Yunchen Du

The electromagnetic property of chemically reduced graphene oxide and its application as microwave absorbing material

The residual defects and groups in chemically reduced graphene oxide cannot only improve the impedance match characteristic and prompt energy transition from contiguous states to Fermi level, but also introduce defect polarization relaxation and groups’ electronic dipole relaxation, which are all in favor of electromagnetic wave penetration and absorption. The chemically reduced graphene oxide shows enhanced microwave absorption compared with graphite and carbon nanotubes, and can be expected to display better absorption than high quality graphene, exhibiting a promising prospect as microwave absorbing material.

Shell Thickness-Dependent Microwave Absorption of Core–Shell Fe3O4@C Composites

Core-shell composites, Fe3O4@C, with 500 nm Fe3O4 microspheres as cores have been successfully prepared through in situ polymerization of phenolic resin on the Fe3O4 surface and subsequent high-temperature carbonization. The thickness of carbon shell, from 20 to 70 nm, can be well controlled by modulating the weight ratio of resorcinol and Fe3O4 microspheres. Carbothermic reduction has not been triggered at present conditions, thus the crystalline phase and magnetic property of Fe3O4 micropsheres can be well preserved during the carbonization process. Although carbon shells display amorphous nature, Raman spectra reveal that the presence of Fe3O4 micropsheres can promote their graphitization degree to a certain extent. Coating Fe3O4 microspheres with carbon shells will not only increase the complex permittivity but also improve characteristic impedance, leading to multiple relaxation processes in these composites, thus the microwave absorption properties of these composites are greatly enhanced. Very interestingly, a critical thickness of carbon shells leads to an unusual dielectric behavior of the core-shell structure, which endows these composites with strong reflection loss, especially in the high frequency range. By considering good chemical homogeneity and microwave absorption, we believe the as-fabricated Fe3O4@C composites can be promising candidates as highly effective microwave absorbers.

Metal organic framework-derived Fe/C nanocubes toward efficient microwave absorption

Composites of magnetic metal nanoparticles and carbon materials are highly desirable for high-performance microwave absorbers due to their compatible dielectric loss and magnetic loss abilities. In this article, novel nanocomposites, Fe/C nanocubes, have been successfully prepared through an in situ route from a metal–organic framework, Prussian blue, by controlled high-temperature pyrolysis. The resultant nanocubes are actually composed of a cubic framework of amorphous carbon and uniformly dispersed core–shell Fe@graphitic carbon nanoparticles. Within the studied pyrolysis temperature range (600–700 °C), the porous structure, iron content, magnetic properties, and graphitization degree of the Fe/C nanocubes can be well modulated. Particularly, the improved carbon graphitization degree, both in amorphous frameworks and graphitic shells, results in enhanced complex permittivity and dielectric loss properties. The homogeneous chemical composition and microstructure stimulate the formation of multiple dielectric resonances by regularizing various polarizations. The synergistic effect of dielectric loss, magnetic loss, matched impedance, and dielectric resonances accounts for the improved microwave absorption properties of the Fe/C nanocubes. The absorption bands of the optimum one obtained at 650 °C are superior to most composites ever reported. By considering the good chemical homogeneity and microwave absorption, we believe that the as-fabricated Fe/C nanocubes will be promising candidates as highly effective microwave absorbers.

Constructing Uniform Core–Shell PPy@PANI Composites with Tunable Shell Thickness toward Enhancement in Microwave Absorption

Highly uniform core-shell composites, polypyrrole@polyaniline (PPy@PANI), have been successfully constructed by directing the polymerization of aniline on the surface of PPy microspheres. The thickness of PANI shells, from 30 to 120 nm, can be well controlled by modulating the weight ratio of aniline and PPy microspheres. PPy microspheres with abundant carbonyl groups have very strong affinity to the conjugated chains of PANI, which is responsible for the spontaneous formation of uniform core-shell microstructures. However, the strong affinity between PPy microspheres and PANI shells does not promote the diffusion or reassembly of two kinds of conjugated chains. Coating PPy microspheres with PANI shells increases the complex permittivity and creates the mechanism of interfacial polarization, where the latter plays an important role in increasing the dielectric loss of PPy@PANI composites. With a proper thickness of PANI shells, the moderate dielectric loss will produce well matched characteristic impedance, so that the microwave absorption properties of these composites can be greatly enhanced. Although PPy@PANI composites herein consume the incident electromagnetic wave by absolute dielectric loss, their performances are still superior or comparable to most PANI-based composites ever reported, indicating that they can be taken as a new kind of promising lightweight microwave absorbers. More importantly, microwave absorption of PPy@PANI composites can be simply modulated not only by the thickness of the absorbers, but also the shell thickness to satisfy the applications in different frequency bands.

Highly Sensitive Surface-Enhanced Raman Spectroscopy (SERS) Platforms Based on Silver Nanostructures Fabricated on Polyaniline Membrane Surfaces

Here, we demonstrate a facile synthesis of homogeneous Ag nanostructures fully covering the polyaniline (PANI) membrane surface simply by introducing organic acid in the AgNO(3) reaction solution, as an improved technique to fabricate well-defined Ag nanostructures on PANI substrates through a direct chemical deposition method [Langmuir2010, 26, 8882]. It is found that the chemical nature of the acid is crucial to create a homogeneous nucleation environment for Ag growth, where, in this case, homogeneous Ag nanostructures that are assembled by Ag nanosheets are produced with the assistance of succinic acid and lactic acid, but only scattered Ag particles with camphorsulfonic acid. Improved surface wettability of PANI membranes after acid doping may also account for the higher surface coverage of Ag nanostructures. The Ag nanostructures fully covering the PANI surface are extremely sensitive in the detection of a target analyte, 4-mercaptobenzoic acid (4-MBA), using surface-enhanced Raman spectroscopy (SERS), with a detection limit of 10(-12) M. We believe the facilely fabricated SERS-active substrates based on conducting polymer-mediated growth of Ag nanostructures can be promising in the trace detection of chemical and biological molecules.

Magnetic CoFe2O4 nanoparticles supported on titanate nanotubes (CoFe2O4/TNTs) as a novel heterogeneous catalyst for peroxymonosulfate activation and degradation of organic pollutants

Magnetic spinel ferrites, as heterogeneous catalysts to generate powerful radicals from peroxymonosulfate (PMS) for the degradation of organic pollutants, have received much attention in recent years due to the characteristic of environmental benefits. In this study, with titanate nanotubes (TNTs) as catalyst support, a novel CoFe2O4/TNTs hybrid was constructed by an impregnation-calcination method. Characterization results revealed that TNTs support could promise small size and good dispersion of CoFe2O4 nanoparticles. Compared to the pure CoFe2O4, the as-prepared CoFe2O4/TNTs not only exhibited better performance in catalytic decomposition of Rhodamine B, but also realized higher total organic carbon removal and less cobalt leaching, which could be attributed to the enhanced catalytic ability from smaller CoFe2O4 nanoparticles and the unique ion-exchange ability from TNTs support. Some influential factors, including reaction temperature, dosages of PMS and CoFe2O4/TNTs, and pH values were investigated and analyzed. Moreover, CoFe2O4/TNTs maintained its catalytic efficiency during the repeated batch experiments and also displayed functional advantages in the catalytic degradation of phenol. We believe the CoFe2O4/TNTs hybrid can be an efficient and green heterogeneous catalyst for the degradation of organic pollutants, and this study provides insights into the rational design and development of alternative catalysts for wastewater treatment.

Synthesis and characterization of polyaniline nanoparticles with enhanced microwave absorption

A series of polyaniline (PANI) materials have been prepared by a reverse dropping method with the assistance of polyvinylpyrrolidone (PVP). It can be found that PVP and the dropping rate play critical roles in determining the morphology evolution of PANI, and the restriction of PVP is highly dependent on the dropping rate. Well dispersed PANI nanoparticles can only be obtained under moderate conditions. Thanks to the unique preparative process, these samples show significant changes in the length and oxidation state of conjugated chains, as proved by the results of UV/vis absorption spectra and FT-IR spectra, which result in their distinguishable conductivity and microwave absorption. Very interestingly, PANI nanoparticles exhibit substantially enhanced microwave absorption properties. In particular the optimum one, PANI-NP2, presents very strong reflection loss (−40.5 dB at 5.8 GHz) and wide response bandwidth (3.2–18 GHz over −10 dB), which are indeed comparable to those composites of PANI with various magnetic particles, implying promising applications as a kind of light-weight and highly effective microwave absorber. By systematically investigating the electromagnetic parameters, it can be concluded that suitable complex permittivity, improved characteristic impedance and multiple relaxation processes in PANI nanoparticles should be responsible for their good microwave absorption.

Bifunctional Nitrogen-Doped Microporous Carbon Microspheres Derived from Poly(o-methylaniline) for Oxygen Reduction and Supercapacitors.

Heteroatom-doped carbon materials have attracted significant attention because of their applications in oxygen reduction reaction (ORR) and supercapacitors. Here we demonstrate a facile poly(o-methylaniline)-derived fabrication of bifunctional microporous nitrogen-doped carbon microspheres (NCMSs) with high electrocatalytic activity and stability for ORR and energy storage in supercapacitors. At a pyrolysis temperature of 900 °C, the highly dispersed NCMSs present a high surface area (727.1 m(2) g(-1)), proper total content of doping N, and high concentration of quaternary N, which exhibit superior electrocatalytic activities for ORR to the commercial Pt/C catalysts, high specific capacitance (414 F g(-1)), and excellent durability, making them very promising for advanced energy conversion and storage. The presented conducting polymer-derived strategy may provide a new way for the fabrication of heteroatom-doped carbon materials for energy device applications.

Fabrication of Thorny Au Nanostructures on Polyaniline Surfaces for Sensitive Surface-Enhanced Raman Spectroscopy

Here we demonstrate, for the first time, the fabrication of Au nanostructures on polyaniline (PANI) membrane surfaces for surface enhanced Raman spectroscopy (SERS) applications, through a direct chemical reduction by PANI. Introduction of acids into the HAuCl(4) solution leads to homogeneous Au structures on the PANI surfaces, which show only sub-ppm detection levels toward the target analyte, 4-mercaptobenzoic acid (4-MBA), because of limited surface area and lack of surface roughness. Thorny Au nanostructures can be obtained through controlled reaction conditions and the addition of a capping agent poly (vinyl pyrrolidone) (PVP) in the HAuCl(4) solution and the temperature kept at 80 °C in an oven. Those thorny Au nanostructures, with higher surface areas and unique geometric feature, show a SERS detection sensitivity of 1 × 10(-9) M (sub-ppb level) toward two different analyte molecules, 4-MBA and Rhodamine B, demonstrating their generality for SERS applications. These highly sensitive SERS-active substrates offer novel robust structures for trace detection of chemical and biological analytes.

Synthesis of nano-sized anatase TiO2 with reactive {001} facets using lamellar protonated titanate as precursor

Nano-sized anatase TiO(2) with exposed {001} facets was synthesized from lamellar protonated titanate precursor. Owing to small size (ca. 11 nm) and high surface area (155 m(2) g(-1)), the crystals with 26.1% {001} facets exhibited markedly superior photoactivity to reference ca. 76 nm anatase TiO(2) nanosheets with 88.4% {001} facets.