Wearable flexible sensor devices have the characteristics of lightweight and miniaturization.Currently,power supply and detection components limit the portability of wearable flexible sensor devices.Meanwhile,conventi...Wearable flexible sensor devices have the characteristics of lightweight and miniaturization.Currently,power supply and detection components limit the portability of wearable flexible sensor devices.Meanwhile,conventional liquid electrolytes are unsuitable for the integration of sensing devices.To address these constraints,wearable biofuel cells and flexible electrochromic displays have been introduced,which can improve integration with other devices,safety,and color-coded display data.Meanwhile,electrode chips prepared through screen printing technology can further improve portability.In this work,a wearable sensor device with screen-printed chips was constructed and used for non-invasive detection of glucose.Agarose gel electrolytes doped with PDA-CNTs were prepared,and the mechanical strength and moisture retention were significantly improved compared with traditional gel electrolytes.Glucose in interstitial fluid was non-invasive extracted to the skin surface using reverse iontophoresis.As a biofuel for wearable biofuel cells,glucose drives self-powered sensor and electrochromic display to produce color change,allowing for visually measurement of glucose levels in body fluids.Accurate detection results can be visualized by reading the RGB value with a cell phone.展开更多
Even in small concentrations,toxic metals like lead,cadmium,and mercury are dangerous to the environment and human health.Environmental monitoring depends on precisely identifying these heavy metals,particularly cadmi...Even in small concentrations,toxic metals like lead,cadmium,and mercury are dangerous to the environment and human health.Environmental monitoring depends on precisely identifying these heavy metals,particularly cadmium ions(Cd(Ⅱ)).In this study,we present a novel screen-printed carbon electrode(SPCE)modified with single crystallineα-Fe_(2)O_(3)nano-hexagons that functions as a sensor for detecting Cd(Ⅱ).The performance of the fabricated sensor was thoroughly assessed and compared with unmodified SPCE using the voltammetric method.The crystalline structure of the synthesizedα-Fe_(2)O_(3)nano-hexagons was confirmed through XRD,and surface analysis revealed an average diameter and thickness of 86 nm and 9 nm,respectively.Theα-Fe_(2)O_(3)modified SPCE yields a 7-fold enhanced response(at pH 5.0 vs.Ag/AgCl)to Cd(Ⅱ)than bare SPCE.The modified electrode effectively detects Cd(Ⅱ)with a linear response range of up to 333.0μmol/L and a detection limit of 0.65 nmol/L under ideal circumstances.This newly fabricated sensor offers significant potential for environmental monitoring applications by providing outstanding practicality,anti-interference ability,and repeatability for detecting Cd(Ⅱ)in water samples.展开更多
CuO nanoparticles were successfully synthesized via a two-jet electrospun method,and then screen-printed on silver-carbon electrodes,forming CuO-modified Ag-C(CuO/Ag-C)disposable strip electrodes.In natural environmen...CuO nanoparticles were successfully synthesized via a two-jet electrospun method,and then screen-printed on silver-carbon electrodes,forming CuO-modified Ag-C(CuO/Ag-C)disposable strip electrodes.In natural environment condition for glucose detection,the obtained CuO/Ag-C electrodes show a high sensitivity of 540 nA·mM^(-1)·cm^(-2),and a low limit of detection(0.68 mM)in a wide linear response range of 0.68 mM and 3 mM(signal/noise=3),respectively.In addition,the CuO/Ag-C electrodes also exhibit excellent anti-interference,air stability and repeatability.As a result,the fabrication of CuO nanoparticles via an electrospun process and the technique of screen-printed electrodes are of great significance for glucose detection.展开更多
A novel electrochemical method for the rapid detection of organophosphorus pesticide residues was realized on a dual-channel screen-printed electrode （DSPE） that was integrated with a portable smartphone-controlled ...A novel electrochemical method for the rapid detection of organophosphorus pesticide residues was realized on a dual-channel screen-printed electrode （DSPE） that was integrated with a portable smartphone-controlled potentiostat. The two carbon working channels of DSPE were first modified by electrodepositing of Prussian blue. The channels were then modified with acetylcholinesterase （ACHE） via Nation. The inhibition ratio of AChE was detected by comparing the electrical current of acetylthiocholine （ATCh） that was catalyzed by the enzyme electrodes with （channel 1） and without （channel 2） organophosphorus pesticide. Inhibition ratios were related with the negative logarithm of the organophosphorus pesticide （trichlorfon, oxamyl, and isocarbophos） concentrations at optimum experimental conditions （pH 6.9 of electrolyte, 0.2V working potential, 2.5μL AChE modification amount, and 15 min inhibition time）. The linear equations were 1%=32.301gC＋ 253.3 （R=0.9750） for isocarbophos, I% = 35.991gC＋ 270.1 （R = 0.9668） for chlorpyrifos, and 1% = 33.701gC＋ 250.5 （R = 0.9606） for trichlorfon. The detection limits were calculated as 10-7 g/mL. Given that the inhibition ratios were only related with pesticide concentration and not with pesticide species, the proposed electrodes and electrometer can rapidly detect universal organophosphorus pesticides and assess pesticide pollution.展开更多
A sensitive and specific immunosensor for the detection of the hormones cortisol and lactate in human or animal biological fluids, such as sweat and saliva, was devised using the label-free electrochemical chronoamper...A sensitive and specific immunosensor for the detection of the hormones cortisol and lactate in human or animal biological fluids, such as sweat and saliva, was devised using the label-free electrochemical chronoamperometric technique. By using these fluids instead of blood,the biosensor becomes noninvasive and is less stressful to the end user, who may be a small child or a farm animal.Electroreduced graphene oxide(e-RGO) was used as a synergistic platform for signal amplification and template for bioconjugation for the sensing mechanism on a screenprinted electrode. The cortisol and lactate antibodies were bioconjugated to the e-RGO using covalent carbodiimide chemistry. Label-free electrochemical chronoamperometric detection was used to analyze the response to the desired biomolecules over the wide detection range. A detection limit of 0.1 ng mL^(-1) for cortisol and 0.1 mM for lactate was established and a correlation between concentration and current was observed. A portable, handheld potentiostat assembled with Bluetooth communication and battery operation enables the developed system for point-of-care applications. A sandwich-like structure containing the sensing mechanisms as a prototype was designed to secure the biosensor to skin and use capillary action to draw sweat or other fluids toward the sensing mechanism. Overall, the immunosensor shows remarkable specificity, sensitivity as well as the noninvasive and point-of-care capabilities and allows the biosensor to be used as a versatile sensing platform in both developed and developing countries.展开更多
Monitoring the concentration of antibiotics in body fluids is essential to optimizing the therapy and minimizing the risk of bacteria resistance,which can be made with electrochemical sensors tailored with appropriate...Monitoring the concentration of antibiotics in body fluids is essential to optimizing the therapy and minimizing the risk of bacteria resistance,which can be made with electrochemical sensors tailored with appropriate materials.In this paper,we report on sensors made with screen-printed electrodes(SPE)coated with fullerene(C60),reduced graphene oxide(rGO)and Nafion(NF)(C60-rGO-NF/SPE)to determine the antibiotic metronidazole(MTZ).Under optimized conditions,the C60-rGO-NF/SPE sensor exhibited a linear response in square wave voltammetry for MTZ concentrations from 2.5×10^(-7) to 34×10^(-6) mol/L,with a detection limit of 2.1×10^(-7) mol/L.This sensor was also capable of detecting MTZ in serum and urine,with recovery between 94%and 100%,which are similar to those of the standard chromatographic method(HPLC-UV).Because the C60-rGO-NF/SPE sensor is amenable to mass production and allows for MTZ determination with simple principles of detection,it fulfills the requirements of therapeutic drug monitoring programs.展开更多
The electrochemical oxidation behavior and voltammetric assay of gemifloxacin were investigated using differential-pulse and cyclic voltammetry on a screen-printed carbon electrode.The effects of pH,scan rates,and con...The electrochemical oxidation behavior and voltammetric assay of gemifloxacin were investigated using differential-pulse and cyclic voltammetry on a screen-printed carbon electrode.The effects of pH,scan rates,and concentration of the drug on the anodic peak current were studied.Voltammograms of gemifloxacin in Tris-HCl buffer（pH 7.0） exhibited a well-defined single oxidation peak.A differential-pulse voltammetric procedure for the quantitation of gemifloxacin has been developed and suitably validated with respect to linearity,limits of detection and quantification,accuracy,precision,specificity,and robustness.The calibration was linear from 0.5 to 10.0 μM,and the limits of detection and quantification were 0.15 and 5.0 μM.Recoveries ranging from 96.26% to 103.64% were obtained.The method was successfully applied to the determination of gemifloxacin in pharmaceutical tablets without any pre-treatment.Excipients present in the tablets did not interfere in the assay.展开更多
An amperometric biosensor based on screen-printed electrodes （SPEs） was developed for the determination of organophosphorus pesticides in water samples. The extent of acetylcholinesterase （AChE） deactivation was d...An amperometric biosensor based on screen-printed electrodes （SPEs） was developed for the determination of organophosphorus pesticides in water samples. The extent of acetylcholinesterase （AChE） deactivation was determined and quantified for pesticide concentrations in water samples. An enzyme immobilization adsorption procedure and polyacrylamide gel matrix polymerization were used for fabrication of the biosensor, with minimal losses in enzyme activity. The optimal conditions for enzyme catalytic reaction on the SPEs surfaces were acetylthiocholine chloride （ATChCl） concentration of 5 mmol/L, pH 7 and reaction time of 4 min. The detection limits for three organophosphorus pesticides （dichlorvos, monocrotophs and parathion） were in the range of 4 to 7 μg/L when an AChE amount of 0.1 U was used for immobilization.展开更多
The screen-printed nanoporous TiO2 thin film was employed to fabricate dye-sensitized solid-state solar cells using CuI as hole-transport materials. The solar cell based on nanoporous TiO2 thin film with large pores f...The screen-printed nanoporous TiO2 thin film was employed to fabricate dye-sensitized solid-state solar cells using CuI as hole-transport materials. The solar cell based on nanoporous TiO2 thin film with large pores formed by the addition of polystyrene balls with diameter of 200 nm to the TiO2 paste exhibits photovoltaic performance enhancement, which is attributed to the good contact of CuI with surface of dye-sensitized thin film due to easy penetration of CuI in the film with large pores.展开更多
We report the fabrication of disposable and flexible Screen-Printed Electrodes (SPEs). This new type of screen-printed electrochemical platform consists of Ag nanoparticles (AgNPs) and graphite composite. For this pur...We report the fabrication of disposable and flexible Screen-Printed Electrodes (SPEs). This new type of screen-printed electrochemical platform consists of Ag nanoparticles (AgNPs) and graphite composite. For this purpose, silver nanoparticles were first synthesized by a chemical reduction method. The morphology and structure of the AgNPs were analyzed using a Scanning Electron Microscope (SEM) and UV-Visible spectroscopy. Graphite was chosen as the working electrode material for the fabrication of a thick-film. The fabrication of a screen-printed hydrogen peroxide biosensor consisting of three electrodes on a polyethylene terephthalate (PET) substrate was performed with a spraying approach (working, counter and reference: enzyme electrode, graphite, pseudo reference: Ag/AgCl). This biosensor was fabricated by immobilizing the peroxidase enzyme (HRP) in a Titania sol-gel membrane which was obtained through a vapor deposition method. The biosensor had electrocatalytic activity in the reduction of H2O2 with linear dependence on H2O2 concentration in the range of 10-5 to 10-3 M;the detection limit was 4.5 × 10-6 M.展开更多
In this study, gold nanoparticles and thermochromic composite films modified screen-printed carbon electrodes (TM-AuNPsSPCEs) were developed as a platform for the simultaneous detection of protein and temperature. The...In this study, gold nanoparticles and thermochromic composite films modified screen-printed carbon electrodes (TM-AuNPsSPCEs) were developed as a platform for the simultaneous detection of protein and temperature. The TM-AuNPs composited film had better sensitivity resulting from the gold nanoparticles amplification effect. A phase transition model analysis of TM-AuNPs films found that the TM-AuNPs films had three-phase transition intervals (<45℃, 45℃ to 80℃ and >80℃) which accommodated the temperature requirements for protein denaturation. When used to detect different concentrations of haemoglobin (Hb) solution, the TM-AuNPs modified SPCEs had a better sensitivity in detecting the different concentrations in comparison to TM and AuNP modified SPCEs which showed no clear sensitivity towards the different Hb concentrations. The dual detection and excellent sensitivity show a good application prospect for the study of the TM-AuNPs composite film.展开更多
The large-scale touch position sensor as a key human-machine interface toolkit holds immense significance in smart city and home construction.However,prior alternatives suffer from high power consumption,material limi...The large-scale touch position sensor as a key human-machine interface toolkit holds immense significance in smart city and home construction.However,prior alternatives suffer from high power consumption,material limitations,and implementation costs.Herein,a self-powered and scalable touch position strategy that integrates contact electrification with a screen-printing technique is proposed.Simply,high-impedance electrodes with stagger patterns are screen-printed onto various substrates before being covered with a dielectric layer.The locating mechanism originates from the touch-generated triboelectric charge shunt effect in the electrodes.The screen-printing parameters that affect the positional accuracy are discussed in detail.Leveraging this strategy,we realize a tailorable and large-scale triboelectric touch position sensor(LTTPS)that offers flexibility,self-powered capability,and a minimized signal channel,making it suitable for various practical scenarios.Demonstrations include an intelligent bookshelf mat with book management functionality,a rollable and foldable film-like keyboard,and a 4 m2 walk-tracking carpet.The LTTPS in this work provides an appealing alternative for large-scale touch positioning and enriches human-machine interaction.展开更多
Nitrate is the primary water-soluble macronutrient essential for plant growth that is converted from excess fish feeds,fish effluents,and degrading biomaterials on the aquaponic pond floor,and when aquacultural malpra...Nitrate is the primary water-soluble macronutrient essential for plant growth that is converted from excess fish feeds,fish effluents,and degrading biomaterials on the aquaponic pond floor,and when aquacultural malpractices occur,large amounts of it retain in the water system causing increase rate in eutrophication and toxifies fish and aquaculture plants.Recent nitrate sensor prototypes still require performing the additional steps of water sample deionization and dilution and were constructed with expensive materials.In response to the challenge of sensor enhancement and aquaponic water quality monitoring,this study developed sensitive,repeatable,and reproducible screen-printed graphite electrodes on polyvinyl chloride and parchment paper substrates with silver as electrode material and 60:40 graphite powder:nail polish formulated conductive ink for electrical traces,integrated with 9-gene genetic expression model as a function of peak anodic current and electrochemical test time for nitrate concentration prediction that is embedded into low-power Arduino ESP32 for in situ nitrate sensing in aquaponic pond water.Five SPE electrical traces were designed on the two types of substrates.Scanning electron microscopy with energy dispersive X-ray confirmed the electrode surface morphology.Electrochemical cyclic voltammetry using 10 to 100 mg/L KNO3 and water from three-depth regions of the actual pond established the electrochemical test time(10.5 s)and electrode potential(0.135 V)protocol necessary to produce peak current that corresponds to the strength of nitrate ions during redox.The findings from in situ testing revealed that the proposed sensors have strong linear predictions(R2=0.968 MSE=1.659 for nSPEv and R2=0.966 MSE=4.697 for nSPEp)in the range of 10 to 100 mg/L and best detection limit of 3.15μg/L,which are comparable to other sensors of more complex construction.The developed three-electrode electrochemical nitrate sensor confirms that it is reliable for both biosensing in controlled solutions and in situ aquaponic pond water systems.展开更多
Electrochemiluminescence(ECL)is nowadays a powerful technique widely used in biosensing and imaging,offering high sensitivity and specificity for detecting and mapping biomolecules.Screen-printed electrodes(SPEs)offer...Electrochemiluminescence(ECL)is nowadays a powerful technique widely used in biosensing and imaging,offering high sensitivity and specificity for detecting and mapping biomolecules.Screen-printed electrodes(SPEs)offer a versatile and cost-effective platform for ECL applications due to their ease of fabrication,disposability,and suitability for large-scale production.This research introduces a novel method for improving the ECL characteristics of screen-printed carbon electrodes(SPCEs)through the application of CO_(2)laser treatment following fabrication.Using advanced ECL microscopy,we analyze three distinct carbon paste-based electrodes and show that low-energy laser exposure(ranging from 7 to 12 mJ·cm^(−2))enhances the electrochemical performance of the electrodes.This enhancement results from the selective removal of surface binders and contaminants achieved by the laser treatment.We employed ECL microscopy to characterize the ECL emission using a bead-based system incorporating magnetic microbeads,like those used in commercial platforms.This approach enabled highresolution spatial mapping of the electrode surface,offering valuable insights into its electrochemical performance.Through quantitative assessment using a photomultiplier tube(PMT),it was observed that GST electrodes could detect biomarkers with high sensitivity,achieving an approximate detection limit(LOD)of 11 antibodies perμm^(2).These findings emphasize the potential of laser-modified GST electrodes in enabling highly sensitive electrochemiluminescent immunoassays and various biosensing applications.展开更多
The solar cell market is predominantly based on textured screen-printed solar cells.Due to parasitic absorption in nanostructures,using plasmonic processes to obtain an enhancement that exceeds 2.5%of the short-circui...The solar cell market is predominantly based on textured screen-printed solar cells.Due to parasitic absorption in nanostructures,using plasmonic processes to obtain an enhancement that exceeds 2.5%of the short-circuit photocurrent density is challenging.In this paper,a 7.2%enhancement in the photocurrent density can be achieved through the integration of plasmonic Al nanoparticles and wrinkle-like graphene sheets.For the first time,we experimentally achieve Al nanoparticle-enhanced solar cells.An innovative thermal evaporation method is proposed to fabricate low-coverage Al nanoparticle arrays on solar cells.Due to the ultraviolet(UV)plasmon resonance of Al nanoparticles,the performance enhancement of the solar cells is significantly greater than that from Ag nanoparticles.Subsequently,we deposit wrinkle-like graphene sheets over the Al nanoparticle-enhanced solar cells.Compared with planar graphene sheets,the bend carbon layer also exhibits a broadband light-trapping effect.Our results exceed the limit of plasmonic light trapping in textured screen-printed silicon solar cells.展开更多
Cadmium(Cd)and lead(Pb)in soil or water environment cause the ecological destruction and environmental deterioration when their contents exceed the natural background values.To trace the concentrations of Cd(II)and Pb...Cadmium(Cd)and lead(Pb)in soil or water environment cause the ecological destruction and environmental deterioration when their contents exceed the natural background values.To trace the concentrations of Cd(II)and Pb(II),a sensitive and selective electrode was developed using disposable screen-printed carbon electrode(SPE)immobilized with a composite film of reduced graphene oxide/carboxylation multi-walled carbon nanotubes/gold nanoparticle hybrid(RGO-MWNT-AuNP)throughπ-πbind.This highly conductive nano-composite layer,“RGO-MWNT-AuNP,”was characterized by scanning electron microscopy,UV-visible spectrometer,cyclic voltammetry,and electrochemical impedance spectroscopy.Square wave stripping voltammetry was applied to RGO-MWNT-AuNP/SPE to electroplate bismuth film and monitor the Cd(II)and Pb(II)simultaneously.To obtain high current responses,the detecting parameters were optimized.Under optimized conditions,the current responses showed a linear relationship with the concentrations of Cd(II)and Pb(II)in the range from 1.0 to 80.0μg/L with a lower detection limit of 0.7μg/L and 0.3μg/L(S/N=3),respectively.Finally,the prepared electrode was further employed to detect Cd(II)and Pb(II)in soil samples with good results.展开更多
Okadaic acid(OA),a small molecule substance derived from shellfish,is one of the most widely distributed marine toxins with acute symptoms of vomiting and diarrhea after accidental ingestion.For this,there is an urgen...Okadaic acid(OA),a small molecule substance derived from shellfish,is one of the most widely distributed marine toxins with acute symptoms of vomiting and diarrhea after accidental ingestion.For this,there is an urgently need for sensitive and reliable methods to detect OA in real shellfish samples.In this study,a simple aptasensor based on screen-printed carbon electrode(SPCE)with modification of chitosan(CS)and gold nanoparticles(Au NPs)was designed for electrochemical determination of OA,and the electrode surface was modified with Au NPs by potential-sweeping electrodeposition,which greatly improved the electrochemical response.The entire detection and characterization process were carried out by cyclic voltammetry(CV)with a linear correlation in the range of 0.01-100 ng/m L and a limit of detection(LOD)of 6.7 pg/m L.Furthermore,recovery rates of 92.3-116%were obtained demonstrating excellent accuracy through the recovery trial of mussel and scallop samples.展开更多
The screen-printed three-electrode system was applied to fabricate a new type of disposable amperometric xanthine oxidase biosensor.Carbon-working,carbon-counter and Ag/AgCl reference electrodes were all manually prin...The screen-printed three-electrode system was applied to fabricate a new type of disposable amperometric xanthine oxidase biosensor.Carbon-working,carbon-counter and Ag/AgCl reference electrodes were all manually printed on the polyethylene terephthalate substrate forming the screen-printed three-electrode system by the conventional screen-printing process.As a mediator,Prussian blue could not only catalyze the electrochemical reduction of hydrogen peroxide produced from the enzyme reaction,but also keep the favorable potential around 0 V.The optimum operational conditions,including pH,potential and temperature,were investigated.The sensitivities of xanthine and hypoxanthine detections were 13.83 mA/M and 25.56 mA/M,respectively.A linear relationship was obtained in the concentration range between 0.10μM and 4.98μM for xanthine and between 0.50μM and 3.98μM for hypoxanthine.The small Michaelis-menten constant value of the xanthine oxidase biosensor was calculated to be 3.90 μM.The results indicate that the fabricated xanthine oxidase biosensor is effective and sensitive for the detection of xanthine and hypoxanthine.展开更多
Developing flexible bioelectronics is essential to the realization of artificial intelligence devices and biomedical applications, such as wearables, but their potential is limited by sustainable energy supply. An enz...Developing flexible bioelectronics is essential to the realization of artificial intelligence devices and biomedical applications, such as wearables, but their potential is limited by sustainable energy supply. An enzymatic biofuel cell(BFC) is promising for power supply, but its use is limited by the challenges of incorporating multiple enzymes and rigid platforms. This paper shows the first example of screen-printable nanocomposite inks engineered for a single-enzyme-based energy-harvesting device and a self-powered biosensor driven by glucose on bioanode and biocathode. The anode ink is modified with naphthoquinone and multiwalled carbon nanotubes(MWCNTs), whereas the cathode ink is modified with Prussian blue/MWCNT hybrid before immobilizing with glucose oxidase. The flexible bioanode and the biocathode consume glucose. This BFC yields an open circuit voltage of 0.45 V and a maximum power density of 266 μW cm-2. The wearable device coupled with a wireless portable system can convert chemical energy into electric energy and detect glucose in artificial sweat. The self-powered sensor can detect glucose concentrations up to 10 mM. Common interfering substances,including lactate, uric acid, ascorbic acid, and creatinine, have no effect on this self-powered biosensor. Additionally, the device can endure multiple mechanical deformations. New advances in ink development and flexible platforms enable a wide range of applications, including on-body electronics, self-sustainable applications, and smart fabrics.展开更多
Supercapacitor diode is a novel ion device that performs both supercapacitor energy storage and ion diode rectification functions.However,previously reported devices are limited by their large size and complex process...Supercapacitor diode is a novel ion device that performs both supercapacitor energy storage and ion diode rectification functions.However,previously reported devices are limited by their large size and complex processes.In this work,we demonstrate a screen-printed micro supercapacitor diode(MCAPode)that based on the insertion of a finger mode with spinel ZnCo_(2)O_(4) as cathode and activated carbon as anode for the first time,and featuring an excellent area specific capacitance(1.21 mF cm^(-2)at 10 mV s^(-1))and high rectification characteristics(rectification ratioⅠof 11.99 at 40 mV s^(-1)).Taking advantage of the ionic gel electrolyte,which provides excellent stability during repeated flexing and at high temperatures.In addition,MCAPode exhibits excellent electrochemical performance and rectification capability in"AND"and"OR"logic gates.These findings provide practical solutions for future expansion of micro supercapacitor diode applications.展开更多
基金supported by the National Natural Science Foundation of China(No.22174055)Key R&D Program of Zhenjiang City(No.NY2022012)。
文摘Wearable flexible sensor devices have the characteristics of lightweight and miniaturization.Currently,power supply and detection components limit the portability of wearable flexible sensor devices.Meanwhile,conventional liquid electrolytes are unsuitable for the integration of sensing devices.To address these constraints,wearable biofuel cells and flexible electrochromic displays have been introduced,which can improve integration with other devices,safety,and color-coded display data.Meanwhile,electrode chips prepared through screen printing technology can further improve portability.In this work,a wearable sensor device with screen-printed chips was constructed and used for non-invasive detection of glucose.Agarose gel electrolytes doped with PDA-CNTs were prepared,and the mechanical strength and moisture retention were significantly improved compared with traditional gel electrolytes.Glucose in interstitial fluid was non-invasive extracted to the skin surface using reverse iontophoresis.As a biofuel for wearable biofuel cells,glucose drives self-powered sensor and electrochromic display to produce color change,allowing for visually measurement of glucose levels in body fluids.Accurate detection results can be visualized by reading the RGB value with a cell phone.
文摘Even in small concentrations,toxic metals like lead,cadmium,and mercury are dangerous to the environment and human health.Environmental monitoring depends on precisely identifying these heavy metals,particularly cadmium ions(Cd(Ⅱ)).In this study,we present a novel screen-printed carbon electrode(SPCE)modified with single crystallineα-Fe_(2)O_(3)nano-hexagons that functions as a sensor for detecting Cd(Ⅱ).The performance of the fabricated sensor was thoroughly assessed and compared with unmodified SPCE using the voltammetric method.The crystalline structure of the synthesizedα-Fe_(2)O_(3)nano-hexagons was confirmed through XRD,and surface analysis revealed an average diameter and thickness of 86 nm and 9 nm,respectively.Theα-Fe_(2)O_(3)modified SPCE yields a 7-fold enhanced response(at pH 5.0 vs.Ag/AgCl)to Cd(Ⅱ)than bare SPCE.The modified electrode effectively detects Cd(Ⅱ)with a linear response range of up to 333.0μmol/L and a detection limit of 0.65 nmol/L under ideal circumstances.This newly fabricated sensor offers significant potential for environmental monitoring applications by providing outstanding practicality,anti-interference ability,and repeatability for detecting Cd(Ⅱ)in water samples.
基金Funded by Cofoe Medical Technology Co.,Ltd and the Scientific Research Start-up Funds of Hexi University(No.KYQD2022006)。
文摘CuO nanoparticles were successfully synthesized via a two-jet electrospun method,and then screen-printed on silver-carbon electrodes,forming CuO-modified Ag-C(CuO/Ag-C)disposable strip electrodes.In natural environment condition for glucose detection,the obtained CuO/Ag-C electrodes show a high sensitivity of 540 nA·mM^(-1)·cm^(-2),and a low limit of detection(0.68 mM)in a wide linear response range of 0.68 mM and 3 mM(signal/noise=3),respectively.In addition,the CuO/Ag-C electrodes also exhibit excellent anti-interference,air stability and repeatability.As a result,the fabrication of CuO nanoparticles via an electrospun process and the technique of screen-printed electrodes are of great significance for glucose detection.
基金financially supported by the Natural Science Foundation of Zhejiang Province(No.LQ17B050002)Analysis and Measurement Foundation of Zhejiang Province(No.2015C37068)
文摘A novel electrochemical method for the rapid detection of organophosphorus pesticide residues was realized on a dual-channel screen-printed electrode （DSPE） that was integrated with a portable smartphone-controlled potentiostat. The two carbon working channels of DSPE were first modified by electrodepositing of Prussian blue. The channels were then modified with acetylcholinesterase （ACHE） via Nation. The inhibition ratio of AChE was detected by comparing the electrical current of acetylthiocholine （ATCh） that was catalyzed by the enzyme electrodes with （channel 1） and without （channel 2） organophosphorus pesticide. Inhibition ratios were related with the negative logarithm of the organophosphorus pesticide （trichlorfon, oxamyl, and isocarbophos） concentrations at optimum experimental conditions （pH 6.9 of electrolyte, 0.2V working potential, 2.5μL AChE modification amount, and 15 min inhibition time）. The linear equations were 1%=32.301gC＋ 253.3 （R=0.9750） for isocarbophos, I% = 35.991gC＋ 270.1 （R = 0.9668） for chlorpyrifos, and 1% = 33.701gC＋ 250.5 （R = 0.9606） for trichlorfon. The detection limits were calculated as 10-7 g/mL. Given that the inhibition ratios were only related with pesticide concentration and not with pesticide species, the proposed electrodes and electrometer can rapidly detect universal organophosphorus pesticides and assess pesticide pollution.
基金the Natural Sciences and Engineering Research Council of Canada (400705) for funding this study
文摘A sensitive and specific immunosensor for the detection of the hormones cortisol and lactate in human or animal biological fluids, such as sweat and saliva, was devised using the label-free electrochemical chronoamperometric technique. By using these fluids instead of blood,the biosensor becomes noninvasive and is less stressful to the end user, who may be a small child or a farm animal.Electroreduced graphene oxide(e-RGO) was used as a synergistic platform for signal amplification and template for bioconjugation for the sensing mechanism on a screenprinted electrode. The cortisol and lactate antibodies were bioconjugated to the e-RGO using covalent carbodiimide chemistry. Label-free electrochemical chronoamperometric detection was used to analyze the response to the desired biomolecules over the wide detection range. A detection limit of 0.1 ng mL^(-1) for cortisol and 0.1 mM for lactate was established and a correlation between concentration and current was observed. A portable, handheld potentiostat assembled with Bluetooth communication and battery operation enables the developed system for point-of-care applications. A sandwich-like structure containing the sensing mechanisms as a prototype was designed to secure the biosensor to skin and use capillary action to draw sweat or other fluids toward the sensing mechanism. Overall, the immunosensor shows remarkable specificity, sensitivity as well as the noninvasive and point-of-care capabilities and allows the biosensor to be used as a versatile sensing platform in both developed and developing countries.
基金The authors gratefully acknowledge the financial support granted by CNPq,INEO,CAPES and FAPESP(Grant Nos.:2018/22214-6,2017/24053-7 and 2016/0991-5).
文摘Monitoring the concentration of antibiotics in body fluids is essential to optimizing the therapy and minimizing the risk of bacteria resistance,which can be made with electrochemical sensors tailored with appropriate materials.In this paper,we report on sensors made with screen-printed electrodes(SPE)coated with fullerene(C60),reduced graphene oxide(rGO)and Nafion(NF)(C60-rGO-NF/SPE)to determine the antibiotic metronidazole(MTZ).Under optimized conditions,the C60-rGO-NF/SPE sensor exhibited a linear response in square wave voltammetry for MTZ concentrations from 2.5×10^(-7) to 34×10^(-6) mol/L,with a detection limit of 2.1×10^(-7) mol/L.This sensor was also capable of detecting MTZ in serum and urine,with recovery between 94%and 100%,which are similar to those of the standard chromatographic method(HPLC-UV).Because the C60-rGO-NF/SPE sensor is amenable to mass production and allows for MTZ determination with simple principles of detection,it fulfills the requirements of therapeutic drug monitoring programs.
文摘The electrochemical oxidation behavior and voltammetric assay of gemifloxacin were investigated using differential-pulse and cyclic voltammetry on a screen-printed carbon electrode.The effects of pH,scan rates,and concentration of the drug on the anodic peak current were studied.Voltammograms of gemifloxacin in Tris-HCl buffer（pH 7.0） exhibited a well-defined single oxidation peak.A differential-pulse voltammetric procedure for the quantitation of gemifloxacin has been developed and suitably validated with respect to linearity,limits of detection and quantification,accuracy,precision,specificity,and robustness.The calibration was linear from 0.5 to 10.0 μM,and the limits of detection and quantification were 0.15 and 5.0 μM.Recoveries ranging from 96.26% to 103.64% were obtained.The method was successfully applied to the determination of gemifloxacin in pharmaceutical tablets without any pre-treatment.Excipients present in the tablets did not interfere in the assay.
基金supported by the National Natural Science Foundation of China (No. 51008026, 40873076 and 41011130204)
文摘An amperometric biosensor based on screen-printed electrodes （SPEs） was developed for the determination of organophosphorus pesticides in water samples. The extent of acetylcholinesterase （AChE） deactivation was determined and quantified for pesticide concentrations in water samples. An enzyme immobilization adsorption procedure and polyacrylamide gel matrix polymerization were used for fabrication of the biosensor, with minimal losses in enzyme activity. The optimal conditions for enzyme catalytic reaction on the SPEs surfaces were acetylthiocholine chloride （ATChCl） concentration of 5 mmol/L, pH 7 and reaction time of 4 min. The detection limits for three organophosphorus pesticides （dichlorvos, monocrotophs and parathion） were in the range of 4 to 7 μg/L when an AChE amount of 0.1 U was used for immobilization.
基金the financial support of this work by the Major State Basic Research Development Program(No.2006CB202605)High-Tech Research and Development of China Program(No.2007AA05Z439)+1 种基金the National Nature Science Foundation of China(No.50221201)Innovative Foundation of the Center for Molecular Science,Chinese Academy of Sciences(No.CMS-CX200718).
文摘The screen-printed nanoporous TiO2 thin film was employed to fabricate dye-sensitized solid-state solar cells using CuI as hole-transport materials. The solar cell based on nanoporous TiO2 thin film with large pores formed by the addition of polystyrene balls with diameter of 200 nm to the TiO2 paste exhibits photovoltaic performance enhancement, which is attributed to the good contact of CuI with surface of dye-sensitized thin film due to easy penetration of CuI in the film with large pores.
文摘We report the fabrication of disposable and flexible Screen-Printed Electrodes (SPEs). This new type of screen-printed electrochemical platform consists of Ag nanoparticles (AgNPs) and graphite composite. For this purpose, silver nanoparticles were first synthesized by a chemical reduction method. The morphology and structure of the AgNPs were analyzed using a Scanning Electron Microscope (SEM) and UV-Visible spectroscopy. Graphite was chosen as the working electrode material for the fabrication of a thick-film. The fabrication of a screen-printed hydrogen peroxide biosensor consisting of three electrodes on a polyethylene terephthalate (PET) substrate was performed with a spraying approach (working, counter and reference: enzyme electrode, graphite, pseudo reference: Ag/AgCl). This biosensor was fabricated by immobilizing the peroxidase enzyme (HRP) in a Titania sol-gel membrane which was obtained through a vapor deposition method. The biosensor had electrocatalytic activity in the reduction of H2O2 with linear dependence on H2O2 concentration in the range of 10-5 to 10-3 M;the detection limit was 4.5 × 10-6 M.
文摘In this study, gold nanoparticles and thermochromic composite films modified screen-printed carbon electrodes (TM-AuNPsSPCEs) were developed as a platform for the simultaneous detection of protein and temperature. The TM-AuNPs composited film had better sensitivity resulting from the gold nanoparticles amplification effect. A phase transition model analysis of TM-AuNPs films found that the TM-AuNPs films had three-phase transition intervals (<45℃, 45℃ to 80℃ and >80℃) which accommodated the temperature requirements for protein denaturation. When used to detect different concentrations of haemoglobin (Hb) solution, the TM-AuNPs modified SPCEs had a better sensitivity in detecting the different concentrations in comparison to TM and AuNP modified SPCEs which showed no clear sensitivity towards the different Hb concentrations. The dual detection and excellent sensitivity show a good application prospect for the study of the TM-AuNPs composite film.
基金National Key Research and Development Program,Grant/Award Number:2021YFA1201602NSFC,Grant/Award Numbers:T2422003,52302219Fundamental Research Funds for the Central Universities,Grant/Award Numbers:2024CDTZCQ-012,2024CDJGF-031。
文摘The large-scale touch position sensor as a key human-machine interface toolkit holds immense significance in smart city and home construction.However,prior alternatives suffer from high power consumption,material limitations,and implementation costs.Herein,a self-powered and scalable touch position strategy that integrates contact electrification with a screen-printing technique is proposed.Simply,high-impedance electrodes with stagger patterns are screen-printed onto various substrates before being covered with a dielectric layer.The locating mechanism originates from the touch-generated triboelectric charge shunt effect in the electrodes.The screen-printing parameters that affect the positional accuracy are discussed in detail.Leveraging this strategy,we realize a tailorable and large-scale triboelectric touch position sensor(LTTPS)that offers flexibility,self-powered capability,and a minimized signal channel,making it suitable for various practical scenarios.Demonstrations include an intelligent bookshelf mat with book management functionality,a rollable and foldable film-like keyboard,and a 4 m2 walk-tracking carpet.The LTTPS in this work provides an appealing alternative for large-scale touch positioning and enriches human-machine interaction.
基金the Philippines’Department of Science and Technology-Engineering Research and Development for Technology program,the Intelligent Systems Laboratory and the iNano Laboratory of the De La Salle University,the Fundação para a Ciência e a Tecnologia(FCT)for funding MARE(Marine and Environmental Sciences Centre,UIDB/04292/2020 and UIDB/04292/2020)ARNET(Aquatic Research Infrastructure Network Associated Laboratory,LA/P/0069/2020)B.Duarte researcher contract(CEECIND/00511/2017).
文摘Nitrate is the primary water-soluble macronutrient essential for plant growth that is converted from excess fish feeds,fish effluents,and degrading biomaterials on the aquaponic pond floor,and when aquacultural malpractices occur,large amounts of it retain in the water system causing increase rate in eutrophication and toxifies fish and aquaculture plants.Recent nitrate sensor prototypes still require performing the additional steps of water sample deionization and dilution and were constructed with expensive materials.In response to the challenge of sensor enhancement and aquaponic water quality monitoring,this study developed sensitive,repeatable,and reproducible screen-printed graphite electrodes on polyvinyl chloride and parchment paper substrates with silver as electrode material and 60:40 graphite powder:nail polish formulated conductive ink for electrical traces,integrated with 9-gene genetic expression model as a function of peak anodic current and electrochemical test time for nitrate concentration prediction that is embedded into low-power Arduino ESP32 for in situ nitrate sensing in aquaponic pond water.Five SPE electrical traces were designed on the two types of substrates.Scanning electron microscopy with energy dispersive X-ray confirmed the electrode surface morphology.Electrochemical cyclic voltammetry using 10 to 100 mg/L KNO3 and water from three-depth regions of the actual pond established the electrochemical test time(10.5 s)and electrode potential(0.135 V)protocol necessary to produce peak current that corresponds to the strength of nitrate ions during redox.The findings from in situ testing revealed that the proposed sensors have strong linear predictions(R2=0.968 MSE=1.659 for nSPEv and R2=0.966 MSE=4.697 for nSPEp)in the range of 10 to 100 mg/L and best detection limit of 3.15μg/L,which are comparable to other sensors of more complex construction.The developed three-electrode electrochemical nitrate sensor confirms that it is reliable for both biosensing in controlled solutions and in situ aquaponic pond water systems.
基金the European Union−Next Generation EU,project MEET codice grant number 20225P4EJC,CUP J53D23014570001support from the Spanish Ministry of Science and Innovation through programs RED2022-134120-T and PID2020-113154RB-C22supported by the Nano-ImmunoEra project that has received funding from the European Union’s MSCA Staff exchange Horizon Europe programme Grant Agreement Number 101086341.
文摘Electrochemiluminescence(ECL)is nowadays a powerful technique widely used in biosensing and imaging,offering high sensitivity and specificity for detecting and mapping biomolecules.Screen-printed electrodes(SPEs)offer a versatile and cost-effective platform for ECL applications due to their ease of fabrication,disposability,and suitability for large-scale production.This research introduces a novel method for improving the ECL characteristics of screen-printed carbon electrodes(SPCEs)through the application of CO_(2)laser treatment following fabrication.Using advanced ECL microscopy,we analyze three distinct carbon paste-based electrodes and show that low-energy laser exposure(ranging from 7 to 12 mJ·cm^(−2))enhances the electrochemical performance of the electrodes.This enhancement results from the selective removal of surface binders and contaminants achieved by the laser treatment.We employed ECL microscopy to characterize the ECL emission using a bead-based system incorporating magnetic microbeads,like those used in commercial platforms.This approach enabled highresolution spatial mapping of the electrode surface,offering valuable insights into its electrochemical performance.Through quantitative assessment using a photomultiplier tube(PMT),it was observed that GST electrodes could detect biomarkers with high sensitivity,achieving an approximate detection limit(LOD)of 11 antibodies perμm^(2).These findings emphasize the potential of laser-modified GST electrodes in enabling highly sensitive electrochemiluminescent immunoassays and various biosensing applications.
文摘The solar cell market is predominantly based on textured screen-printed solar cells.Due to parasitic absorption in nanostructures,using plasmonic processes to obtain an enhancement that exceeds 2.5%of the short-circuit photocurrent density is challenging.In this paper,a 7.2%enhancement in the photocurrent density can be achieved through the integration of plasmonic Al nanoparticles and wrinkle-like graphene sheets.For the first time,we experimentally achieve Al nanoparticle-enhanced solar cells.An innovative thermal evaporation method is proposed to fabricate low-coverage Al nanoparticle arrays on solar cells.Due to the ultraviolet(UV)plasmon resonance of Al nanoparticles,the performance enhancement of the solar cells is significantly greater than that from Ag nanoparticles.Subsequently,we deposit wrinkle-like graphene sheets over the Al nanoparticle-enhanced solar cells.Compared with planar graphene sheets,the bend carbon layer also exhibits a broadband light-trapping effect.Our results exceed the limit of plasmonic light trapping in textured screen-printed silicon solar cells.
基金This work was supported by the International Research Exchange Scheme of the Marie Curie Program of the 7th Framework Program(Ref.PIRSES-GA-2013-612659)Chinese National Natural Science Foundation(No.31671578)+1 种基金the Fundamental Research Funds for the Central Universities(Grant No.2016 XD001)the Shandong Provincial Natural Science Foundation of China(No.ZR2015CM016).
文摘Cadmium(Cd)and lead(Pb)in soil or water environment cause the ecological destruction and environmental deterioration when their contents exceed the natural background values.To trace the concentrations of Cd(II)and Pb(II),a sensitive and selective electrode was developed using disposable screen-printed carbon electrode(SPE)immobilized with a composite film of reduced graphene oxide/carboxylation multi-walled carbon nanotubes/gold nanoparticle hybrid(RGO-MWNT-AuNP)throughπ-πbind.This highly conductive nano-composite layer,“RGO-MWNT-AuNP,”was characterized by scanning electron microscopy,UV-visible spectrometer,cyclic voltammetry,and electrochemical impedance spectroscopy.Square wave stripping voltammetry was applied to RGO-MWNT-AuNP/SPE to electroplate bismuth film and monitor the Cd(II)and Pb(II)simultaneously.To obtain high current responses,the detecting parameters were optimized.Under optimized conditions,the current responses showed a linear relationship with the concentrations of Cd(II)and Pb(II)in the range from 1.0 to 80.0μg/L with a lower detection limit of 0.7μg/L and 0.3μg/L(S/N=3),respectively.Finally,the prepared electrode was further employed to detect Cd(II)and Pb(II)in soil samples with good results.
基金supported by Beijing University of Chemical Technology-China-Japan Friendship Hospital Biomedical Translation Engineering Research Center Joint Project(RZ2020-02)the National Key Research and Development Program of China(2016YFF0203703)
文摘Okadaic acid(OA),a small molecule substance derived from shellfish,is one of the most widely distributed marine toxins with acute symptoms of vomiting and diarrhea after accidental ingestion.For this,there is an urgently need for sensitive and reliable methods to detect OA in real shellfish samples.In this study,a simple aptasensor based on screen-printed carbon electrode(SPCE)with modification of chitosan(CS)and gold nanoparticles(Au NPs)was designed for electrochemical determination of OA,and the electrode surface was modified with Au NPs by potential-sweeping electrodeposition,which greatly improved the electrochemical response.The entire detection and characterization process were carried out by cyclic voltammetry(CV)with a linear correlation in the range of 0.01-100 ng/m L and a limit of detection(LOD)of 6.7 pg/m L.Furthermore,recovery rates of 92.3-116%were obtained demonstrating excellent accuracy through the recovery trial of mussel and scallop samples.
基金supported by Science and Technology Commission of Shanghai Municipality (09391911500)
文摘The screen-printed three-electrode system was applied to fabricate a new type of disposable amperometric xanthine oxidase biosensor.Carbon-working,carbon-counter and Ag/AgCl reference electrodes were all manually printed on the polyethylene terephthalate substrate forming the screen-printed three-electrode system by the conventional screen-printing process.As a mediator,Prussian blue could not only catalyze the electrochemical reduction of hydrogen peroxide produced from the enzyme reaction,but also keep the favorable potential around 0 V.The optimum operational conditions,including pH,potential and temperature,were investigated.The sensitivities of xanthine and hypoxanthine detections were 13.83 mA/M and 25.56 mA/M,respectively.A linear relationship was obtained in the concentration range between 0.10μM and 4.98μM for xanthine and between 0.50μM and 3.98μM for hypoxanthine.The small Michaelis-menten constant value of the xanthine oxidase biosensor was calculated to be 3.90 μM.The results indicate that the fabricated xanthine oxidase biosensor is effective and sensitive for the detection of xanthine and hypoxanthine.
基金supported by National Research Council of Thailand NRCT (grant number: N41A640129), Prince of Songkla University, Hat Yai, Thailandthe Talent Management Project of Prince of Songkla Universitythe Center of Excellence for Innovation in Chemistry (PERCH-CIC), Ministry of Higher Education, Science, Research, and Innovation (MHESI)。
文摘Developing flexible bioelectronics is essential to the realization of artificial intelligence devices and biomedical applications, such as wearables, but their potential is limited by sustainable energy supply. An enzymatic biofuel cell(BFC) is promising for power supply, but its use is limited by the challenges of incorporating multiple enzymes and rigid platforms. This paper shows the first example of screen-printable nanocomposite inks engineered for a single-enzyme-based energy-harvesting device and a self-powered biosensor driven by glucose on bioanode and biocathode. The anode ink is modified with naphthoquinone and multiwalled carbon nanotubes(MWCNTs), whereas the cathode ink is modified with Prussian blue/MWCNT hybrid before immobilizing with glucose oxidase. The flexible bioanode and the biocathode consume glucose. This BFC yields an open circuit voltage of 0.45 V and a maximum power density of 266 μW cm-2. The wearable device coupled with a wireless portable system can convert chemical energy into electric energy and detect glucose in artificial sweat. The self-powered sensor can detect glucose concentrations up to 10 mM. Common interfering substances,including lactate, uric acid, ascorbic acid, and creatinine, have no effect on this self-powered biosensor. Additionally, the device can endure multiple mechanical deformations. New advances in ink development and flexible platforms enable a wide range of applications, including on-body electronics, self-sustainable applications, and smart fabrics.
基金the financial support from the Key Project of National Natural Science Foundation of China(12131010)the National Natural Science Foundation of China(22279166)+2 种基金the Special Project for Marine Economy Development of Guangdong Province(GDNRC[2023]26)the International Cooperation Base of Infrared Reflection Liquid Crystal Polymers and Device(2015B050501010)the Guangdong Basic and Applied Basic Research Foundation(2022B1515120019)。
文摘Supercapacitor diode is a novel ion device that performs both supercapacitor energy storage and ion diode rectification functions.However,previously reported devices are limited by their large size and complex processes.In this work,we demonstrate a screen-printed micro supercapacitor diode(MCAPode)that based on the insertion of a finger mode with spinel ZnCo_(2)O_(4) as cathode and activated carbon as anode for the first time,and featuring an excellent area specific capacitance(1.21 mF cm^(-2)at 10 mV s^(-1))and high rectification characteristics(rectification ratioⅠof 11.99 at 40 mV s^(-1)).Taking advantage of the ionic gel electrolyte,which provides excellent stability during repeated flexing and at high temperatures.In addition,MCAPode exhibits excellent electrochemical performance and rectification capability in"AND"and"OR"logic gates.These findings provide practical solutions for future expansion of micro supercapacitor diode applications.
