Sodium storage properties of thin phosphorus-doped graphene layers developed on the surface of nanodiamonds under hot pressing conditions

Abstract

Phosphorus-doped graphene layers have been formed on the surface of nanodiamond (ND) particles by hot pressing of a mixture of purified detonation ND powder and triphenylphosphine (TPP) at 1000?°C and 100?bar. X-ray photoelectron spectroscopy detected about 1.7 at.% of phosphorus in the product, most of which was in the oxidized form. The same treatment conditions of the ND powder without the addition of TPP resulted in the only partial covering of some ND particles by sp²-hybridized carbon layers. The tests in Na-ion half-cells found that the pure carbon sample can reversibly sustain 42 mAh g^?1 at a current density of 0.1?A g^?1. For the phosphorus-doped sample, this value increases up to 54 mAh g^?1 due to mainly accumulation of sodium at various defects created in the graphitic layers as a result of phosphorus incorporation. Taking into account inertness of inner diamond cores, specific capacity values are 417 mAh g^?1 for phosphorus-doped graphene layers and 587 mAh g^?1 for non-doped ones.     

Transparent Electrothermal Film Defoggers and Antiicing Coatings based on Wrinkled Graphene

Fog, frost, ice, and other natural phenomena can inevitably affect human life and the function of equipment. Therefore, removal or prevention is an urgent problem to be solved. As a new type of 2D material, graphene possesses great application potential in defogging and antiicing. In this work, a graphene film with intentionally increased defects and uniformly distributed wrinkles is synthesized on copper–zinc alloy substrates by chemical vapor deposition, and transparent electrothermal film defoggers are prepared based on such material. The defoggers can completely remove fog within 5 s when supplying a safe voltage of 28 V. The surface resistance of the defoggers is sensitive to humidity and it can monitor the defogging process in real time. Such outstanding performance is attributed to the ultrafast evaporation mechanism, which can prevent excessive water accumulation. The antiicing performance of wrinkled graphene (WG) is further studied. The antiicing coatings can delay freezing for 1.25 h at ?15 °C or 2.8 h at ?10 °C. The superior performance of WG can be explained by its unique surface structure and nanoscale roughness. Taken together, WG is expected to be used in antifog glass, rearview mirror defogging, aircraft surface deicing, and other applications.     

Nanocrystalline transition metal oxides and their composites with reduced graphene oxide and carbon nanotubes for photocatalytic applications

Transition metal oxide nanoparticles (CuO, ZnO & Fe₂O₃) and mixed metal oxides CuO. ZnO.Fe₂O₃ were fabricated by facile co-precipitation approach for photocatalytic treatment of organic dyes. The structural features, phase purity, crystallite size and morphology of individual and mixed metal oxides were analysed by X-rays diffraction patterns (XRD) and scanning electron microscopic (SEM) analysis. Electrical behaviour of CuO, ZnO, Fe₂O₃ and mixed metal oxides CuO. ZnO.Fe₂O₃ was explored by current-voltage (I-V) measurements. Functional groups present in the synthesized metal oxides were investigated by Fourier transform infrared spectroscopy (FTIR) which ensures the existence of M-O functional groups in the samples. The optical bandgap analysis was carried out by UV–visible spectroscopic technique which revealed that the blend of three different transition metal oxides reduced the bandgap energy of mixed metal oxides. The reason behind this reduced bandgap energy is formation of new electronic state which arises due to the metal-oxygen interactions. Moreover, the nanocomposites of CuO.ZnO.Fe₂O₃ with reduced graphene oxide (rGO) and carbon nanotubes (CNTs) were prepared to study the effect of the carbonaceous materials on the rate of photodegradation. These carbonaceous nanomaterials have plethora properties which can bring advancement in sector of photocatalytic treatment of wastewater. The photocatalytic experiments were performed using methylene blue (MB) as standard dye for comparative study of metal oxides and their composites with rGO and CNTs. The percentage degradation of methylene blue (MB) by nanocomposite CuO.ZnO.Fe₂O₃/rGO is 87% which is prominent among all samples. This result ascribed the photocatalytic aspects of reduced graphene oxide along with mixed metal oxides.     

The role of Pt loading on reduced graphene oxide support in the polyol synthesis of catalysts for oxygen reduction reaction

Common carbon-blacks have shown insufficient stability as cathodic catalyst supports for proton exchange membrane fuel cells (PEMFCs). In this regard, alternative supports have been proposed and, specifically graphene or reduced graphene oxide (rGO), have attracted special attention. Herein, a set of electrocatalysts using reduced graphene oxide (rGO) as support is synthetized by a modified polyol method. The influence of Pt loading on the support is studied and compared with conventional supports, considering Pt particle morphologies and oxygen reduction reaction (ORR) performance in rotating disk electrode (RDE). Despite Pt average particle size typically increases with the Pt loading, 30 wt% of Pt on rGO is the optimal Pt loading, yielding the highest ORR activity among the rGO-supported electrocatalysts. These results show that both Pt loading and type of support greatly impact on the morphology and electrochemical performance of Pt nanoparticles.     

Highly Stretchable and Sensitive SBS/Graphene Composite Fiber for Strain Sensors

Flexible strain sensors have attracted tremendous interests due to the emergence of intelligent wearable technology. Electrically conductive fibers are desirable candidates for flexible strain sensors, but up til now, there still exist enormous challenges to obtain conductive fibers exhibiting simultaneously high stretchability and high strain sensitivity. This paper introduces a poly (styrene‐butadiene‐styrene) (SBS)/graphene (Gr) composite fiber‐based flexible strain sensor fabricated by a facile and highly scalable wet spinning method. The results demonstrate that the graphene content has significant influence on the morphology, mechanical properties, and electromechanical properties of the composite fibers. The fibers with 5 wt% graphene have a wide response range of up to 100% strain, a high electrical sensitivity with the gauge factor of 10083.98 at 100% strain, and meanwhile, a high level of stability for 2100 stretching–releasing cycles under an applied strain of 20%. Furthermore, the SBS‐5%Gr composite fibers display excellent sensing performance in detecting human upper limb movements at different joints including hand joints, wrist joints, elbow joints, and shoulder joints.     

GO@TA-Fe/PVDF纳米复合材料制备与介电性能

为降低氧化石墨烯（GO）/聚偏氟乙烯（PVDF）体系的介电损耗，本文采用单宁酸-铁配合物（TA-Fe）修饰GO表面，将改性GO和PVDF复合后制得了GO@TA-Fe/PVDF纳米复合电介质材料，研究了GO@TA-Fe对PVDF复合材料的微观形貌及介电性能影响。研究结果表明，TA-Fe包覆层强化了GO与PVDF基体间界面相容性及界面作用力，促进了GO在基体中均匀分散；TA-Fe界面层的存在显著降低了GO/PVDF漏导电流及损耗，归因于绝缘界面层有效阻止了GO之间直接接触，抑制漏导电流；TA-Fe用量对体系介电性能有明显影响，随TA-Fe用量增大，体系的介电损耗和电导率显著降低。与GO/PVDF相比，质量分数2%的GO@TA-Fe/PVDF在100Hz下介电常数为1000，而介电损耗由19.8降低为0.08。本研究制备的高介电常数及低损耗的柔性GO@TA-Fe/PVDF纳米电介质材料在电子器件及电力设备领域具有潜在应用。     

On‐the‐Spot Immobilization of Quantum Dots,Graphene Oxide,and Proteins via Hydrophobins

Class I hydrophobin Vmh2, a peculiar surface active and versatile fungal protein, is known to self‐assemble into chemically stable amphiphilic films, to be able to change wettability of surfaces, and to strongly adsorb other proteins. Herein, a fast, highly homogeneous and efficient glass functionalization by spontaneous self‐assembling of Vmh2 at liquid–solid interfaces is achieved (in 2 min). The Vmh2‐coated glass slides are proven to immobilize not only proteins but also nanomaterials such as graphene oxide (GO) and quantum dots (QDs). As models, bovine serum albumin labeled with Alexa 555 fluorophore, anti‐immunoglobulin G antibodies, and cadmium telluride QDs are patterned in a microarray fashion in order to demonstrate functionality, reproducibility, and versatility of the proposed substrate. Additionally, a GO layer is effectively and homogeneously self‐assembled onto the studied functionalized surface. This approach offers a quick and simple alternative to immobilize nanomaterials and proteins, which is appealing for new bioanalytical and nanobioenabled applications.