these seeds, thin ZSM-5 zeolite membranes were prepared on the outer surface of a porous α-alumina tube with a pore size of 2 μm in a gel system by varying-concentration synthesis with organic-free template. The first composition synthesis sol-gel was the same as seeds of molar composition and the second one was 12Na2O∶100SiO2∶2Al2O3∶5000H2O at 180 ℃ for 10 h, respectively. XRD shows that the film consists of well-crystallized ZSM-5 zeolite. SEM investigation indicats that the zeolite films on the supports are defect free and the film thickness is approximately 8 μm. The permeances for H2, N2, CH4 and CO2 are 8.94×10-7, 3.27×10-7, 3.9×10-7, 3.14×10-7 and 0.874×10-7 mol·m2·s-1·Pa-1, respectively. The ideal selectivity of membrane at room temperature for H2/CO2, H2/N2, H2/CH4 are 2.84, 2.73 and 2.29, respectively.

Environmentally benign synthesis of crystalline nanosized molecular sieves

Zeolites and zeo-type materials with nanosized dimensions are of great practical interest owing to their favorable transport properties,faster adsorption kinetics,and large external surface area.This mini-review presents recent developments in the organic template-free synthesis of nanosized zeolites and related materials.The advantages and challenges of these methods are addressed with particular attention to the green synthesis of nanozeolites.

Self-assembled Synthesis of Porous TiO_2 Film on the Electrophoretic-deposited Titanate Nanoribbon Film

The porous TiOz film was self-assembled on the surface of electrophoretic-deposited titanate nanoribbon film without the addition of templates by using TiF4 as the precursor. It was found that the hydrolysis of TiF4 was accompanied with the self-assembly processes of TiO2 nanoparticles on the surface of electrophoretic-deposited titanate nanoribbon film, resulting in the formation of porous TiO2 structures. Titanate nanoribbon film was demonstrated to provide the active sites for the effective self-assembly of porous TiO2 nanostructures owing to a large amount of hydroxyl groups. Compared with the nonporous TiO2 film, the prepared porous TiO2 films obviously showed an enhanced photocatalytic activity, which could be attributed to the rapider diffusion and more efficient transport of various reactants and products during photocatalytic reaction in the t^orous structures.

Polydopamine Modified Biomimetic Gold Nanoparticles for Dual Photothermal Therapy

Our study producted Polydopamine modified gold nanoflowers with controlled morphology for anti-tumor photothermal therapy.The branch structure containsabundant(Au NFs).By adjusting the reduction rate,the dosage of reducing agent(sodium borohydride)and the reduction temperature,we can adjust tthe morphology and particle size of Au NFs.We found that the lower reaction temperature is,the more abundant the surface branching structure of gold nanoflowers is,by adjusting the reaction temperature.and the largest specific surface area of golden nanopowder was found at 0℃.The results of TEM indicated that with the increase of sodium borohydride,the diameter of gold nano flowers gold nanoflowers decreased and was in the range of 60~100nm,and it has good EPR effect After that,we modify poly(dopamine)(PDA)biomimetic layer on the surface of golden nanoparticles to obtain Au NFS@PDA.Poly(dopamine)has the ability,of photothermal conversion,which can enhance the plasma resonance ability and biocompatibility of gold nanoflowers in the near infrared region.We can control the thickness of polydopamine layer on the surface of gold nanoflowers between 7~15nm by adjusting dopamine DA concentrationgold nanoflowers.Au NFS@PDA was characterized by its morphology and physical properties.We detect(UV-Vis)spectra in the near infrared region.And it showed obvious absorption peaks in the near infrared region of 575~650nm.Under the 808nm irradiation laser,the photothermal conversion of gold nanoflowers and polydopamine can be rapidly increased to 57°C.Fourier Transform Infrared Absorption Spectroscopy(FTIR)and X-ray Diffraction(XRD)analysis showed that polydopamine was modified successfully,Au NFS@PDA and Au NFs had no obvious difference in crystal form.The cell viability test showed that the bionic Au NFS@PDA had good biocompatibility and showed good antitumor activity against HeLa cells under NIR irradiation.The cell viability was only 12%.Therefore,we can use Au NFS@PDA with good biocompatibility as a promising photothermal conversion agent in tumor therapy.