Search

Controlling the morphology and magnetic properties of CoFe2O4 nanoparticles is crucial for the synthesis of compatible materials for different applications. CoFe2O4 nanoparticles were synthesized by a solvothermal method using cobalt nitrate, iron nitrate as precursors, and oleic acid as a surfactant. The formation of CoFe2O4 nanoparticles was systematically observed by adjusting synthesis process conditions including reaction temperature, reaction time, and oleic acid concentration. Nearly spherical, monodispersed CoFe2O4 nanoparticles were formed by changing the reaction time and reaction temperature. The oleic acid-coated CoFe2O4 nanoparticles inhibited the growth of particle size after 1 h and, therefore, the particle size of CoFe2O4 nanoparticles did not change significantly as the reaction time increased. Both without and with low oleic acid concentration, the large-sized cubic CoFe2O4 nanoparticles showing ferromagnetic behavior were synthesized, while the small-sized CoFe2O4 nanoparticles with superparamagnetic properties were obtained for the oleic acid concentration higher than 0.1 M. This study will become a basis for further research in the future to prepare the high-functional CoFe2O4 magnetic nanoparticles by a solvothermal process, which can be applied to bio-separation, biosensors, drug delivery, magnetic hyperthermia, etc.

This review provides a comprehensive overview of the recent advances in the various typical spinel ferrite-based thin films with controlled synthesis, their performances, applications in multifunctional material fields, fundamental scientific challenges, and beyond. Firstly, the crystal structures of spinel ferrite-based thin films are introduced. Secondly, recent progress in traditional synthesizing and novel methods for preparation of spinel ferrite-based films are highlighted. Thirdly, their magnetism, electricity, optics performances, and applications in advanced information technology, energy storage and conversion, and environmental conservation fields are also summarized and discussed in-depth. Some effective strategies for optimizing performances and further applications are summarized. Finally, the present review work ends with a short discussion concerning the challenges, opportunities, and future prospects of spinel ferrite-based thin films.

Since the very recent discovery of ferroic ordering under two dimensional limit, novel devices based on 2D ferroelectricity or ferromagnetism has attracted a lot of interests and are promising for next generation electronic and optoelectronic applications. We find that, below the transition temperature Tc ~320 K, ultrathin CuInP2S6 (CIPS) nanoflakes down to bilayer are still pyroelectric. Changing the temperature will lead to charge modification at the surface of CIPS. 2D pyroelectric nanogenerator is fabricated which can efficiently convert the pyroelectric charges into electrical current. This work will facilitate novel applications of pyroelectric and ferroelectric materials, including pyroelectric devices, thermal sensors, ultrathin nanogenerators and various van der Waals (vdW) heterostructure at room temperature. Ministry of Education (MOE) National Research Foundation (NRF) Accepted version This work was supported by the National Research Foundation Singapore under NRF award number NRF-RF2013-08, Tier 2 MOE2017-T2-2-136, Tier 2 MOE2016-T2-2-153, MOE2015-T2-2-007, Tier 1 RG7/18, Tier 1 RG4/17. X.F.L thanks the support from the Ministry of Science and Technology (2017YFA0205004 and 2016YFA0200700), National Natural Science Foundation of China (21673054 and 11874130), Natural Science Foundation of Beijing Municipality (4182076 and 4184109).

In this paper, we propose for the first time the synthesis of α-MoO3 nanorods in a one-step procedure at mild temperatures. By changing the growth parameters, the microstructure and controllable morphology of the resulting products can be customized. The average diameter of the as-prepared nanorods is about 200 nm. The electrochromic and capacitance properties of the synthesized products were studied. The results show that the electrochromic properties of α-MoO3 nanorods at 550 nm have 67% high transmission contrast, good cycle stability and fast response time. The MoO3 nanorods also exhibit a stable supercapacitor performance with 98.5% capacitance retention after 10,000 cycles. Although current density varies sequentially, the nanostructure always exhibits a stable capacitor to maintain 100%. These results indicate the as-prepared MoO3 nanorods may be good candidates for applications in electrochromic devices and supercapacitors.

Controlled synthesis of hollow polymeric nanocapsules has attracted significant attention in a wide range of applications. This paper reports a facile method for the synthesis of hybrid starch nanocapsules decorated with silver nanoparticles using the inverse miniemulsion polyaddition technique. Silver nanoparticles are formed and embedded in the shell of the nanocapsules during the polyaddition process without using any additional reducing agents. We found that silver also acts as a lipophobe that builds up osmotic pressure in the droplets facilitating the formation of stable round shaped nanocapsules. The nanocapsules' shell thickness could be tuned from 13 to 29 nm by varying the amount of cross-linker. We investigated the minimum inhibitory concentration (MIC) of the nanocapsules against Staphylococcus epidermidis ATCC 35984 and Escherichia coli ATCC 25922 which are two bacteria of medical relevance. The silver nanoparticle decorated nanocapsules showed antibacterial properties against both bacteria at the MIC of 2.315 mu g mL(-1) while control nanocapsules without silver had no antibacterial activity. Refereed/Peer-reviewed

Zinc oxide (ZnO) nanoparticles have gained widespread interest due to their unique properties, making them suitable for a range of applications. Several methods for their production are available, and of these, controlled synthesis techniques are particularly favourable. Large-scale culturing of Chlorella vulgaris produces secretory carbohydrates as a waste product, which have been shown to play an important role in directing the particle size and morphology of nanoparticles. In this investigation, ZnO nanorods were produced through a controlled synthesis approach using secretory carbohydrates from C. vulgaris, which presents a cost-effective and sustainable alternative to the existing techniques. Fourier transform infrared (FTIR) spectroscopy, X-ray powder diffraction (XRD) analysis, transmission electron microscopy (TEM), and UV-Vis spectroscopy were used to characterise the nanorods. The prepared nanorods exhibited a broad range of UV absorption, which suggests that the particles are a promising broadband sun blocker and are likely to be effective for the fabrication of sunscreens with protection against both UVB (290&ndash, 320 nm) and UVA (320&ndash, 400 nm) radiations. The antimicrobial activity of the prepared nanorods against Gram-positive and Gram-negative bacteria was also assessed. The nanostructures had a crystalline structure and rod-like appearance, with an average length and width of 150 nm and 21 nm, respectively. The nanorods also demonstrated notable antibacterial activity, and 250 &mu, g/mL was determined to be the most effective concentration. The antibacterial properties of the ZnO nanorods suggest its suitability for a range of antimicrobial uses, such as in the food industry and for various biomedical applications.

Listeria monocytogenes (L. monocytogenes) has been recognized as one of the extremely hazardous and potentially life-threatening food-borne pathogens, its real-time monitoring is of great importance to human health. Herein, a simple and effective method based on platinum sensitized tin dioxide semiconductor gas sensors has been proposed for selective and rapid detection of L. monocytogenes. Pt doped SnO2 nanospheres with particular mesoporous hollow structure have been synthesized successfully through a robust and template-free approach and used for the detection of 3-hydroxy-2-butanone biomarker of L. monocytogenes. The steady crystal structure, unique micromorphology, good monodispersit, and large specific surface area of the obtained materials have been confirmed by X-ray diffraction (XRD), Raman spectroscopy, Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM), X-ray Photoelectron Spectroscopy (XPS), Brunauer-Emmett-Teller (BET), and Photoluminescence spectra (PL). Pt doped SnO2 mesoporous hollow nanosphere sensors reach the maximum response of 3-hydroxy-2-butanone at 250°C. Remarkably, sensors based on SnO2 mesoporous hollow nanospheres with 0.16 wt% Pt dopant exhibit excellent sensitivity (Rair/Rgas = 48.69) and short response/recovery time (11/20 s, respectively) to 10 ppm 3-hydroxy-2-butanone at the optimum working temperature. Moreover, 0.16 wt% Pt doped SnO2 gas sensors also present particularly low limit of detection (LOD = 0.5 ppm), superb long-term stability and prominent selectivity to 3-hydroxy-2-butanone. Such a gas sensor with high sensing performance foresees its tremendous application prospects for accurate and efficient detection of foodborne pathogens for the food security and public health.

Organolead halide perovskites (e.g., CH3NH3PbI3) have caught tremendous attention for their excellent optoelectronic properties and applications, especially as the active material for solar cells. Perovskite crystal quality and dimension is crucial for the fabrication of high-performance optoelectronic and photovoltaic devices. Herein the controlled synthesis of organolead halide perovskite CH3NH3PbI3 nanoplatelets on SiO2/Si substrates is investigated via a convenient two-step vapor transport deposition technique. The thickness and size of the perovskite can be well-controlled from few-layers to hundred nanometers by altering the synthesis time and temperature. Raman characterizations reveal that the evolutions of Raman peaks are sensitive to the thickness. Furthermore, from the time-resolved photoluminescence measurements, the best optoelectronic performance of the perovskite platelet is attributed with thickness of ≈30 nm to its dominant longest lifetime (≈4.5 ns) of perovskite excitons, which means lower surface traps or defects. This work supplies an alternative to the synthesis of high-quality organic perovskite and their possible optoelectronic applications with the most suitable materials. Accepted version

Pt nanoparticles (Pt NPs) supported on carbon have been widely employed as electrocatalysts toward oxygen reduction reaction. The development of more efficient electrocatalysts that enable one to reduce or even not require the use of Pt is a central challenge. In addition to the control over the physical and chemical features of Pt NPs, metal support interactions can be employed to enhance activities via the generation and exposure of surface-active sites. In this context, we report herein the development of electrocatalysts composed of Pt NPs supported on TiO2 microspheres, that were subsequently impregnated onto carbon. We have found that, by optimizing the loading of Pt at the TiO2 surface, the electrocatalytic activity toward the ORR could be improved compared to that of the commercial Pt/C (E-TEK) material, even at lower Pt loadings. The enhancement in activities could be assigned to the balance between Pt loading and generation of reactive surface sites, such as adsorbed oxygenated species. Moreover, the utilization of TiO2 as support enabled improved stabilities relative to Pt/C (E-TEK). We believe that the results described herein may inspire the development of electrocatalysts for the ORR with improved activities and stabilities.

The present review focuses on the proteins and peptides at the interfaces of nanostructured metals and semiconductors as a result of their use in synthesis in-situ and functionalization of nanostructures. We start the review with an introduction about the peculiar properties of nanostructured materials and their applications. In the following, the chemical and structural properties of peptides and proteins that allow their use as reducing, stabilizing, and functionalization agents are discussed. P roteins and peptides have not only the chemical groups for the metal ion reducing but also provide templates for directing the crystalline growing of nanostructures to the desired shapes and sizes. Proteins and peptides are also used mainly for the stabilization and functionalization of a diversity of nanostructured materials providing properties such as biocompatibility, plasmon-enhanced catalysis, sensing, micro/nanomotors, spin filters, and others. Nanostructured materials of metal oxides have mainly been functionalized with proteins and peptides to gain specific properties such as light harvesting and spin filters. Herein, we described the synthesis and functionalization of some types of nanostructured materials by using peptides and proteins. In the last part of the review, it is discussed the perspectives and challenges for the use of proteins and peptides in Nanotechnology.

Most methods controlling size and shape of metal nanoparticles are chemical methods, and little work has been done using only plasma methods. Size- and shape-controlled synthesis of silver nanoparticles (Ag NPs) is proposed based on adjusting the gas bubble formation produced between two silver electrodes. The application of a voltage waveform with three different pulse widths during a plasma process in water can generate different gas bubble formations. Transmission electron microscopy (TEM) and scanning electron microscopy (SEM) images of Ag NPs synthesized using three different bubble formations reveal that spherical Ag NPs are synthesized when very tiny bubbles are generated between two electrodes or when only the grounded electrode is enveloped with large gas bubbles, but Ag nanoplates are synthesized when both electrodes are completely enveloped with large gas bubbles.

Magnetic nanoparticles provide a unique nanosystem for various smart therapy applications because of their biocompatibility, their nanostructures which can be prepared controllably to match with the interest of study and, specifically, their responses to an external magnetic field. Interests in utilizing magnetic nanoparticles for biomedical treatments originate from their external controllability of transportation and movement inside biological objects and magnetic heat generation which provide tremendous advantages for targeted drug delivery and controlled drug release as well as magnetic hyperthermia. Recent progress in synthesis and functionalization has led to the formation of various functional magnetic nanoparticles with controlled magnetic properties based on controlling their particle size, shape and composition. In this review, we focus on the synthesis, protection and functionalization of iron oxide-based magnetic nanoparticles in order to control magnetic properties of nanostructured systems. We also highlight the recent advances in the development of multifunctional therapeutic nanosystems combining magnetic nanoparticles and drugs as well as their superior efficacy in biomedical treatments with smart performance by including therapy and modulated drug delivery and release through magnetic heating.

Lack of control on the chirality or diameter of single-wall carbon nanotubes (SWCNTs) during synthesisis a major impediment in the path of their widespread commercialization. We demonstrate that the humble technique of catalytic chemical vapor deposition of methane, without any sophisticated catalyst preparation, can provide significant control on the diameter of the synthesized SWCNTs. The catalyst used is a solid solution of the bimetals Fe-Mo or Co-Mo in MgO. The radial breathing modes (RBMs) in the Raman spectra of SWCNTs were used to find out the diameters. Kataura plot along with RBMs was used to study the chirality of the tubes. High concentration of the catalysts (Co: Mo: MgO = 1:0.5: 15 and Fe: Mo: MgO = 1: 0.5: 30) resulted in high yields. However, most of these carbonaceous materials were impurities. Reducing the concentration not only improved the purity and crystallinity (I-D/I-G ratio similar to 0.1), but most importantly reduced the diameter spread of the SWCNTs. Majority of the SWCNTs grown using the low concentration catalysts (Co: Mo: MgO = 1: 0.5: 300 and Fe: Mo: MgO = 1: 0.5: 200) were estimated to have diameters lying between 1.13 and 1.65 nm. This narrowing of diameter spread happened for both Fe and Co catalyst systems and depended only on the concentration of the catalyst. (C) 2014 Elsevier B.V. All rights reserved.

Controlled synthesis of CuO nanoparticles with various morphologies were achieved by a wet chemical method by the reduction of copper acetate with NaOH. Influence of surfactant, alkaline concentration and solvent medium on the morphology of nanoparticles was investigated. Our studies reveal that these parameters alter the aggregation-growth processes and hence the morphology. Sodium dodecyl sulphate (SDS) as a structure-guiding agent has a strong impact on the morphology of nanostructure. By adjusting the rate of hydrolysis, two dimensional netted structures consisting of bundles of nanorods were obtained, formed by oriented attachment mechanism. Moreover, well defined and dispersed CuO nanoparticles were produced by manipulating the solvent medium. Optical properties were studied using UV-Vis absorption and Raman spectroscopy. Morphology and size of nanoparticles have a profound effect on the nature of multi-phonon band observed in the Raman spectra of CuO nanostructures. � 2014 Elsevier B.V. All rights reserved.

Printable electronics and the increased use of nanoparticle products (e.g. quantum dots) has resulted in the rapid development of nanoparticle inks. Microfl uidic reactors ‐ or microreactors ‐ show promise to provide advanced control over size, size distribution and shape for commercial-scale synthesis of nanoparticles. Compared to batch-wise synthesis techniques primarily in use today, microfl uidic technology can provide better control of the reaction conditions, which is the key to controlling the product characteristics. [ 1 ] Handling small volumes of liquid allows better control of mixing, and hence yields more uniform chemical composition. For thermally activated syntheses, reagents can be heated and cooled rapidly and uniformly, avoiding the large thermal gradients typically found throughout the reaction volume in batch techniques. Several high-temperature microreactors for synthesizing nanoparticles have been described in the literature. [ 2 ] Almost all microreactors described to date have a

Van der Waals (vdW) solids, as a new type of artificial materials that consist of alternating layers bonded by weak interactions, have shed light on fascinating optoelectronic device concepts. As a result, a large variety of vdW devices have been engineered via layer-by-layer stacking of two-dimensional materials, although shadowed by the difficulties of fabrication. Alternatively, direct growth of vdW solids has proven as a scalable and swift way, highlighted by the successful synthesis of graphene/h-BN and transition metal dichalcogenides (TMDs) vertical heterostructures from controlled vapor deposition. Here, we realize high-quality organic and inorganic vdW solids, using methylammonium lead halide (CH3NH3PbI3) as the organic part (organic perovskite) and 2D inorganic monolayers as counterparts. By stacking on various 2D monolayers, the vdW solids behave dramatically different in light emission. Our studies demonstrate that h-BN monolayer is a great complement to organic perovskite for preserving its original optical properties. As a result, organic/h-BN vdW solid arrays are patterned for red light emitting. This work paves the way for designing unprecedented vdW solids with great potential for a wide spectrum of applications in optoelectronics.

In the present research, large iron oxide microparticles with large sizes in the range of 1–5 μm have been facilely synthesized by a modified polyol method with NaBH4 as a versatile strong reducing agent. We found that the highly homogeneous iron oxide microparticles' novel structure is the best pure crystal phase of α-Fe2O3 in terms of polyhedral morphology and shape in existence. There are no diffraction peaks of other crystal phases from impurities in α-Fe2O3 microparticle products in the crystal growth. Interestingly, a new method of heat treatment or atomic surface deformation allowed for the discovery of a new large α-Fe2O3 structure with controlled specific α-Fe2O3 oxide grains in the crystal structure. The severe surface deformation of sharp, polyhedral, large α-Fe2O3 microparticles under a sintering treatment was found to give un-sharp, polyhedral large α-Fe2O3 microparticles with specific grains and boundaries.

We present our results obtained in the Rh-catalyzed carbene copolymerization of diazomethane and diazoesters as a new approach to functional polymer synthesis. Copolymerization reactions were successful, and high-Mw ethylene-acrylate type copolymers were obtained with a large variation in functional group content, which proved to be tunable by varying the monomer feed ratio and the way of addition. Polymer yields decrease strongly with increasing incorporation of diazomethane due to rapid β-hydride elimination. Sequential insertions of polar monomers were observed to a large extent, giving rise to copolymers with a blocky microstructure, which is a unique feature of this polymerization technique. The copolymer properties are demonstrated to be highly dependent on the functional group content and can therefore easily be varied in the window between the properties of both homopolymers.