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
The slow oxygen reaction kinetics of air electrodes impair the performance of reversible protonic ceramic electrochemical cells(R-PCECs);hence,it is imperative to design novel air electrodes featuring excellent cataly...The slow oxygen reaction kinetics of air electrodes impair the performance of reversible protonic ceramic electrochemical cells(R-PCECs);hence,it is imperative to design novel air electrodes featuring excellent catalytic activity and endurance.Here,we report an Rb-doped double perovskite PrBa_(0.8)Ca_(0.1)Rb_(0.1)Co_(2)O_(5+δ)(denoted as PBCR_(0.1)C)as an air electrode for R-PCECs,displaying a low polarization resistance of 0.044Ωcm^(2) at 700℃ and excellent stability during exposure to humid air(3 vol%H_(2)O).The high performance is attributed to the high electrical conductivity,high concentration of oxygen vacancies,and fast surface exchange,as verified by the analyses of X-ray photoelectron spectroscopy,thermogravimetric testing,and conductivity tests.The R-PCECs with the PBCR_(0.1)C air electrode demonstrate an encouraging performance at 700℃:a peak power density of 2.32 W cm^(-2) in a fuel cell(FC)mode and an electrolysis current density of-3.55 A cm^(-2) at 1.3 V in an electrolysis(EL)mode.At 30 vol%steam concentration,a Faraday efficiency of 87.80%and a corresponding H_(2) production rate of 3.05 mL min^(-1) cm^(-2) at a current density of-0.5 A cm^(-2) at 650℃.Additionally,the durability of the cell in the FC mode(120 h),EL mode(120 h),and cycling FC/EL mode(100 h)at 650℃ suggests the great potential of PBCR_(0.1)C as the highly reactive and robust air electrodes of R-PCECs.展开更多
Developing an industrially relevant electrode with high catalytic activity,stability,and tunable composition/size for large-scale water electrolysis is a significant challenge.We have created an integrated elec-trode(...Developing an industrially relevant electrode with high catalytic activity,stability,and tunable composition/size for large-scale water electrolysis is a significant challenge.We have created an integrated elec-trode(NFM30-N)for the oxygen evolution reaction(OER)using a facile top-down approach that combines arc melting with dealloying-oxidation.Due to the dealloying-oxidation effect,the asderived porous amorphous M-O,M-OH,and M-OOH(M=Ni,Fe)nanocones cover the basic NiFeMn alloy.This integrated design enables NFM30-N to exhibit outstanding OER performance at high current densities,requiring low overpotentials of only 282 and 323 mV to achieve large current densities of 100 and 500 mA cm^(-2),respectively.It also displays a small Tafel slope of 44.1 mV dec^(-1) and remarkable stability for over 100 h at 100 and 500 mA cm^(-2).When used as an anode,a two-electrode electrolyzer cell with NFM30-N at 500 mA cm^(-2) only requires a cell voltage of 1.619 V and exhibits excellent stability,with almost no performance degradation after continuous chronopotentiometry test for each 100 h at 500 and 100 mA cm^(-2).This exceptional OER electrocatalytic performance is attributed to the integrated structure providing high electrical conductivity and stability,the presence of numerous active sites due to dealloying and the amorphous structure,and the promotion of the OER process by M-O,M-OH,and M-OOH species.This work offers a novel idea for fabricating integrated,industrially relevant electrocatalytic electrodes through traditional metallurgy combined with dealloying-oxidation.展开更多
This study investigates the impact of oxide bottom electrode(BE)material and orientation on the resistive switching(RS)characteristics of Al/ZrO_(2)-based ReRAM devices.Devices with different oxide BEs,including(400)-...This study investigates the impact of oxide bottom electrode(BE)material and orientation on the resistive switching(RS)characteristics of Al/ZrO_(2)-based ReRAM devices.Devices with different oxide BEs,including(400)-and(222)-oriented ITO BEs deposited under pure argon and argon–oxygen(20%O_(2))sputtering atmospheres,as well as SrRuO_(3)(SRO),show distinct RS behaviors.The Al/ZrO_(2)/(400)-ITO and Al/ZrO_(2)/SRO devices demonstrate stable bipolar RS performance,with(400)-ITO enabling an abrupt reset process,a wider memory window(>10^(4)),and superior stability,while SRO devices exhibit gradual reset transitions with lower power consumption.Furthermore,the crystallographic orientation control applied to ITO BE significantly affects the V_(O) dynamics and RS performance,with(222)-ITO devices exhibiting irreversible RS behavior.It is irrefutable that BE material and its orientation can strongly influence RS performance by modulating the V_(O) dynamics,electric field distribution,and conductive filament behavior.These findings underscore the importance of BE properties in optimizing ReRAM performance and provide valuable guidance for the development of high-efficiency memory devices.展开更多
The hierarchically porous carbons （HPCs） were prepared by sol-gel selassembly technology in different surfactant concentrations and were used as the potential electrode for lithium oxygen batteries. The physical and...The hierarchically porous carbons （HPCs） were prepared by sol-gel selassembly technology in different surfactant concentrations and were used as the potential electrode for lithium oxygen batteries. The physical and electrochemical properties of the as-prepared HPCs were investigated by filed emission scanning electron microscopy （FE-SEM）, transmission electron microscopy （TEM）, nitrogen adsorption-desorption isotherm and galvanostatic charge/discharge. The results indicate that all of the HPCs mainly possess mesoporous structure with nearly similar pore size distribution. Using the HPCs as the electrode, a high discharge capacity for lithium oxygen battery can be achieved, and the discharge capacity increases with the specific surface area. Especially, the HPCs-3 oxygen electrode with CTAB concentration of 0.27 mol/L exhibits good capacity retention through controlling discharge depth to 800 mA·h/g and the highest discharge capacity of 2050 mA·h/g at a rate of 0.1 mA/cm2.展开更多
Dry-spun Carbon Nanotube(CNT)fibers were surface-modified by atmospheric pressure oxygen plasma functionalization using a well controlled and continuous process.The fibers were characterized by scanning electron micro...Dry-spun Carbon Nanotube(CNT)fibers were surface-modified by atmospheric pressure oxygen plasma functionalization using a well controlled and continuous process.The fibers were characterized by scanning electron microscopy(SEM),Raman spectroscopy,and X-ray Photoelectron Spectroscopy(XPS).It was found from the conducted electrochemical measurements that the functionalized fibers showed a 132.8% increase in specific capacitance compared to non-functionalized fibers.Dye-adsorption test and the obtained Randles-Sevcik plot demonstrated that the oxygen plasma functionalized fibers exhibited increased surface area.It was further established by Brunauer-Emmett-Teller(BET)measurements that the surface area of the CNT fibers was increased from 168.22 m^2/g to 208.01 m^2/g after plasma functionalization.The pore size distribution of the fibers was also altered by this processing.The improved electrochemical data was attributed to enhanced wettability,increased surface area,and the presence of oxygen functional groups,which promoted the capacitance of the fibers.Fiber supercapacitors were fabricated from the oxygen plasma functionalized CNT fiber electrodes using different electrolyte systems.The devices with functionalized electrodes exhibited excellent cyclic stability(93.2% after 4000 cycles),flexibility,bendability,and good energy densities.At 0.5 m A/cm^2,the EMIMBF4 device revealed a specific capacitance,which is 27% and 65%greater than the specific capacitances of devices using EMIMTFSI and H2SO4 electrolytes,respectively.The practiced in this work plasma surface processing can be employed in other applications where fibers,yarns,ribbons,and sheets need to be chemically modified.展开更多
Oxygen electrocatalysis,exemplified by the oxygen reduction reaction(ORR)and oxygen evolution reaction(OER),is central to energy storage and conversion technologies such as fuel cells,metal-air batteries,and water ele...Oxygen electrocatalysis,exemplified by the oxygen reduction reaction(ORR)and oxygen evolution reaction(OER),is central to energy storage and conversion technologies such as fuel cells,metal-air batteries,and water electrolysis.However,highly effective and inexpensive earth-abundant materials are sought after to replace the noble metal-based electrocatalysts currently in use.Recently,metal-organic frameworks(MOFs)and carbon-based MOF derivatives have attracted considerable attention as efficient catalysts due to their exceedingly tunable morphologies,structures,compositions,and functionalization.Here,we report two-dimensional(2D)MOF/MOF derivative coupled arrays on nickel foam as binder-free bifunctional ORR/OER catalysts with enhanced electrocatalytic activity and stability.Their remarkable electrochemical properties are primarily attributed to fully exposed active sites and facilitated charge-transfer kinetics.The coupled and hierarchical nanosheet arrays produced via our growth-pyrolysis-regrowth strategy offer promise in the development of highly active electrodes for energy-related electrochemical devices.展开更多
High quality Sb-doped SnO_(2)electrode,with high oxygen evolution potential of 3.0 V,was successfully synthesized on the Ti substrates by in situ hydrothermal synthesis method.
To improve both oxygen evolution efficiency and stability at high temperatures, Mn, Mn+Mo, Mn+Mo+V, and Mn+Fe+V oxide electrodes were prepared on a Ti substrate, with an intermediate layer of IrO_2, by an anodic depos...To improve both oxygen evolution efficiency and stability at high temperatures, Mn, Mn+Mo, Mn+Mo+V, and Mn+Fe+V oxide electrodes were prepared on a Ti substrate, with an intermediate layer of IrO_2, by an anodic deposition method. The crystal structure, surface morphology, pore size distribution, specific surface area, and voltammetric charge were then characterized for each electrode. The results demonstrated that for Mn-O electrodes, the preferential orientation of the(100) crystal plane and the mesopore structure played negative roles in the oxygen evolution reaction. On the basis of the electrocatalytic properties of MnO2-based electrodes in seawater, the outer surface voltammetric charge at a scan rate of 500 mV·s-1 was shown to effectively indicate whether oxygen evolution reactions were preferred over chlorine evolution reactions. The Mn-O electrode exhibited oxygen evolution efficiency of only 47.27%, whereas the Mn+Mo, Mn+Mo+V and Mn+Fe+V oxide electrodes displayed oxygen evolution efficiency of nearly 100%. This means that adding Mo, V, and Fe elements to the electrode can improve its crystal structure and morphology as well as further enhancing its oxygen evolution efficiency.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
Transition metal-based electrocatalysts are a promising alternative to noble metal catalysts for electrochemical upgrading of biomass-derived 5-hydroxymethylfurfural(HMF)into high-value 2,5-furandicarboxylic acid(FDCA...Transition metal-based electrocatalysts are a promising alternative to noble metal catalysts for electrochemical upgrading of biomass-derived 5-hydroxymethylfurfural(HMF)into high-value 2,5-furandicarboxylic acid(FDCA).However,the rational design of efficient electrocatalysts with precisely tailored structure-activity correlations remains a critical challenge.Herein,we report a hierarchically structured self-supporting electrode(Vo-NiCo(OH)_(2)-NF)synthesized through in situ electrochemical reconstruction of NiCo-Prussian blue analogue(NiCo-PBA)precursor,in which oxygen vacancy(Vo)-rich Co-doped Ni(OH)_(2)nanosheet arrays are vertically aligned on nickel foam(NF),creating an interconnected conductive network.When evaluated for the HMF oxidation reaction(HMFOR),Vo-NiCo(OH)_(2)-NF exhibits exceptional electrochemical performance,achieving near-complete HMF conversion(99%),ultrahigh FDCA Faradaic efficiency(97.5%),and remarkable product yield(96.2%)at 1.45 V,outperforming conventional Co-doped Ni(OH)_(2)(NiCo(OH)_(2)-NF)and pristine Ni(OH)_(2)(Ni(OH)_(2)-NF)electrodes.By combining in situ spectroscopic characterization and theoretical calculations,we elucidate that the synergistic effects of Co-doping and oxygen vacancy engineering effectively modulate the electronic structure of Ni active centers,favor the formation of high-valent Ni^(3+)species,and optimize HMF adsorption,thereby improving the HMFOR performance.This work provides valuable mechanistic insights for catalyst design and may inspire the development of advanced transition metal-based electrodes for efficient biomass conversion systems.展开更多
Electrochemical water splitting has attracted tremendous interest as a promising approach for generating sustainable hydrogen for transportation and other industrial applications.However,the oxygen evolution reaction(...Electrochemical water splitting has attracted tremendous interest as a promising approach for generating sustainable hydrogen for transportation and other industrial applications.However,the oxygen evolution reaction(OER)significantly limits the efficiency of electrochemical water splitting because of the sluggish reaction kinetics derived from the intrinsic four-electron-transfer process.In addition,the stability of OER electrocatalysts encounters significant challenges during long-term operation under harsh conditions.To overcome these challenges,we demonstrate that monolithic electrodes composed of medium-entropy alloys(MEAs)containing Fe,Co,Cr,and Ni can be used as efficient and stable OER catalysts in alkaline solutions.The monolithic FeCoCrNi alloy electrode exhibited a remarkably low overpotential of 237 mV at a current density of 10 mA/cm^(2) in a 1 mol/L KOH solution.Significantly,the monolithic alloy electrode can operate stably for more than 2000 h at a practical current density of 1 A/cm^(2).The enhanced activity and stability of the alloy electrode are ascribed to surface reconstruction.This work presents a novel and effective approach for fabricating high-performance electrodes with excellent stability for the oxygen evolution reaction.展开更多
The state-of-the-art anion-exchange membrane water electrolyzers(AEMWEs)require highly stable electrodes for prolonged operation.The stability of the electrode is closely linked to the effective evacuation of H_(2) or...The state-of-the-art anion-exchange membrane water electrolyzers(AEMWEs)require highly stable electrodes for prolonged operation.The stability of the electrode is closely linked to the effective evacuation of H_(2) or O_(2) gas generated from electrode surface during the electrolysis.In this study,we prepared a superhydrophilic electrode by depositing porous nickel–iron nanoparticles on annealed TiO_(2) nanotubes(NiFe/ATNT)for rapid outgassing of such nonpolar gases.The super-hydrophilic NiFe/ATNT electrode exhibited an overpotential of 235 mV at 10 mA cm^(−2) for oxygen evolution reaction in 1.0 M KOH solution,and was utilized as the anode in the AEMWE to achieve a current density of 1.67 A cm^(−2) at 1.80 V.In addition,the AEMWE with NiFe/ATNT electrode,which enables effective outgassing,showed record stability for 1500 h at 0.50 A cm^(−2) under harsh temperature conditions of 80±3℃.展开更多
In order to achieve the high capacities of carbonaceous oxygen diffusion electrodes for aprotic lithiumoxygen batteries(Li-O2 batteries),most efforts currently focus on the design of rational porous architectures.Only...In order to achieve the high capacities of carbonaceous oxygen diffusion electrodes for aprotic lithiumoxygen batteries(Li-O2 batteries),most efforts currently focus on the design of rational porous architectures.Only few works study the surface chemistry effect that might be a critical factor influencing the capacities of carbonaceous electrodes.In addition,the surface chemistry effect is very difficult to be studied in composite electrodes due to the influences of binders and additives.Herein,we propose chemically activated carbon cloth(CACC) as an ideal model to investigate the effect of surface functional groups on the discharge capacities of carbonaceous oxygen electrodes for Li-O2 batteries.The intrinsic surface chemistry effect on the performance of carbonaceous cathode is directly observed for the first time without the influences of binders and additives.Results indicate that the surface carboxyl groups introduced by the chemical treatment not only function as the appropriate nucleation sites for Li2 O2 but also induce the formation of toroid-like Li2 O2.Thus,the surface carboxyl modification enhances the discharge capacities from 0.48 mAh/cm^2 of pristine carbon cloth to 1.23 mAh/cm^2 of CACC.This work presents an effective way to further optimize the carbonaceous oxygen electrodes via surface functional group engineering.展开更多
The proton ceramic electrochemical cell(PCEC),distinguished by its robust all-solid-state construction,emerges as a particularly promising contender in the realm of hydrogen production technologies.However,inadequate ...The proton ceramic electrochemical cell(PCEC),distinguished by its robust all-solid-state construction,emerges as a particularly promising contender in the realm of hydrogen production technologies.However,inadequate water-storage capability(hydration)and limited proton mobility within conventional PCEC oxygen electrodes hinder the efficiency of water splitting to oxygen,thereby restricting the broader application of PCECs.Here,we report a Ni-doped perovskite oxygen electrode Sr_(2)Fe_(1.4)Ni_(0.1)Mo_(1.5)O_(6-δ)(SFNM),where the incorporation of nickel can effectively amplify the concentration of oxygen vacancies while synergistically enhancing the hydration interaction between water molecules and the perovskite lattice.The enhanced hydration capacity facilitates proton-defect formation and lowers the energy barrier for proton migration.Benefiting from these synergistic enhancements,SFNM demonstrates a substantially reduced polarization resistance of approximately 0.078Ωcm^(2)at700℃under humidified conditions(pH_(2)O=0.1 atm).A PCEC utilizing the SFNM electrode achieves a remarkable current density of 2.60 A cm^(2)with an applied voltage of 1.3 V at 700℃.Furthermore,the PCEC exhibits favorable stability over a duration of 200 h.These outstanding results emphasize the potential of Ni doping to substantially improve both the hydration efficiency and proton mobility within perovskite electrode materials,positioning them as excellent candidates for high-performance PCECs.展开更多
Cyclic voltammetry was used to investigate the reaction of erythromycin （EM） with dissolved oxygen on gold nanopartiele-modified electrodes prepared via electrodeposition. A well-defined reduction peak at -0.420 V a...Cyclic voltammetry was used to investigate the reaction of erythromycin （EM） with dissolved oxygen on gold nanopartiele-modified electrodes prepared via electrodeposition. A well-defined reduction peak at -0.420 V and a reoxidation peak at -0.055 V were observed. With the addition of EM into the NaOH solution containing dissolved oxygen, the oxidation peak at -0.055 V was still indiscernible. However, a new oxidation peak at 0.200 V appeared, which suggests the interaction between EM and dissolved oxygen. Therefore, this method can be used for the analysis of EM in tablets. The present method is simple, reproducible, and does not require complex analytical instruments.展开更多
The thermal equilibrium state of the reference electrode was investigated. The results show that the temperature difference between the inside and the outside of zirconia tube was very small and the Seebeck effect can...The thermal equilibrium state of the reference electrode was investigated. The results show that the temperature difference between the inside and the outside of zirconia tube was very small and the Seebeck effect can be ignored after the sensor was dipped into liquid steel for more than 2 s. A special sensor was designed to test the relation between the EMF （electromotive force） of sensor and the thermal equilibrium state of the reference elec- trode. Based on these results, it is suggested that the peak in EMF curve was caused by the change of oxygen potential in reference electrode before the thermal equilibrium was reached. If NiO was added by 2 M- 5 M to the Cr/Cr2O3 reference electrode, the peak in EMF curve could be eliminated.展开更多
The synthesis of low-cost and highly active electrodes for both oxygen evolution reaction(OER)and hydrogen evolution reaction(HER)is very important for water splitting.In this work,the novel amorphous iron-nickel phos...The synthesis of low-cost and highly active electrodes for both oxygen evolution reaction(OER)and hydrogen evolution reaction(HER)is very important for water splitting.In this work,the novel amorphous iron-nickel phosphide(FeP-Ni)nanocone arrays as efficient bifunctional electrodes for overall water splitting have been in-situ assembled on conductive three-dimensional(3D)Ni foam via a facile and mild liquid deposition process.It is found that the FeP-Ni electrode demonstrates highly efficient electrocatalytic performance toward overall water splitting.In 1 M KOH electrolyte,the optimal FeP-Ni electrode drives a current density of 10 mA cm^(-2) at overpotential of 218 mV for the OER and120 mV for the HER,and can attain such current density for 25 h without performance regression.Moreover,a two-electrode electrolyzer comprising the FeP-Ni electrodes can afford 10 mA cm^(-2) electrolysis current at a low cell voltage of 1.62 V and maintain long-term stability,as well as superior to that of the coupled RuO_(2)/NFk Pt/C/NF cell.Detailed characterizations confirm that the excellent electrocatalytic performances for water splitting are attributed to the unique 3D morphology of nanocone arrays,which could expose more surface active sites,facilitate electrolyte diffusion,and benefit charge transfer and also favorable bubble detachment behavior.Our work presents a facile and cost-effective pathway to design and develop active self-supported electrodes with novel 3D morphology for water electrolysis.展开更多
The development of a simple, efficient and sensitive sensor for dissolved oxygen is proposed using a novel type of porous carbon composite membrane/glassy carbon electrode based on the low-cost common filter paper by ...The development of a simple, efficient and sensitive sensor for dissolved oxygen is proposed using a novel type of porous carbon composite membrane/glassy carbon electrode based on the low-cost common filter paper by a simple method. The resulting device exhibited excellent electrocatalytic activities toward the oxygen reduction reaction. Scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy and electrochemical measurements demonstrated that the porous morphology and uniformly dispersed Fe;C nanoparticles of the PCCM play an important role in the oxygen reduction reaction. A linear response range from 2mmol/L up to 110 mmol/L and a detection limit of 1.4 mmol/L was obtained with this sensor. The repeatability of the proposed sensor,evaluated in terms of relative standard deviation, was 3.0%. The successful fabrication of PCCM/GC electrode may promote the development of new porous carbon oxygen reduction reaction material for the oxygen reduction sensor.展开更多
There has been a continuous need for high active, excellently durable and low-cost electrocatalysts for rechargeable zinc-air batteries. Among many low-cost metal based candidates, transition metal oxides with the CNT...There has been a continuous need for high active, excellently durable and low-cost electrocatalysts for rechargeable zinc-air batteries. Among many low-cost metal based candidates, transition metal oxides with the CNTs composite have gained increasing attention. In this paper, the 3-D hollow sphere MnO_2 nanotube-supported Co_3O_4 nanoparticles and its carbon nanotubes hybrid material(Co_3 O_4/MnO_2-CNTs) have been synthesized via a simple co-precipitation method combined with post-heat treatment. The morphology and composition of the catalysts are thoroughly analyzed through SEM, TEM, TEM-mapping, XRD, EDX and XPS. In comparison with the commercial 20% Pt/C, Co_3O_4/MnO_2,bare MnO_2 nanotubes and CNTs, the hybrid Co_3O_4/MnO_2-CNTs-350 exhibits perfect bi-functional catalytic activity toward oxygen reduction reaction and oxygen evolution reaction under alkaline condition(0.1 M KOH). Therefore, high cell performances are achieved which result in an appropriate open circuit voltage(～1.47 V),a high discharge peak power density(340 mW cm^(-2)) and a large specific capacity(775 mAh g^(-1) at 10 mA cm^(-2)) for the primary Zn-air battery, a small charge-discharge voltage gap and a high cycle-life(504 cycles at 10 mA cm^(-2) with 10 min per cycle) for the rechargeable Zn-air battery. In particular, the simple synthesis method is suitable for a large-scale production of this bifunctional material due to a green, cost effective and readily available process.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.
文摘The slow oxygen reaction kinetics of air electrodes impair the performance of reversible protonic ceramic electrochemical cells(R-PCECs);hence,it is imperative to design novel air electrodes featuring excellent catalytic activity and endurance.Here,we report an Rb-doped double perovskite PrBa_(0.8)Ca_(0.1)Rb_(0.1)Co_(2)O_(5+δ)(denoted as PBCR_(0.1)C)as an air electrode for R-PCECs,displaying a low polarization resistance of 0.044Ωcm^(2) at 700℃ and excellent stability during exposure to humid air(3 vol%H_(2)O).The high performance is attributed to the high electrical conductivity,high concentration of oxygen vacancies,and fast surface exchange,as verified by the analyses of X-ray photoelectron spectroscopy,thermogravimetric testing,and conductivity tests.The R-PCECs with the PBCR_(0.1)C air electrode demonstrate an encouraging performance at 700℃:a peak power density of 2.32 W cm^(-2) in a fuel cell(FC)mode and an electrolysis current density of-3.55 A cm^(-2) at 1.3 V in an electrolysis(EL)mode.At 30 vol%steam concentration,a Faraday efficiency of 87.80%and a corresponding H_(2) production rate of 3.05 mL min^(-1) cm^(-2) at a current density of-0.5 A cm^(-2) at 650℃.Additionally,the durability of the cell in the FC mode(120 h),EL mode(120 h),and cycling FC/EL mode(100 h)at 650℃ suggests the great potential of PBCR_(0.1)C as the highly reactive and robust air electrodes of R-PCECs.
基金the National Natural Science Foundation of China(Nos.52174365,52004155,52334009 and 52130204)the National Key R&D Program of China(Nos.2023YFB3506701 and 2022YFB3706801)the Science and Technology Commission of Shanghai Municipality(No.21DZ1208900).
文摘Developing an industrially relevant electrode with high catalytic activity,stability,and tunable composition/size for large-scale water electrolysis is a significant challenge.We have created an integrated elec-trode(NFM30-N)for the oxygen evolution reaction(OER)using a facile top-down approach that combines arc melting with dealloying-oxidation.Due to the dealloying-oxidation effect,the asderived porous amorphous M-O,M-OH,and M-OOH(M=Ni,Fe)nanocones cover the basic NiFeMn alloy.This integrated design enables NFM30-N to exhibit outstanding OER performance at high current densities,requiring low overpotentials of only 282 and 323 mV to achieve large current densities of 100 and 500 mA cm^(-2),respectively.It also displays a small Tafel slope of 44.1 mV dec^(-1) and remarkable stability for over 100 h at 100 and 500 mA cm^(-2).When used as an anode,a two-electrode electrolyzer cell with NFM30-N at 500 mA cm^(-2) only requires a cell voltage of 1.619 V and exhibits excellent stability,with almost no performance degradation after continuous chronopotentiometry test for each 100 h at 500 and 100 mA cm^(-2).This exceptional OER electrocatalytic performance is attributed to the integrated structure providing high electrical conductivity and stability,the presence of numerous active sites due to dealloying and the amorphous structure,and the promotion of the OER process by M-O,M-OH,and M-OOH species.This work offers a novel idea for fabricating integrated,industrially relevant electrocatalytic electrodes through traditional metallurgy combined with dealloying-oxidation.
基金supported in part by the National Natural Science Foundation of China(Grant Nos.51602160 and 61605086)the Natural Science Foundation of Jiangsu Province,China(Grant No.BK20150842)the Talent Project of Nanjing University of Posts and Telecommunications(NUPTSF)(Grant No.NY222127)。
文摘This study investigates the impact of oxide bottom electrode(BE)material and orientation on the resistive switching(RS)characteristics of Al/ZrO_(2)-based ReRAM devices.Devices with different oxide BEs,including(400)-and(222)-oriented ITO BEs deposited under pure argon and argon–oxygen(20%O_(2))sputtering atmospheres,as well as SrRuO_(3)(SRO),show distinct RS behaviors.The Al/ZrO_(2)/(400)-ITO and Al/ZrO_(2)/SRO devices demonstrate stable bipolar RS performance,with(400)-ITO enabling an abrupt reset process,a wider memory window(>10^(4)),and superior stability,while SRO devices exhibit gradual reset transitions with lower power consumption.Furthermore,the crystallographic orientation control applied to ITO BE significantly affects the V_(O) dynamics and RS performance,with(222)-ITO devices exhibiting irreversible RS behavior.It is irrefutable that BE material and its orientation can strongly influence RS performance by modulating the V_(O) dynamics,electric field distribution,and conductive filament behavior.These findings underscore the importance of BE properties in optimizing ReRAM performance and provide valuable guidance for the development of high-efficiency memory devices.
基金Projects (51272221,51072173,21203161) supported by the National Natural Science Foundation of ChinaProject (10CY005) supported by Industrial Project of Colleges and Universities of Hunan Province,China
文摘The hierarchically porous carbons （HPCs） were prepared by sol-gel selassembly technology in different surfactant concentrations and were used as the potential electrode for lithium oxygen batteries. The physical and electrochemical properties of the as-prepared HPCs were investigated by filed emission scanning electron microscopy （FE-SEM）, transmission electron microscopy （TEM）, nitrogen adsorption-desorption isotherm and galvanostatic charge/discharge. The results indicate that all of the HPCs mainly possess mesoporous structure with nearly similar pore size distribution. Using the HPCs as the electrode, a high discharge capacity for lithium oxygen battery can be achieved, and the discharge capacity increases with the specific surface area. Especially, the HPCs-3 oxygen electrode with CTAB concentration of 0.27 mol/L exhibits good capacity retention through controlling discharge depth to 800 mA·h/g and the highest discharge capacity of 2050 mA·h/g at a rate of 0.1 mA/cm2.
基金funded by a NASA Grant NNX13AF46Apartly by the National Institute for Occupational Safety and Health through the UC Pilot Research Project Training Program ERC Grant #T42OH008432
文摘Dry-spun Carbon Nanotube(CNT)fibers were surface-modified by atmospheric pressure oxygen plasma functionalization using a well controlled and continuous process.The fibers were characterized by scanning electron microscopy(SEM),Raman spectroscopy,and X-ray Photoelectron Spectroscopy(XPS).It was found from the conducted electrochemical measurements that the functionalized fibers showed a 132.8% increase in specific capacitance compared to non-functionalized fibers.Dye-adsorption test and the obtained Randles-Sevcik plot demonstrated that the oxygen plasma functionalized fibers exhibited increased surface area.It was further established by Brunauer-Emmett-Teller(BET)measurements that the surface area of the CNT fibers was increased from 168.22 m^2/g to 208.01 m^2/g after plasma functionalization.The pore size distribution of the fibers was also altered by this processing.The improved electrochemical data was attributed to enhanced wettability,increased surface area,and the presence of oxygen functional groups,which promoted the capacitance of the fibers.Fiber supercapacitors were fabricated from the oxygen plasma functionalized CNT fiber electrodes using different electrolyte systems.The devices with functionalized electrodes exhibited excellent cyclic stability(93.2% after 4000 cycles),flexibility,bendability,and good energy densities.At 0.5 m A/cm^2,the EMIMBF4 device revealed a specific capacitance,which is 27% and 65%greater than the specific capacitances of devices using EMIMTFSI and H2SO4 electrolytes,respectively.The practiced in this work plasma surface processing can be employed in other applications where fibers,yarns,ribbons,and sheets need to be chemically modified.
文摘Oxygen electrocatalysis,exemplified by the oxygen reduction reaction(ORR)and oxygen evolution reaction(OER),is central to energy storage and conversion technologies such as fuel cells,metal-air batteries,and water electrolysis.However,highly effective and inexpensive earth-abundant materials are sought after to replace the noble metal-based electrocatalysts currently in use.Recently,metal-organic frameworks(MOFs)and carbon-based MOF derivatives have attracted considerable attention as efficient catalysts due to their exceedingly tunable morphologies,structures,compositions,and functionalization.Here,we report two-dimensional(2D)MOF/MOF derivative coupled arrays on nickel foam as binder-free bifunctional ORR/OER catalysts with enhanced electrocatalytic activity and stability.Their remarkable electrochemical properties are primarily attributed to fully exposed active sites and facilitated charge-transfer kinetics.The coupled and hierarchical nanosheet arrays produced via our growth-pyrolysis-regrowth strategy offer promise in the development of highly active electrodes for energy-related electrochemical devices.
基金supported by the National Natural Science Foundation of China(No.20607015)Program for Young Excellent Talents in Tongji University(No.2006KJ057).
文摘High quality Sb-doped SnO_(2)electrode,with high oxygen evolution potential of 3.0 V,was successfully synthesized on the Ti substrates by in situ hydrothermal synthesis method.
基金Funded by National Natural Science Foundation of China(No.51301070)Scientific and Technological Project of Henan Province(No.182102210068)
文摘To improve both oxygen evolution efficiency and stability at high temperatures, Mn, Mn+Mo, Mn+Mo+V, and Mn+Fe+V oxide electrodes were prepared on a Ti substrate, with an intermediate layer of IrO_2, by an anodic deposition method. The crystal structure, surface morphology, pore size distribution, specific surface area, and voltammetric charge were then characterized for each electrode. The results demonstrated that for Mn-O electrodes, the preferential orientation of the(100) crystal plane and the mesopore structure played negative roles in the oxygen evolution reaction. On the basis of the electrocatalytic properties of MnO2-based electrodes in seawater, the outer surface voltammetric charge at a scan rate of 500 mV·s-1 was shown to effectively indicate whether oxygen evolution reactions were preferred over chlorine evolution reactions. The Mn-O electrode exhibited oxygen evolution efficiency of only 47.27%, whereas the Mn+Mo, Mn+Mo+V and Mn+Fe+V oxide electrodes displayed oxygen evolution efficiency of nearly 100%. This means that adding Mo, V, and Fe elements to the electrode can improve its crystal structure and morphology as well as further enhancing its oxygen evolution efficiency.
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.
基金financial support of the National Natural Science Foundation of China(NSFC)(22372039 and 22305247)the Natural Science Foundation of Fujian Province of China(2021J06010)the Fuzhou University Testing Fund of Precious Apparatus(2025T022)。
文摘Transition metal-based electrocatalysts are a promising alternative to noble metal catalysts for electrochemical upgrading of biomass-derived 5-hydroxymethylfurfural(HMF)into high-value 2,5-furandicarboxylic acid(FDCA).However,the rational design of efficient electrocatalysts with precisely tailored structure-activity correlations remains a critical challenge.Herein,we report a hierarchically structured self-supporting electrode(Vo-NiCo(OH)_(2)-NF)synthesized through in situ electrochemical reconstruction of NiCo-Prussian blue analogue(NiCo-PBA)precursor,in which oxygen vacancy(Vo)-rich Co-doped Ni(OH)_(2)nanosheet arrays are vertically aligned on nickel foam(NF),creating an interconnected conductive network.When evaluated for the HMF oxidation reaction(HMFOR),Vo-NiCo(OH)_(2)-NF exhibits exceptional electrochemical performance,achieving near-complete HMF conversion(99%),ultrahigh FDCA Faradaic efficiency(97.5%),and remarkable product yield(96.2%)at 1.45 V,outperforming conventional Co-doped Ni(OH)_(2)(NiCo(OH)_(2)-NF)and pristine Ni(OH)_(2)(Ni(OH)_(2)-NF)electrodes.By combining in situ spectroscopic characterization and theoretical calculations,we elucidate that the synergistic effects of Co-doping and oxygen vacancy engineering effectively modulate the electronic structure of Ni active centers,favor the formation of high-valent Ni^(3+)species,and optimize HMF adsorption,thereby improving the HMFOR performance.This work provides valuable mechanistic insights for catalyst design and may inspire the development of advanced transition metal-based electrodes for efficient biomass conversion systems.
基金supported by the Strategic Priority Research Program of the Chinese Academy of Sciences(No.XDB0450302)the National Natural Science Foundation of China(Nos.52072358,51902304,22209162,U21A2082)+2 种基金the Fundamental Research Funds for the Central Universities(Nos.YD2060002043,WK2060000048)the Hefei Municipal Natural Science Foundation(No.BJ2060000042)the financial support from the R&D Department of Petro China。
文摘Electrochemical water splitting has attracted tremendous interest as a promising approach for generating sustainable hydrogen for transportation and other industrial applications.However,the oxygen evolution reaction(OER)significantly limits the efficiency of electrochemical water splitting because of the sluggish reaction kinetics derived from the intrinsic four-electron-transfer process.In addition,the stability of OER electrocatalysts encounters significant challenges during long-term operation under harsh conditions.To overcome these challenges,we demonstrate that monolithic electrodes composed of medium-entropy alloys(MEAs)containing Fe,Co,Cr,and Ni can be used as efficient and stable OER catalysts in alkaline solutions.The monolithic FeCoCrNi alloy electrode exhibited a remarkably low overpotential of 237 mV at a current density of 10 mA/cm^(2) in a 1 mol/L KOH solution.Significantly,the monolithic alloy electrode can operate stably for more than 2000 h at a practical current density of 1 A/cm^(2).The enhanced activity and stability of the alloy electrode are ascribed to surface reconstruction.This work presents a novel and effective approach for fabricating high-performance electrodes with excellent stability for the oxygen evolution reaction.
基金supported by the National Research Foundation of Korea(RS-2023-00207831,RS-2024-00346153).
文摘The state-of-the-art anion-exchange membrane water electrolyzers(AEMWEs)require highly stable electrodes for prolonged operation.The stability of the electrode is closely linked to the effective evacuation of H_(2) or O_(2) gas generated from electrode surface during the electrolysis.In this study,we prepared a superhydrophilic electrode by depositing porous nickel–iron nanoparticles on annealed TiO_(2) nanotubes(NiFe/ATNT)for rapid outgassing of such nonpolar gases.The super-hydrophilic NiFe/ATNT electrode exhibited an overpotential of 235 mV at 10 mA cm^(−2) for oxygen evolution reaction in 1.0 M KOH solution,and was utilized as the anode in the AEMWE to achieve a current density of 1.67 A cm^(−2) at 1.80 V.In addition,the AEMWE with NiFe/ATNT electrode,which enables effective outgassing,showed record stability for 1500 h at 0.50 A cm^(−2) under harsh temperature conditions of 80±3℃.
基金supported by grants from the National Natural Science Foundation of China (Nos.21673169,51672205)the National Key R&D Program of China (No.2016YFA0202602)+1 种基金the Research Start-Up Fund from Wuhan University of Technologythe Fundamental Research Funds for the Central Universities (WUT:Nos.2019IB003,2016IVA083)
文摘In order to achieve the high capacities of carbonaceous oxygen diffusion electrodes for aprotic lithiumoxygen batteries(Li-O2 batteries),most efforts currently focus on the design of rational porous architectures.Only few works study the surface chemistry effect that might be a critical factor influencing the capacities of carbonaceous electrodes.In addition,the surface chemistry effect is very difficult to be studied in composite electrodes due to the influences of binders and additives.Herein,we propose chemically activated carbon cloth(CACC) as an ideal model to investigate the effect of surface functional groups on the discharge capacities of carbonaceous oxygen electrodes for Li-O2 batteries.The intrinsic surface chemistry effect on the performance of carbonaceous cathode is directly observed for the first time without the influences of binders and additives.Results indicate that the surface carboxyl groups introduced by the chemical treatment not only function as the appropriate nucleation sites for Li2 O2 but also induce the formation of toroid-like Li2 O2.Thus,the surface carboxyl modification enhances the discharge capacities from 0.48 mAh/cm^2 of pristine carbon cloth to 1.23 mAh/cm^2 of CACC.This work presents an effective way to further optimize the carbonaceous oxygen electrodes via surface functional group engineering.
基金financially supported by the National Key R&D Program of China(No.2022YFB4002501)the National Natural Science Foundation of China(No.52202208)
文摘The proton ceramic electrochemical cell(PCEC),distinguished by its robust all-solid-state construction,emerges as a particularly promising contender in the realm of hydrogen production technologies.However,inadequate water-storage capability(hydration)and limited proton mobility within conventional PCEC oxygen electrodes hinder the efficiency of water splitting to oxygen,thereby restricting the broader application of PCECs.Here,we report a Ni-doped perovskite oxygen electrode Sr_(2)Fe_(1.4)Ni_(0.1)Mo_(1.5)O_(6-δ)(SFNM),where the incorporation of nickel can effectively amplify the concentration of oxygen vacancies while synergistically enhancing the hydration interaction between water molecules and the perovskite lattice.The enhanced hydration capacity facilitates proton-defect formation and lowers the energy barrier for proton migration.Benefiting from these synergistic enhancements,SFNM demonstrates a substantially reduced polarization resistance of approximately 0.078Ωcm^(2)at700℃under humidified conditions(pH_(2)O=0.1 atm).A PCEC utilizing the SFNM electrode achieves a remarkable current density of 2.60 A cm^(2)with an applied voltage of 1.3 V at 700℃.Furthermore,the PCEC exhibits favorable stability over a duration of 200 h.These outstanding results emphasize the potential of Ni doping to substantially improve both the hydration efficiency and proton mobility within perovskite electrode materials,positioning them as excellent candidates for high-performance PCECs.
基金Project(2005037207) supported by Postdoctoral Science Foundation of China
文摘Cyclic voltammetry was used to investigate the reaction of erythromycin （EM） with dissolved oxygen on gold nanopartiele-modified electrodes prepared via electrodeposition. A well-defined reduction peak at -0.420 V and a reoxidation peak at -0.055 V were observed. With the addition of EM into the NaOH solution containing dissolved oxygen, the oxidation peak at -0.055 V was still indiscernible. However, a new oxidation peak at 0.200 V appeared, which suggests the interaction between EM and dissolved oxygen. Therefore, this method can be used for the analysis of EM in tablets. The present method is simple, reproducible, and does not require complex analytical instruments.
文摘The thermal equilibrium state of the reference electrode was investigated. The results show that the temperature difference between the inside and the outside of zirconia tube was very small and the Seebeck effect can be ignored after the sensor was dipped into liquid steel for more than 2 s. A special sensor was designed to test the relation between the EMF （electromotive force） of sensor and the thermal equilibrium state of the reference elec- trode. Based on these results, it is suggested that the peak in EMF curve was caused by the change of oxygen potential in reference electrode before the thermal equilibrium was reached. If NiO was added by 2 M- 5 M to the Cr/Cr2O3 reference electrode, the peak in EMF curve could be eliminated.
基金supported by the National Natural Science Foundation of China(No.21878204)Key R&D program of Shanxi Province(International Cooperation,201903D421073)。
文摘The synthesis of low-cost and highly active electrodes for both oxygen evolution reaction(OER)and hydrogen evolution reaction(HER)is very important for water splitting.In this work,the novel amorphous iron-nickel phosphide(FeP-Ni)nanocone arrays as efficient bifunctional electrodes for overall water splitting have been in-situ assembled on conductive three-dimensional(3D)Ni foam via a facile and mild liquid deposition process.It is found that the FeP-Ni electrode demonstrates highly efficient electrocatalytic performance toward overall water splitting.In 1 M KOH electrolyte,the optimal FeP-Ni electrode drives a current density of 10 mA cm^(-2) at overpotential of 218 mV for the OER and120 mV for the HER,and can attain such current density for 25 h without performance regression.Moreover,a two-electrode electrolyzer comprising the FeP-Ni electrodes can afford 10 mA cm^(-2) electrolysis current at a low cell voltage of 1.62 V and maintain long-term stability,as well as superior to that of the coupled RuO_(2)/NFk Pt/C/NF cell.Detailed characterizations confirm that the excellent electrocatalytic performances for water splitting are attributed to the unique 3D morphology of nanocone arrays,which could expose more surface active sites,facilitate electrolyte diffusion,and benefit charge transfer and also favorable bubble detachment behavior.Our work presents a facile and cost-effective pathway to design and develop active self-supported electrodes with novel 3D morphology for water electrolysis.
基金the National Natural Science Foundation of China (No.21273097)the project from the State Key Laboratory of Electroanalytical Chemistry (No.2013)the Science Foundation of Jilin Province (No.20130204003GX)
文摘The development of a simple, efficient and sensitive sensor for dissolved oxygen is proposed using a novel type of porous carbon composite membrane/glassy carbon electrode based on the low-cost common filter paper by a simple method. The resulting device exhibited excellent electrocatalytic activities toward the oxygen reduction reaction. Scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy and electrochemical measurements demonstrated that the porous morphology and uniformly dispersed Fe;C nanoparticles of the PCCM play an important role in the oxygen reduction reaction. A linear response range from 2mmol/L up to 110 mmol/L and a detection limit of 1.4 mmol/L was obtained with this sensor. The repeatability of the proposed sensor,evaluated in terms of relative standard deviation, was 3.0%. The successful fabrication of PCCM/GC electrode may promote the development of new porous carbon oxygen reduction reaction material for the oxygen reduction sensor.
基金financial support from the National Natural Science Foundation of China (U1510120, 91645110)the Project of Introducing Overseas Intelligence High Education of China (2017-2018)+1 种基金the Graduate Thesis Innovation Foundation of Donghua University (EG2016034)the College of Environmental Science and Engineering, State Environmental Protection Engineering Center for Pollution Treatment and Control in Textile Industry, Donghua University
文摘There has been a continuous need for high active, excellently durable and low-cost electrocatalysts for rechargeable zinc-air batteries. Among many low-cost metal based candidates, transition metal oxides with the CNTs composite have gained increasing attention. In this paper, the 3-D hollow sphere MnO_2 nanotube-supported Co_3O_4 nanoparticles and its carbon nanotubes hybrid material(Co_3 O_4/MnO_2-CNTs) have been synthesized via a simple co-precipitation method combined with post-heat treatment. The morphology and composition of the catalysts are thoroughly analyzed through SEM, TEM, TEM-mapping, XRD, EDX and XPS. In comparison with the commercial 20% Pt/C, Co_3O_4/MnO_2,bare MnO_2 nanotubes and CNTs, the hybrid Co_3O_4/MnO_2-CNTs-350 exhibits perfect bi-functional catalytic activity toward oxygen reduction reaction and oxygen evolution reaction under alkaline condition(0.1 M KOH). Therefore, high cell performances are achieved which result in an appropriate open circuit voltage(～1.47 V),a high discharge peak power density(340 mW cm^(-2)) and a large specific capacity(775 mAh g^(-1) at 10 mA cm^(-2)) for the primary Zn-air battery, a small charge-discharge voltage gap and a high cycle-life(504 cycles at 10 mA cm^(-2) with 10 min per cycle) for the rechargeable Zn-air battery. In particular, the simple synthesis method is suitable for a large-scale production of this bifunctional material due to a green, cost effective and readily available process.
