Development of next-generation sensor devices is gaining tremendous attention in both academia and industry because of their broad applications in manufacturing processes, food and environment control, medicine, disease diagnostics, security and defense, aerospace, and so forth. Current challenges include the development of low-cost, ultrahigh, and user-friendly sensors, which have high selectivity, fast response and recovery times, and small dimensions. The critical demands of these new sensors are typically associated with advanced nanoscale sensing materials. Among them, graphene and its derivatives have demonstrated the ideal properties to overcome these challenges and have merged as one of the most popular sensing platforms for diverse applications. A broad range of graphene assemblies with different architectures, morphologies, and scales (from nano-, micro-, to macrosize) have been explored in recent years for designing new high-performing sensing devices. Herein, this study presents and discusses recent advances in synthesis strategies of assembled graphene-based superstructures of 1D, 2D, and 3D macroscopic shapes in the forms of fibers, thin films, and foams/aerogels. The fabricated state-of-the-art applications of these materials in gas and vapor, biomedical, piezoresistive strain and pressure, heavy metal ion, and temperature sensors are also systematically reviewed and discussed, and their sensing performance is compared.

Here, we report a new method to prepare graphene from graphite by the liquid phase exfoliation process with sonication using graphene oxide (GO) as a dispersant. It was found that GO nanosheets act a as surfactant to the mediated exfoliation of graphite into a GO-adsorbed graphene complex in the aqueous solution, from which graphene was separated by an additional process. The preparation of isolated graphene from a single to a few layers is routinely achieved with an exfoliation yield of up to higher than 40% from the initial graphite material. The prepared graphene sheets showed a high quality (C/O ∼ 21.5), low defect (ID/IG ∼ 0.12), and high conductivity (6.2 × 10(4) S/m). Moreover, the large lateral size ranging from 5 to 10 μm of graphene, which is believed to be due to the shielding effect of GO avoiding damage under ultrasonic jets and cavitation formed by the sonication process. The thin graphene film prepared by the spray-coating technique showed a sheet resistance of 668 Ω/sq with a transmittance of 80% at 550 nm after annealing at 350 °C for 3 h. The transparent electrode was even greater with the resistance only 66.02 Ω when graphene is deposited on an interdigitated electrode (1 mm gap). Finally, a flexible sensor based on a graphene spray-coating polydimethylsiloxane (PDMS) is demonstrated showing excellent performance working under human touch pressure (<10 kPa). The graphene prepared by this method has some distinct properties showing it as a promising material for applications in electronics including thin film coatings, transparent electrodes, wearable electronics, human monitoring sensors, and RFID tags.

Present and past anthropogenic pollution of the hydrosphere and lithosphere is a growing concern around the world for sustainable development and human health. Current industrial activity, abandoned contaminated plants and mining sites, and even everyday life is a pollution source for our environment. There is therefore a crucial need to clean industrial and municipal effluents and remediate contaminated soil and groundwater. Nanosized zero-valent iron (nZVI) is an emerging material in these fields due to its high reactivity and expected low impact on the environment due to iron’s high abundance in the earth crust. Currently, there is an intensive research to test the effectiveness of nZVI in contaminant removal processes from water and soil and to modify properties of this material in order to fulfill specific application requirements. The number of laboratory tests, field applications, and investigations for the environmental impact are strongly increasing. The aim of the present review is to provide an overview of the current knowledge about the catalytic activity, reactivity and efficiency of nZVI in removing toxic organic and inorganic materials from water, wastewater, and soil and groundwater, as well as its toxic effect for microorganisms and plants.

The early diagnosis of diseases, e.g., Parkinson’s and Alzheimer’s disease, diabetes, and various types of cancer, and monitoring the response of patients to the therapy plays a critical role in clinical treatment; therefore, there is an intensive research for the determination of many clinical analytes. In order to achieve point-of-care sensing in clinical practice, sensitive, selective, cost-effective, simple, reliable, and rapid analytical methods are required. Biosensors have become essential tools in biomarker sensing, in which electrode material and architecture play critical roles in achieving sensitive and stable detection. Carbon nanomaterials in the form of particle/dots, tube/wires, and sheets have recently become indispensable elements of biosensor platforms due to their excellent mechanical, electronic, and optical properties. This review summarizes developments in this lucrative field by presenting major biosensor types and variability of sensor platforms in biomedical applications.

The lithium mediated reduction of N 2 is one of the only available approaches to electrochemical ammonia production at significant yields under ambient conditions. However, much remains to be investigated about the various electrochemical processes and side reactions that are involved. Herein, we have examined the effects of parameters including electrode potential, convection, N 2 pressure, and water content to refine and control the process. We demonstrate that a closely linear ammonia yield can be maintained during experiments up to 60 h in length, with approximately constant faradaic efficiency. This steady state operation appears to be preceded by a coating of the electrode surface with the products of the reductive electrolyte decomposition, such as LiF. We demonstrate ammonia yield rates above 1 nmol s −1 cm −2 and faradaic efficiencies as high as 60% through the improved control of the reaction conditions.

The condensation of complex silicates with pyroxene and olivine composition at conditions prevailing in molecular clouds has been experimentally studied. For this purpose, molecular species comprising refractory elements were forced to accrete on cold substrates representing the cold surfaces of surviving dust grains in the interstellar medium. The efficient formation of amorphous and homogeneous magnesium iron silicates at temperatures of about 12 K has been monitored by IR spectroscopy. The gaseous precursors of such condensation processes in the interstellar medium are formed by erosion of dust grains in supernova shock waves. In the laboratory, we have evaporated glassy silicate dust analogs and embedded the released species in neon ice matrices that have been studied spectroscopically to identify the molecular precursors of the condensing solid silicates. A sound coincidence between the 10 µm band of the interstellar silicates and the 10 µm band of the low-temperature siliceous condensates can be noted.

For the first time: Thiofulminic acid (HCNS), the parent member of the nitrile sulfide family of reactive intermediates and potential interstellar species, was produced and characterized by IR spectroscopy for the first time. HCNS was generated in cryogenic matrices by 254 nm UV irradiation of 1,2,5‐thiadiazole (see figure).

Carbon microsphere-supported Cu nanoparticles were fabricated, characterized, and applied for synthesis.