Chemical Sensors Research Articles

Blind cavefish evolved higher foraging responses to chemo- and mechanostimuli.

In nature, animals must navigate to forage according to their sensory inputs. Different species use different sensory modalities to locate food efficiently. For teleosts, food emits visual, mechanical, chemical, and/or possibly weak-electrical signals, which can be detected by optic, auditory/lateral line, and olfactory/taste buds sensory systems. However, how fish respond to and use different sensory inputs when locating food, as well as the evolution of these sensory modalities, remain unclear. We examined the Mexican tetra, Astyanax mexicanus, which is composed of two different morphs: a sighted riverine (surface fish) and a blind cave morph (cavefish). Compared with surface fish, cavefish have enhanced non-visual sensory systems, including the mechanosensory lateral line system, chemical sensors comprising the olfactory system and taste buds, and the auditory system to help navigate toward food sources. We tested how visual, chemical, and mechanical stimuli evoke food-seeking behavior. In contrast to our expectations, both surface fish and cavefish did not follow a gradient of chemical stimulus (food extract) but used it as a cue for the ambient existence of food. Surface fish followed visual cues (red plastic beads and food pellets), but, in the dark, were likely to rely on mechanosensors-the lateral line and/or tactile sensor-as cavefish did. Our results indicate cavefish used a similar sensory modality to surface fish in the dark, while affinity levels to stimuli were higher in cavefish. In addition, cavefish evolved an extended circling strategy to forage, which may yield a higher chance to capture food by swimming-by the food multiple times instead of once through zigzag motion. In summary, we propose that ancestors of cavefish, similar to the modern surface fish, evolved extended food-seeking behaviors, including circling motion, to adapt to the dark.

Efficient fabrication of high quality SU-8 photoresist based microsphere lasers via emulsion

SU-8 photoresist is a highly important material in the field of microfabrication and photonics owing to its low cost, excellent chemical and mechanical durability, high refractive index and transparency in the visible range. As a result, SU-8 photoresist has been employed as a cavity matrix for microsphere lasers. However, the current fabrication technique of SU-8 based microsphere lasers is complex and time-consuming. Here, we demonstrate a novel, cost-effective fabrication method for dye-doped SU-8 microspheres with diameters ranging from about 15–100 µm. These microspheres exhibit efficient lasing emission under optical pulse excitation. Lasing thresholds of 20–30 µJ mm−2 and quality factors ranging from 1500 to 3000 are achieved. The size dependence of lasing characteristics indicates that the lasing mechanism is due to whispering gallery mode. Interestingly, these microsphere lasers can work in water, presenting promising application prospects in the fields of biological and chemical sensors.

Synthesis of silica inverse opal and evaluation of its potential as an optical chemical sensor for detection of metal salts

In this paper, SiO2 inverse opal photonic crystals, made by the co-assembly of SiO2 and polymethylmethacrylate (PMMA) microspheres, were used to detect 20 different metal salts with a concentration of 0.002 mol/L. Surprisingly, two different behaviors were observed. Some metal salts caused a redshift in photonic bandgap (PBG) while the others led to a PBG’s blueshift. The observed different behaviors of salts are due to their distinct influence on the lattice constant of the inverse structures which was precisely investigated by analyzing the field emission scanning electron microscopy (FESEM) images and ultraviolet–visible (UV–Vis) spectroscopy. It has been revealed that the competition between the hydrophilicity of SiO2 and the hygroscopicity of metal salts led to a shift of PBG toward blue or red. The maximum shift in the PBG range was observed for mercury (II) nitrate salt (19 nm), which indicates a sensitivity of 9.5 nm per concentration unit (mM). Furthermore, the lowest displacement of the PBG was observed for the sodium nitrate salt (5 nm), which represents a sensitivity of 2.5 nm/mM. The lowest and highest values of the detection limit (LOD) for mercury (II) nitrate salt and sodium nitrate salt equal 0.193 mmol/L and 0.887 mmol/L, respectively. In addition, according to the calibration curve, with a regression coefficient of R2 > 0.95, there is a linear relationship between the salt concentration and the displacement of the PBG of the structure. Based on the results illustrating the sensitivity of the synthesized inverse opal to the type and concentration of the salts, inverse opal can be regarded as a promising structure to create a new perspective in the field of chemical sensing.

Liquid-Phase Exfoliated Graphene and Polytetrafluoroethylene for Highly Durable and Reusable Chemical Leak Detection Sensors

Graphene-based chemical sensors hold promise across diverse applications owing to their exceptional sensitivity and selectivity. However, achieving their long-term durability and reusability while preserving high sensitivity remains a significant challenge, particularly in harsh environments where exposure to strong chemicals is inevitable. This paper presents a novel approach to address this challenge by synergistically integrating liquid-phase exfoliated graphene (LPEG) with polytetrafluoroethylene (PTFE) within a single sensing strip. Through a comprehensive experimental investigation, we demonstrate the fabrication of highly durable and reusable chemical leak detection sensors by combining LPEG and PTFE. Furthermore, we explore the sensing mechanism, highlighting the roles of LPEG and PTFE in enhancing sensitivity and selectivity, along with durability and reusability. Performance evaluation reveals the sensors’ robustness against mechanical and chemical degradation, coupled with excellent recyclability. This innovative approach holds promise for applications in environmental monitoring, industrial safety, and healthcare, thus advancing the field of graphene-based chemical leak detection sensors.

Tetrazole-functionalized Organoboranes Exhibiting Dynamic Intramolecular N→B-Coordination and Cyanide-selective Anion Binding.

Starting from two different cyano-functionalized organoboranes, we demonstrate that 1,3-dipolar [3+2] azide-nitrile cycloaddition can serve to generate libraries of alkyl-tetrazole-functionalized compounds capable of intramolecular NàB-Lewis adduct formation. Due to the relatively low basicity of tetrazoles, structures can be generated that exhibit weak and labile NàB-coordination. The reaction furnishes 1- and 2-alkylated regio-isomers that exhibit different effective Lewis-acidities at the boron centers, and vary in their optical absorption and fluorescence properties. Indeed, we identified derivatives capable of selectively binding cyanide over fluoride, as confirmed by 11B NMR. This finding demonstrates the potentialities of this synthetic strategy to systematically fine-tune the properties of lead structures that are of interest as chemical sensors.

Development of an innovative colorimetric optical sensor for the detection of silver ions in environmental and biological samples

ABSTRACT A recently developed optical chemical sensor for silver assessment relies on polymer inclusion membranes (PIM) and avoids the use of plasticisers. This innovative optical sensor is constructed through a physical immobilisation process known as the encapsulation technique, resulting in an optical chemical membrane. The suggested PIM integrates 2-(2`-hydroxynaphthylazo)benzo-thiazole (HNABT) was used as a colorimetric reagent, polyvinyl chloride (PVC) as the foundational polymer, and dinonyl naphthalene sulphonic acid (DNNS) as an extractant. The created PIM demonstrates heightened responsiveness within the described approach, credited to the sensor membrane, in contrast to the optical sensor without PIM. The achieved results demonstrated that the sensor response was based on some factors such as plasticiser, film thickness, stirring effect, HNABT concentration, DNNS concentration and pH of the aqueous solution. Within the measurement range spanning from 7.5 to 250 ng mL−1 of Ag+ at pH 7.75, the absorbance response exhibits a notable correlation, achieving detection and quantification limits of 2.3 and 7.3 ng mL−1, respectively. The λmax for the PIM-based sensor registers at 577 nm. Additionally, the reproducibility and repeatability of the system are characterised by RSD of 2.25% and 1.13%, respectively, with a swift response time of approximately 3.0 min. The optode membrane’s selectivity is scrutinised in pH-buffered solutions concerning Ag+ ions. The proposed sensor is effectively applied for Ag+ assessment in food, water, environmental, and biological samples. The obtained results are corroborated by the FAAS procedure.

High Q/V single-mode nanobeam-grating resonator, functional in the ultra-high sensitive label-free lab-on-a-chip chemical sensor

High Q/V single-mode nanobeam-grating resonator, functional in the ultra-high sensitive label-free lab-on-a-chip chemical sensor

A hydroxyl-rich covalent organic framework for the precisely selective fluorescence sensing of explosives with high sensitivity

Covalent organic Frameworks (COFs) have become a new platform for functional research and material design. A novel covalent organic skeleton (DHB-TFP COF) was synthesized from 2-hydroxybenzene-1,3,5-tricarbaldehyde and 3,3′-dihydroxybenzidine using Schiff base reaction. DHB-TFP COF is a highly stable porous crystalline material and exhibits exceptional thermal and chemical resistance. DHB-TFP COF exhibited a selective and sensitive “turn-off” fluorescence response to 4-NP in ethanol, and TNP not only significantly quenched the fluorescence of DHB-TFP COF but also caused the obvious red-shift. The fluorescence intensity of DHB-TFP COF exhibited a linear correlation with the concentration of 4-NP with a detection limit of 0.40 μM. Furthermore, the maximum fluorescence peak observed for DHB-TFP COF demonstrated a linear relationship with TNP concentration with a detection limit of 11.15 μM. DHB-TFP COF exhibited satisfactory recovery in the detection of 4-NP and TNP in actual water sample indicating its practical application potential. The O atoms of rich hydroxyl and N atoms of C = N present on the surface of DHB-TFP COF scaffold can establish strong hydrogen bonds with 4-NP and TNP, facilitating their mutual interaction. The spectra studies indicated that the fluorescence quenching mechanism can be attributed to the absorption competitive quenching (ACQ) and fluorescence resonance energy transfer (FRET) mechanism. This study not only proposed the approach for synthesizing novel structured organic frameworks, but also developed a highly selective and sensitive fluorescence chemical sensor for identifying and detecting 4-NP and TNP.

CdTe@ZnS quantum dots for rapid detection of organophosphorus pesticide in agricultural products

Organophosphorus pesticides (OPPs) constitute the most widely employed class of pesticides. However, the prevalent use of OPPs, while advantageous, raises concerns due to their toxicity, posing serious threats to food safety. Chemical sensors utilizing quantum dots (QDs) demonstrate promising applications in rapidly detecting OPPs residues, thereby facilitating efficient inspection of agricultural products. In this study, we employ an aqueous synthesis approach to prepare low toxic CdTe@ZnS QDs with stable fluorescence properties. To mitigate the risk of imprecise measurements stemming from the inherent susceptibility of fluorescence to quenching, we have adopted the principle of fluorescence resonance energy transfer (FRET) for the construction of the turn-on quantum dot sensor. With a detection limit for chlorpyrifos as low as 10 ppb (10 μg/L), the QDs sensor exhibits notable resistance to interference from various pesticides. Application of this system to detect organophosphorothioate pesticides in apples produced results consistent with those obtained from high-performance liquid chromatography (HPLC) detection, affirming the promising application prospects of this sensing system for the rapid detection of OPPs residues.

Chiral Metal-Organic Frameworks with Spectroscopic Methods: Towards Chemical Sensor Devices.

Chiral Metal-Organic Frameworks (CMOFs) are a rapidly growing field reflecting their potential as selective and sensitive chemical sensors for chiral analytes. The highly tuneable nature of CMOFs enables the size, shape, and non-covalent interactions to be optimised towards specific analytes to engender strong intermolecular interactions and sensing responses. While CMOFs as chiral chemical sensor devices have been explored with electrochemical methods including differential pulse voltammetry (DPV), bipolar and chemiresistive sensing techniques, the CMOFs as chiral chemical sensors using spectroscopic methods has received significantly less attention. This review examines the synthesis of CMOFs for chemical sensors with spectroscopic methods such as photoluminescence, circular dichroism, and solid-state nuclear magnetic resonance with a view towards their incorporation into chemical sensor devices. Future directions of the field are highlighted for the generation of functional devices.

Intrinsically stretchable jellyfish-like gold nanowires film as multifunctional wearable chemical and physical sensors

We report on an intrinsically stretchable jellyfish-like gold nanowires film as a multifunctional wearable platform that can detect both chemical and physical biometrics. The film inherently exhibits multifunctionality, serving directly as an electrochemical electrode, strain sensor, temperature sensor, pressure sensor, and noncontact humidity sensor without the need of any additional materials. Our results highlight the excellent electrochemical properties, evidenced by a large electrochemical active surface area (EASA) of approximately 22.39 cm2 and the ability to withstand significant strain values up to 70 %. Leveraging these attributes, a stretchable electrochemical glucose biosensor was further designed with high sensitivity (45.40μA·mM−1·cm−2) and low limit of detection (10 μM). In addition, its sensing applications in strain, temperature, pressure and noncontact humidity were systematically explored. Impressively, the gold film is capable of monitoring multiple human motions and physiological signals, including joints bending, pulse motions, throat motions (e.g., drinking, speaking, swallowing and pronunciation recognition) and breathing. Furthermore, the film exhibited great versatility by integrating with 3D printing hydrogels, enabling customized patterning. The results demonstrate that our gold nanowires coating approach represent a new route to design multimodal soft wearable platforms for applications in personalized medicine and next-generation healthcare systems.

Application of pfg NMR diffusometry to study diffusion and ionization phenomena in plasticized polymeric membranes doped with ionic liquids

Ionic liquids (ILs) are increasingly used as promising organic solvents for a variety of applications, including electrochemical processes, novel separation techniques and innovative methods of synthesis, due to their low volatility, excellent solvation properties, high ionic conductivity and electrochemical stability. Moreover, the tunable properties of ILs determined by their composition make them favorable candidates as dopants for composite and/or functional polymeric materials, e.g. in the membranes of chemical sensors. To effectively use ILs in polymeric materials and control the characteristics of the latter, one should develop a complete understanding of the properties of ILs in the polymeric phase, such as their diffusion and ionic behavior.In our previous work, we applied pulsed field gradient (PFG) NMR technique to verify the results of a chronopotentiometric method conventionally used to determine the diffusion coefficients and electrolytic properties of electrolytes in plasticized poly(vinyl chloride) (PVC) membranes of chemical sensors. The results obtained with these two independent methods were in good agreement, confirming that PEG NMR diffusometry is a viable technique for assessing the diffusion properties of species even in highly viscous polymeric media of low polarity.Here we report a comprehensive study of the transport and ionic behavior of IL 1-hexyl-3-methyl-1H-imidazolium bis[(trifluoromethyl)sulfonyl]amide ([C6Meim][NTf2]) in a poly(vinyl chloride) matrix, performed in situ by means of PFG NMR diffusometry. A number of sets of spectra for the 1H and 19F nuclei of the [C6Meim][NTf2] ionic liquid in PVC membranes doped with the plasticizer bis(2-ethylhexyl)sebacate were registered at different amplitudes of the magnetic field gradient. The mobility of both individual ions of the IL and the formed ion associates was investigated over a broad range of IL concentrations in the PVC matrix; in addition, the ionization degree and dissociation constant of [C6Meim][NTf2] were determined and their dependence on the IL content was traced.

Role of Silica, Carbon, and ZnO Nanomaterials in the Fabrication of Electrochemical Sensors for the Detection of Water Contaminants and Food Dye

AbstractSilica‐based nanomaterials have attracted huge attention for maximizing their safety and efficacy due to their nontoxicity, chemical and thermal stability, size tunability, and versatile functionality. Nanosilica with ZnO or carbon in a composite has excellent usage as an electrochemical sensor. Recent technological progression in nanotechnology and nanoscience has seen a number of applications of zinc oxide (ZnO) nanomaterials ranging from electronics, and sensing to environmental, and biomedical applications because of its various applications, multifunction, high specific surface area, stability, biocompatibility, nontoxicity, electrochemical activities, and so on. Carbon also has various advantageous properties like renewability, low ohmic resistance, and very stable response due to which carbon paste electrodes have attracted attention in the fabrication of electrochemical sensors. Electrochemical sensors are inexpensive, portable, and have excellent ability in detecting water contaminants, pesticides, disinfectants, pathogens, and different molecules. Artificial dyes are usually mixed with vegetable sauces, drinks, and other food items, which can cause cancer in human body. Voltametric methods with electrochemical sensors can be used to detect them in food samples. In this review, the present applications of ZnO and carbon nanomaterial‐based chemical sensors are meticulously studied to detect water contaminants and food dyes where nanosilica plays an important role as a sensor modifier.

Integrated imaging and proteomics sensors detect proteome aggregation induced by platinum-based chemotherapy drugs in living cells and mice model

Proteome aggregation is challenging to analyze given its loss of defined 3-D structures to develop chemo- and bio-sensors. Herein, we present integrated chemical sensors to image the occurrence of proteome aggregation and dissect its proteomic composition. Via these combinative sensors, we systematically reveal for the first time platinum-based drugs can deteriorate proteome stability, compromise protein homeostasis (proteostasis) network, and consequently cause proteome aggregation. Fluorescent protein aggregation imaging sensors (AggStain and AggRetina) not only confirms these drugs generally induce intracellular proteome aggregation but also quantifies the compactness (polarity) heterogeneity inside these aggregates. Chemical proteomics sensor (AggLink) further captures and profiles the composition of aggregated proteome, which uncovers the fluctuations of proteostasis network and metabolic pathways. In mice model, proteome aggregation and oxidative stress are imaged in multi-organs with platinum enrichment. Together, we integrate imaging and proteomics sensors to provide an alternative mechanism-of-action for platinum-based drugs’ anti-cancer function in addition to their common DNA intercalation mechanism.

Boron-nitride nanostructures for the detection of harmful gases (CO, CO2, H2S, N2O, and SO2)

Boron-nitride (BN) structures are considered materials with several applications, including sensing platforms. Through density functional theory calculations based on the PBE-D3/6-311G(d,p) level of theory, we propose the boron-nitride nanosheet, armchair nanotube (5,5), and fullerene as possible sensors for the harmful gases CO, CO2, H2S, N2O, and SO2. According to our results, the systems exhibit adsorption energies of −0.10 eV to −1.26 eV, and remarkable electronic parameters such as chemical potential, energy gap, and HOMO and LUMO energies, ideal for serving as chemical sensors of such pollutant gases. The nanostructures can be selective to sense a particular gas, mainly CO, N2O, and SO2. Additionally, we note a dramatic change in the electrical conductivity up to 2.14 eV, and low recovery time from 15 μs to 6.2 s. Finally, the BNNS-SO2, BNNT-N2O, BNNT-SO2, and BNF-CO are the more promissory systems to be used as chemical sensors of SO2, N2O, and CO.

Feasibility study of coffee husk char-derived carbon dots to enhance solar photovoltaic-thermal applications

Coffee is one of the most traded commodities in the world. Coffee husk makes up the majority of the solid debris generated during the dry processing of coffee, which is between 30% and 50%. Pyrolysis is a reliable and feasible technology to valorise the coffee husk. The present study proposes and investigates a novel method for producing carbon dots from coffee husk char through pyrolysis. Nanomaterials are becoming more popular to improve the thermal and optical properties of working fluids used in solar photovoltaic and thermal conversion systems. The coffee husk-char derived carbon dot (CHC-CD) nanofluids are prepared with different char concentrations (1%, 2%, 3% and 4%). The chemical and optical properties of the nanofluid produced from coffee husk char (CHC-CD nanofluid) are investigated. The morphology, size and particle size distribution of the CHC-CD particles were studied using field emission scanning electron microscopy (FESEM) and high-resolution transmission electron microscopy (HRTEM). The particles were found to have an average size of 5.38 nm. The CHC-CD nanofluid had a basic pH and negative zeta potential, which was found to decrease with an increase in the char concentration and pH. The nanofluid prepared with 2% char was found to have a zeta potential of −61.4 mV. It was evident from the UV–vis transmittance spectra that the CHC-CD nanofluid prepared with a char concentration of 2% had very limited transmittance in the UV region and good transmittance above 735 nm. This transmittance range is found to be favourable for the smooth and efficient operation of silicon-based solar PV cells. The CHC-CD nanofluid also showed a maximum intensity emission wavelength of 522 nm at an excitation wavelength of 450 nm. Characterisation of the carbon phase, surface functional groups, and surface defects was also done using XRD, FTIR, and Raman spectroscopy, respectively. The optical and chemical properties indicate that the developed CHC-CD nanofluid can find application not only in solar photovoltaic and thermal systems but also in applications in biomedical and chemical sensor applications.

Inductance coil high-frequency contactless chemical sensor: Systematic study of its cationic sensitivity

Contactless sensors for chemical analysis, based on inexpensive and widely available electronic components, are a promising alternative to existing routine laboratory methods. We have proposed a novel type of a contactless sensor, composed of three simple components: an alternate current generator, an inductance coil, and a receiver. The sample, placed into the coil as a core of the inductor, modifies the current passing through the coil. Previously, we have demonstrated that this contactless sensor may have numerous applications for chemical analysis. In this work, we have explored the performance of the coil-based measuring platform further and performed the first systematic study of the response of inductance coil sensor to metal cations in aqueous solutions. Sixteen metal cations with different charge and radii were studied. Linear response ranges, sensitivity values and the comparison between univariate and multivariate regression modeling are presented. The largest linear response range was observed for transition metal cations Ni2+, Cu2+, Pb2+ and Nd3+ (10-3 – 10-1 M), the narrowest – for Li+ and Gd3+ (10-2 – 3.2x10-1 M) with R2 values larger than 0.94. The dependence of the response on the radius and the charge of the cation are discussed. The analytical characteristics of the device show its potential in contactless and low-cost chemical analysis and set the ground for the future research.

Aerosol-Synthesized Surfactant-Free Single-Walled Carbon Nanotube-Based NO2 Sensors: Unprecedentedly High Sensitivity and Fast Recovery.

This study pioneers a chemical sensor based on surfactant-free aerosol-synthesized single-walled carbon nanotube (SWCNT) films for detecting nitrogen dioxide (NO2). Unlike conventional CNTs, the SWCNTs used in this study exhibit one of the highest surface-to-volume ratios. They show minimal bundling without the need for surfactants and have the lowest number of defects among reported CNTs. Furthermore, the dry-transferrable and facile one-step lamination resultsin promising industrial viability. When applied to devices, the sensor shows excellent sensitivity (41.6% at 500ppb), rapid response/recovery time (14.2/120.8s), a remarkably low limit of detection (below ≈0.161ppb), minimal noise, repeatability for more than 50 cycles without fluctuation, and long-term stability for longer than 6months. This is the best performance reported for a pure CNT-based sensor. In addition, the aerosol SWCNTs demonstrate consistent gas-sensing performance even after 5000 bending cycles, indicating their suitability for wearable applications. Based on experimental and theoretical analyses, the proposed aerosol CNTs are expected to overcome the limitations associated with conventional CNT-based sensors, thereby offering a promising avenue for various sensor applications.

MEMS Resonant Beam with Outstanding Uniformity of Sensitivity and Temperature Distribution for Accurate Gas Sensing and On-Chip TGA.

Micromechanical resonators have aroused growing interest as biological and chemical sensors, and microcantilever beams are the main research focus. Recently, a resonant microcantilever with an integrated heater has been applied in on-chip thermogravimetric analysis (TGA). However, there is a strong relationship between the mass sensitivity of a resonant microcantilever and the location of adsorbed masses. Different sampling positions will cause sensitivity differences, which will result in an inaccurate calculation of mass change. Herein, an integrated H-shaped resonant beam with uniform mass sensitivity and temperature distribution is proposed and developed to improve the accuracy of bio/chemical sensing and TGA applications. Experiments verified that the presented resonant beam possesses much better uniformity of sensitivity and temperature distribution compared with resonant microcantilevers. Gas-sensing and TGA experiments utilizing the integrated resonant beam were also carried out and exhibited good measurement accuracy.

All‐Printed Electrically Driven Lighting via Electrochemiluminescence

AbstractElectrochemiluminescence (ECL) has attracted significant attention as a promising light‐emitting technology owing to its simple configuration and solution processability. ECL has wide applications in biological and chemical sensors, lighting, and displays. ECL lighting devices are fabricated as sandwiched structures with a transparent electrode on top, which limits their widespread adoption. Intricate structures with high precision and customizable designs can be directly fabricated using 3D printing. However, 3D printing of ECL devices is challenging because of poor printability and structural integrity of ECL luminophore inks. Here, all‐printed electrically driven lighting is demonstrated using the direct ink writing method. The ECL reactive layer and electrodes are directly printed using a side‐by‐side electrode configuration. A 3D printable ECL ink is developed by incorporating silica nanoparticles as rheological modifiers to realize well‐defined patterns with high structural integrity. Graphene is introduced on Ag multilayer electrodes to embrace both the electrical conductivity and electrochemical stability for efficient ECL operation. This all‐printing approach allows the fabrication of ECL devices with complex designs, such as combs and spirals. Moreover, it facilitates seamless printing on various substrate materials, making this technology an asset in the fields of biology, chemistry, and electronics.