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1. Nanostructured Diamond Composites for Multifunctional Sensing Applications

   https://doi.org/10.3390/chemosensors10110488  

   Li, Eric Y. ; Pacheco, Elluz ; Zhou, Andrew F. ; Feng, Peter X. ( November 2022 , Chemosensors)

   We report studies of multifunctional, nanostructured diamond composites that were fabricated using chemical vapor deposition (CVD) techniques. Grain sizes from micrometer, to submicron, nano, and ultrananocrystalline diamond (UNCD) were controlled by varying CH4, hydrogen, and argon gas concentrations during the syntheses. Scanning electron microscopy (SEM) and Raman scattering spectroscopy were used to investigate the morphologies, composites, and crystallinities of the films. Four multifunctional sensor prototypes were designed, fabricated, and tested, based on the four diamond materials of different grain sizes. The responses of the four prototypes to either pollution gas or UV light illumination were systematically investigated at different operating temperatures. Experimental data indicated the obtained UNCD composite from the low-cost simple CVD fabrication technique appeared to have very good sensitivities when exposed to low concentrations of H2 or NH3 gas with a decent response and fast recovery time. Furthermore, highly induced photocurrents from both microdiamond- and UNCD-based prototypes to deep UV illumination were also demonstrated, with responsivities up to 2750 mA/W and 550 mA/W at 250 nm wavelength, respectively. Overall, the fabricated UNCD prototypes displayed a good balance in performance for multifunctional sensor applications in terms of responsivity, stability, and repeatability.

    

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2. Gallium Nitride (GaN) Nanostructures and Their Gas Sensing Properties: A Review

   https://doi.org/10.3390/s20143889  

   Khan, Md Ashfaque ; Rao, Mulpuri V. ( July 2020 , Sensors)

   null (Ed.)

   In the last two decades, GaN nanostructures of various forms like nanowires (NWs), nanotubes (NTs), nanofibers (NFs), nanoparticles (NPs) and nanonetworks (NNs) have been reported for gas sensing applications. In this paper, we have reviewed our group’s work and the works published by other groups on the advances in GaN nanostructures-based sensors for detection of gases such as hydrogen (H2), alcohols (R-OH), methane (CH4), benzene and its derivatives, nitric oxide (NO), nitrogen dioxide (NO2), sulfur-dioxide (SO2), ammonia (NH3), hydrogen sulfide (H2S) and carbon dioxide (CO2). The important sensing performance parameters like limit of detection, response/recovery time and operating temperature for different type of sensors have been summarized and tabulated to provide a thorough performance comparison. A novel metric, the product of response time and limit of detection, has been established, to quantify and compare the overall sensing performance of GaN nanostructure-based devices reported so far. According to this metric, it was found that the InGaN/GaN NW-based sensor exhibits superior overall sensing performance for H2 gas sensing, whereas the GaN/(TiO2–Pt) nanowire-nanoclusters (NWNCs)-based sensor is better for ethanol sensing. The GaN/TiO2 NWNC-based sensor is also well suited for TNT sensing. This paper has also reviewed density-functional theory (DFT)-based first principle studies on the interaction between gas molecules and GaN. The implementation of machine learning algorithms on GaN nanostructured sensors and sensor array has been analyzed as well. Finally, gas sensing mechanism on GaN nanostructure-based sensors at room temperature has been discussed. 

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3. Recent Advances in Electrochemical Sensors for Detecting Toxic Gases: NO2, SO2 and H2S

   https://doi.org/10.3390/s19040905  

   Khan, Md ; Rao, Mulpuri ; Li, Qiliang ( February 2019 , Sensors)

   null (Ed.)

   Toxic gases, such as NOx, SOx, H2S and other S-containing gases, cause numerous harmful effects on human health even at very low gas concentrations. Reliable detection of various gases in low concentration is mandatory in the fields such as industrial plants, environmental monitoring, air quality assurance, automotive technologies and so on. In this paper, the recent advances in electrochemical sensors for toxic gas detections were reviewed and summarized with a focus on NO2, SO2 and H2S gas sensors. The recent progress of the detection of each of these toxic gases was categorized by the highly explored sensing materials over the past few decades. The important sensing performance parameters like sensitivity/response, response and recovery times at certain gas concentration and operating temperature for different sensor materials and structures have been summarized and tabulated to provide a thorough performance comparison. A novel metric, sensitivity per ppm/response time ratio has been calculated for each sensor in order to compare the overall sensing performance on the same reference. It is found that hybrid materials-based sensors exhibit the highest average ratio for NO2 gas sensing, whereas GaN and metal-oxide based sensors possess the highest ratio for SO2 and H2S gas sensing, respectively. Recently, significant research efforts have been made exploring new sensor materials, such as graphene and its derivatives, transition metal dichalcogenides (TMDs), GaN, metal-metal oxide nanostructures, solid electrolytes and organic materials to detect the above-mentioned toxic gases. In addition, the contemporary progress in SO2 gas sensors based on zeolite and paper and H2S gas sensors based on colorimetric and metal-organic framework (MOF) structures have also been reviewed. Finally, this work reviewed the recent first principle studies on the interaction between gas molecules and novel promising materials like arsenene, borophene, blue phosphorene, GeSe monolayer and germanene. The goal is to understand the surface interaction mechanism. 

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4. Microbial nanowires with genetically modified peptide ligands to sustainably fabricate electronic sensing devices

   https://doi.org/10.1016/j.bios.2023.115147  

   Lekbach, Yassir ; Ueki, Toshiyuki ; Liu, Xiaomeng ; Woodard, Trevor ; Yao, Jun ; Lovley, Derek R. ( April 2023 , Biosensors and Bioelectronics)

   Nanowires have substantial potential as the sensor component in electronic sensing devices. However, surface functionalization of traditional nanowire and nanotube materials with short peptides that increase sensor selectivity and sensitivity requires complex chemistries with toxic reagents. In contrast, microorganisms can assemble pilin monomers into protein nanowires with intrinsic conductivity from renewable feedstocks, yielding an electronic material that is robust and stable in applications, but also biodegradable. Here we report that the sensitivity and selectivity of protein nanowire-based sensors can be modified with a simple plug and play genetic approach in which a short peptide sequence, designed to bind the analyte of interest, is incorporated into the pilin protein that is microbially assembled into nanowires. We employed a scalable Escherichia coli chassis to fabricate protein nanowires that displayed either a peptide previously demonstrated to effectively bind ammonia, or a peptide known to bind acetic acid. Sensors comprised of thin films of the nanowires amended with the ammonia-specific peptide had a ca. 100-fold greater response to ammonia than sensors made with unmodified protein nanowires. Protein nanowires with the peptide that binds acetic acid yielded a 4-fold higher response than nanowires without the peptide. The protein nanowire-based sensors had greater responses than previously reported sensors fabricated with other nanomaterials. The results demonstrate that protein nanowires with enhanced sensor response for analytes of interest can be fabricated with a flexible genetic strategy that sustainably eliminates the energy, environmental, and health concerns associated with other common nanomaterials. 

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5. Multipurpose made colorimetric materials for amines, pH change and metal ion detection

   https://doi.org/10.1039/d1ra07811a  

   Bao, Lihong ; Jones, Leighton O. ; Garrote Cañas, Ana M. ; Yan, Yunhan ; Pask, Christopher M. ; Hardie, Michaele J. ; Mosquera, Martin A. ; Schatz, George C. ; Sergeeva, Natalia N. ( January 2022 , RSC Advances)

   Sensors are routinely developed for specific applications, but multipurpose sensors are challenging, due to stability and poor functional design. We report organic materials that operate in solution and gas phase. They show a strong response behaviour to at least three types of environmental changes: pH, amine and metal ion binding/detection. We have confirmed and validated our findings using various analytical and computational methods. We found that the changes in polarity of the solvent and pH not only red shift the tail of the absorption spectra, but also extend the peak optical absorption of these structures by up to 100 nm, with consequential effects on the optical gap and colour changes of the materials. Acid–base response has been studied by spectrophotometric titrations with trifluoroacetic acid (TFA) and triethyl amine (TEA). The experiments show excellent reversibility with greater sensitivity to base than acid for all compounds. Analysis into metal sensing using Zn( ii ) and Cu( ii ) ions as analytes show that the materials can successfully bind the cations forming stable complexes. Moreover, a strong suppression of signal with copper gives an operative modality to detect the copper ion as low as 2.5 × 10 −6 M. The formation of the metal complexes was also confirmed by growing crystals using a slow diffusion method; subsequent single crystal X-ray analysis reveals the ratio of ligand to metal to be 2 to 1. To test sensitivity towards various amine vapours, paper-based sensors have been fabricated. The sensors show a detection capability at 1 ppm of amine concentration. We have employed CIE L * a * b * colour space as the evaluation method, this provides numeric comparison of the samples from different series and allows comparison of small colour differences, which are generally undetectable by the human-eye. It shows that the CIE L * a * b * method can assess both sensitivity to a particular class of analytes and a specificity response to individual amines in this subclass offering an inexpensive and versatile methodology. 

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