Exploring impedance spectrum for lithium-ion batteries diagnosis and prognosis:A comprehensive review

Lithium-ion batteries have extensive usage in various energy storage needs,owing to their notable benefits of high energy density and long lifespan.The monitoring of battery states and failure identification are indispensable for guaranteeing the secure and optimal functionality of the batteries.The impedance spectrum has garnered growing interest due to its ability to provide a valuable understanding of material characteristics and electrochemical processes.To inspire further progress in the investigation and application of the battery impedance spectrum,this paper provides a comprehensive review of the determination and utilization of the impedance spectrum.The sources of impedance inaccuracies are systematically analyzed in terms of frequency response characteristics.The applicability of utilizing diverse impedance features for the diagnosis and prognosis of batteries is further elaborated.Finally,challenges and prospects for future research are discussed.

Construction of a broadband impedance spectrum and synchronous DC voltammetry measurement system for solar cells

The current impedance spectroscopy measurement techniques face difficulties in diagnosing solar cell faults due to issues such as cost,complexity,and accuracy.Therefore,a novel system was developed for precise broadband impedance spectrum measurement of solar cells,which was composed of an oscilloscope,a signal generator,and a sampling resistor.The results demonstrate concurrent accurate measurement of the impedance spectrum(50 Hz-0.1 MHz)and direct current voltametric characteristics.Comparative analysis with Keithley 2450 data yields a global relative error of approximately 6.70%,affirming the accuracy.Among excitation signals(sine,square,triangle,pulse waves),sine wave input yields the most accurate data,with a root mean square error of approximately 13.3016 and a global relative error of approximately 4.25%compared to theoretical data.Elevating reference resistance expands the half circle in the impedance spectrum.Proximity of reference resistance to that of the solar cell enhances the accuracy by mitigating line resistance influence.Measurement error is lower in high-frequency regions due to a higher signal-to-noise ratio.

Battery impedance spectrum prediction from partial charging voltage curve by machine learning

Electrochemical impedance spectroscopy(EIS) is an effective technique for Lithium-ion battery state of health diagnosis, and the impedance spectrum prediction by battery charging curve is expected to enable battery impedance testing during vehicle operation. However, the mechanistic relationship between charging curves and impedance spectrum remains unclear, which hinders the development as well as optimization of EIS-based prediction techniques. In this paper, we predicted the impedance spectrum by the battery charging voltage curve and optimized the input based on electrochemical mechanistic analysis and machine learning. The internal electrochemical relationships between the charging curve,incremental capacity curve, and the impedance spectrum are explored, which improves the physical interpretability for this prediction and helps define the proper partial voltage range for the input for machine learning models. Different machine learning algorithms have been adopted for the verification of the proposed framework based on the sequence-to-sequence predictions. In addition, the predictions with different partial voltage ranges, at different state of charge, and with different training data ratio are evaluated to prove the proposed method have high generalization and robustness. The experimental results show that the proper partial voltage range has high accuracy and converges to the findings of the electrochemical analysis. The predicted errors for impedance spectrum are less than 1.9 mΩ with the proper partial voltage range selected by the corelative analysis of the electrochemical reactions inside the batteries. Even with the voltage range reduced to 3.65–3.75 V, the predictions are still reliable with most RMSEs less than 4 mO.

Fault Diagnosis of Proton Exchange Membrane Fuel Cell Based on Nonlinear Impedance Spectrum

Electrochemical impedance spectroscopy(EIS)contributes to developing the fault diagnosis tools for fuel cells,which is of great significance in improving service life.The conventional impedance measurement techniques are limited to linear responses,failing to capture high-order harmonic responses.However,nonlinear electrochemical impedance analysis incorporates additional nonlinear information,enabling the resolution of such responses.This study proposes a novel multi-stage fault diagnosis method based on the nonlinear electrochemical impedance spectrum(NEIS).First,the impact of alternating current excitation amplitude on NEIS is analyzed.Then,a series of experiments are conducted to obtain NEIS data under various fault conditions,encompassing recoverable faults like flooding,drying,starvation,and their mixed faults,spanning different degrees of fault severity.Based on these experiments,both EIS and NEIS datasets are established,and principal component analysis is utilized to extract the main features,thereby reducing the dimensionality of the original data.Finally,a fault diagnosis model is constructed with the support vector machine(SVM)and random forest algorithms,with model hyperparameters optimized by a hybrid genetic particle swarm optimization(HGAPSO)algorithm.The results show that the diagnostic accuracy of NEIS is higher than that of traditional EIS,with the HGAPSO-SVM model achieving a 100%accurate diagnosis under the NEIS dateset and self-defined fault labels.

Electrochemical Impedance Spectroscopy Study on Novel Carbon-Sulfur Nano-Composite Cathodes in Lithium Rechargeable Batteries

Carbon-sulfur nano-composite cathodes for lithium rechargeable batteries were investigated by electrochemical impedance spectroscopy (EIS). The novel carbon-sulfur nano-composite material was synthesized by heating sublimed sulfur and high surface area activated carbon (HSAAC) in certain conditions. Equivalent circuits were used to fit the spectra at different discharge states. The variations of impedance spectra, charge-transfer resistance and double layer capacitance were discussed. The changes of EIS with potential were analyzed based on a plausible electrical equivalent circuit model, and some parameters were measured and analyzed about electrochemical performance and state of charge and discharge of the electrode. The good accuracy in fitting values of the model to the experimental data indicates that the mathematical model gives out a satisfying description upon the mechanism of high rate of capacity fade in lithium-sulfur battery.

Spectrum and Electrochemical Properties of Nanosized Ce_(1-x)Bi_xO_(2-δ) Solid Solutions

Ce1-xBixO2-δ （x = 0.00, 0.03, 0.05, 0.07, 0.10, 0.15, 0.30） solid solutions were synthesized via a hydrothermal method. The structure, spectra and electrochemical transport properties of the samples were characterized systematically. The powder X-ray diffraction analysis showed that all of the doped samples exhibited single phase fluorite structure. The particle sizes decreased from 18 to 9 nm and the lattice parameters increased gradually with the dopant content increasing from x = 0.03 to x = 0.30. The Bi^3＋ doping also induced the F2g Raman peak to shift from 463 to 455 cm^-1, and caused a red shift of the band gap energies calculated from UV-Vis spectra. The impedance plots at different temperature demonstrated that the boundary resistance was much larger than the grain resistance, and two activation energy values were obtained in different temperature range.

Effects of complexing agents on acidic electroless nickel deposition

Our previous study reported the influences of different complexing agents on electroless nickel （EN） by examining the properties of the deposits. In the present work, the effects of four common-used complexing agents on EN deposition rate and the stability of solution pH values were examined, either with an acetic pH buffer agent or absent of them. It is indicated that the pH buffeting effect of them is dominative when the EN solution is lack of the pH buffer. Under this situation, the EN deposition rate increases with the concentration of complexing agents increasing. The EN deposition rate decreases with fin＇ther adding the complexing agent when the solution already has enough pH buffer capability. Electrochemical impedance spectroscopy obtained during EN deposition illustrates that, in this case, the enhanced reaction resistance is the main reason for a lower deposition rate. However, the influence of polarization caused by mass transfer is not negligible at high complex ratio for sodium citrate and malic acid EN solutions.

Effects of Nano Pigments on the Corrosion Resistance of Alkyd Coating

Alkyd coatings embedded with nano-TiO2 and nano-ZnO pigments were prepared. The effects of nano pigments on anticorrosion performance of alkyd coatings were investigated using electrochemical impedance spectrum （EIS）. For the sake of comparison, the corrosion protection of alkyd coatings with conventional TiO2 and ZnO was also studied. It was found that nano-TiO2 pigment improved the corrosion resistance as well as the hardness of alkyd coatings. The optimal amount of nano-TiO2 in a colored coating for corrosion resistance was 1%. The viscosities of alkyd coatings with nanometer TiO2 and ZnO and conventional TiO2 and ZnO pigments were measured and the relation between viscosity and anticorrosion performance was discussed.

Fabrication and performance of La(0.8)Sr(0.2)MnO3/YSZ graded composite cathodes for SOFC

The performance of multi-layer （1 -x）La0.8Sr0.2MnO3/xYSZ graded composite cathodes was studied as electrode materials for intermediate solid oxide fuel cells （SOFC）. The thermal expansion coefficient, electrical conductivity, and electrochemical performance of multi-layer composite cathodes were investigated. The thermal expansion coefficient and electrical conductivity decreased with the increase in YSZ content. The （1 -x）Lao.sSr0.EMnO3/xYSZ composite cathode greatly increased the length of the active triple phase boundary line （TPBL） among electrode, electrolyte, and gas phase, leading to a decrease in polarization resistance and an increase in polarization current density. The polarization current density of the triple-layer graded composite cathode （0.77 A/cm2） was the highest and that of the monolayer cathode （0.13 A/cm2） was the lowest. The polarization resistance （Rp） of the triple-layer graded composite cathode was only 0.182 Ω·cm2 and that of the monolayer composite cathode was 0.323 Ω·cm2. The power density of the triple-layer graded composite cathode was the highest and that of the monolayer composite cathode was the lowest. The triple-layer graded composite cathode had superior performance.

Corrosion Behavior of Anodic Oxidized TiO_2 Film in Seawater

TiO2 films were formed on metallic titanium substrates by the anodic oxidation method in H2SO4 solution under the 80V D.C..Phase component and microstructure were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM).Water contact angles on titanium oxide film surface were measured under both dark and sunlight illumination conditions.Corrosion tests were carried out in seawater under different illumination conditions by electrochemistry impedance spectrum (EIS) and polarization curves.The result showed that the TiO2 film prepared by the anodic oxidation method was anatase with a uniform structure and without obvious pores or cracks on its surface.The average water contact angle of the film was 116.4? in dark, in contrast to an angle of 42.7? under the UV illumination for 2 hours, which demonstrates good hydrophobic property.The anti-corrosion behavior of the TiO2 film was declining with the extended immersion time.Under dark conditions, however, the hydrophobic TiO2 film retarded the water infiltrating into the substrate.The impedance changed slowly and the corrosion current density was 2 orders of magnitude lower than that with the film illuminated by sunlight.All of those mentioned above indicate that the TiO2 film possesses much better performance under dark condition, and it can be applied as an engineering material under dark seawater environment.

The Conductivity of Co-dopant Ceria Electrolyte

A kind of novel ceria electrolyte was examined.Various trivalent oxides were added as co-dopants to Ce 0.8Gd 0.2O 1.9,and their effects on the conductivity of ceria electrolyte were discussed.It has been found that the co-dopant of trivalent oxides of Sm,Nd,La and Y improves the ionic conductivity notably.Furthermore,the fine original powders,co-dopant and higher sintering temperature may hasten the sintering.

Effect of Nano Silver Modification on the Dielectric Properties of Ag@TiO_(2)/PVDF Composites

To get a dielectric material with a high dielectric permittivity and suppressed dielectric loss,nano-Ag with a particle size of 20 nm and Ag@TiO_(2)core-shell particles with diameters of approximately 70-120 nm were embedded in polyvinylidene fluoride(PVDF)to fabricate nano-Ag/Ag@TiO_(2)/PVDF composites.After being modified by nano-Ag with 3 vol%optimal amount,the relative permittivity(ε_r)at 100 Hz of 50 vol%Ag@TiO_(2)/PVDF composites was 61,and the dielectric loss can be suppressed to 0.04,almost 96.4%lower than that of unmodified composites,and a higher frequency stability of bothε_r and loss has also been found.The underlying mechanism of the reduced loss was attributed to Maxwell-Wagner polarization and the Coulomb blockade effect caused by the introduction of a small amount of nano-Ag,which will block the movement of electrons between metal nanoparticles and composites.The space charge polarization and conductance loss are weakened at lower and higher Ag@TiO_(2)filling ratios,respectively,thus leading to a very low loss of the composites.

Electrochemical Corrosion Study in H2SO4 of NiAl with Cu Additions, Microstructure and Micro-Hardness at Room Temperature

For many years, intermetallic materials promise applications in a wide variety of technology areas. NiAl intermetallic compound is material that exhibits important characteristics such as high corrosion resistance and low density besides its ability to retain strength and stiffness at elevated temperatures. However NiAl intermetallic is too hard, brittle and exhibits very low ductility at room temperature being the reason because this material is not yet available for structural applications. In order to increase the ductility of the NiAl intermetallic compound, the addition of a third alloying element has been proved, nevertheless it is important to determine if such additions decrease or increase the hardness and the corrosion resistance of the alloy. So, the present investigation reports the corrosion performance of the NiAl intermetallic compound modified with Cu, emphasizing the EIS analysis and the relation between physical parameters and the modelling equations used in the Equivalent Electric Circuit. It was found that the addition of Cu promotes the formation of the γ’-Ni3Al phase in Cu contents greater than 15 at. %, in addition to a decrease in micro hardness and an increment in the Icorr values. In this way, the electrochemical characterization evidenced a high corrosion resistance of these intermetallic alloys.

Coulometric Response of H-Selective Solid-Contact Ion-Selective Electrodes and Its Application in Flexible Sensors+

The analytical performance of H+-selective solid-contact ion-selective electrodes(SCISEs)based on solid contact polyaniline doped with chloride(PANI(Cl))and poly(3,4-ethylenedioxythiophene)doped with poly(styrene sulfonate)(PEDOT(PSS))was characterized by a developed coulometric signal transduction method.PEDOT(PSS)solid contact is covered by PVC based H+-selective membrane.The obtained coulometric signal demonstrates that the cumulated charge can be amplified by increasing the capacitance of solid contact.SCISEs covered with spin-coated membrane behave faster amperometric response than electrodes with drop-cast mem-brane.In contrast to earlier works,the amperometric response and impedance spectrum demonstrates H+transfer through SCISEs is independent from the thickness of membrane.The exceptional behavior of PANI(Cl)H+-SCISEs shows that the capacitance estimated from impedance spectrum at low frequency 10 mHz and coulometric signal of PANI(Cl)based SCISEs is influenced by the applied po-tentials,whereas PEDOT(PSS)solid contact is independent from the chosen applied potentials.Furthermore,preliminary investiga-tions of coulometric signal transduction on flexible pH sensor implies its potential applications in wearable sensors for sweat ion concentration detection.

Inhibition roles of molybdate and borate on Q235 steel corrosion in resistance reducing agent

The effects of Na_(2)MoO_(4) and Na_(2)B_(4)O_(7) on corrosion behavior of Q235 steel in resistance reducing agent(RRA)containing sodium bentonite were studied by mass loss,scanning electron microscopy and electrochemical measurement.The results showed that both the independent and mixed additions of Na_(2)MoO_(4) and/or Na_(2)B_(4)O_(7),can reduce the corrosion rate of Q235 steel in RRA containing sodium bentonite.And the inhibition effect of Na_(2)MoO_(4) and/or Na_(2)B_(4)O_(7)increased with their dosage increase.With the same dosage,the inhibition efficiency of the mixed addition of Na_(2)MoO_(4) and Na_(2)B_(4)O_(7),was higher than that of their independent addition.The passivation effect of Q235 steel was easy to obtain in the RRA with the mixed addition of Na_(2)MoO_(4) and Na_(2)B_(4)O_(7).The optimized inhibitor for the RRA containing sodium bentonite was the mixture of Na_(2)B_(4)O_(7) and Na_(2)MoO_(4) with a total concentration of 1.5 wt.%.Furthermore,the increase in corrosion potential E_(corr) and the decrease in corrosion current density i_(cor) in carbon steel were one of the important criteria for the formation of passivation film.

LOSS DETERMINATION METHODOLOGY FOR A PIEZOELECTRIC CERAMIC:NEW PHENOMENOLOGICAL THEORY AND EXPERIMENTAL PROPOSALS

The key factor to the miniaturization of piezoelectric devices is power density,which is limited by the heat generation or loss mechanisms.There are three loss components in general in piezoelectric vibrators/resonators,i.e.,dielectric,elastic and piezoelectric losses.The mechanical quality factor,determined by these three factors,is the Figure Of Merit(FOM)in the sense of loss or heat generation.In this paper,we introduce a new loss phenomenology and innovative measuring methods based on the theory.First,quality factors at resonance and antiresonance for the k31,k33,kt and k15 vibration modes are derived theoretically,and the methodology for determining loss factors in various orientations(i.e.,loss anisotropy)is provided.For simplicity,we focus on materials with 1mm(equivalent to 6 mm)crystal symmetry for deriving the loss factors of a polycrystalline ceramic,and 14 different loss factors among 20 in total can be obtained from the measurements.Second,we propose the experimental methods for measuring both mechanical quality factors QA and QB at the resonance and antiresonance modes:a continuous admittance/impedance spectrum measuring method(traditional with temperature rise)and a burst mode(to circumvent the temperature effect).

Influence of Cr on the Electronic Properties of Passive Film on B30 Alloy in NaOH Solution

The influence of Cr on the electronic properties of the passive film on B30 alloy in NaOH solution was studied via electrochemical impedance spectra（EIS）, potentiodynamic curve and Mott-Schottky plot. The Cr doped in the passive film on B30 alloy was detected by X-ray photoelectron spectroscopy（XPS）. XPS results show that Cr203 appeared on the passive film, which implied the enhanced anti-corrosion of B30 alloy. The passive film showed a p-type semi-conductive character. The acceptor density（NA） was in an order of magnitude of 1022 cm-3, and NA de- creased with the increment of Cr. EIS results show that the film resistance（Rf） increased with increasing the amount of Cr. The diffusion coefficient（D0） was calculated to be in a range of 10^-16---10^-17 cm-2/s on the basement of point defect modcl（PDM）.