Multicomponent Gd_(1−x)Sm_(x)Ba_(0.5)Sr_(0.5)CoCuO_(5+δ)double perovskites are optimized for application in terms of chemical composi-tion and morphology for the use as oxygen electrodes in solid oxide cells.Structur...Multicomponent Gd_(1−x)Sm_(x)Ba_(0.5)Sr_(0.5)CoCuO_(5+δ)double perovskites are optimized for application in terms of chemical composi-tion and morphology for the use as oxygen electrodes in solid oxide cells.Structural studies of other physicochemical properties are con-ducted on a series of materials obtained by the sol-gel method with different ratios of Gd and Sm cations.It is documented that changing the x value,and the resulting adjustment of the average ionic radius,have a significant impact on the crystal structure,stability,as well as on the total conductivity and thermomechanical properties of the materials,with the best results obtained for the Gd_(0.75)Sm_(0.2)5Ba_(0.5)Sr_(0.5)CoCuO_(5+δ)composition.Oxygen electrodes are prepared using the selected compound,allowing to obtain low polarization resistance values,such as 0.086Ω·cm^(2)at 800℃.Systematic studies of electrocatalytic activity are conducted using La_(0.8)Sr_(0.2)Ga_(0.8)Mg_(_(0.2))O_(3−δ)as the electrolyte for all electrodes,and Ce_(0.8)Gd_(0.2)O_(2−δ)electrolyte for the best performing Gd_(0.75)Sm_(0.2)5Ba_(0.5)Sr_(0.5)CoCuO_(5+δ)electrodes.The electrochemical data are analyzed using the distribution of relaxation times method.Also,the influence of the preparation method of the electrode material is in-ve`stigated using the electrospinning technique.Finally,the performance of the Gd_(0.75)Sm_(0.2)5Ba_(0.5)Sr_(0.5)CoCuO_(5+δ)electrodes is tested in a Ni-YSZ(yttria-stabilized zirconia)anode-supported cell with a Ce_(0.8)Gd_(0.2)O_(2−δ)buffer layer,in the fuel cell and electrolyzer operating modes.With the electrospun electrode,a power density of 462 mW·cm^(−2)is obtained at 700℃,with a current density of ca.0.2 A·cm^(−2)at 1.3 V for the electrolysis at the same temperature,indicating better performance compared to the sol-gel-based electrode.展开更多
Solid oxide cells(SOCs)are attractive electrochemical energy conversion/storage technologies for electricity/green hydrogen production because of the high efficiencies,all-solid structure,and superb reversibility.Neve...Solid oxide cells(SOCs)are attractive electrochemical energy conversion/storage technologies for electricity/green hydrogen production because of the high efficiencies,all-solid structure,and superb reversibility.Nevertheless,the widespread applications of SOCs are remarkably restricted by the inferior stability and high material costs induced by the high operational temperatures(600-800℃).Tremendous research efforts have been devoted to suppressing the operating temperatures of SOCs to decrease the overall costs and enhance the long-term durability.However,fuel electrodes as key components in SOCs suffer from insufficient(electro)catalytic activity and inferior impurity tolerance/redox resistance at reduced temperatures.Nanostructures and relevant nanomaterials exhibit great potential to boost the performance of fuel electrodes for low-temperature(LT)-SOCs due to the unique surface/interface properties,enlarged active sites,and strong interaction.Herein,an in-time review about advances in the design and fabrication of nanostructured fuel electrodes for LT-SOCs is presented by emphasizing the crucial role of nanostructure construction in boosting the performance of fuel electrodes and the relevant/distinct material design strategies.The main achievements,remaining challenges,and research trends about the development of nanostructured fuel electrodes in LT-SOCs are also presented,aiming to offer important insights for the future development of energy storage/conversion technologies.展开更多
Solid oxide cells(SOCs)are emerging devices for efficient energy storage and conversion.However,during SOC operation,gaseous chromium(Cr)species released from Fe-Cr alloy interconnect can lead to Cr deposition and poi...Solid oxide cells(SOCs)are emerging devices for efficient energy storage and conversion.However,during SOC operation,gaseous chromium(Cr)species released from Fe-Cr alloy interconnect can lead to Cr deposition and poisoning of air electrodes,causing substantial degradation in electrochemical performance and compromising the longterm stability of SOCs.This mini-review examines the mechanism of Cr deposition and poisoning in air electrodes under both fuel-cell and electrolysis modes.Furthermore,emphasis is placed on the recent advancements in strategies to mitigate Cr poisoning,offering insights into the rational design and development of active and Cr-tolerant air electrodes for SOCs.展开更多
Reversible solid oxide cell(RSOC)is a new energy conversion device with significant applications,especially for power grid peaking shaving.However,the reversible conversion process of power generation/energy storage p...Reversible solid oxide cell(RSOC)is a new energy conversion device with significant applications,especially for power grid peaking shaving.However,the reversible conversion process of power generation/energy storage poses challenges for the performance and stability of air electrodes.In this work,a novel high-entropy perovskite oxide La_(0.2)Pr_(0.2)Gd_(0.2)Sm_(0.2)Sr_(0.2)Co_(0.8)Fe_(0.2)O_(3−δ)(HE-LSCF)is proposed and investigated as an air electrode in RSOC.The electrochemical behavior of HE-LSCF was studied as an air electrode in both fuel cell and electrolysis modes.The polarization impedance(Rp)of the HE-LSCF electrode is only 0.25Ω·cm^(2) at 800℃ in an air atmosphere.Notably,at an electrolytic voltage of 2 V and a temperature of 800℃,the current density reaches up to 1.68 A/cm^(2).The HE-LSCF air electrode exhibited excellent reversibility and stability,and its electrochemical performance remains stable after 100 h of reversible operation.With these advantages,HE-LSCF is shown to be an excellent air electrode for RSOC.展开更多
Developing highly active and stable air electrodes remains challenging for reversible solid oxide cells(R-SOCs).Herein,we re-port an A-site high-entropy engineered perovskite oxide,La_(0.2)Pr_(0.2)Nd_(0.2)Ba_(0.2)Sr_(...Developing highly active and stable air electrodes remains challenging for reversible solid oxide cells(R-SOCs).Herein,we re-port an A-site high-entropy engineered perovskite oxide,La_(0.2)Pr_(0.2)Nd_(0.2)Ba_(0.2)Sr_(0.2)Co_(0.8)Fe_(0.2)O_(3−δ)(HE-LSCF),and its electrocatalytic activity and stability property are systematically probed for tubular R-SOCs.The HE-LSCF air electrode exhibits excellent oxygen reduction reac-tion(ORR)activity with a low polarization resistance of 0.042Ω·cm^(2)at 700℃,which is much lower than that of La0.6Sr0.4Co_(0.8)Fe_(0.2)O_(3−δ)(LSCF),indicating the excellent catalytic activity of HE-LSCF.Meanwhile,the tubular R-SOCs with HE-LSCF shows a high peak power density of 1.18 W·cm^(−2)in the fuel cell mode and a promising electrolysis current density of−0.52 A·cm^(−2)at 1.5 V in the electrolysis mode with H_(2)(~10%H_(2)O)atmosphere at 700℃.More importantly,the tubular R-SOCs with HE-LSCF shows favorable stability under 180 h reversible cycling test.Our results show the high-entropy design can significantly enhance the activity and robustness of LSCF electrode for tubular R-SOCs.展开更多
Monolayer ultra-large graphene oxide （UL-GO） sheets with diameter up to about 100 μm were synthesized based on a chemical method. Transparent conductive films were produced using the UL-GO sheets that were deposite...Monolayer ultra-large graphene oxide （UL-GO） sheets with diameter up to about 100 μm were synthesized based on a chemical method. Transparent conductive films were produced using the UL-GO sheets that were deposited layer-by-layer on a substrate by the Langmuir-Blodgett （L-B） assembly technique. The films produced from UL-GO sheets with a close-packed flat structure exhibit exceptionally high electrical conductivity and transparency after thermal reduction. A remarkable sheet resistance of 605 -/sq at 86% transparency is obtained, which outperforms the graphene films grown on a Ni substrate by chemical vapor deposition. The technique used to produce transparent conductive films is facile, inexpensive and tunable for mass production.展开更多
This work describes the discharge characteristics and acetone degradation with plasma under different electric fields based on a coaxial cylindrical dielectric barrier discharge(DBD)device energized by pulsed power.It...This work describes the discharge characteristics and acetone degradation with plasma under different electric fields based on a coaxial cylindrical dielectric barrier discharge(DBD)device energized by pulsed power.It is found that the segmented electrodes with appropriate spacing in coaxial cylindrical DBD are beneficial to the plasma ionization.In this work,the plasma distribution,discharge thermal effect,ionization of reactive species,and acetone degradation performance in coaxial cylindrical DBD with different segmented electrodes are systematically investigated.The experimental results show that segmented electrodes with a certain distance can cause additional ionization in the non-electrode-covered region between adjacent electrodes,thus enlarging the plasma region compared with a single electrode with equivalent total electrode length.The additional ionization involved the inner volume discharge between the quartz tubes and the outer surface discharge along the surface of the external quartz tube.The spatial distributions of the inner volume discharge and external surface discharge were predominantly governed by the radial and axial components of the inter-electrode electric field,respectively.The external surface discharge exhibited significant suppression when the electrode spacing was<1.5 mm,and it reached its maximum length at 3 mm spacing.When the electrode distance increased to 7-9 mm,a weak ionizing region appeared in the middle of the adjacent electrodes,which could be attributed to the gradual attenuation of the radial component with the increasing electrode spacing.A higher thermal effect and better oxidation of acetone to CO_(x)(CO and CO_(2))were achieved with the segmented electrode;the dual-segment configuration(3 mm per electrode)achieved a reactor temperature of 63.4℃,representing a 10℃enhancement over comparable single-electrode systems.Similarly,the CO_(2)and CO concentration reached 328.8 mg/m3and 105.7 mg/m3,respectively,in two 3 mm long segmented electrodes,which was an increase of 12.2%and 25.6%,respectively,compared with the single electrode.Notably,considering the equivalent ionization of the inner discharge with different electrodes,the enhanced thermal effects and CO_(x)conversion efficiency directly correlate with the expanded plasma zone induced by electrode segmentation.This work provides critical insights into optimizing electrode configurations for efficient plasma-assisted volatile organic compound degradation systems.展开更多
In recent times,there has been a surge of attention towards advanced high-performance materials for storing energy,specifically in supercapacitors.One encouraging method involves utilizing nanocomposites based on tran...In recent times,there has been a surge of attention towards advanced high-performance materials for storing energy,specifically in supercapacitors.One encouraging method involves utilizing nanocomposites based on transition metal oxides/graphene which have demonstrated significant potential for improving capacitance.The electrochemical properties of titanium oxide doped graphene in current research have been improved through the incorporation of rare earth metals.The hydrothermal technique was chosen for the fabrication of nanocomposites as electrode materials.X-ray diffraction(XRD),Raman spectroscopy,Fourier transform infrared spectroscopy(FT-IR),and scanning electron microscopy(SEM) approaches were employed for the characterization of nanocomposites.Ternary and quaternary nanocomposites with 2 wt% rare earth elements doped with titanium oxide and graphene were synthesized with various ratios of lanthanum and cerium as dopants.In 2 wt% La:Ce-TiO_(2)/rGO,lanthanum,and cerium were doped in 1:1,1:3,and 1:5 ratios.2 wt% La:Ce(1:5)-TiO_(2)/rGO among co-doped composites exhibits better capacitive performance as determined through cyclic voltammetry and galvanostatic charge-discharge.Among all the nanocomposites 422 F/g was the maximum depicted by 2 wt%La:Ce(1:5)-TiO_(2)/rGO at a scan rate of 10 mV/s(potential window from-0.4 to+0.6 V) and 1895 F/g at1 mV/s(potential window-0.6 to+0.6 V).specific capacitance was also determined via GCD,and a maximum capacitance of 486 F/g is depicted by 2 wt% La:Ce(1:5)-TiO_(2)/rGO.The same composites have also served as promising electrode materials in terms of columbic efficiency,power,and energy density.展开更多
High-entropy oxides(HEOs),offering reversible lithium storage and moderate operating potential,are considered promising negative electrodes.However,the intricate lithium storage mechanism within HE polycationic system...High-entropy oxides(HEOs),offering reversible lithium storage and moderate operating potential,are considered promising negative electrodes.However,the intricate lithium storage mechanism within HE polycationic systems remains challenging.Here,we conduct comprehensive investigations into the electrochemical properties and structu ral evolution of(CrMnCoNiZn)_(3)O_(4)(HESO)to clarify lithium storage mechanisms.Density functional theory(DFT)calculations reveal that polycationic synergy modulates the electronic structure and d-band centers of HESO,delivering fast electrode kinetics.Exhaustive in-and exsitu analyses demonstrate that the residual crystalline phases acting as seed crystals maintain the spinel/rock-salt lattice persistence under the entropy stabilization effect,lattice distortion effect,and cation synergy,which guide cation crystallization upon the electric field to drive reversible lithium storage.Such properties underlie the HESO electrode with an exceptional rate and long-term capability.This work clarifies the roles of cationic synergy and seed-crystal-driven structural reversibility,providing a blueprint for designing high-performance HEO negative electrodes for next-generation lithium-ion batteries(LIBs).展开更多
The insufficient stability and poor surface reaction kinetics(i.e.,oxygen reduction reaction(ORR)and oxygen evolution reaction(OER))of air electrodes are significant factors hindering the development of reversible sol...The insufficient stability and poor surface reaction kinetics(i.e.,oxygen reduction reaction(ORR)and oxygen evolution reaction(OER))of air electrodes are significant factors hindering the development of reversible solid oxide cells(R-SOCs).The high-entropy strategy offers a new direction to optimize air electrodes.We introduce a high-entropy air electrode,(La_(0.12)Pr_(0.12)Nd_(0.12)Sm_(0.12)Gd_(0.12))Sr_(0.4)Co_(0.2)Fe_(0.8)O_(3-δ)(LPNSGSrCF),demonstrating a low polarization resistance(0.15Ωcm^(2))and good durability(1.3×10^(-3)Ωcm^(2)h^(-1)),superior to those of La_(0.6)Sr_(0.4)Co_(0.2)Fe_(0.8)O_(3-δ)(0.31Ωcm^(2),2.0×10^(-3)Ωcm^(2)h^(-1))at 650℃.The elevated activity may be a result of the substantial concentration of oxygen vacancies and rapid reaction kinetics,as verified by X-ray photoelectron spectroscopy,electrochemical impedance spectroscopy,and distribution of relaxation times studies.Specifically,an R-SOC with LPNSGSrCF air electrode achieves a peak power density of 1.05 W cm^(-2)in fuel cell mode and a current density of0.89 A cm^(-2)at 1.3 V in electrolysis cell mode(with 30%H_(2)O)at 700℃.Moreover,the cells with LPNSGSrCF electrode can be stably operated in both modes for over 100 h.展开更多
The sandwich-like structure of reduced graphene oxide/polyaniline （RGO/PANI） hybrid electrode was prepared by electrochemical deposition. Both the voltage windows and electrolytes for electrochemical deposition of P...The sandwich-like structure of reduced graphene oxide/polyaniline （RGO/PANI） hybrid electrode was prepared by electrochemical deposition. Both the voltage windows and electrolytes for electrochemical deposition of PANI and RGO were optimized. In the composites, PANI nanofibers were anchored on the surface of the RGO sheets, which avoids the re-stacking of neighboring sheets. The R（;O/PANI composite electrode shows a high specific capacitance of 466 F/g at 2 mA/cm2 than that of previously reported RGO/PANI composites. Asymmetric flexible supercapacitors applying RGO/PANI as positive electrode and carbon fiber cloth as negative electrode can be cycled reversibly in the high-voltage region of 0-1.6 V and displays intriguing performance with a maximum specific capacitance of 35.5 mF cm^-2. Also, it delivers a high energy density of 45.5 mW h cm^-2 at power density of 1250 mW cm^-2. Furthermore, the asymmetric device exhibits an excellent long cycle life with 97.6Z initial capacitance retention after 5000 cycles. Such composite electrode has a great potential for applications in flexible electronics, roll-up display, and wearable devices.2017 Published by Elsevier Ltd on behalf of The editorial office of Journal of Materials Science ＆ Technology.展开更多
Effects of flaky rare earth oxide additives including Er2O3,Tm2O3,and Yb2O3,Lu2O3 on high temperature and high rate discharge performance of nickel electrodes were investigated.The discharge efficiency at 0.2C reached...Effects of flaky rare earth oxide additives including Er2O3,Tm2O3,and Yb2O3,Lu2O3 on high temperature and high rate discharge performance of nickel electrodes were investigated.The discharge efficiency at 0.2C reached 96% at 60 oC for electrodes with 1 at.% flaky rare earth oxides.The high rate discharge performance for electrodes with flaky rare earth oxides were improved significantly,for example,discharge efficiency at 5C improved from 50% to 70%.The results showed that the end charging potential of the ...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
Recent advances in the preparation and application of perovskite-type oxides as bifunctional electrocatalysts for oxygen reaction and oxygen evolution reaction in rechargeable metal-air batteries are presented in this...Recent advances in the preparation and application of perovskite-type oxides as bifunctional electrocatalysts for oxygen reaction and oxygen evolution reaction in rechargeable metal-air batteries are presented in this review.Various fabrication methods of these oxides are introduced in detail,and their advantages and disadvantages are analyzed.Different preparation methods adopted have great influence on the morphologies and physicochemical properties of perovskite-type oxides.As a bifunctional electrocatalyst,perovskite-type oxides are widely used in rechargeable metal-air batteries.The relationship between the preparation methods and the performances of oxygen/air electrodes are summarized.This work is concentrated on the structural stability,the phase compositions,and catalytic performance of perovskite-type oxides in oxygen/air electrodes.The main problems existing in the practical application of perovskite-type oxides as bifunctional electrocatalysts are pointed out and possible research directions in the future are recommended.展开更多
The Ti base PbO 2 electrode prepared by electrodeposition of PbO 2 on the surface of titanium was used for electro catalytic oxidation of phenol in waste water. The experimental results show that the electrodeposition...The Ti base PbO 2 electrode prepared by electrodeposition of PbO 2 on the surface of titanium was used for electro catalytic oxidation of phenol in waste water. The experimental results show that the electrodeposition of PbO 2 at a higher current density for a short time, then followed by a lower current density can get a compact and combinative PbO 2 layer. The properties of a Ti/PbO 2 electrode with an interlayer of oxide are the best. When this kind of electrode is used to treat phenol containing waste water, the phenol removal rate is higher and the slot voltage is lower. In addition, by using the phenol removal rate as an index, the influences of electrolysis current density, mass transfer condition and pH were studied and the optimal condition was confirmed.展开更多
The present work explores the application of La_(0.5)Sr_(0.5)Co_(0.95)Nb_(0.05)O_(3-δ)(LSCNO)perovskite as electrode material for the symmetric solid oxide fuel cell.Symmetric solid oxide fuel cells of thin-film LSCN...The present work explores the application of La_(0.5)Sr_(0.5)Co_(0.95)Nb_(0.05)O_(3-δ)(LSCNO)perovskite as electrode material for the symmetric solid oxide fuel cell.Symmetric solid oxide fuel cells of thin-film LSCNO electrodes were prepared to study the oxygen reduction reaction at intermediate temperature.The Rietveld refinement of syn-thesized material shows a hexagonal structure with the R-3c space group of the prepared perovskite material.Lattice parameter and fractional coordinates were utilized to calculate the oxygen ion diffusion coefficient for molecular dynamic simulation.At 973 K,the oxygen ion diffusion of LSCNO was 1.407×10^(-8)cm^(2)s^(-1) higher by order of one magnitude than that of the La_(0.5)Sr_(0.5)Co_(0.95)Nb_(0.05)O_(3-δ)(7.751×10^(-9)cm^(2)^(-1)).The results suggest that the Nb doping provide the structural stability which improves oxygen anion diffusion.The enhanced structural stability was analysed by the thermal expansion coefficient calculated experimentally and from molecular dynamics simulations.Furthermore,the density functional theory calculation revealed the role of Nb dopant for oxygen vacancy formation energy at Sr-0 and La-O planes is lower than the undoped structure.To understand the rate-limiting process for sluggish oxygen diffusion kinetics,80 nm and 40 nm thin films were fabricated using radio frequency magnetron sputtering on gadolinium doped ceria electrolyte substrate.The impedance was observed to increase with an increasing thickness,suggesting the bulk diffusion as a rate-limiting step for oxygen ion diffu-sion.The electrochemical performance was analysed for the thin-flm symmetric solid oxide fuel cell,which achieved a peak power density of 390 mW cm^(-2) at 1.02 V in the presence of H_(2) fuel on the anode side and air on the cathode side.展开更多
Solid oxide cells(SOCs)have attracted great attention in the past decades because of their high conversion efficiency,low environmental pollution and diversified fuel options.Nickel-based catalysts are the most widely...Solid oxide cells(SOCs)have attracted great attention in the past decades because of their high conversion efficiency,low environmental pollution and diversified fuel options.Nickel-based catalysts are the most widely used fuel electrode materials for SOCs due to the low price and high activity.However,when hydrocarbon fuels are employed,nickel-based electrodes face serious carbon deposition challenges,leading to a rapid decline of cell performance.Great efforts have been devoted to understanding the occurrence of the coking reaction,and to improving the stability of the electrodes in hydrocarbon fuels.In this review,we summarize recent research progress of utilizing surface modification to improve the stability and activity of Ni-based electrodes for SOCs by preventing carbon coking.The review starts with a briefly introduction about the reaction mechanism of carbon deposition,followed by listing several surface modification technologies and their working principles.Then we introduce representative works using surface modification strategies to prevent carbon coking on Ni-based electrodes.Finally,we highlight future direction of improving electrode catalytic activity and anti-coking performance through surface engineering.展开更多
Reversible solid oxide cells(SOCs)are very efficient and clean for storage and regeneration of renewable electrical energy by switching between electrolysis and fuel cell modes.One of the most critical factors governi...Reversible solid oxide cells(SOCs)are very efficient and clean for storage and regeneration of renewable electrical energy by switching between electrolysis and fuel cell modes.One of the most critical factors governing the efficiency and durability of SOCs technology is the stability of the interface between oxygen electrode and electrolyte,which is conventionally formed by sintering at a high temperature of~1000–1250℃,and which suffers from delamination problem,particularly for reversibly operated SOCs.On the other hand,our recent studies have shown that the electrode/electrolyte interface can be in situ formed by a direct assembly approach under the electrochemical polarization conditions at 800℃and lower.The direct assembly approach provides opportunities for significantly simplifying the cell fabrication procedures without the doped ceria barrier layer,enabling the utilization of a variety of high-performance oxygen electrode materials on barrier layer–free yttria-stabilized zirconia(YSZ)electrolyte.Most importantly,the in situ polarization induced interface shows a promising potential as highly active and durable interface for reversible SOCs.The objective of this progress report is to take an overview of the origin and research progress of in situ fabrication of oxygen electrodes based on the direct assembly approach.The prospect of direct assembly approach in the development of effective SOCs and in the fundamental studies of electrode/electrolyte interface reactions is discussed.展开更多
Direct carbon solid oxide fuel cells(DC-SOFCs)are promising,green,and efficient power-generating devices that are fueled by solid carbons and comprise all-solid-state structures.Developing suitable anode materials for...Direct carbon solid oxide fuel cells(DC-SOFCs)are promising,green,and efficient power-generating devices that are fueled by solid carbons and comprise all-solid-state structures.Developing suitable anode materials for DC-SOFCs is a substantial scientific challenge.Herein we investigated the use of La_(0.75)Sr_(0.25)Cr_(0.5)Mn_(0.5)O_(3)-δ−Ce_(0.8)Gd_(0.2)O_(1.9)(LSCM−GDC)composite electrodes as anodes for La_(0.9)Sr_(0.1)Ga_(0.8)Mg_(0.2)O_(3)-δelectrolyte-based DC-SOFCs,with Camellia oleifera shell char as the carbon fuel.The LSCM−GDC-anode DC-SOFC delivered a maximum power density of 221 mW/cm^(2) at 800℃ and it significantly improved to 425 mW/cm^(2) after Ni nanoparticles were introduced into the LSCM−GDC anode through wet impregnation.The microstructures of the prepared anodes were characterized,and the stability of the anode in a DC-SOFC and the influence of catalytic activity on open circuit voltage were studied.The above results indicate that LSCM–GDC anode is promising to be applied in DC-SOFCs.展开更多
基金funded by the National Science Centre,Poland,on the basis of the decision number UMO-2020/37/B/ST8/02097supported by the program“Excellence Initiative-Research University”for the AGH University of Krakow(IDUB AGH,No.501.696.7996,Action 4,ID 9880).
文摘Multicomponent Gd_(1−x)Sm_(x)Ba_(0.5)Sr_(0.5)CoCuO_(5+δ)double perovskites are optimized for application in terms of chemical composi-tion and morphology for the use as oxygen electrodes in solid oxide cells.Structural studies of other physicochemical properties are con-ducted on a series of materials obtained by the sol-gel method with different ratios of Gd and Sm cations.It is documented that changing the x value,and the resulting adjustment of the average ionic radius,have a significant impact on the crystal structure,stability,as well as on the total conductivity and thermomechanical properties of the materials,with the best results obtained for the Gd_(0.75)Sm_(0.2)5Ba_(0.5)Sr_(0.5)CoCuO_(5+δ)composition.Oxygen electrodes are prepared using the selected compound,allowing to obtain low polarization resistance values,such as 0.086Ω·cm^(2)at 800℃.Systematic studies of electrocatalytic activity are conducted using La_(0.8)Sr_(0.2)Ga_(0.8)Mg_(_(0.2))O_(3−δ)as the electrolyte for all electrodes,and Ce_(0.8)Gd_(0.2)O_(2−δ)electrolyte for the best performing Gd_(0.75)Sm_(0.2)5Ba_(0.5)Sr_(0.5)CoCuO_(5+δ)electrodes.The electrochemical data are analyzed using the distribution of relaxation times method.Also,the influence of the preparation method of the electrode material is in-ve`stigated using the electrospinning technique.Finally,the performance of the Gd_(0.75)Sm_(0.2)5Ba_(0.5)Sr_(0.5)CoCuO_(5+δ)electrodes is tested in a Ni-YSZ(yttria-stabilized zirconia)anode-supported cell with a Ce_(0.8)Gd_(0.2)O_(2−δ)buffer layer,in the fuel cell and electrolyzer operating modes.With the electrospun electrode,a power density of 462 mW·cm^(−2)is obtained at 700℃,with a current density of ca.0.2 A·cm^(−2)at 1.3 V for the electrolysis at the same temperature,indicating better performance compared to the sol-gel-based electrode.
基金supported by the National Key R&D Program of China(No.2022YFB4002502)the National Natural Science Foundation of China(No.22279057)。
文摘Solid oxide cells(SOCs)are attractive electrochemical energy conversion/storage technologies for electricity/green hydrogen production because of the high efficiencies,all-solid structure,and superb reversibility.Nevertheless,the widespread applications of SOCs are remarkably restricted by the inferior stability and high material costs induced by the high operational temperatures(600-800℃).Tremendous research efforts have been devoted to suppressing the operating temperatures of SOCs to decrease the overall costs and enhance the long-term durability.However,fuel electrodes as key components in SOCs suffer from insufficient(electro)catalytic activity and inferior impurity tolerance/redox resistance at reduced temperatures.Nanostructures and relevant nanomaterials exhibit great potential to boost the performance of fuel electrodes for low-temperature(LT)-SOCs due to the unique surface/interface properties,enlarged active sites,and strong interaction.Herein,an in-time review about advances in the design and fabrication of nanostructured fuel electrodes for LT-SOCs is presented by emphasizing the crucial role of nanostructure construction in boosting the performance of fuel electrodes and the relevant/distinct material design strategies.The main achievements,remaining challenges,and research trends about the development of nanostructured fuel electrodes in LT-SOCs are also presented,aiming to offer important insights for the future development of energy storage/conversion technologies.
基金supported by National Natural Science Foundation of China(22279018)National Natural Science Foundation of China(22005055)Natural Science Foundation of Fujian Province(2022J01085).
文摘Solid oxide cells(SOCs)are emerging devices for efficient energy storage and conversion.However,during SOC operation,gaseous chromium(Cr)species released from Fe-Cr alloy interconnect can lead to Cr deposition and poisoning of air electrodes,causing substantial degradation in electrochemical performance and compromising the longterm stability of SOCs.This mini-review examines the mechanism of Cr deposition and poisoning in air electrodes under both fuel-cell and electrolysis modes.Furthermore,emphasis is placed on the recent advancements in strategies to mitigate Cr poisoning,offering insights into the rational design and development of active and Cr-tolerant air electrodes for SOCs.
基金supported by Fundamental Research Funds for the Central Universities(2023KYJD1008)the Science Research Projects of the Anhui Higher Education Institutions of China(2022AH051582).
文摘Reversible solid oxide cell(RSOC)is a new energy conversion device with significant applications,especially for power grid peaking shaving.However,the reversible conversion process of power generation/energy storage poses challenges for the performance and stability of air electrodes.In this work,a novel high-entropy perovskite oxide La_(0.2)Pr_(0.2)Gd_(0.2)Sm_(0.2)Sr_(0.2)Co_(0.8)Fe_(0.2)O_(3−δ)(HE-LSCF)is proposed and investigated as an air electrode in RSOC.The electrochemical behavior of HE-LSCF was studied as an air electrode in both fuel cell and electrolysis modes.The polarization impedance(Rp)of the HE-LSCF electrode is only 0.25Ω·cm^(2) at 800℃ in an air atmosphere.Notably,at an electrolytic voltage of 2 V and a temperature of 800℃,the current density reaches up to 1.68 A/cm^(2).The HE-LSCF air electrode exhibited excellent reversibility and stability,and its electrochemical performance remains stable after 100 h of reversible operation.With these advantages,HE-LSCF is shown to be an excellent air electrode for RSOC.
基金support provided by the National Key R&D Program of China(No.2024YFE0101500)the National Natural Science Foundation of China(No.52272257)the Natural Science Foundation of Jiangsu Province(No.BK20240109).
文摘Developing highly active and stable air electrodes remains challenging for reversible solid oxide cells(R-SOCs).Herein,we re-port an A-site high-entropy engineered perovskite oxide,La_(0.2)Pr_(0.2)Nd_(0.2)Ba_(0.2)Sr_(0.2)Co_(0.8)Fe_(0.2)O_(3−δ)(HE-LSCF),and its electrocatalytic activity and stability property are systematically probed for tubular R-SOCs.The HE-LSCF air electrode exhibits excellent oxygen reduction reac-tion(ORR)activity with a low polarization resistance of 0.042Ω·cm^(2)at 700℃,which is much lower than that of La0.6Sr0.4Co_(0.8)Fe_(0.2)O_(3−δ)(LSCF),indicating the excellent catalytic activity of HE-LSCF.Meanwhile,the tubular R-SOCs with HE-LSCF shows a high peak power density of 1.18 W·cm^(−2)in the fuel cell mode and a promising electrolysis current density of−0.52 A·cm^(−2)at 1.5 V in the electrolysis mode with H_(2)(~10%H_(2)O)atmosphere at 700℃.More importantly,the tubular R-SOCs with HE-LSCF shows favorable stability under 180 h reversible cycling test.Our results show the high-entropy design can significantly enhance the activity and robustness of LSCF electrode for tubular R-SOCs.
基金Project (51102170) supported by the National Natural Science Foundation of ChinaProject (2010CB234609) supported by the National Basic Research Program of China
文摘Monolayer ultra-large graphene oxide （UL-GO） sheets with diameter up to about 100 μm were synthesized based on a chemical method. Transparent conductive films were produced using the UL-GO sheets that were deposited layer-by-layer on a substrate by the Langmuir-Blodgett （L-B） assembly technique. The films produced from UL-GO sheets with a close-packed flat structure exhibit exceptionally high electrical conductivity and transparency after thermal reduction. A remarkable sheet resistance of 605 -/sq at 86% transparency is obtained, which outperforms the graphene films grown on a Ni substrate by chemical vapor deposition. The technique used to produce transparent conductive films is facile, inexpensive and tunable for mass production.
文摘This work describes the discharge characteristics and acetone degradation with plasma under different electric fields based on a coaxial cylindrical dielectric barrier discharge(DBD)device energized by pulsed power.It is found that the segmented electrodes with appropriate spacing in coaxial cylindrical DBD are beneficial to the plasma ionization.In this work,the plasma distribution,discharge thermal effect,ionization of reactive species,and acetone degradation performance in coaxial cylindrical DBD with different segmented electrodes are systematically investigated.The experimental results show that segmented electrodes with a certain distance can cause additional ionization in the non-electrode-covered region between adjacent electrodes,thus enlarging the plasma region compared with a single electrode with equivalent total electrode length.The additional ionization involved the inner volume discharge between the quartz tubes and the outer surface discharge along the surface of the external quartz tube.The spatial distributions of the inner volume discharge and external surface discharge were predominantly governed by the radial and axial components of the inter-electrode electric field,respectively.The external surface discharge exhibited significant suppression when the electrode spacing was<1.5 mm,and it reached its maximum length at 3 mm spacing.When the electrode distance increased to 7-9 mm,a weak ionizing region appeared in the middle of the adjacent electrodes,which could be attributed to the gradual attenuation of the radial component with the increasing electrode spacing.A higher thermal effect and better oxidation of acetone to CO_(x)(CO and CO_(2))were achieved with the segmented electrode;the dual-segment configuration(3 mm per electrode)achieved a reactor temperature of 63.4℃,representing a 10℃enhancement over comparable single-electrode systems.Similarly,the CO_(2)and CO concentration reached 328.8 mg/m3and 105.7 mg/m3,respectively,in two 3 mm long segmented electrodes,which was an increase of 12.2%and 25.6%,respectively,compared with the single electrode.Notably,considering the equivalent ionization of the inner discharge with different electrodes,the enhanced thermal effects and CO_(x)conversion efficiency directly correlate with the expanded plasma zone induced by electrode segmentation.This work provides critical insights into optimizing electrode configurations for efficient plasma-assisted volatile organic compound degradation systems.
文摘In recent times,there has been a surge of attention towards advanced high-performance materials for storing energy,specifically in supercapacitors.One encouraging method involves utilizing nanocomposites based on transition metal oxides/graphene which have demonstrated significant potential for improving capacitance.The electrochemical properties of titanium oxide doped graphene in current research have been improved through the incorporation of rare earth metals.The hydrothermal technique was chosen for the fabrication of nanocomposites as electrode materials.X-ray diffraction(XRD),Raman spectroscopy,Fourier transform infrared spectroscopy(FT-IR),and scanning electron microscopy(SEM) approaches were employed for the characterization of nanocomposites.Ternary and quaternary nanocomposites with 2 wt% rare earth elements doped with titanium oxide and graphene were synthesized with various ratios of lanthanum and cerium as dopants.In 2 wt% La:Ce-TiO_(2)/rGO,lanthanum,and cerium were doped in 1:1,1:3,and 1:5 ratios.2 wt% La:Ce(1:5)-TiO_(2)/rGO among co-doped composites exhibits better capacitive performance as determined through cyclic voltammetry and galvanostatic charge-discharge.Among all the nanocomposites 422 F/g was the maximum depicted by 2 wt%La:Ce(1:5)-TiO_(2)/rGO at a scan rate of 10 mV/s(potential window from-0.4 to+0.6 V) and 1895 F/g at1 mV/s(potential window-0.6 to+0.6 V).specific capacitance was also determined via GCD,and a maximum capacitance of 486 F/g is depicted by 2 wt% La:Ce(1:5)-TiO_(2)/rGO.The same composites have also served as promising electrode materials in terms of columbic efficiency,power,and energy density.
基金supported by the National Natural Science Foundation of China(No.22271101)the R&D Program of Guangzhou(2024A04J2497)+1 种基金the Key Laboratory of Polymer Chemistry&Physics of Ministry of Educationsupported by the High Performance Computing Platform of SCUT。
文摘High-entropy oxides(HEOs),offering reversible lithium storage and moderate operating potential,are considered promising negative electrodes.However,the intricate lithium storage mechanism within HE polycationic systems remains challenging.Here,we conduct comprehensive investigations into the electrochemical properties and structu ral evolution of(CrMnCoNiZn)_(3)O_(4)(HESO)to clarify lithium storage mechanisms.Density functional theory(DFT)calculations reveal that polycationic synergy modulates the electronic structure and d-band centers of HESO,delivering fast electrode kinetics.Exhaustive in-and exsitu analyses demonstrate that the residual crystalline phases acting as seed crystals maintain the spinel/rock-salt lattice persistence under the entropy stabilization effect,lattice distortion effect,and cation synergy,which guide cation crystallization upon the electric field to drive reversible lithium storage.Such properties underlie the HESO electrode with an exceptional rate and long-term capability.This work clarifies the roles of cationic synergy and seed-crystal-driven structural reversibility,providing a blueprint for designing high-performance HEO negative electrodes for next-generation lithium-ion batteries(LIBs).
基金supported by the National Key R&D Program of China(2022YFB4003601)the National Natural Science Foundation of China(22179039)+4 种基金the Introduced Innovative R&D Team of Guangdong(2021ZT09L392)the Guangzhou Science and Technology Project(2024A04J3079)the Guangdong Basic and Applied Basic Research Foundation(2024A1515010448)the Pearl River Talent Recruitment Program(2019QN01C693)Zijin Mining Group Co.,Ltd(5405-ZC-2023-00008).
文摘The insufficient stability and poor surface reaction kinetics(i.e.,oxygen reduction reaction(ORR)and oxygen evolution reaction(OER))of air electrodes are significant factors hindering the development of reversible solid oxide cells(R-SOCs).The high-entropy strategy offers a new direction to optimize air electrodes.We introduce a high-entropy air electrode,(La_(0.12)Pr_(0.12)Nd_(0.12)Sm_(0.12)Gd_(0.12))Sr_(0.4)Co_(0.2)Fe_(0.8)O_(3-δ)(LPNSGSrCF),demonstrating a low polarization resistance(0.15Ωcm^(2))and good durability(1.3×10^(-3)Ωcm^(2)h^(-1)),superior to those of La_(0.6)Sr_(0.4)Co_(0.2)Fe_(0.8)O_(3-δ)(0.31Ωcm^(2),2.0×10^(-3)Ωcm^(2)h^(-1))at 650℃.The elevated activity may be a result of the substantial concentration of oxygen vacancies and rapid reaction kinetics,as verified by X-ray photoelectron spectroscopy,electrochemical impedance spectroscopy,and distribution of relaxation times studies.Specifically,an R-SOC with LPNSGSrCF air electrode achieves a peak power density of 1.05 W cm^(-2)in fuel cell mode and a current density of0.89 A cm^(-2)at 1.3 V in electrolysis cell mode(with 30%H_(2)O)at 700℃.Moreover,the cells with LPNSGSrCF electrode can be stably operated in both modes for over 100 h.
基金supported by the Qing Lan Project of Jiangsu Provincethe Natural Science Foundation of Jiangsu Province (BK20161289)+4 种基金the Natural Science Foundation of Higher Education of Jiangsu Province (17KJB610009)the Research Innovation Program for College Graduates and Students of Jiangsu Province (KYZZ15 0043)the Foundation of Nantong Vocational University (1512102)the College Students Innovation and Entrepreneurship Training Program of Jiangsu Province (201612684001Y)333 Talents Program of Jiangsu Province (BRA2016195)
文摘The sandwich-like structure of reduced graphene oxide/polyaniline （RGO/PANI） hybrid electrode was prepared by electrochemical deposition. Both the voltage windows and electrolytes for electrochemical deposition of PANI and RGO were optimized. In the composites, PANI nanofibers were anchored on the surface of the RGO sheets, which avoids the re-stacking of neighboring sheets. The R（;O/PANI composite electrode shows a high specific capacitance of 466 F/g at 2 mA/cm2 than that of previously reported RGO/PANI composites. Asymmetric flexible supercapacitors applying RGO/PANI as positive electrode and carbon fiber cloth as negative electrode can be cycled reversibly in the high-voltage region of 0-1.6 V and displays intriguing performance with a maximum specific capacitance of 35.5 mF cm^-2. Also, it delivers a high energy density of 45.5 mW h cm^-2 at power density of 1250 mW cm^-2. Furthermore, the asymmetric device exhibits an excellent long cycle life with 97.6Z initial capacitance retention after 5000 cycles. Such composite electrode has a great potential for applications in flexible electronics, roll-up display, and wearable devices.2017 Published by Elsevier Ltd on behalf of The editorial office of Journal of Materials Science ＆ Technology.
基金supported by the 863 National Research and Development Project Foundation of China (2006AA11A151)
文摘Effects of flaky rare earth oxide additives including Er2O3,Tm2O3,and Yb2O3,Lu2O3 on high temperature and high rate discharge performance of nickel electrodes were investigated.The discharge efficiency at 0.2C reached 96% at 60 oC for electrodes with 1 at.% flaky rare earth oxides.The high rate discharge performance for electrodes with flaky rare earth oxides were improved significantly,for example,discharge efficiency at 5C improved from 50% to 70%.The results showed that the end charging potential of the ...
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.
基金Projects(51504212,21573184,51703061)supported by the National Natural Science Foundation of ChinaProject(2018J01521)supported by the Natural Science Foundation of Fujian Province,ChinaProject(fma2017202)supported by the Open Fund of Fujian Provincial Key Laboratory of Functional Materials and Applications(Xiamen University of Technology),China
文摘Recent advances in the preparation and application of perovskite-type oxides as bifunctional electrocatalysts for oxygen reaction and oxygen evolution reaction in rechargeable metal-air batteries are presented in this review.Various fabrication methods of these oxides are introduced in detail,and their advantages and disadvantages are analyzed.Different preparation methods adopted have great influence on the morphologies and physicochemical properties of perovskite-type oxides.As a bifunctional electrocatalyst,perovskite-type oxides are widely used in rechargeable metal-air batteries.The relationship between the preparation methods and the performances of oxygen/air electrodes are summarized.This work is concentrated on the structural stability,the phase compositions,and catalytic performance of perovskite-type oxides in oxygen/air electrodes.The main problems existing in the practical application of perovskite-type oxides as bifunctional electrocatalysts are pointed out and possible research directions in the future are recommended.
文摘The Ti base PbO 2 electrode prepared by electrodeposition of PbO 2 on the surface of titanium was used for electro catalytic oxidation of phenol in waste water. The experimental results show that the electrodeposition of PbO 2 at a higher current density for a short time, then followed by a lower current density can get a compact and combinative PbO 2 layer. The properties of a Ti/PbO 2 electrode with an interlayer of oxide are the best. When this kind of electrode is used to treat phenol containing waste water, the phenol removal rate is higher and the slot voltage is lower. In addition, by using the phenol removal rate as an index, the influences of electrolysis current density, mass transfer condition and pH were studied and the optimal condition was confirmed.
文摘The present work explores the application of La_(0.5)Sr_(0.5)Co_(0.95)Nb_(0.05)O_(3-δ)(LSCNO)perovskite as electrode material for the symmetric solid oxide fuel cell.Symmetric solid oxide fuel cells of thin-film LSCNO electrodes were prepared to study the oxygen reduction reaction at intermediate temperature.The Rietveld refinement of syn-thesized material shows a hexagonal structure with the R-3c space group of the prepared perovskite material.Lattice parameter and fractional coordinates were utilized to calculate the oxygen ion diffusion coefficient for molecular dynamic simulation.At 973 K,the oxygen ion diffusion of LSCNO was 1.407×10^(-8)cm^(2)s^(-1) higher by order of one magnitude than that of the La_(0.5)Sr_(0.5)Co_(0.95)Nb_(0.05)O_(3-δ)(7.751×10^(-9)cm^(2)^(-1)).The results suggest that the Nb doping provide the structural stability which improves oxygen anion diffusion.The enhanced structural stability was analysed by the thermal expansion coefficient calculated experimentally and from molecular dynamics simulations.Furthermore,the density functional theory calculation revealed the role of Nb dopant for oxygen vacancy formation energy at Sr-0 and La-O planes is lower than the undoped structure.To understand the rate-limiting process for sluggish oxygen diffusion kinetics,80 nm and 40 nm thin films were fabricated using radio frequency magnetron sputtering on gadolinium doped ceria electrolyte substrate.The impedance was observed to increase with an increasing thickness,suggesting the bulk diffusion as a rate-limiting step for oxygen ion diffu-sion.The electrochemical performance was analysed for the thin-flm symmetric solid oxide fuel cell,which achieved a peak power density of 390 mW cm^(-2) at 1.02 V in the presence of H_(2) fuel on the anode side and air on the cathode side.
基金This work was supported by the National Natural Science Foundation of China(91745203)the State Key Laboratory of Pulp and Paper Engineering(2020C01)the Guangdong Pearl River Talent Program(2017GC010281).
文摘Solid oxide cells(SOCs)have attracted great attention in the past decades because of their high conversion efficiency,low environmental pollution and diversified fuel options.Nickel-based catalysts are the most widely used fuel electrode materials for SOCs due to the low price and high activity.However,when hydrocarbon fuels are employed,nickel-based electrodes face serious carbon deposition challenges,leading to a rapid decline of cell performance.Great efforts have been devoted to understanding the occurrence of the coking reaction,and to improving the stability of the electrodes in hydrocarbon fuels.In this review,we summarize recent research progress of utilizing surface modification to improve the stability and activity of Ni-based electrodes for SOCs by preventing carbon coking.The review starts with a briefly introduction about the reaction mechanism of carbon deposition,followed by listing several surface modification technologies and their working principles.Then we introduce representative works using surface modification strategies to prevent carbon coking on Ni-based electrodes.Finally,we highlight future direction of improving electrode catalytic activity and anti-coking performance through surface engineering.
基金The authors thank the funding support by National Natural Science Foundation of China(21875038 and 22005055)Joint Independent Innovation Fund of Tianjin University and Fuzhou University(TF2020-10)and Australian Research Council(DP180100731 and DP180100568).
文摘Reversible solid oxide cells(SOCs)are very efficient and clean for storage and regeneration of renewable electrical energy by switching between electrolysis and fuel cell modes.One of the most critical factors governing the efficiency and durability of SOCs technology is the stability of the interface between oxygen electrode and electrolyte,which is conventionally formed by sintering at a high temperature of~1000–1250℃,and which suffers from delamination problem,particularly for reversibly operated SOCs.On the other hand,our recent studies have shown that the electrode/electrolyte interface can be in situ formed by a direct assembly approach under the electrochemical polarization conditions at 800℃and lower.The direct assembly approach provides opportunities for significantly simplifying the cell fabrication procedures without the doped ceria barrier layer,enabling the utilization of a variety of high-performance oxygen electrode materials on barrier layer–free yttria-stabilized zirconia(YSZ)electrolyte.Most importantly,the in situ polarization induced interface shows a promising potential as highly active and durable interface for reversible SOCs.The objective of this progress report is to take an overview of the origin and research progress of in situ fabrication of oxygen electrodes based on the direct assembly approach.The prospect of direct assembly approach in the development of effective SOCs and in the fundamental studies of electrode/electrolyte interface reactions is discussed.
基金Project(2019YFC1907405)supported by the National Key R&D Program of ChinaProject(GJJ200809)supported by the Education Department Project Fund of Jiangxi Province,ChinaProject(2020BAB214021)supported by the Natural Science Foundation of Jiangxi Province,China。
文摘Direct carbon solid oxide fuel cells(DC-SOFCs)are promising,green,and efficient power-generating devices that are fueled by solid carbons and comprise all-solid-state structures.Developing suitable anode materials for DC-SOFCs is a substantial scientific challenge.Herein we investigated the use of La_(0.75)Sr_(0.25)Cr_(0.5)Mn_(0.5)O_(3)-δ−Ce_(0.8)Gd_(0.2)O_(1.9)(LSCM−GDC)composite electrodes as anodes for La_(0.9)Sr_(0.1)Ga_(0.8)Mg_(0.2)O_(3)-δelectrolyte-based DC-SOFCs,with Camellia oleifera shell char as the carbon fuel.The LSCM−GDC-anode DC-SOFC delivered a maximum power density of 221 mW/cm^(2) at 800℃ and it significantly improved to 425 mW/cm^(2) after Ni nanoparticles were introduced into the LSCM−GDC anode through wet impregnation.The microstructures of the prepared anodes were characterized,and the stability of the anode in a DC-SOFC and the influence of catalytic activity on open circuit voltage were studied.The above results indicate that LSCM–GDC anode is promising to be applied in DC-SOFCs.
