Solid-state Sensors Research Articles

Brownian Motion Paving the Way for Molecular Translocation in Nanopores.

Tracing fast nanopore-translocating analytes requires a high-frequency measurement system that warrants a temporal resolution better than 1µs. This constraint may practically shift the challenge from increasing the sampling bandwidth to dealing with the rapidly growing noise with frequencies typically above 10kHz, potentially making it still uncertain if all translocation events are unambiguously captured. Here, a numerical simulation model is presented as an alternative to discern translocation events with different experimental settings including pore dimension, bias voltage, the charge state of the analyte, salt concentration, and electrolyte viscosity. The model allows for simultaneous analysis of forces exerting on a large analyte cohort along their individual trajectories; these forces are responsible for the analyte movement leading eventually to the nanopore translocation. Through tracing the analyte trajectories, the Brownian force is found to dominate the analyte movement in electrolytes until the last moment at which the electroosmotic force determines the final translocation act. The mean dwell time of analytes mimicking streptavidin decreases from ≈6 to ≈1µs with increasing the bias voltage from ±100 to ±500mV. The simulated translocation events qualitatively agree with the experimental data with streptavidin. The simulation model is also helpful for the design of new solid-state nanopore sensors.

Solid-state real-time colorimetric sensing of ultra-trace copper ions using aqueous compatible chromatic probe imbued porous polymer monolithic sensor

In this work, we design an aqua-compatible and sustainable chromatic sensor for the selective detection of copper ions in aqueous solutions for application in industrial quality control and environmental analysis. The solid-state chromatic sensor is fabricated through the uniform decoration of an indigenously synthesized unique chromoionophoric probe (TMAP), i.e., (2,2′-(((1E,1′E)-thiophene-2,5-diylbis(methaneylylidene)) bis(azaneylylidene))diphenol) onto a bimodal macro-/meso‑porous polymer monolith, poly(2VP-co-DVB), i.e., poly(2vinylpyridine-co-divinylbenzene), to exploit the possibility of solid-state colorimetric ion sensing. The polymer monolith and sensor materials' topography and morphology are characterized through p-XRD, FE-SEM, XPS, EDX, TEM, SAED, TGA, FT-IR and BET/BJH analysis. The ion-sensing is accompanied by a discernible color transition from vivid yellow to subdued red, with a detection and quantification limit value of 0.20 and 0.51 μg/L for Cu2+, respectively. The sensor affirms a fast detection (≤60 s) for Cu2+, with a linear signal/colorimetric response in the concentration range of 3–100 μg/L. The parameters such as sensor dosage, chromatic receptor dose, pH, temperature, sensing kinetics and reusability are optimized for reliable and reproducible ion-sensing. The solid-state sensor reveals excellent selectivity and sensitivity for Cu2+, and its practical utility with environmental/industrial samples proves its utility as a portable sensor kit for real-time on-site analysis for ultra-trace Cu2+.

Simple and ultrasensitive solid-state electrochemiluminescence sensor based on g-C3N4 and Au NPs for detection of Doxorubicin

A simple and ultrasensitive solid-state electrochemiluminescence (ECL) sensor was developed for the detection of doxorubicin (DOX). The sensor was constructed by coating the electrode with graphitic carbon nitride (g-C3N4) and a complex substance called Au NPs@HAP@CS, which consists of Au nanoparticles (Au NPs), hydroxylaptite (HAP), and chitosan (CS). The luminescent reagent, g-C3N4, obtained from high temperature pyrolysis of melamine, produced a relatively sensitive but unstable ECL signal in a K2S2O8 solution (pH 8.0). The introduced Au NPs, with their high negative potential, enhanced electron transport and captured and store excess electrons injected into g-C3N4, thereby improving the ECL signal and its stability. The non-toxic green HAP, serving as a carrier of Au NPs, further enhanced the ECL signal, and the addition of CS improved the stability of the sensor. Under optimal conditions, the fabricated ECL sensor demonstrated sensitive determination of DOX, with a linear range of 5.0 × 10−15 ∼ 1.0 × 10−8 mol/L and a detection limit as low as 1.67 × 10−15 (S/N = 3). Notably, the resulting sensor exhibited good stability, high sensitivity, and reliable reproducibility, making it suitable for the detection of trace DOX in human serum.

Online Calibration of Extrinsic Parameters for Solid-State LIDAR Systems.

This work addresses the challenge of calibrating multiple solid-state LIDAR systems. The study focuses on three different solid-state LIDAR sensors that implement different hardware designs, leading to distinct scanning patterns for each system. Consequently, detecting corresponding points between the point clouds generated by these LIDAR systems-as required for calibration-is a complex task. To overcome this challenge, this paper proposes a method that involves several steps. First, the measurement data are preprocessed to enhance its quality. Next, features are extracted from the acquired point clouds using the Fast Point Feature Histogram method, which categorizes important characteristics of the data. Finally, the extrinsic parameters are computed using the Fast Global Registration technique. The best set of parameters for the pipeline and the calibration success are evaluated using the normalized root mean square error. In a static real-world indoor scenario, a minimum root mean square error of 7 cm was achieved. Importantly, the paper demonstrates that the presented approach is suitable for online use, indicating its potential for real-time applications. By effectively calibrating the solid-state LIDAR systems and establishing point correspondences, this research contributes to the advancement of multi-LIDAR fusion and facilitates accurate perception and mapping in various fields such as autonomous driving, robotics, and environmental monitoring.

Ultrasensitive solid-state electrochemiluminescence sensor based on lotus root shaped carbon fiber, CdSe QDs and Fe3O4 synergically amplify Ru(bpy)32+ luminophore signal for detection of cyfluthrin.

An efficient and innovative electrochemiluminescence (ECL) sensor was developed for trace detection of cyfluthrin.The sensor utilized materials such as lotus root shaped carbon fiber (Co CNFs), cadmium selenide quantum dots (CdSe QDs), and Fe3O4 to amplify Ru(bpy)32+ signals. Co CNFs, with its large specific surface area and porosity, served the purpose of not only enhancing the stability of the sensor by fixing CdSe QDs and Ru(bpy)32+ on the Co CNFs/GCE, but also facilitating electron transfer. CdSe QDs was involved in the luminescence reaction and collaborated with Ru(bpy)32+ to enhance the sensor's sensitivity, while Fe3O4 promoted electron transfer in the system due to its large surface area. The solid-state ECL sensor achieved satisfactory signal under the synergistic action of these components. The ECL signal of the sensor was quenched by cyfluthrin, and a favorable linear relationship was observed between the sensor and cyfluthrin in the concentration range 1 × 10-12 to 1 × 10-6 M. The detection limit of the sensor was 3.3 × 10-13 M (S/N = 3). The utilization of lotus root shaped carbon fiber, CdSe QDs, and Fe3O4 in the Ru(bpy)32+ system demonstrated a synergistic effect for cyfluthrin detection, presenting a new approach for the rapid determinationanalysis of pesticide residues in foods.

Development of green and sustainable ammonia sensor from xanthohumol extract-immobilized polylactic acid nanofibers

Ammonia is a significant industrial gaseous agent that is colorless. However, long exposure to ammonia gas can cause organ damages or even death. This study describes the preparation of a solid-state vapochromic sensor for gaseous and aqueous ammonia using eco-friendly smart colorimetric polylactic acid nanofibers. Xanthohumol (XMOL) is a natural spectroscopic probe that can be found in the common hop (Humulus lupulus L.) plant. Nanoparticles of mordant/xanthohumol (M/XMOL) coordinated complex were synthesized by immobilizing the xanthohumol direct dyestuff into polylactic acid nanofibers in the presence of a mordant (potassium aluminum sulfate). Xanthohumol can be described as an appropriate sensor for gaseous and aqueous ammonia due to its tiny molecular size and high water-solubility. Both of CIE Lab color parameters and absorbance spectra were used to inspect the color shift of the xanthohumol-finished polylactic acid nanofibers from yellow to colorless upon exposure to ammonia. This could be attributed to the intramolecular charge transfer caused by molecular switching of xanthohumol. In a fraction of second, the polylactic acid nanofibrous fabric showed a colorimetric change with a detection limit of 10–450 mg/L. The absorption spectra of the xanthohumol probe exhibited hypsochromic shift with a wavelength change from 465 nm to 315 nm (isosbestic point of 370 nm) in response to an aqueous solution of ammonia. Transmission electron microscopic (TEM) images showed that M/XMOL particles were 13–27 nm in diameter, whereas scanning electron microscopic (TEM) images demonstrated that the polylactic acid nanofibers were 150–450 nm in diameter. We observed no significant differences in air-permeability and bending-length of the nanofibrous fabric after immobilization of M/XMOL into polylactic acid nanofibers. In addition, the colorfastness properties of the treated polylactic acid nanofibers were investigated.

Imaging electromagnetic boundary of microdevice using a wide field quantum microscope.

Imaging of electronic device surface or sub-surface electromagnetic fields under operating conditions is important for device design and diagnosis. In this study, we proposed a method to characterize specific magnetic field properties of electromagnetic devices at micron-scale using a solid-state quantum sensor, namely diamond nitrogen-vacancy (NV) centers. By employing a wide-field magnetic field measurement technique based on NV centers, we rapidly obtain the first-order magnetic field distribution of anomalous regions. Furthermore, we approximate the second-order magnetic field (magnetic gradient tensor) using the differential gradient method. To visualize the electromagnetic anomalous regions boundary, we utilize the tensor invariants of the magnetic gradient tensor components, along with their nonlinear combinations. The identification error rate of the anomalous regions is within 12.5%. Additionally, the electromagnetic field of anomalous regions is simulated showing the measurement accuracy. Our study shows that the experimental results are very similar to the theoretical simulation of the electromagnetic field (error: 7%). This work is essential for advancing electromagnetic field characterization of electronic devices and the advancement of quantum magnetic sensor applications.

Sustainable and reusable probe-encapsulated porous poly(AMST-co-TRIM) monolithic sensor for the selective and ultra-sensitive detection of toxic cadmium(II) from industrial/environmental wastewater

This study focuses on a new type of fast responsive solid-state visual colorimetric sensor, custom engineered with dual-entwined porous polymer imbued with chromoionophoric 4-(sec-butyl)− 2-((5-mercapto-1,3,4-thiadiazol-2-yl)diazenyl)phenol (SMDP) probe for selective and ultra-sensitive colorimetric sensing of Cd(II). The polymer monolith, i.e., poly(aminostyrene-co-trimethylolpropanetrimethacrylate) denoted as poly(AMST-co-TRIM), is designed through a stoichiometric blending of monomer, crosslinker, and porogens leading to superior surface area, pore and adsorption properties for the voluminous incorporation of SMDP probe for target specific ion sensing. The porosity, surface and structural characteristics of the poly(AMST-co-TRIM)monolith and poly(AMST-co-TRIM)SMDP sensor are investigated using p-XRD, XPS, TG-DTA, FT-IR, BET/BJH, FE-SEM, HR-TEM, EDAX, and SAED techniques. The poly(AMST-co-TRIM)SMDP sensor reveals a frozen geometrical orientation of SMDP molecules to bind selectively with Cd(II), forming stable charge-transfer complexes by exhibiting transitional visible color shifts from light yellow to dark green (λmax 608 nm). The sensor imposes a linear response from 0–200 ppb, with quantification and detection limits of 0.95 and 0.28 ppb. The fabricated sensor material is cost-effective and versatile in its solid-state naked-eye sensing, with excellent reusability. The sensor performance has been verified using various environmentally contaminated water and commercial cigarette samples, with a recovery of ≥ 99.12% and an RSD of ≤ 1.95%, thus reflecting exceptional data reproducibility/reliability.

Microfabricated potentiometric sensor based on a carbon nanotube transducer layer for selective Bosentan determination

Abstract In this work, a solid-state electrochemical sensor relying on potentiometric transduction was constructed and optimized to detect Bosentan (BOS) in its pharmaceutical dosage form and human plasma. BOS is useful in pulmonary hypertension management as a nonselective endothelin receptor antagonist. A printed circuit board has been constructed and used as a substrate for microfabricated Cu electrodes. In comparison to a microfabricated control (Cu/ISM) electrode, the sensor potential signal drift was enhanced, and the response time was reduced by using multi-walled carbon nanotubes (MWCNTs) as an ion-to-electron transducer layer. According to IUPAC requirements, the suggested BOS sensors have been electrochemically characterized, and the linear dynamic range is (1.0 × 10−8 to 1.0 × 10−5) M with a limit of detection of 6.28 × 10−9 M and 6.12 × 10−9 M for MWCNT-based sensor (Cu/CNT-NC/ISM) and control sensor (Cu/ISM), respectively. The described sensors have been used successfully to selectively determine BOS in dosage form and human plasma without any pre-treatment steps.

Predicting Ozone Depletion using BIn2O3 With RH based Solid Conductometric Sensor

<p>Ozone depletion arises due to the presence of gases like chlorofluorocarbons and halons which are liberated into the atmosphere. The region of earth’s atmosphere named as ozone shield, in which absorbs the ultra violet radiations of the sun. Although, its thickness varies periodically, this layer is primarily located in the lower stratosphere between 15 to 35 kms above the earth. Due to this, the ultraviolet rays directly enter into the earth causes harmful effects little by little on both living and non-living organisms. In this paper, BIn2O3 with rh sensor in co precipitation method is used to detect the ozone depletion and it is based on the solid-state gas sensors. To achieve the excellent performance of an ozone depletion detecting branch like BIn2O3 with rh, this was designed using a simple precipitation method. The coprecipitation method had deposited in BIn2O3 with a thickness of 45 to 50 nanometer. The detection limit of ozone reduced as 30 parts per billion. Further, the gas detector demonstrated high sensitivity and selectivity of the device. The rhodium covers the surface areas ranges from 0 to 0.1. It reaches the accuracy of 96%. According to the degree of rhodium coverage, the sensors will be response to the ozone gas. The oxygen chemisorbed ability and a coverage of a great surface area of BIn2O3 with rhodium highly related to the excellent sensing behavior. This study paves the way for an exact sensing and ppb level detection ozone gas.</p>

A Stimuli-Responsive Dual-Emitting Covalent Organic Framework Shows Selective Sensing of Highly Corrosive Acidic Media via Fluorescence Turn-On Signal with White Light Emission.

Luminescent covalent organic frameworks (LCOFs) have been employed as platforms for sensing analytes. Judicial incorporation of appropriate functional units inside the framework leads to the different electronic states in the presence of external stimuli, e.g., temperature, pH, etc. We report herein a new COF (TPEPy) as a solid-state acid sensor specific for the highly acidic environments that range from pH ∼0.5 to ∼3.0. This COF shows a protonation-induced reversible color change from bright yellow to deep red upon decreasing the pH from 3 to 0.5 and vice versa. No visual color change was, however, observed above pH 3.0. Photoluminescence (PL) studies show that the intrinsic emission peak of the TPEPy COF at 530 nm is shifted to 420 nm owing to the N-protonation of the imine nitrogen of COF within this pH range. Extensive studies demonstrate that the protonation behavior of the COF is counterion dependent. This was revealed when different acids, e.g., HCl, HNO3, HBr, and HI, were employed. The intensity of the proton-induced emission peak at 420 nm depends significantly upon the counterions with the order of HCl > HNO3 > HBr > HI. These anions interact with the protonated TPEPy COF by cation-anion and H-bonding interactions. Further, the pristine COF showed near white light emission at a particular pH of 2.5 (CIE coordinates 0.27, 0.32). From the PL spectrophotometric titrations, the deprotonation pKa was experimentally found to be 1.8 ± 0.02 for the TPEPy COF. The sensor reported herein is reversible, reusable, and regenerable and is useful for assessing pH fluctuations within a strongly acidic range via digital signaling.

A Review of Development of Chemical Sensors

A comprehensive summary of the most recentre search concentrating on chemical sensors utilizing nano tubes,Nano rods,Nano belts, and nano wiresis given in this article. The experimental principle, sensor device design,sensor mechanism, and multiple significant conclusionsreceivethevastmajorityofourattention.Thefollowingfoursectionsprovide additional information on the creation of chemical sensors based on nanostructured materials: nanotube sensors, Nano rod sensors, Nano belt sensors and Nano wire sensors. Weconcludethisreviewwithpersonalperspectivesonthedirectionstowardswhichfuture research on nanostructured sensors might be directed. At ambient temperature, the nanotube sensors show a far faster response time and a significantly higher sensitivity than the current solid-state sensors. Reversibility of the sensor can be obtained by heating it to a high temperature or by slowly recovering under ambient conditions. Over the past decade, synthesized nanomaterial’s, such as carbon nanotube, nanoparticle, quantum dot, and nanowire, have already made breakthroughs in various fields, including biomedical sensors. Enormous surface area-to-volume ratio of the Nano materials increases sensitivity dramatically compared with macro-sized material. Herein we present a comprehensive review about the working principle and fabrication process of nanowire sensors. Then anotube sensor sex hibit a fast response and asubstantially higher sensitivity than thatofexistingsolid-statesensorsatroomtemperature.Sensorreversibilityisachievedbyslow recovery under ambient conditions or by heating to high temperatures.Synthesized Nano materials, including carbon nanotubes, nanoparticles, quantum dots, and nanowires, have already achieved significant advances in a number of sectors, including biological sensors, during the last ten years. When compared to macro-sized material, the nanoparticles' enormous surface area-to-volume ratio significantly boosts sensitivity. We provide a thorough overview of the fabrication process and operating principle of the nanowire sensor here. Recent advances including self-powering, reusability, sensitivity in high ionic strength solvent,andlong-term stabilityaresurveyedandhighlightedas well.Nanowire isexpectedtolead significant improvement of biomedical sensor in the near future.Advantages and disadvantages of the sensors are provided along with brief descriptions. An electrical device that monitors changes in a quantity, such as voltage, temperature, pressure, or humidity, is called a sensor. As a result, classification is done according to the attribute that a sensor measures. A temperature sensor detects even the smallest variations in its environment or shifts in temperature, such as hot or cold weather. Microelectronic manufacturing techniques have been used to manufacture chemical and electrochemical sensors.Thedevelopment ofchemical sensors has been spurred forward by the recentadvancesinmicromachingtechnology.Chemicalsensorresearchhasadvancedthanksto micro machining methods like sacrificiallayers, plasmaetching, andchemicalanisotropicetching. These methods enable the creation of low mass, low power driven devices as well as controlled working conditions and temperature. Researchersbecameinterestedinthesecarefullychoseninvitronanostructureswhentheywere combined with nanomaterials because the improved properties of these nanostructures led to advances inthe analytical performance of chemical and biosensors. Thisstudycoversthe latest advancements in recognition elements that are integrated in to chemical sensors and bio sensors used in the food, medical, and environmental domains. These elements include both traditional ones like enzymes and antibodies as well as more modern ones like aptomers and phages.Cyclic voltammetry and electron microscopy are frequently used in the characterization of chemically modified sensors and biosensors because they enable the confirmation of electrode mechanisms and surface morphologies. X-ray photoelectron spectroscopy (XPS), among other methods, is a special tool for obtaining information on the sensor surface that is qualitative, quantitative/semi-quantitative, and speciation-related. However, XPS is still not widely applied in this industry. The purpose of this work is to review a few selected studies that demonstrate how wellXPSperformswhencharacterizingthetopsurfacelayersofbiosensorsandchemically Modified sensors. The reader is provided with the necessary background information in a brief introduction to X-ray photoelectron spectroscopy. The use of XPS to characterize sensors appropriate for environmental and food analysis is highlighted.

CRISPR-assisted solid-state nanopore sensor for rapid and sensitive point-of-care amendable of monkeypox virus detection via RPA amplification

CRISPR-assisted solid-state nanopore sensor for rapid and sensitive point-of-care amendable of monkeypox virus detection via RPA amplification

Targeted Analysis of the Size Distribution of Heavy Chain-Modified Hyaluronan with Solid-State Nanopores.

The glycosaminoglycan hyaluronan (HA) plays important roles in diverse physiological functions where the distribution of its molecular weight (MW) can influence its behavior and is known to change in response to disease conditions. During inflammation, HA undergoes a covalent modification in which heavy chain subunits of the inter-alpha-inhibitor family of proteins are transferred to its structure, forming heavy chain-HA (HC•HA) complexes. While limited assessments of HC•HA have been performed previously, determining the size distribution of its HA component remains a challenge. Here, we describe a selective method for extracting HC•HA from mixtures that yields material amenable to MW analysis with a solid-state nanopore sensor. After demonstrating the approach in vitro, we validate extraction of HC•HA from osteoarthritic human synovial fluid as a model complex biological matrix. Finally, we apply our technique to pathophysiology by measuring the size distributions of HC•HA and total HA in an equine model of synovitis.

An azo-receptor immobilized mesoporous honeycomb silica framework as a solid-state chromogenic sensor for capturing ultra-trace cadmium ions from environmental/industrial samples

A solid-state naked-eye sensor composed of a mesoporous honeycomb structured silica monolith impregnated with a DMTHBD receptor offers a simple, rapid and eco-benign approach for the selective sensing of trace Cd2+, with brilliant color transitions.

Fabrication of an all-in-one self-enhanced solid-state electrochemiluminescence sensing platform for the selective detection of spermine.

The fabrication of an all-in-one solid-state ECL sensing platform is beneficial not only for expediting the miniaturization of sensing devices, but also, more importantly, for enabling point-of-care applications. In the present work, a self-enhanced solid-state ECL sensing platform is fabricated using newly synthesised silica polyethylene nanoparticles (SiO2-PEI NPs) which generate a co-reactant in situ and easily self-assemble with Ru(bpy)32+ and shows selective and sensitive detection of spermine at physiological pH (7.4). Spermine induces the maximum ECL emission intensity compared to other biogenic amines due to the presence of two secondary amines. A possible ECL reaction mechanism has been proposed based on CV and ECL experiments, DFT calculations, and in situ ECL spectrum analysis. The developed solid-state sensor showed a linear increase in ECL intensity with increasing spermine concentration in the range of 10 nM to 100 nM with an LOD of 12.2 nM. Compared to other biogenic amines in previous works, chemically synthesised SiO2-PEI NPs used in the present study act as an effective label- and enzyme-free sensor, and the new method is observed to be simple and cost-effective, to overcome various limitations of solution-phase ECL and to avoid the usage of any noble metals.

The highly selective rhodol-based putrescine probe and visual sensors for on-site detection of putrescine in food spoilage

Putrescine (Butane-1,4-diamine) has been regarded as a vital marker of spoiling protein-rich foods, especially meat and seafood. The detection of putrescine in food is considered a convenient and powerful method for evaluating the degree of spoilage of protein-rich foods. Herein, a novel rhodol-based fluorescent probe RSMA (formyl-rhodol Schiff base with methoxyaniline) was developed to detect putrescine. RSMA exhibited excellent linearity (R2 = 0.9912) in the concentration range of 0–45 μM of putrescine with a detection limit as low as 0.45 μM. Although RSMA had moderate responses to some aliphatic diamines, the selectivity of RSMA for putrescine was one of the best reported in the literature so far. Moreover, RSMA was successfully fabricated to solid-state sensors for on-site detection of putrescine in shrimp, that demonstrated its application in monitoring food spoilage.

Silicon photomultipliers for the SST camera of the Cherenkov Telescope Array

The Cherenkov Telescope Array Observatory (CTAO) will be the major global observatory for gamma-ray astronomy over the next decade and beyond. It will consist of two arrays of telescopes of different sizes, one for each hemisphere, and will be sensitive to gamma rays in the energy range from a few tens of GeV to hundreds of TeV. The Small-Sized Telescopes (SSTs) are a crucial component of the southern array, as they will extend the sensitivity of the observatory to the highest energies. Their focal plane will be equipped with 2048 Silicon Photomultiplier (SiPM) pixels, each one read independently by a state-of-the-art full waveform sampling readout. These solid-state sensors offer advantages over the traditional photomultiplier tubes, such as lower operating voltage, higher photon detection efficiency, and tolerance to bright illumination. In particular, they are the best choice for a small and compact camera such as the SST one. After a detailed comparative study, LVR3-type SiPMs from Hamamatsu Photonics were selected, with an active area of 6 mm × 6 mm, a microcell of 50 μm and without a protective coating, for optimum performance. The sensors demonstrated to have a higher photon detection efficiency and a lower crosstalk compared to the competitors, alongside a low dark count rate. In this contribution, we present the selection process and the latest measurements performed on the SiPMs mounted on the SST Camera module.

Enhanced detection of acrylamide using a versatile solid-state upconversion sensor through spectral and visual analysis

Acrylamide (AM) generally forms in high-temperature processes and has been classified as a potential carcinogen. In this study, we put forward a maneuverable solid-state luminescence sensor using polydimethylsiloxane (PDMS) as the matrix coupled with upconversion nanoparticles as the indicator. The core-shell upconversion nanoparticles emitting cyan light were uniformly encapsulated in PDMS. Then it was further modified with complementary DNA of AM aptamer. The nanocrystalline fluorescein isothiocyanate isomer (FITC), coupled with AM aptamer, was attached to the surface of PDMS. FITC effectively quenched the upconversion luminescence through fluorescence resonance energy transfer (FRET). The introduction of AM resulted in preferentially bound to aptamer caused the separation of the quencher and the donor, and led to luminescence recovery. The developed sensor was applied for both spectral and visual monitoring, demonstrating a detection limit (LOD) of 1.00 nM and 1.07 nM, respectively. Importantly, in the actual foodstuffs detection, there is no obvious difference between the results of this study and the standard method, which indicates the developed method has good accuracy. Therefore, this solid-state sensor has the potential for on-site detection using a smartphone device and an Android application.

(Invited) Magneto-Mechanical Micro-Nano Devices with Electrodeposited Magnetostriction Films

Microsystems play an important role in IoT sensors and actuators in the recent information and communication society. Among these, actuators are important elements used in transmitters, acoustic devices, and optical elements, and for those devices, piezoelectric thin films have been used widely. Magnetostrictive materials are expected to have even greater actuation performance than that of the piezoelectric films, but in the magnetostrictive films integration technologies with a high performance have not yet been fully developed. We have developed the film deposition technologies for magnetostriction materials by electrodeposition and apply them to actuators and sensors [1,2]. The FeGa, TbDyFe, and FeCo magnetic materials are known as giant magnetostriction materials [3]. In this study, the film deposition method for these materials have been developed by electrodeposition. Tbe electrodeposition of rare earth elements is generally considered to be difficult, but in this study, by using Fe chelate as a catalyst, the magnetic films containing Fe and rare earth elements have been successfully deposited, and large magnetostriction are achieved. The TbDyFe films show magnetostriction of ~1000 [1]. In addition, large volume magnetostriction has been observed in these amorphous materials. The magnetostrictive materials are known to have a reverse magnetostriction effect, in which the magnetization of the magnetic material changes when it is subjected to strain. They are known to work as strain sensors based on magnetic measurements. In order to demonstrate the strain sensing, a bi-material cantilever of FeGa/Si with a Si Hall sensor integrated on the support has been developed, as shown in Fig. 1 [2]. The vibration of the cantilever can be detected from the magnetization change using the integrated Hall sensor. On the other hand, magnetostrictive actuators generally require an electromagnet to drive them, making them difficult to miniaturize the system. Therefore, an attempt has been made to drive magnetostrictive thin films by injecting spins into them using the spin Hall effect, giving angular momentum to the spins of magnetic materials and changing the spin fluctuations [4]. It is found that a large strain can be generated by spin injection into the TbDyFe film. The above results show that high-performance magnetostrictive films can be deposited by electrodeposition and can be applied to strain sensors and spin-current driven actuators, and are expected to be applied to the development of novel sensors and actuators [5].References H. Shim, K. Sakamoto, N. Inomata, M. Toda, N. V. Toan and T. Ono, Magnetostrictive Performance of Electrodeposited TbxDy(1−x)Fey Thin Film with Microcantilever Structures, Micromachines 11, 5 (2020) 523.T. Ezura, N. Inomata, T. Ono, Integration of Magnetostrictive Microsensor With Hall Element for Microstructure Resonant Detection, 21st International Conference on Solid-State Sensors, Actuators and Microsystems (Transducers), (2021) 418-421.Mohammad Akita Indianto, Masaya Toa, Takahito Ono, Comprehensive study of magnetostriction-based MEMS magnetic sensor of a FeGa/PZT cantilever, Sensors and Actuators A 331, (2021) 112985.H. Arisawa, H. Shim, S. Daimon, T. Kikkawa, Y. Oikawa, S. Takahashi, T. Ono, E. Saitoh, Observation of spin-current striction in a magnet, Nature Communication 13 (2022) 2400.M. A. Indianto, M. Toda, T. Ono, Development of assembled microchannel resonator as an alternative fabrication method of a microchannel resonator for mass sensing in flowing liquid, Biomicrofluidics 14, (2020) 064111. Figure 1