Ohmic Resistance Research Articles

Dual doped fluorite oxide enabling enhanced performance for low-temperature ceramic fuel cells

Ceria-based electrolyte materials are of great interest for solid oxide fuel cell applications because they exhibit low ohmic resistance and high ionic conductivity, especially at a low temperature of 550oC. Consequently, we have designed a very interesting electrolyte Al and Nd dual-doped SDC (Sm0.1Ce0.9O2) using the sol–gel technique to function as an electrolyte for LT–CFCs (low-temperature ceramic fuel cells). The AN–SDC (Al0.15N0.15-Sm0.1Ce0.6O2) as an electrolyte shows a maximum power output of 1085 mW/cm2 with a high ionic conductivity of 0.22 S/cm at 550oC. This high performance is mainly because of the co-doping into SDC, which facilitates many oxygen vacancies, enabling faster stabilized ion transportation through the AN–SDC lattice. The low resistance of either the ohmic and grain boundary resistance + the microstructure features of AN–SDC contribute to achieving higher fuel cell performance. In addition, dual doping into SDC might build a synergistic effect, which further improves devices’ performance. The ionic conduction mechanism has been explained based on the dual doping of the incorporation of Al and Nd into the SDC. Dual doping is a promising, feasible avenue for designing electrolytes to enhance the performance of LT–CFC devices.

Reducing Ohmic Resistances in Membrane Capacitive Deionization Using Micropatterned Ion‐Exchange Membranes, Ionomer Infiltrated Electrodes, and Ionomer‐Coated Nylon Meshes

Membrane capacitive deionization (MCDI) is an emerging water desalination platform that is compact, electrified, and does not require high‐pressure piping. Herein, highly conductive poly(phenylene alkylene) ion‐exchange membranes (IEMs) are micropatterned with different surface geometries for MCDI. The micropatterned membranes increase the interfacial area with the liquid stream leading to a 700 mV reduction in cell voltage when operating at constant current (2 mA cm−2; 2000 ppm NaCl feed) while improving the energy normalized adsorbed salt (ENAS) value by 1.4 times. Combining the micropatterned poly(phenylene alkylene) IEMs with poly(phenylene alkylene) ionomer‐filled electrodes reduces the cell voltage by 1000 mV and improves the ENAS values by 2.3 times relative to the base case. This reduction in cell voltage allows for higher current density operation (i.e., 3–4 mA cm−2) . The reduction in cell voltage is ascribed to the ameliorating ohmic resistances related to ion transport at the membrane‐process stream interface and in the carbon cloth electrode. Finally, porous ionic conductors are implemented into the spacer channel with flat and micropatterned IEM configurations and ionomer infiltrated electrodes. For the configuration with flat IEMs, the porous ionic conductor improves ENAS values across the current density regime (2–4 mA cm−2), while for micropatterned IEMs it gets improved only at 4 mA cm−2.

Comprehensive study of high-temperature calendar aging on cylinder Li-ion battery

Calendar aging at high temperature is tightly correlated to the performance and safety behavior of lithium-ion batteries. However, the mechanism study in this area rarely focuses on multi-level analysis from cell to electrode. Here, a comprehensive study from centimeter-scale to nanometer-scale on high-temperature aged battery is carried out. After short-time high-temperature aging, measurements of electrochemical performance show notable decay of capacity and increase of internal resistance. The thermal safety behavior is studied through accelerating rate calorimeter (ARC), which indicates that the heat output of the aged battery during thermal runaway is largely increased. The aging mechanism of high temperature is investigated under various scales. Incremental capacity (IC) curves depict the deterioration of electrodes and increase of ohmic resistance. Computational Tomography (CT) reveals structure evolution of aged battery at millimeter scale, indicating gas generation after high-temperature aging. Scanning electron microscope (SEM) shows thickened solid-state-electrolyte (SEI) on anode and cracks on cathode at sub-micrometer scale. X-ray diffraction (XRD) patterns present crystallographic evolution of both anode and cathode. Thus, the cell degradation-mechanism after high-temperature aging is interpreted at multi-level, that high temperature induces deterioration of electrodes, formation of SEI and evolution of gas.

Enhanced performance of solid oxide fuel cells using highly conductive Ca2+ and F− co-doped Gd0.2Ce0.8O1.9 buffer layer

Gadolinium-doped ceria (GDC) is the most widely used buffer layer to prevent the reaction between YSZ electrolyte and La0.6Sr0.4Co0.2Fe0.8O3-δ (LSCF) cathode for commercial solid oxide fuel cell (SOFC). However, conductivity and sintering activity are vital to cell performance. In this paper, Ca2+ and F− co-doped GDC (Ca0.03Gd0.17Ce0.8F0.06O1.84-δ, CGDCF) is used as a buffer layer to improve the performance and stability of SOFC. The co-doped F− and Ca2+ significantly improve the sintering properties and oxygen ion transport of traditional GDC material. Meanwhile, the optimized sintering temperature is 1300 °C, with the lowest ohmic resistance. The peak power density of a cell with a CGDCF buffer layer reaches 1.809 W cm−2 at 850 °C, which is 37 % higher than that of GDC. In addition, the cell with the CGDCF buffer layer exhibits excellent stability during the 150 h test owing to the lower migration of La and Sr elements. Thus, the Ca2+ and F− co-doped GDC oxide emerges as a promising material for buffer layer applications.

Anticipating the lifespan: Predicting the durability of an anode-supported solid oxide fuel cell short stack over 50,000 h

In the present study, the operational lifetime of a solid oxide fuel (SOFC) short stack is predicted by investigating the performance degradation of both the short stack and its cells throughout 1000 ​h at 800 ​°C. The short stack and integral cell voltages are continuously measured during the long-term test, with electrochemical impedance spectroscopy (EIS) conducted every 200 ​h. The short stack voltage decreased rapidly for the initial 200–300 ​h and afterwards, it decreased at a slow rate due to the increase in the Ohmic and polarization resistances in the same manner. Scanning electron microscopy results show that there is no delamination or cracking among constituent layers of the short-stack cells. The single degradation effects of the Ni coarsening in the anode, cation migration and surface segregation in cathode and oxide scale growth in metallic interconnect mesh are successfully integrated into a comprehensive lifetime prediction model. The experimentally measured voltage degradation data of the short stack fits well with the developed mathematical model and allows the successful prediction of the lifetime up to 50,000 ​h.

Impact of string connection and contact defects on electrical current distribution in solar cells and modules: A model validated by magnetic field imaging

AbstractModeling of solar modules and their components is essential to quantify geometrical, optical, and electrical losses and to improve the designs and technologies in terms of performance. In most loss analysis models, the current share among the busbars of the solar cell is assumed to be equal since a symmetrical distribution of the metallization is given. The impact of string terminal connection on the current distribution among the ribbons and the resulting changes in ohmic losses has not been studied yet. In this study, a MATLAB model is developed to consider the impact of the string connector terminal position on the current distribution and the ohmic losses in the ribbons and in string connector. The model allows for the analysis of the impact of contact defects scenarios in ribbons and string connectors on the current distribution. Results show that the highest current flows at the closest busbar to the string connector terminal while the current decreases at the busbars farther away from the terminal due to higher ohmic resistance of the current path. The higher the ohmic resistance of the string connector, the more inhomogeneous the current share at busbars. Simulating a 9 busbar M6 half‐cell with 1 × 0.08 mm2 string connector, positioning the string connector terminal at the leftmost or rightmost ribbon results in 0.4 W less power compared to center connection configuration, where the string connector terminal is positioned at the center ribbon. Furthermore, simulation results show that inhomogeneity of current causes about 2.1% reduction in module power compared to the case of evenly distributed cell current, considering a 120‐haf‐cell module with the same string connector. Regarding contact defect analysis, exemplary simulations show the impact of the position of detached ribbons on the power or efficiency loss. Considering left or right connection configuration, detaching the leftmost or rightmost ribbon results in higher power loss compared to other ribbons. Detaching one cell ribbon completely from the string connector results in about 0.2%abs decrease in cell efficiency, while detaching the outer ribbon along all strings of a 120‐half‐cell module results in power loss of about 0.8%. The developed model is validated by performing magnetic field imaging (MFI) measurements, in which the magnetic flux density induced by the current carried by the ribbons is measured.

Impact of eliminating ungated access regions on DC and thermal performance of GaN-based MIS-HEMT

The impacts of eliminating access regions (AR) on DC and thermal performance of GaN-based MIS-HEMT have been studied using a device of 4 µm gate length. Nominal absence of ARs was achieved by a metal-organic chemical vapor deposition-regrown heavily n-doped GaN contact region extended to the two-dimensional electron gas (2DEG) channel (with sheet resistance as low as 14 Ω/ ◻ and ohmic contact resistance of 0.20 Ω⋅ mm) and 22-nm-thick AlN/Al2O3/HfO2 insulator layers acting as both gate dielectrics and sidewall spacers. As a result, a low knee voltage (2.5 V @ VGS = +2 V) comparable to deeply-scaled devices was attained, revealing the dominant role of ARs in knee voltages. High linearity at lower supply voltages (gate voltage swing of 7.3 V @ VDS = 5 V) and a faster GVS saturation trend with V DS increasing were observed, benefiting from the improved utility of applied lateral voltage. Moreover, a much lower thermal resistance compared to that of the conventional MIS-HEMT structure (146 vs. 202 K W−1) was extracted by a static-pulsed I-V measurement method. Simplified TCAD simulations were conducted to explain the underlying mechanisms, demonstrating that the enhanced surface heat flow covered by the gate metal as well as the more uniform electric field along the 2DEG channel accounts for the better capability of heat management in the device free of ARs. Our results indicate the size of DC and thermal performance enhancements obtained by eliminating ARs in a GaN-based MIS-HEMT structure.

Unravelling the La dopant induced physicochemical changes and the electrical behaviour on BaFeO3 under oxidising and reducing atmospheres

Electroceramic oxides like La-doped BaFeO3 garner greater interest owing to their tunability of mixed ionic conduction. However, reports on the effect of La on the microstructural changes, the type of conduction mechanism under different atmospheres and the negative charge transfer influenced by the Fe-O hybridization in Ba1−xLaxFeO3−δ are hardly available. Doping La induces cation vacancies and Fe reduction, creating nanorod decorated surface after the high-temperature treatment. Conductivity studies expose the rate-limiting steps for hydrogen oxidation reaction (HOR) and oxygen reduction reaction (ORR) as the ohmic resistances and Ba segregation effects. Among the samples studied, Ba0.9La0.1FeO3−δ performs better at 800 °C with an activation energy of ∼0.35 eV under both oxidizing and reducing atmospheres. Surface analysis after EIS reveals Fe and O with different oxidation states that enhance the total conductivity. The amount of hydroxyl species retained (23.66% for Ba0.9La0.1FeO3−δ ) and the ratio of the adsorbed to the lattice oxygen (15.33% for Ba0.9La0.1FeO3−δ ) gives insight on HOR and ORR activities. Also, computational studies validated the negative charge transfer mechanism of the samples under thermally assisted oxidation. The results indicate Ba0.9La0.1FeO3−δ as a tuneable electrode for solid oxide cells.

Electrical conductivity enhancement of rGO-MoS2 composite electrode for inverted PSC by parameter optimization

Carbon-based electrodes are widely used in photovoltaic, metal-ion batteries, supercapacitors, and sensors due to their low ohmic resistance and ability to integrate modifiers. Reduced graphene oxide (rGO) represents a promising alternative to graphite in carbon-based electrodes because of its high electrical conductivity, large surface area, and robust mechanical properties. This study aimed to optimize the fabrication parameters of rGO-MoS2 composite electrodes prepared via a one-pot hydrothermal method, focusing on maximizing their electrical conductivity for potential electronic applications. Taguchi analysis was employed to evaluate the impact of three key factors: rGO-MoS2 mixing ratio, annealing temperature, and annealing time. The novelty of this work lies in the systematic optimization approach using the Taguchi method, which allowed for the identification of the most significant factors and their optimal levels. The optimal combination was found to be a 1:1 ratio, 75 °C annealing temperature, and 15-min annealing time, resulting in an impressive electrical conductivity of 11 800 S m⁻1. This optimized rGO-MoS2 composite electrode exhibited an approximate 11 % reduction in sheet resistance compared to the unoptimized composite. Furthermore, all samples show an improvement in sheet resistance values compared to pure rGO and MoS2, which were 82.5 Ω/sq and 48.9 Ω/sq. Numerical simulations further revealed a 13.23 % improvement in device performance when the optimized rGO-MoS2 composite was implemented as the top electrode in an inverted perovskite solar cell, demonstrating the significant potential of this material for various electronic applications.

Synergistic effects of dimethyl sulfoxide-treatment and aramid nanofiber addition on performance enhancement of the PEDOT: PSS-based supercapacitor

Charge storage performance of the poly (3,4-ethylenedioxythiophene): poly (styrene sulfonate) (PEDOT: PSS, PH1000)-based supercapacitor is greatly enhanced by dimethyl sulfoxide (DMSO)-treatment and addition of aramid nanofibers (ANFs), but the underlying mechanism is unclear. To reveal it, we synthesized the films of PH1000, DMSO-treated PH1000 (D-P) and DMSO-treated PH1000-20 wt%ANF (D-PA) to construct the in-plane supercapacitors. A comparative study of electrochemical performance was firstly conducted to identify the specific contribution of DMSO-treatment and ANF components. Electrochemical impedance spectroscopy (EIS) was then analyzed, and the results demonstrated that the reduction of the ohmic resistance of the device was mainly attributed to the DMSO-treatment, while the addition of ANFs was found to contribute more to the decrease of Warburg resistance. The effects of DMSO-treatment and ANF components on the electrical propertíe and microstructure of PH1000 film were analyzed based on the square resistance results and AFM/SEM images, respectively. Dynamic permeation processes of the hydrogel electrolyte on the films were further recorded, vividly showing that the electrolyte permeability is highly dependent on the microstructure of the film. Through these analyses, a deep insight into the synergistic effects of DMSO-treatment and ANF addition on the electrochemical performance of the PH1000-based supercapacitor has been reached.

Analysis of Kinetic and Ohmic Resistances in PEM Water Electrolysis through Reference Electrode Measurements

We investigated a three electrode setup utilized in a temperature variation study to extract the activation energy for the half-cell reactions in PEM water electrolysis and the contributions of electronic resistances to ohmic resistance. The reference electrode configuration used in this investigation is an improved version of a setup previously introduced by our group. Enhancements have been made to minimize the influence of the reference electrode and improve the accuracy of electrochemical impedance spectroscopy.

Electrochemical Analysis of an Electrolyte-Supported Solid Oxide Cell-Based MK35x Stack during Long-Term Electrolysis Operation

The currently ongoing scale-up of high-temperature solid oxide electrolysis (SOEL) requires an understanding of the underlying dominant degradation mechanisms to enable continuous progress in increasing stack durability. In the present study, the degradation behavior of SOEL stacks of the type “MK35x” with chromium-iron-yttrium (CFY) interconnects and electrolyte-supported cells (ESC) developed at Fraunhofer IKTS was investigated. For this purpose, the initial electrochemical performance of a 10-cell stack was characterized in various operating conditions in both fuel cell and electrolysis mode. Degradation was evaluated during galvanostatic steady-state steam electrolysis operation for more than 3000 h at an oxygen side outlet temperature of 816 °C and a current density of −0.6 A cm−2 and showed an average voltage evolution rate of −0.3%/kh demonstrating high stability. Initial and final characterization at the part load operating point at −0.39 A cm−2 and 800 °C led to the determination of a positive overall degradation rate of 0.4%/kh showing a considerable impact of the operating conditions on the degradation rate. By means of electrochemical impedance spectroscopy analysis it was shown that the stack’s ohmic resistance increased whereas the polarization resistance decreased most likely due to an enhancement in LSMM’/ScSZ oxygen electrode performance.

Enhancing protonic ceramic electrolysis cell performance through electrolyte composition optimization

Polarization resistance, chemical stability against high steam, and faradaic efficiency (FE) are important parameters for steam electrolysis using protonic ceramic electrolysis cells (PCEC) at an intermediate temperature range of approximately 500 °C. To investigate the effects of electrolyte composition on these parameters, PCECs were fabricated using two electrolyte compositions: one without Zr, Ba(Ce0.8Y0.1Yb0.1)O3-δ (BCYYb), and one with Zr, Ba(Ce0.3Zr0.5Y0.1Yb0.1)O3-δ (BCZYYb), as well as a double-layered electrolyte BCYYb/BCZYYb. Although Zr in BCZYYb is required for chemical stability, BCYYb without Zr can also be chemically stable against high steam at 500 °C. Additionally, BCYYb has a higher conductivity compared to BCZYYb, which contributes to lower ohmic resistance and the highest peak power density in H2 fuel at 700 °C (2.04 W/cm2) among the cells with three different electrolytes. However, the BCYYb electrolyte exhibits a slightly higher polarization resistance than BCZYYb. In PCEC operation at 500 °C, the electrolyte composition significantly affects the FE. At a high current density (0.8 A/cm2), the FE of the PCEC with the BCYYb electrolyte (85 %) is significantly larger than that with BCZYYb (68 %).

Role of Silica, Carbon, and ZnO Nanomaterials in the Fabrication of Electrochemical Sensors for the Detection of Water Contaminants and Food Dye

AbstractSilica‐based nanomaterials have attracted huge attention for maximizing their safety and efficacy due to their nontoxicity, chemical and thermal stability, size tunability, and versatile functionality. Nanosilica with ZnO or carbon in a composite has excellent usage as an electrochemical sensor. Recent technological progression in nanotechnology and nanoscience has seen a number of applications of zinc oxide (ZnO) nanomaterials ranging from electronics, and sensing to environmental, and biomedical applications because of its various applications, multifunction, high specific surface area, stability, biocompatibility, nontoxicity, electrochemical activities, and so on. Carbon also has various advantageous properties like renewability, low ohmic resistance, and very stable response due to which carbon paste electrodes have attracted attention in the fabrication of electrochemical sensors. Electrochemical sensors are inexpensive, portable, and have excellent ability in detecting water contaminants, pesticides, disinfectants, pathogens, and different molecules. Artificial dyes are usually mixed with vegetable sauces, drinks, and other food items, which can cause cancer in human body. Voltametric methods with electrochemical sensors can be used to detect them in food samples. In this review, the present applications of ZnO and carbon nanomaterial‐based chemical sensors are meticulously studied to detect water contaminants and food dyes where nanosilica plays an important role as a sensor modifier.

Enhancing proton exchange membrane water electrolysis by building electron/proton pathways

Proton exchange membrane water electrolysis (PEMWE) plays a critical role in practical hydrogen production. Except for the electrode activities, the widespread deployment of PEMWE is severely obstructed by the poor electron-proton permeability across the catalyst layer (CL) and the inefficient transport structure. In this work, the PEDOT:F (Poly(3,4-ethylenedioxythiophene):perfluorosulfonic acid) ionomers with mixed proton-electron conductor (MPEC) were fabricated, which allows for a homogeneous anodic CL structure and the construction of a highly efficient triple-phase interface. The PEDOT:F exhibits strong perfluorosulfonic acid (PFSA) side chain extensibility, enabling the formation of large hydrophilic ion clusters that form proton-electron transport channels within the CL networks, thus contributing to the surface reactant water adsorption. The PEMWE device employing membrane electrode assembly (MEA) prepared by PEDOT:F-2 demonstrates a competitive voltage of 1.713 ​V under a water-splitting current of 2 ​A ​cm−2 (1.746 ​V at 2A cm−2 for MEA prepared by Nafion D520), along with exceptional long-term stability. Meanwhile, the MEA prepared by PEDOT:F-2 also exhibits lower ohmic resistance, which is reduced by 23.4 ​% and 17.6 ​% at 0.1 ​A ​cm−2 and 1.5 ​A ​cm−2, respectively, as compared to the MEA prepared by D520. The augmentation can be ascribed to the superior proton and electron conductivity inherent in PEDOT:F, coupled with its remarkable structural stability. This characteristic enables expeditious mass transfer during electrolytic reactions, thereby enhancing the performance of PEMWE devices.

The internal resistance of a non-ideal inductor in an RLC series circuit at resonance

The measured voltage at the inductor in an RLC series circuit connected to a sinusoidal electromotive force depends on the current and the impedance. The latter does not only include the inductive reactance only but also the ohmic resistance of the inductor. This fact has a clear consequence on the result of the measurement as the measured voltage at the inductor is not in counterphase with the measured voltage at the capacitance as shown in theory where ideal inductors are usually considered. In this work, the resistance of a coil in an RLC circuit is obtained from the direct measurements of the phase of the voltage at the coil at resonance and the resonant frequency for different values of capacitance. This value is compared with the resistance of the coil determined directly with an ohmmeter. The agreement between both values is very good. The conventional signal generator has been replaced by a smartphone which is a very familiar device for the students. The smartphone can provide the necessary voltage supply for the experiment to be carried out successfully.

Electrochemical Investigation of Lithium Perchlorate-Doped Polypyrrole Growing on Titanium Substrate

Lithium perchlorate-doped polypyrrole growing on titanium substrate (LiClO4-PPy/Ti) has been fabricated to act as electroactive electrode material for feasible electrochemical energy storage. A theoretical and experimental investigation is adopted to disclose the conductivity, electroactivity properties and interfacial interaction-dependent capacitance of LiClO4-PPy/Ti electrode. The experimental measurement results disclose that LiClO4-PPy/Ti reveals lower ohmic resistance (0.2226 Ω cm−2) and charge transfer resistance (2116 Ω cm−2) to exhibit higher electrochemical conductivity, a more reactive surface, and feasible ion diffusion to present higher double-layer capacitance (0.1930 mF cm−2) rather than LiClO4/Ti (0.3660 Ω cm−2, 65,250 Ω cm−2, 0.0334 mF cm−2). LiClO4-PPy/Ti reveals higher Faradaic capacitance caused by the reversible doping and dedoping process of perchlorate ion on PPy than the electrical double-layer capacitance of LiClO4/Ti caused by the reversible adsorption and desorption process of the LiClO4 electrolyte on Ti. Theoretical simulation calculation results prove that a more intensive electrostatic interaction of pyrrole N···Ti (2.450 Å) in LiClO4-PPy/Ti rather than perchlorate O···Ti (3.537 Å) in LiClO4/Ti. LiClO4-PPy/Ti exhibits higher density of states (57.321 electrons/eV) at Fermi energy and lower HOMO-LUMO molecule orbital energy gap (0.032 eV) than LiClO4/Ti (9.652 electrons/eV, 0.340 eV) to present the enhanced electronic conductivity. LiClO4-PPy/Ti also exhibits a more declined interface energy (−1.461 × 104) than LiClO4/Ti (−5.202 × 103 eV) to present the intensified interfacial interaction. LiClO4-PPy/Ti accordingly exhibits much higher specific capacitances of 0.123~0.0122 mF cm−2 at current densities of 0.01~0.10 mA cm−2 rather than LiClO4/Ti (0.010~0.0095 mF cm−2, presenting superior electroactivity and electrochemical capacitance properties. LiClO4-PPy/Ti could well act as the electroactive supercapacitor electrode for feasible energy storage.

Development of Nanostructured Lanthanum Strontium Cobalt Ferrite/Gadolinian-Doped Ceria Composite Electrodes of Solid Oxide Cells Formed by In Situ Polarization.

In the development of nanoscale oxygen electrodes of high-temperature solid oxide cells (SOCs), the interface formed between the nanoelectrode particles and the electrolyte or electrolyte scaffolds is the most critical. In this work, a new synthesis technique for the fabrication of nanostructured electrodes via in situ electrochemical polarization treatment is reported. The lanthanum strontium cobalt ferrite (LSCF) precursor solution is infiltrated into a gadolinia-doped ceria (GDC) scaffold presintered on a yttria-stabilized zirconia (YSZ) electrolyte, followed by in situ polarization current treatment at SOC operation temperatures. Electrode ohmic and polarization resistances decrease with an increase in the polarization current treatment. Detailed microstructure analysis indicates the formation of a convex-shaped interface between the LSCF nanoparticles (NPs) and the GDC scaffold, very different from the flat contact between LSCF and GDC observed after heating at 800 °C with no polarization current treatment. The embedded LSCF NPs on the GDC scaffold contribute to the superior stability under both fuel cell and electrolysis operation conditions at 750 °C and a high peak power density of 1.58 W cm-2 at 750 °C. This work highlights a novel and facile route to in situ construct a stable and high-performing nanostructured electrode for SOCs.

Synergetic effect of spontaneous Fe diffusion for enabling immediately switchable operations in NiFe-supported solid oxide cells

Solid oxide cells (SOCs) are highly efficient energy conversion systems, offering switchable capabilities for power and fuel production. NiFe metal-supported structures in SOCs show promising advantages in structural stability and scalability. This study explores the synergistic effect of spontaneous Fe diffusion in NiFe-supported SOCs, enhancing alloy catalyst formation in the electrode and improving the sinterability of the zirconia-based electrolyte. This results in increased activity for carbon fuel reactions, resistance to coking, and a remarkably low ohmic resistance of 0.06 Ω cm2 at 800 °C. The NiFe support also enhances structural stability, enabling reversible and multifuel operation. The single cell achieves exceptional maximum power densities of 2.6 and 2.0 W cm−2 in fuel cell mode (3 % H2O/H2 and dry CO) and current densities of − 1.51 and − 1.38 A cm−2 in electrolysis cell mode (1.3 V, 20 % H2O/H2 and 20 % CO2/CO) at 800 °C, respectively.

Interface Engineering to Operate Reversible Protonic Ceramic Electrochemical Cells Below 500 °C

AbstractThe low‐temperature (<500 °C) operation of reversible protonic ceramic electrochemical cells (PCECs) is desirable in achieving efficient and sustainable electricity generation, as well as green hydrogen production. However, significant interfacial resistance, which contributes to both ohmic and polarization resistance, remains a hurdle in lowering the operating temperature. In this study, PrBa0.5Sr0.5Co1.5Fe0.5O5+δ (PBSCF) and BaZr0.4Ce0.4Y0.1Yb0.1O3‐δ (BZCYYb) mono‐grain composite interlayers are introduced, which significantly extend the electrode/electrolyte interface and increase the concentration of vertically aligned oxygen vacancies along the heterointerface. This unique design achieves the lowest ohmic and polarization resistances among previously reported values in solid electrolyte‐based electrochemical cells. As a result, the PCEC can operate at extremely low temperature of 350 °C with an exceptional peak power density of 0.50 W cm−2 in fuel cell mode and current density of 0.25 A cm−2 at 1.3 V in electrolysis cell mode. Furthermore, it demonstrates high energy conversion efficiency and excellent stability under static and dynamic operating conditions.