Binary Metal Oxide Adsorbed Graphene Modified Glassy Carbon Electrode for Detection of Riboflavin

Tungsten oxide (W) decorated titanium oxide (T) adsorbed onto a graphene (Gr) and modified the glassy carbon electrode for the electrochemical quantification of riboflavin (RF) in edible food and pharmaceuticals. For comparison, nanocomposites are formed using graphene oxide (GO), reduced graphene oxide (rGO) and pure graphite (G) sheets to study the electrochemical activities towards riboflavin. The ternary WTGr modified GCE shows the highest electrocatalytic activity due to synergetic interactions between the metal oxide and graphene. The electrochemical observations are supported by the SEM, HRTEM, XRD, UV-Vis, Zeta potential (ζ) and size data. The sensor shows a wide linear range 20 nM–2.5 μM with a detection limit 25.24 nM and sensitivity (4.249×10⁻⁸ A/nM). The fabricated sensor is validated in real samples.     

A New Nanocomposite Based on Pt-rGO Embedded Polymelamine Formaldehyde Nanocomposite for Reduction of Carbon Dioxide

Here, polymelamine formaldehyde was decorated on the surface of reduced graphene oxide whose surface was then electrodeposited with a sub-monolayer of platinum nanoparticles. The nanocomposite thus prepared was characterized using several spectroscopic methods. Using the nanocomposite as a potential electrocatalyst for carbon dioxide reduction, the products were detected by Raman spectroscopy, gas chromatography, ¹³C-NMR spectroscopy, and gas chromatography-mass spectrometry. The analytical results identified methanol as the main product of CO₂ reduction. Moreover, analysis of the liquid products confirmed methanol as the predominant product with a current density of 0.4 mA/cm and a Faradaic efficiency of 93 %.     

Stages of melting of graphene model in two-dimensional space

Spontaneous melting of a perfect crystalline graphene model in 2D space is studied via molecular dynamics simulation. Model containing 10⁴ atoms interacted via long-range bond-order potential (LCBOP) is heated up from 50 to 8,450 K in order to see evolution of various thermodynamic quantities, structural characteristics and occurrence of various structural defects. We find that spontaneous melting of our graphene model in 2D space exhibits a first-order behaviour of the transition from solid 2D graphene sheet into a ring-like structure 2D liquid. Occurrence and clustering of Stone–Wales defects are the first step of melting process followed by breaking of C–C bonds, occurrence/growth of various types of vacancies and multi-membered rings. Unlike that found for melting of a 2D crystal with an isotropic bonding, these defects do not occur homogeneously throughout the system, they have a tendency to aggregate into a region and liquid phase initiates/grows from this region via tearing-like or crack-propagation-like mechanism. Spontaneous melting point of our graphene model occurs at T_m = 7,750 K. The validity of classical nucleation theory and Berezinsky–Kosterlitz–Thouless–Nelson–Halperin–Young (BKTNHY) one for the spontaneous melting of our graphene model in strictly 2D space is discussed.     

Electro‐optic switching with liquid crystal graphene

Graphene oxide (GO) particles in aqueous dispersions can form liquid crystal (LC) phases at extremely low concentrations due to the extremely high aspect ratio of the flakes and noticeably, they possess an extremely large Kerr coefficient attractive for low power consumption electro‐optic devices. Reduced graphene does not easily form LC phases in water due to its hydrophobic nature but here we show that stable dispersions of reduced graphene oxide can be realized with surfactants and that they exhibit birefringence upon shearing as well as under application of electric fields. The performance of the system is largely superior to GO LC possessing longer time stability and drastically improved electro‐optic properties with an induced birefringence twice as large at the same field strength thanks to the almost recovery of graphene properties upon reduction. (© 2016 WILEY‐VCH Verlag GmbH &Co. KGaA, Weinheim)     

Graphene screen‐printed radio‐frequency identification devices on flexible substrates

Despite the great promise of printed flexible electronics from 2D crystals, and especially graphene, few scalable applications have been reported so far that can be termed roll‐to‐roll compatible. Here we combine screen printed graphene with photonic annealing to realize radio‐frequency identification devices with a reading range of up to 4 meters. Most notably our approach leads to fatigue resistant devices showing less than 1% deterioration of electrical properties after 1000 bending cycles. The bending fatigue resistance demonstrated on a variety of technologically relevant plastic and paper substrates renders the material highly suitable for various printable wearable devices, where repeatable dynamic bending stress is expected during usage. All applied printing and post‐processing methods are compatible with roll‐to‐roll manufacturing and temperature sensitive flexible substrates providing a platform for the scalable manufacturing of mechanically stable and environmentally friendly graphene printed electronics.

     

Coulomb screening effects on the optoelectronic far-infrared properties of spatially separated few-layer graphene

We investigate the longitudinal optical conductivity of spatially separated few-layer graphene analytically and numerically. Each layer could be monolayer or bilayer graphene. The density–density correlation function has been screened by the dielectric function using the random phase approximation, which includes the inter-layer Coulomb coupling. In the presence of the potential function between the layers, the carrier densities in each layer can be tuned respectively. In these two-dimensional layered structures, the main contributions to the optical conductivity are from the intra- and inter-band transition channels in a same layer. In the infrared region, the Drude optical conductivity was observed by the unscreened intra-band transition process. But in the presence of the inter-layer Coulomb interaction, one peak structure of the optical conductivity is observed which can be modified by the dielectric environment. From the number of turning points and the turning positions, the carrier density, the Fermi wavevector, and the layered structure can be determined.     

Advances in two-dimensional heterostructures by mono-element intercalation underneath epitaxial graphene

Two-dimensional (2D) materials have displayed many remarkable physical properties, including 2D superconductivity, magnetism, and layer-dependent bandgaps. However, it is difficult for a single 2D material to meet complex practical requirements. Heterostructures obtained by vertically stacking different kinds of 2D materials have extensively attracted researchers’ attention because of their rich electronic features. With heterostructures, the constraints of lattice matching can be overcome. Meanwhile, high application potential has been explored for electronic and optoelectronic devices, including tunneling transistors, flexible electronics, and photodetectors. Specifically, graphene-based van der Waals heterostructures (vdWHs) by intercalation are emerging to realize various functional heterostructures-based electronic devices. Intercalating atoms under epitaxial graphene can efficiently decouple graphene from the substrate, and is expected to realize rich novel electronic properties in graphene. In this study, we systematically review the progress of the mono-element intercalation in graphene-based vdWHs, including the intercalation mechanism, intercalation-modified electronic properties, and the practical applications of 2D intercalated heterostructures. This work would inspire edge-cutting ideas in the scientific frontiers of 2D materials.     

Cross‐sectional structural characterization of the surface of exfoliated HOPG using HRTEM‐EELS

We analyzed the surface atomic structure of highly oriented pyrolytic graphite (HOPG) substrate exfoliated with adhesive tape, using high‐resolution transmission electron microscopy and scanning transmission electron microscopy‐electron energy‐loss spectroscopy (STEM‐EELS). The surface step height of the exfoliated HOPG substrate was determined using high‐angle annular dark‐field‐scanning transmission electron microscopy (HAADF‐STEM) images and the depth profiles of the EELS spectra of a cross‐sectioned thin foil specimen prepared via focused ion beam milling. The exfoliated surface of the HOPG substrate presented disordered and curved graphene layers. The STEM‐EELS measurements indicated that upon exfoliation, the surface of the HOPG substrate reacted with atmospheric water and oxygen molecules.     

激光诱导三维网状石墨烯的一步法制备及应用

三维多孔石墨烯作为一种优异的石墨烯碳材料, 其独特的多孔结构使得材料在具有较大比表面积的同时还保持着足够高的电子迁移率和机械稳定性, 在电子器件中得到了广泛的应用. 本文介绍的激光诱导石墨烯是一种以一步法直接制备得到的三维网状石墨烯材料, 该技术将三维石墨烯的制备和图案化相结合, 无需进行湿化学反应处理, 制作方法更简便, 材料性能更优异. 目前研究主要集中在通过掺杂提高性能和利用转移法实现不同基底器件的制备. 激光诱导石墨烯自身特有的属性如多孔微纳米结构和大的比表面积等使其在超级电容器和传感器等领域拥有较高的应用价值.     

Sc,Ti,V修饰B/N掺杂单缺陷石墨烯的储氢研究

3d过渡金属修饰是改善石墨烯储氢性能的最有效途径, 但仍存在金属团聚和H₂解离导致难以脱附的问题. 提出了B/N掺杂单缺陷石墨烯(BMG/NMG)的策略来避免以上两个问题. 密度泛函理论计算结果表明, N掺杂可以使Sc, Ti, V与石墨烯的结合能提高3~4倍, B掺杂可以将Sc与石墨烯的结合能提高3倍. Sc/BMG和Sc/NMG吸附的第一个H₂不会解离. Sc/BMG中Sc吸附5个H₂, 平均氢分子结合能为-0.18～-0.43 eV, 并且可以通过在同侧锚定多个Sc原子形成Sc/C₃B₂五元环增加H₂吸附位点. Sc/NMG中每个Sc吸附6个H₂, 平均氢分子结合能为-0.17～-0.29 eV, 还可以通过在异侧修饰形成Sc/N₃/Sc单元进一步提高储氢能力. 研究结果将为设计基于3d过渡金属修饰碳材料的储氢材料提供理论基础.