Accurate measurement of temperatures with low power consumption with the highest sensitivity and smallest possible elements is still a challenge. The thermal, electrical, and mechanical properties of carbon nanotubes (CNTs) have suggested that their use as a very sensitive sensing element will allow the creation of different sensors, far superior to other devices of similar size. In this paper, we present a short review of different constructive designs of CNTs based resistive sensors used for temperature measurement, available in literature, assembled using different processes, such as self-assembly, drop-casting from a solution, thin films obtained by gluing, printing, spraying, or filtration over a special membrane. As particular cases, temperature sensors obtained from CNT-polymer nanocomposite structures, CNTs filled with uniformly dispersed Fe3O4 nanoparticles or with gallium, and carbon nanotube wires (CNWs) hybrids are presented. Using these preparation procedures, mixtures of CNTs with different dimensions and chirality, as well as with a variable level of impurities and structural defects, can be produced. The sensors’ performance charts are presented, highlighting a number of aspects regarding the applicability of CNT structures for temperature measurement ranging from cryogenic temperatures to high temperatures, the limitations they have, their characteristics and advantages, as well as the special situations that may arise given the particular structure of these new types of materials, together with basic relationships and parameters for CNTs characterization. Further research will be required to develop the techniques of manipulating and depositing individual CNTs on supports and electrodes for the development of temperature sensors.

Three-dimensional graphene foam (3D-GrFoam) is a highly porous structure and sustained lattice formed by graphene layers with sp² and sp³ hybridized carbon. In this work, chemical vapor deposition (CVD)—grown 3D-GrFoam was nitrogen-doped and platinum functionalized using hydrothermal treatment with different reducing agents (i.e., urea, hydrazine, ammonia, and dihydrogen hexachloroplatinate (IV) hydrate, respectively). X-ray photoelectron spectroscopy (XPS) survey showed that the most electrochemically active nitrogen-doped sample (GrFoam3N) contained 1.8 at % of N, and it exhibited a 172 mV dec⁻¹ Tafel plot associated with the Volmer–Heyrovsky hydrogen evolution (HER) mechanism in 0.1 M KOH. By the hydrothermal process, 0.2 at % of platinum was anchored to the graphene foam surface, and the resultant sample of GrFoamPt yielded a value of 80 mV dec⁻¹ Tafel associated with the Volmer–Tafel HER mechanism. Furthermore, Raman and infrared spectroscopy analysis, as well as scanning electron microscopy (SEM) were carried out to understand the structure of the samples.

This paper presents the preparation of platinum on a reduced graphene oxide matrix (PtrGO) using the microwave-assisted method with three different pH solutions. The platinum concentration determined by energy-dispersive X-ray analysis (EDX) was 4.32 (weight%), 2.16 (weight %) and 5.70 (weight%), corresponding to pH 3.3, 11.7 and 7.2, respectively. Pt functionalization of reduced graphene oxide (rGO) decreased the rGO specific surface, as shown by Brunauer, Emmett and Teller (BET) analysis. An XRD spectrum of platinum-decorated reduced graphene oxide (rGO) showed the presence of the associated phases of rGO and centered cubic platinum peaks. An oxygen reduction reaction (ORR) electrochemical characterization performed using the rotating disk electrode (RDE) method showed that in PtGO1 synthetized in an acidic environment, with 4.32 Pt (weight%) determined by EDX, platinum is much more dispersed, which explains its better electrochemical oxygen reduction reaction performance. Koutecky–Levich (K-L) plots calculated at different potentials prove a good linear relationship. Electron transfer numbers (n) determined from the K-L plots are between 3.1 and 3.8, which confirms that the ORR for all the samples can be regarded as first-order reaction kinetics of O₂ concentration formed on the Pt surface during ORR.

Iodine-doped graphene oxide is attracting great attention as fuel cell (FC) electrocatalysts with a high activity for the oxygen reduction reaction (ORR). However, most of the reported preparation techniques for iodine-doped graphene (I/rGO) could be transposed into practice as multiple step procedures, a significant disadvantage for scale-up applications. Herein, we describe an effective, eco-friendly, and fast technique for synthesis by a microwave-tuned one-stage technique. Structural and morphological characterizations evidenced the obtaining of nanocomposite sheets, with iodine bonded in the graphene matrix. The ORR performance of I/rGO was electrochemically investigated and the enhancement of the cathodic peak was noted. Based on the noteworthy electrochemical properties for ORR activity, the prepared I/rGO can be considered an encouraging alternative for a more economical electrode for fuel cell fabrication and commercialization. In this perspective, the iodine-based catalysts synthesis can be considered a step forward for the metal-free electrocatalysts development for the oxygen reduction reaction in fuel cells.

The objective of this investigation is to study silica-doped/sulfonated poly(2,6-dimethyl-1,4-phenylene oxide) (PPO) composite membranes for operation in hydrogen/oxygen proton-exchange membrane fuel cells ranging from room temperature (RT) up to 120 °C. The sulfonated PPO composite membranes were prepared using a sol–gel process employing reaction with tetra-ethoxysilane (TEOS) followed by heat treatment at 60, 90, and 120 °C, respectively. The presence of silicon oxide in the composite membranes was evaluated using FTIR spectroscopy, while thermal properties were studied using thermal gravimetric analysis-differential scanning calorimetric (TGA-DSC) measurements. Additionally, ion exchange capacity, water uptake, and proton conductivity characterizations were also carried out. It was observed that water uptake for 75% PPO sulfonated composite membrane treated at 120 °C is higher than that of Nafion^TM membrane and the proton conductivity value measured at 120 °C is 0.35·10⁻¹ S/cm. Therefore, the composite membranes are potentially suitable for high temperature fuel cell applications.

New Energy Storage and Hydrogen Technologies Cryogenic Technologies Material Science for Energy and Environment Isotopes in Environmental Studies and Life Quality Applications