The concerns related to particulate matter’s health effects alongside the increasing demands from citizens for more participatory, timely, and diffused air quality monitoring actions have resulted in increasing scientific and industrial interest in low-cost particulate matter sensors (LCPMS). In the present paper, we discuss 50 LCPMS models, a number that is particularly meaningful when compared to the much smaller number of models described in other recent reviews on the same topic. After illustrating the basic definitions related to particulate matter (PM) and its measurements according to international regulations, the device’s operating principle is presented, focusing on a discussion of the several characterization methodologies proposed by various research groups, both in the lab and in the field, along with their possible limitations. We present an extensive review of the LCPMS currently available on the market, their electronic characteristics, and their applications in published literature and from specific tests. Most of the reviewed LCPMS can accurately monitor PM changes in the environment and exhibit good performances with accuracy that, in some conditions, can reach R² values up to 0.99. However, such results strongly depend on whether the device is calibrated or not (using a reference method) in the operative environment; if not, R² values lower than 0.5 are observed.

The crystal structure of graphene flakes is expected to significantly affect their sensing properties. Here we report an experimental investigation on the crystalline structure of graphene aimed at exploring the effects on the gas sensing properties. The morphology of graphene, prepared via Chemical Vapor Deposition (CVD), Liquid Phase Exfoliation (LPE) and Mechanical Exfoliation (ME), is inspected through Raman spectroscopy, Atomic Force Microscopy (AFM) and Scanning Electron Microscopy (SEM). CVD and LPE-graphene structures are found to be more defective with respect to ME-graphene. The defects are due to the jagged morphology of the films rather than originating from intrinsic disorder. The flatness of ME-graphene flakes, instead, explains the absence of defects. Chemiresistors based on the three different graphene preparation methods are subsequently exposed to NO₂ in the concentration range 0.1–1.5 ppm (parts per million). The device performance is demonstrated to be strongly and unambiguously affected by the material structure: the less defective the material is, the higher the response rate is. In terms of signal variation, at 1.5 ppm, for instance, ME-graphene shows the highest value (5%) among the three materials. This study, comparing simultaneously graphene and sensors prepared via different routes, provides the first experimental evidence of the role played by the graphene level of defectiveness in the interaction with analytes. Moreover, these findings can pave the path for tailoring the sensor behavior as a function of graphene morphology.

This paper presents a review of the current research activities in the field of gas nanosensors. Nanomaterials are characterized by physical and chemical properties that differ from their macroscopic counterparts and, in particular, by an enhanced chemical reactivity even at room temperature. This effect has stimulated the development of chemical sensors based on several different nanomaterials. Here we focus most attention on carbon nanotubes, silicon and metal oxide nanoparticles and metal nanowires. After introducing a few general definitions a discussion on the fundamental properties of the nanostate used in the sensor field is presented and several nanosensors, based on the aforementioned nanomaterials, are discussed. Finally, some personal conclusions will be drawn.

The aim of this work is to investigate the degradation of perovskite solar cells (PSCs) by means of impedance spectroscopy, a highly sensitive characterization technique used to establish the electrical response of a device in a nondestructive manner. In this paper, PSCs with two different electron transport layers (ETLs) are studied: PSCs with undoped SnO₂ as an ETL are compared to PSCs with an ETL composed of graphene-doped SnO₂ (G-SnO₂). Experimental data were collected immediately after fabrication and after one week, monitoring both impedance spectroscopy and dark current-voltage (I-V) curves. It was observed that, in the case of the undoped PSCs, the degradation of the solar cells affected both the AC behavior of the devices, modifying the associated Nyquist plots, and the DC behavior, observable from the dark I-V measurements. Conversely, the solar cells with G-SnO₂ showed no variation. Considering the Nyquist plots, a quantitative analysis was performed by comparing the parameters of a proper equivalent circuit model. The results were coherent with those achieved in the DC analysis, thus proving that the analysis of impedance spectra, supported with dark I-V curves, allows one to gain a deeper knowledge of the degradation phenomena of perovskite solar cells. This study opens the door for further improvement of these devices through a better understanding of their electrical behavior.