A novel bismuth (Bi)-biopolymer (chitosan) nanocomposite screen-printed carbon electrode was developed using a Bi and chitosan co-electrodepositing technique for detecting multiple heavy metal ions. The developed sensor was fabricated with environmentally benign materials and processes. In real wastewater, heavy metal detection was evaluated by the developed sensor using square wave anodic stripping voltammetry (SWASV). The nanocomposite sensor showed the detection limit of 0.1 ppb Zn²⁺, 0.1 ppb Cd²⁺ and 0.2 ppb Pb²⁺ in stock solutions. The improved sensitivity of the Bi-chitosan nanocomposite sensor over previously reported Bi nanocomposite sensors was attributed to the role of chitosan. When used for real wastewater samples collected from a mining site and soil leachate, similar detection limit values with 0.4 ppb Cd²⁺ and 0.3 ppb Pb²⁺ were obtained with relative standard deviations (RSD) ranging from 1.3% to 5.6% (n = 8). Temperature changes (4 and 23 °C) showed no significant impact on sensor performance. Although Zn²⁺ in stock solutions was well measured by the sensor, the interference observed while detecting Zn²⁺ in the presence of Cu²⁺ was possibly due to the presence of Cu-Zn intermetallic species in mining wastewater. Overall, the developed sensor has the capability of monitoring multiple heavy metals in contaminated water samples without the need for complicated sample preparation or transportation of samples to a laboratory.

Flexible sensors with low fabrication cost, high sensitivity, and good stability are essential for the development of smart devices for wearable electronics, soft robotics, and electronic skins. Herein, we report a nanocomposite material based on carbon nanotube and metal oxide semiconductor for ultraviolet (UV) sensing applications, and its sensing behavior. The sensors were prepared by a screen-printing process under a low-temperature curing condition. The formation of a conducting string node and a sensing node could enhance a UV sensing response, which could be attributed to the uniform mixing of functionalized multi-walled carbon nanotubes and zinc oxide nanoparticles. A fabricated device has shown a fast response time of 1.2 s and a high recovery time of 0.8 s with good mechanical stability.

In this paper, a chitosan biopolymer-coated planar carbon electrode was developed for in situ determination of heavy metals (Zn ²⁺ and Pb ²⁺ ) using square-wave anodic stripping voltammetry. The experimental conditions were optimized with respect to deposition time, amplitude, and frequency. With 300-s deposition time, the heavy metal stripping was conducted at 0.05-V pulse amplitude, 20-Hz pulse frequency, and 0.004-V square-wave step voltage in 0.1-M acetate buffer at pH 4.6. Two distinguished peaks were observed at -0.86 and -0.37 V, which are associated with the stripping of Zn ²⁺ and Pb ²⁺ , respectively. The limit of detection was 0.6 and 1 ppb for Zn ²⁺ and Pb ²⁺ , respectively, and the relative standard deviations for repetitive measurements of Zn ²⁺ and Pb ²⁺ were in the range of 4.8%-5.4% (n = 30 with two identical electrodes). The chitosan biopolymer-coated carbon electrode was successfully applied for detecting Pb ²⁺ in tap water, mining wastewater, and soil leachate, and showed a reliable performance for measuring heavy metals with acceptable reproducibility. Overall, the developed biopolymer-coated carbon electrode exhibited excellent representativeness and reproductivity for in situ multiheavy metal ions detection in spiked samples, holding a great promise for on-site testing of heavy metals in drinking water.

Even at low levels heavy metal pollutants significantly threaten the quality of life, posing long-term risks. Current laboratory instrument-based measurement techniques have their limitations due to lengthy preparation and analysis steps. In this study, we introduce a screen-printed electrochemical sensor utilizing non-toxic, biodegradable sodium alginate grafted with 2-acrylamido-2-methyl propane sulfonic acid (AMPS) and conductive fillers for a trace-level lead ion detection in water. The presence of anionic functional groups facilitates chelation through electrostatic interactions, enabling them to preferentially bind to positive lead ions. With the proposed sensor, a low detection limit of 0.1 ppb was obtained by square wave anodic stripping voltammetry. This work demonstrates the effectiveness of an eco-friendly, sustainable sensor construct that takes advantage of enhanced organo-metallic interactions.

A layer of self-assembled 1-octadecanethiol was used to fabricate a palladium (Pd)/zinc oxide (ZnO) nanoparticle-based flexible hydrogen sensor with enhanced response and high selectivity at room temperature. A palladium film was first deposited using DC sputtering technique and later annealed to form palladium nanoparticles. The formation of uniform, surfactant-free palladium nanoparticles contributed to improved sensor response towards hydrogen gas at room temperature. The obtained sensor response was higher than for previously reported room temperature Pd/ZnO sensors. Furthermore, the use of the polymer membrane suppressed the sensor’s response to methane, moisture, ethanol, and acetone, resulting in the selective detection of hydrogen in the presence of the common interfering species. This study shows a viable low-cost fabrication pathway for highly selective room temperature flexible hydrogen sensors for hydrogen-powered vehicles and other clean energy applications.

Silver nanoparticle-based electrodes were studied extensively in recent years as an electrode material for wearable and flexible electronics due to their stability and conductivity. A wet chemical deposition technique is considered as a low-cost scalable technique. The current wet chemical-based nanoparticle deposition techniques include electrospray deposition, drop casting, spin coating, and the inkjet printing process. These techniques generally require a separate postdeposition annealing step. This can be a problem for substrates with a low melting point. In addition, some of the above-mentioned methods require physical contact, which increases the probability of cross-contamination. In this research, we present a technique that combines electrospray and laser radiation to deposit and sinter nanoparticles simultaneously on a rigid or flexible substrate. In this process, the microdroplets of aqueous silver nanoparticle suspension ejected in what is known as the microdripping mode from a metallic capillary nozzle, which can be controlled by an electric potential. A conical hollow laser beam is used to vaporize the liquid and sinter the nanoparticles at desired locations on a substrate. This is a promising technique compared to the traditional methods to fabricate conductive micropatterns due to its simplified one step deposition, suppressed cross-contamination, and applicability to various surfaces. Thin-film micropatterns of silver nanoparticles were fabricated using a Nd:YAG laser with powers from 5 to 13 W. The correlation between the grain size distribution, composition, and electrical resistivity was studied using a scanning electron microscope, energy-dispersive x ray, and four-point probe analysis. The results are comparable to the conventional thermal sintering method.