Design of liquid level detection circuit based on sampling probe structure capacitance.

Liquid level detection system is an essential core functional component of automatic clinical medical testing instrument. The conventional liquid level detection method has low detection accuracy and sensitivity, and may have the problem of false detection, which may lead to the inaccurate test results. This paper presents a high sensitivity liquid level detection system based on the principle of variable capacitance. When the sampling probe contacts the liquid level, the probe capacitance will change. The liquid level detection circuit board judges whether the probe contacts the liquid level by sensing the change of probe capacitance. When judging the liquid level signal, the combination of slope detection and amplitude detection is used. The liquid level detection circuit board takes the phase-locked loop(PLL) circuit as the center to detect the change of the capacitance. The reference signal of the PLL is set as a square wave of 375kHz. The double tube probe is used as a part of the tuning capacitor of the voltage controlled oscillator to control the frequency of the output signal, which can realize the rapid phase locking. The experimental results show that the system has accurate detection results, high sensitivity, stable and reliable operation, good dynamic response performance in the case of large and small liquid volume. Compared with other liquid level detection methods based on machine vision, ultrasonic, optics and so on, the proposed liquid level detection system has simpler structure and lower cost, it can avoid the problems of collision, carryover contamination and empty suction by controlling the depth of sampling needle inserted into liquid.

Optical and electronic properties of MgPc-Ch-diisoQ blend organic thin film as an active layer for photovoltaic cells.

Organic photovoltaic cells are a promising technology for generating renewable energy from sunlight. These cells are made from organic materials, such as polymers or small molecules, and can be lightweight, flexible, and low-cost. Here, we have created a novel mixture of magnesium phthalocyanine (MgPc) and chlorophenyl ethyl diisoquinoline (Ch-diisoQ). A coating unit has been utilized in preparing MgPc, Ch-diisoQ, and MgPc-Ch-diisoQ films onto to FTO substrate. The MgPc-Ch-diisoQ film has a spherical and homogeneous surface morphology with a grain size of 15.9 nm. The optical absorption of the MgPc-Ch-diisoQ film was measured, and three distinct bands were observed at 800-600 nm, 600-400 nm, and 400-250 nm, with a band gap energy of 1.58 eV. The current density-voltage and capacitance-voltage measurements were performed to analyze the photoelectric properties of the three tested cells. The forward current density obtained from our investigated blend cell is more significant than that for each material by about 22%. The photovoltaic parameters (Voc, Isc, and FF) of the MgPc-Ch-diisoQ cell were found to be 0.45 V, 2.12 µA, and 0.4, respectively. We believe that our investigated MgPc-Ch-diisoQ film will be a promising active layer in organic solar cells.

Co/P co-doped bamboo-based woodceramics with a sandwich structure modified by carbon nanotube electrodeposition as supercapacitor electrodes.

Exploring new electrode structures and co-doped composite biomass material electrodes is considered to be an effective way of developing cheap, efficient carbon-based supercapacitors. A bamboo-based sandwich-structured matrix was prepared from thin bamboo veneer and bamboo fiber by pretreatment with H3PO4 and Co2+-catalyzed graphitization. The pore structure was modulated by hydrothermal activation with NaOH and electrodeposition of carbon nanotubes (CNTs) to obtain CNTs modified, Co/P co-doped sandwich-structured woodceramics electrode (CNT@Co/P). It not only has an obvious sandwich structure, but also retains the natural structural characteristics of bamboo. The specific capacitance of the resulting electrode (CNT@Co/P-20) is as high as 453.72F/g using 1 wt% of carboxylated multi-walled carbon nanotubes (CMWCNT) solution as the deposition electrolyte at a current density of 0.2 A/g for 20 min at room temperature. When the power density is 500 W/kg, the energy density reaches 21.3Wh /kg, showing a good electrochemical performance.

Photoinduced charge generation of nanostructured carbon derived from human hair biowaste for performance enhancement in polyvinylidene fluoride based triboelectric nanogenerator.

Carbon nanostructures derived from human hair biowaste are incorporated into polyvinylidene fluoride (PVDF) polymer to enhance the energy conversion performance of a triboelectric nanogenerator (TENG). The PVDF filled with activated carbon nanomaterial from human hair (AC-HH) exhibits improved surface charge density and photoinduced charge generation. These remarkable properties are attributed to the presence of graphene-like nanostructures in AC-HH, contributing to the augmented performance of PVDF@AC-HH TENG. The correlation of surface morphologies, surface charge potential, charge capacitance properties, and TENG electrical output of the PVDF composites at various AC-HH loading is studied and discussed. Applications of the PVDF@AC-HH TENG as a power source for micro/nanoelectronics and a movement sensor for detecting finger gestures are also demonstrated. The photoresponse property of the fabricated TENG is demonstrated and analyzed in-depth. The analysis indicates that the photoinduced charge carriers originate from the conductive reduced graphene oxide (rGO), contributing to the enhanced surface charge density of the PVDF composite film. This research introduces a novel approach to enhancing TENG performance through the utilization of carbon nanostructures derived from human biowaste. The findings of this work are crucial for the development of innovative energy-harvesting technology with multifunctionality, including power generation, motion detection, and photoresponse capabilities.

Kenaf-based activated carbon: A sustainable solution for high-performance aqueous symmetric supercapacitors.

This study presents an innovative method for synthesizing activated carbon with an exceptionally high surface area (3359 m2 g-1) using kenaf fiber-based biochar through chemical activation. The achieved specific surface area surpasses activated carbon derived from other reported fiber-based precursors. The resulting activated carbon was investigated as electrodes for supercapacitors, revealing a remarkable maximum capacitance of 312 F g-1 at a current density of 0.5 A g-1. An aqueous symmetric supercapacitor employing these high-surface-area electrodes exhibited an outstanding energy density of 18.9 Wh kg-1 at a power density of 250 W kg-1. Notably, the supercapacitor retained exceptional capacitance, maintaining 93% of its initial capacitance even after 5000 charge-discharge cycles.

Capacitive Bionic Magnetic Sensors Based on One-Step Biointerface Preparation.

Magnetic biomolecule-based bionic magnetic field sensors are anticipated to open up novel pathways for magnetic field detection. The detection range and accuracy of current bionic magnetic field sensors are limited, and little work is based on the capacitive response principle. We successfully developed a biochemical interface with an extralarge target-receptor size ratio, which can be manufactured in a single step for weak magnetic field detection across a wide frequency range, and we used electrochemical capacitance as a magnetic field change conduction strategy. The thickness-controllable nanoscale bovine serum albumin/graphene layer on an indium tin oxide working electrode combines with the one-step preparation method to immobilize the MagR/Cry4 complex. This capacitive bionic magnetic sensor can achieve the detection range of 0-120 mT. This biointerface design strategy obtains the further improvement of the performance of this bionic magnetic field sensor. Furthermore, the biointerface construction and optimization methodology in this proposal has potential applications in the design of other medical biosensors.

Soluble starch-derived porous carbon microspheres with interconnected and hierarchical structure by a low dosage KOH activation for ultrahigh rate supercapacitors.

The developed porous structure and high density are essential to enhance the bulk performance of carbon-based supercapacitors. Nevertheless, it remains a significant challenge to optimize the balance between the porous structure and the density of carbon materials to realize superior gravimetric and areal electrochemical performance. The soluble starch-derived interconnected hierarchical porous carbon microspheres were prepared through a simple hydrothermal treatment succeeded by chemical activation with a low dosage of KOH. Due to the formation of interconnected spherical morphology, hierarchical porous structure, reasonable mesopore volume (0.33 cm3 g-1) and specific surface area (1162 m2 g-1), the prepared carbon microsphere has an ultrahigh capacitance of 394 F g-1 @ 1 A g-1 and a high capacitance retention of 62.7 % @ 80 A g-1. The assembled two-electrode device displays good cycle stability after 20,000 cycles and an ultra-high energy density of 11.6 Wh kg-1 @ 250 W kg-1. Moreover, the sample still exhibits a specific capacitance of 165 F g-1 @ 1 A g-1 at a high mass loading of 10 mg cm-2, resulting in a high areal capacitance of 1.65 F cm-2. The strategy proposed in this study, via a low-dose KOH activation process, provides the way for the synthesis of high-performance porous carbon materials.

Enhancing capacitive performance of magnetite-reduced graphene oxide nanocomposites through magnetic field-assisted ion migration.

The transition towards renewable energy sources necessitates efficient energy storage systems to meet growing demands. Electrochemical capacitors, particularly electric double-layer capacitors (EDLCs), show promising performance due to their superior properties. However, the presence of resistance limits their performance. This study explores using an external magnetic field to mitigate ion transfer resistance and enhance capacitance in magnetite-reduced graphene oxide (M-rGO) nanocomposites. M-rGO nanocomposites with varying weight ratios of magnetite were synthesized and comprehensively characterized. Characterization highlighted the difference in certain parameters such as C/O ratio, the Id/Ig ratio, surface area and particle size that contribute towards alteration of M-rGO's capacitive behaviour. Electrochemical studies demonstrated that applying a magnetic field increased specific capacitance by approximately 20% and reduced resistance by 33%. Notably, a maximum specific capacitance of 16.36 F/g (at a scan rate of 0.1 V/s) and 27.24 F/g (at a current density of 0.25 A/g) was achieved. These improvements were attributed to enhanced ion transportation and migration at the electrode/electrolyte interface, lowering overall resistance. However, it was also observed that the aforementioned parameters can also limit the M-rGO's performance, resulting in saturated capacitive state despite a reduced resistance. The integration of magnetic fields enhances energy storage in nanocomposite systems, necessitating further investigation into underlying mechanisms and practical applications.

Waste polyethylene terephthalate plastic derived Zr-MOF for high performance supercapacitor applications.

The chemical conversion of plastic waste into metal-organic framework (MOF) materials has emerged as a significant research field in addressing issues associated to the environment and the economy. The significant advantages of MOFs as electrode material for energy/supercapacitors arises from their extensive surface area and notable porosity. The present study involved the synthesis of Zirconium-Metal Organic Frameworks (Zr-MOF) by the solvothermal method, utilizing plastic waste in the form of Polyethylene terephthalate (PET) bottles. The morphological and structural characteristics of the Zr-MOF were inspected through several analytical techniques, including scanning electron microscopy, transmission electron microscopy, X-ray diffraction, and Fourier-transform infrared spectroscopy analysis. The as prepared Zr-MOF demonstrated very high specific surface area of 927.567 m2 g-1 with mesoporous nature of the materials estimate by BJH method. The electrochemical characteristics of the Zr-MOF in 3-electrode system exhibited a notable specific capacitance of 822 F g-1 when subjected to a low scan rate of 2 mV S-1, while the specific capacitance estimated through galvanostatic charge-discharge exhibited an enhanced value of 890 F g-1 at a current density of 0.5 A g-1. Additionally, the working electrode composed of Zr-MOF demonstrated noteworthy capacitance retention of 92% after 5000 charge discharge cycles. This research presents novel opportunities for the utilization of waste PET bottles in fabrication of highly functional Zr-MOF, aiming to advance the development of next-generation supercapacitors and environmental remediation.

Fringe-fields-modulated double-gate tunnel-FET biosensor.

This paper aims to evaluate a groundbreaking bio-TFET that utilizes the fringe fields capacitance concept to detect neutral and charged biomolecules. While facilitating fabrication process and scalability, this innovative bio-TFET is able to rival the conventional bio-TFET which relies on carving cavities in the gate oxide. The cavities of the proposed device are carved in the spacers over the source region and in the vicinity of the gate metal. Inserting biomolecules in the cavities of our bio-TFET modifies the fringe fields arising out of the gate metal. As a result, these spacers modulate tunneling barrier width at the source-channel tunneling junction. We have assessed our proposed device's DC/RF performance using the calibrated Silvaco ATLAS device simulator. For further evaluation of the reliability of our bio-TFET, non-idealities, such as trap-assisted tunneling and temperature, are also studied. The device we propose is highly suitable for biosensing applications, as evidenced by the parameters of [Formula: see text] = 1.21 × 103, SSS = 0.365, and [Formula: see text] = 1.63 × 103 at VGS = 1 V.

Lignosulfonate sodium assisted PEDOT-based all-gel supercapacitors with enhanced supercapacitance and wide temperature tolerance.

Conducting polymer hydrogels are typically employed in all-gel supercapacitors; however, Poly[3,4-ethylene-dioxythiophene] (PEDOT)-based hydrogel supercapacitors still suffer from low capacitance because of the low packing density of PEDOT in the electrodes. Here, we demonstrate lignosulfonate sodium (LS) as an excellent template to synthesize various LS-PEDOT conductive nanofillers for high mass-loading LS-PEDOT/PAAM hydrogel electrodes. Then, the optimum LS-PEDOT/PAAM electrode was assembled with a redox-active LS/PAAM/Fe3+ hydrogel electrolyte to form sandwich-structured all-gel supercapacitors, which could deliver a high specific capacitance of 672.5 mF/cm2 and an energy efficiency of 60 µWh/cm2, which are three times higher than the 220 mF/cm2 and 19.5 µWh/cm2 of the device without Fe3+ at the same condition. Such a device shows excellent temperature tolerance from -30 to 100 °C. Besides, the LS-PEDOT/PAAM electrode has excellent photothermal conversion effects under simulated solar illumination. The sluggish electrochemical performance of the SC under low temperatures could be significantly boosted by ~50 % under simulated solar light. All of these findings demonstrate that the capacitance performance of the PEDOT-based hydrogel device is successfully improved not only at room temperature but also under subzero conditions.

Biomass-derived multifunctional nanoscale carbon fibers toward fire warning sensors, supercapacitors and moist-electric generators.

Nowadays, great effort has been devoted to designing biomass-derived nanoscale carbon fibers with controllable fibrous morphology, high conductivity, big specific surface area and multifunctional characteristics. Herein, a green and renewable strategy is performed to prepare the biomass-based nanoscale carbon fibers for fire warning sensor, supercapacitor and moist-electric generator. This preparation strategy thoroughly gets over the dependence of petroleum-based polymeride, and effectually improves the energy storage capacity, sensing sensitivity, humidity power generation efficiency of the obtaining biomass-based carbon nanofibers. Without the introduction of any active components or pseudocapacitive materials, the specific capacitance and energy density for biomass-based nanoscale carbon fibers achieve 143.58 F/g and 19.9 Wh/kg, severally. The biomass-based fire sensor displays excellent fire resistance, stability, and flame sensitivity with a response time of 2 s. Furthermore, the biomass-based moist-electric generator shows high power generation efficiency. The output voltage and current of five series connected and parallel-connected biomass-based moist-electric generators reaches 4.30 V and 43 µA, respectively. Notably, as the number of biomass-based moist-electric generators in series or parallel increases, the overall output voltage and current of the device system have a linear relationship. This work proposes a self-powered fire prediction system based on nanoscale carbon fibers that integrates sensing, power generation, and energy storage functions.

High-Performing and Capacitive-Matched Triboelectric Implants Driven by Ultrasound.

In implantable bioelectronics, which aim for semipermanent use of devices, biosafe energy sources and packaging materials to protect devices are essential elements. However, research so far has been conducted in a direction where they cannot coexist. Here, the development of capacitance-matched triboelectric implants driven is reported by ultrasound under 500 mW cm-2 safe intensity and realize a battery-free, miniatured, and wireless neurostimulator with full titanium (Ti) packaging. The triboelectric implant with high dielectric composite, which has ultralow output impedance, can efficiently deliver sufficient power to generate the stimulation pulse without an energy-storing battery, despite ultrasound attenuation due to the Ti, and has the highest energy transmission efficiency among those reported so far. In vivo study using a rat model demonstrated that the proposed device system is an effective solution for relieving urinary symptoms. These achievements provide a significant step toward permanently implantable devices for controlling human organs and treating various diseases.

Starch-based carbon aerogels prepared by an innovative KOH activation method for supercapacitors.

Biomass-based carbon aerogels hold promising application prospect in the field of supercapacitors. In this research, starch was selected as a raw material for preparing carbon aerogels. The preparation process of starch hydrogels was simplified by using KOH, which can change starch suspension into hydrogels at room temperature. Moreover, the molecular mixing of KOH and starch was realized, so that KOH can be fully utilized in the activation process. The specific surface area of the starch-based carbon aerogels prepared by this method was 1349 m2/g, and the proportion of micropores was 43.7 %. Remarkably, as electrode materials for supercapacitors, the starch-based carbon aerogels exhibited outstanding electrochemical performance. In a three-electrode system, the carbon aerogels exhibited specific capacitance of 211.5 F/g at 0.5 A/g and 138.5 F/g at 10 A/g, suggesting their suitability for high-current applications. In a symmetrical supercapacitor configuration, the materials exhibited an energy density of 11.3 Wh/kg at a power density of 0.5 kW/kg and the specific capacitance can maintain 98.91 % after 10,000 cycles. Overall, this work provides a new method for mixing activators, which will foster potential advances in starch based carbon aerogels.

Ion-Electron Transduction Layer of the SnS2-MoS2 Heterojunction to Elevate Superior Interface Stability for All-Solid Sodium-Ion Selective Electrode.

The high selectivity and fast ion response of all-solid sodium ion selective electrodes were widely applied in human sweat analysis. However, the potential drift due to insufficient interfacial capacitance leads to the deterioration of its stability and ultimately affects the potential accuracy of ion analysis. Designing a novel ion-electron transduction layer between the electrode and the ion selective membrane is an effective method to stabilize the interfacial potential. Herein, the SnS2-MoS2 heterojunction material was constructed by doping Sn in MoS2 nanosheets and used as the ion electron transduction layers of an all-solid sodium ion selective electrode for the first time, achieving the stable and efficient detection of Na+ ions. The proposed electrode exhibited a Nernst slope of 57.86 mV/dec for the detection of Na+ ions with a detection limit of 10-5.7 M in the activity range of 10-6-10-1 M. Via the electronic interaction at the heterojunction interfaces between SnS2 and MoS2 materials, the micro-nanostructure of the SnS2-MoS2 heterojunction was changed and SnS2-MoS2 as the ion-electron transduction layer acquired excellent capacitance (699 µF) and hydrophobicity (132°), resulting in a long-term potential stability of 1.37 µV/h. It was further proved that the large capacitance and high hydrophobicity of the ion-electron transduction layer are primary reasons for the excellent stability of the all-solid sodium ion selective electrode toward Na+ ions.

Synthesis of novel nanocomposite of g-C3N4 coated ZnO-MoS2 for energy storage and photocatalytic applications.

Fabrication of heterostructures for energy storage and environmental remedial applications is an interesting subject of research that has been undertaken in this present investigation. The incorporation of g-C3N4 into ZnO:MoS2 heterojunction nanocomposite was accomplished by wet-chemical route and characterized by various techniques to ascertain its structure, morphology, and study its potential electro-optical characteristics. The g-C3N4@ZnO:MoS2 sample was investigated by x-ray diffraction (XRD) which reveals the co-existence of the ZnO, MoS2 and C3N4 phases linked to characteristic crystallographic planes in the spectrum, validating the formation of ternary nanocomposite. The XRD patterns of the pristine samples were also considered as reference to understand the structural evolution and phase transformations. Field emission scanning electron microscopy (FESEM) study states the formation of heterogeneous nanostructures having nanoparticles embedded on 2-D nanosheets like structures. Studies using energy dispersive spectroscopy (EDS) and elemental mapping show that all the elements that are linked to the above hybrid nanocomposite are present. Transmission electron microscopy (TEM) provided clear insights on the microstructure as we can identify the distribution of ZnO and MoS2 nanostructures on layered g-C3N4 nanosheets. The chemical composition and oxidation states of elements were elucidated by X-ray photoelectron spectroscopy (XPS) study, which added another layer of confirmation on the structural evolution of the ternary nanocomposite. Fourier transformed infrared (FTIR) study revealed the layered structure of sp2 hybridized bonding features of C and N in g-C3N4, besides Zn-O and Mo-S stretching vibrations. The nanocomposite demonstrated improved photodegradation efficacy and decomposed alizarin red and methylene blue dyes significantly with better stability and reusability. MoS2 as a co-catalyst acts as an electron acceptor/accelerator in the Z-scheme composite photocatalysis leading to improved photocatalytic efficiency. The resulting heterostructured material delivered a higher specific capacitance of 10.85 F/g with good capacitance retention. Electrochemical study revealed the energy storage capability of the hybrid system.

Unlocking Bimetallic Active Centers via Heterostructure Engineering for Exceptional Phosphate Electrosorption: Internal Electric Field-Induced Electronic Structure Reconstruction.

Development of electrode materials exhibiting exceptional phosphate removal performance represents a promising strategy to mitigate eutrophication and meet ever-stricter stringent emission standards. Herein, we precisely designed a novel LaCeOx heterostructure-decorated hierarchical carbon composite (L8C2PC) for high-efficiency phosphate electrosorption. This approach establishes an internal electric field within the LaCeOx heterostructure, where the electrons transfer from Ce atoms to neighboring La atoms through superexchange interactions in La-O-Ce coordination units. The modulatory heterostructure endows a positive shift of the d band of La sites and the increase of electron density at Fermi level, promoting stronger orbital overlap and binding interactions. The introduction of oxygen vacancies during the in situ nucleation process reduces the kinetic barrier for phosphate-ion migration and supplies additional active centers. Moreover, the hierarchical carbon framework ensures electrical double-layer capacitance for phosphate storage and interconnected ion migration channels. Such synergistically multiple active centers grant the L8C2PC electrode with high-efficiency record in phosphate electrosorption. As expected, the L8C2PC electrode demonstrates the highest removal capability among the reported electrode materials with a saturation capacity of 401.31 mg P g-1 and a dynamic capacity of 91.83 mg P g-1 at 1.2 V. This electrochemical system also performs well in the dephosphorization in natural water samples with low concentration that enable effluent concentration to meet the first-class discharge standard for China (0.5 mg P L-1). This study advances efficient dephosphorization techniques to a new level and offers a deep understanding of the internal electric field that regulates metal orbitals and electron densities in heterostructure engineering.

Four minutes of capacitive and resistive electric transfer therapy increased jump performance.

Capacitive and resistive electric transfer (CRET) therapy can improve flexibility and increase muscle activity and may be useful as a warm-up technique. This study examined the effects of short-time CRET on jump performance. Thirty healthy men (age range, 20-40 years) were randomly divided into passive (n = 15) and active (n = 15) warm-up groups. The participants and statisticians were blinded to the participant allocation. The passive warm-up group underwent 4 min of CRET therapy on their posterior lower legs. The active warm-up group performed stretching and jogging for 4 min. Calf muscle temperature and rebound jump (RJ) index were measured before and after the intervention. The mean (± standard deviation) muscle temperature increased by 2.0 ± 0.5°C and 1.4 ± 0.6°C in the passive and active warm-up groups, respectively (p < 0.05). RJ index increased significantly in both groups (p < 0.05). Therefore, passive warm-up using CRET may help avoid energy loss while increasing the muscle temperature in a short time when compared with traditional active warm-up techniques.

Capacitive and resistive electric transfer (CRET) is a device with deep thermal effect. CRET therapy can improve flexibility and increase muscle activity and may be useful as a warm-up technique. This study examined the effects of short-time CRET on jump performance. Thirty healthy men (age range, 20­40 years) were randomly divided into passive (n=15) and active (n=15) warm-up groups. The passive warm-up group underwent 4min of CRET therapy on their calf. The active warm-up group performed stretching and jogging for 4min. Calf muscle temperature and jump performance were measured before and after the intervention. The mean (± standard deviation) muscle temperature increased by 2.0±0.5°C and 1.4±0.6°C in the passive and active warm-up groups, respectively (p<0.05). Jump performance increased significantly in both groups (p<0.05). Therefore, passive warm-up using CRET may help avoid energy loss while increasing the muscle temperature in a short time when compared with traditional active warm-up techniques.

Maintenance-Free Smart Hand Dynamometer.

Grip strength measurement is one of the most accessible methods for measuring overall muscle strength, and many studies have shown a link between low grip strength and future diseases. In recent years, devices for grip strength measurements that can connect to digital devices for automatic data recording have been developed. However, such devices have high development costs and require daily maintenance. Therefore, this we propose a grip strength measurement method using the capacitance sensor of a smartphone and no electronic parts on the measurement device side.

Characterization and Correction of Low Frequency Artifacts in Segmental Bioimpedance Measurements.

Bioimpedance analysis can be used for remote monitoring of volume status for various conditions such as congestive heart failure. The measurement is typically performed with four electrodes, two of them driving an alternating current through the tissue and the other two sensing the resulting voltage. Issues with the measurement setup such as stray capacitance or electrode mismatch can cause artifacts that impact Cole parameters used for volume estimation. While previous research has focused on mitigating high frequency artifacts, little research has been done to understand the cause and impact of low frequency artifacts, nor how to mitigate the impact of these artifacts. These artifacts are most prevalent in wearable segmental bioimpedance systems, especially using textile electrodes, so future research in this area is needed for these systems to be viable. The present study uses simulations to identify the potential sources of low frequency artifacts, and explores techniques to minimize the impact of these artifacts on Cole parameters. Theoretical analysis and simulations show that the mismatch of the voltage electrodes causes artifacts at low frequency. These artifacts are highly dependent on the impedance of the negative current injecting electrode. Averaging measurements of the mismatch of both voltage electrodes and limiting high frequency measurements to 200 kHz can reduce errors due to these artifacts from over 137% to less than 3%. The results of this study suggest the impact of low frequency artifacts can be significantly reduced, enabling future development of wearable bioimpedance systems.Clinical relevance- Reducing the impact of low frequency artifacts on Cole parameter estimation enables wearable segmental bioimpedance systems that can be used for remote monitoring of volume status in home environments.