β-PbO2 electrodes were prepared by electro-deposition and characterized by scanning electron microscopy,X-ray diffraction,X-ray photoelectron spectroscopy,and linear sweep voltammetry.We confirmed pure β-PbO2 crysta...β-PbO2 electrodes were prepared by electro-deposition and characterized by scanning electron microscopy,X-ray diffraction,X-ray photoelectron spectroscopy,and linear sweep voltammetry.We confirmed pure β-PbO2 crystals were on the electrode and it had a high oxygen evolution potential.The photoactivity and photoelectrochemical（PEC） properties of the β-PbO2 electrode were investigated under visible light irradiation（λ 〉 420 nm） for the decolorization of Methylene Blue.Pseudo first-order kinetics parameter（Kapp） for dye decolorization using the β-PbO2 electrode achieved 6.71×10-4 min-1 under visible light irradiation,which indicated its excellent visible light-induced photoactivity.The Kapp of the PEC process was as much as 1.41×10-3 min-1 and was 1.71 times that of visible light irradiation or electrolysis even in the presence of the β-PbO2 electrode.A significant synergetic effect was observed in the PEC system.We also employed TiO2 modified β-PbO2 electrodes in this test,which revealed that the TiO2 immobilized on the β-PbO2 electrode inhibited the visible light-induced PEC efficiency despite the amount of TiO2 used for electrode preparation.The β-PbO2 electrode was also superior to the dimensionally stable anode（Ti/Ru0.3Ti0.7O2） in visible light-induced photoactivity and PEC efficiency.展开更多
The acid-proof anode Ti/SnO2+Mn2O3/PbO2 doped with Ce was prepared by thermal decomposition and electrodeposition combination technology, the effect of Ce on the morphology and structure of anode was also studied in t...The acid-proof anode Ti/SnO2+Mn2O3/PbO2 doped with Ce was prepared by thermal decomposition and electrodeposition combination technology, the effect of Ce on the morphology and structure of anode was also studied in this paper. The results obtained by cyclic voltammetry (CV), electrochemical impedance spectroscopic (EIS), X-ray Diffraction (XRD) and scanning electron microscopy (SEM) indicated that PbO2 crystal grains presented honeycomb structure were formed on the electrode surface by doping with Ce. The specific surface areas and catalytic active sites of the Ce-PbO2 doped electrode were increased and the catalytic activity was evidently greater than the undoped one. However, when Ce was doped into the intermediate layer (SnO2+Mn2O3), a more cracked surface structure formed, thus leading electrode deactivation by passivation of the Ti-substrate. So the anodic stability was decreased according to the accelerated life tests.展开更多
Al/α-PbO2/β-PbO2 composite electrodes doped with rare earth oxide （CeO2） were prepared by anodic oxidation method investigate the influence of nano-CeO2 dopants on the properties of Al/α-PbO2/β-PbO2-CeO2 electro...Al/α-PbO2/β-PbO2 composite electrodes doped with rare earth oxide （CeO2） were prepared by anodic oxidation method investigate the influence of nano-CeO2 dopants on the properties of Al/α-PbO2/β-PbO2-CeO2 electrodes and the impact of α-PbO2 as the intermediate layer. The results show that using α-PbO2 as the intermediate layer will benefit the crystallization of β-PbO2 and β-PbO2 is more suitable as the surface layer than α-PbO2. CeO2 dopants change the crystallite size and crystal structure, enhance the catalytic activity, and even change the deposition mechanism of PbO2. The doping of CeO2 in the PbO2 electrodes can enhance the electro-catalytic activity, which is helpful for oxygen evolution, and therefore reduce the cell voltage.展开更多
Al/conductive coating/α-Pb O2-Ce O2-Ti O2/β-PbO 2-MnO 2-WC-Zr O2 composite electrode material was prepared on Al/conductive coating/α-PbO 2-Ce O2-Ti O2 substrate by electrochemical oxidation co-deposition technique...Al/conductive coating/α-Pb O2-Ce O2-Ti O2/β-PbO 2-MnO 2-WC-Zr O2 composite electrode material was prepared on Al/conductive coating/α-PbO 2-Ce O2-Ti O2 substrate by electrochemical oxidation co-deposition technique. The effects of current density on the chemical composition, electrocatalytic activity, and stability of the composite anode material were investigated by energy dispersive X-ray spectroscopy（EDXS）, anode polarization curves, quasi-stationary polarization（Tafel） curves, electrochemical impedance spectroscopy（EIS）, scanning electron microscopy（SEM）, and X-ray diffraction（XRD）. Results reveal that the composite electrode obtained at 1 A/dm2 possesses the lowest overpotential（0.610 V at 500 A/m2） for oxygen evolution, the best electrocatalytic activity, the longest service life（360 h at 40 °C in 150 g/L H2SO4 solution under 2 A/cm2）, and the lowest cell voltage（2.75 V at 500 A/m2）. Furthermore, with increasing current density, the coating exhibits grain growth and the decrease of content of Mn O2. Only a slight effect on crystalline structure is observed.展开更多
A novel nano crystalline Ag2O2-PbO2 film chemically modified electrode (CME) was prepared and the CME was characterized by X-ray diffractometer (XRD) and atomic force microscope (AFM). By chronoamperometry, the nano A...A novel nano crystalline Ag2O2-PbO2 film chemically modified electrode (CME) was prepared and the CME was characterized by X-ray diffractometer (XRD) and atomic force microscope (AFM). By chronoamperometry, the nano Ag2O2-PbO2 CME was used as bioelectro- chemical sensor to determine the population of Escherichia coli (E. coli) in water. Compared with conventional methods, it is found that the technique we used is fast and convenient in counting E. coli.展开更多
Membrane electrode assembly(MEA)is widely considered to be the most promising type of electrolyzer for the practical application of electrochemical CO_(2) reduction reaction(CO_(2)RR).In MEAs,a square-shaped cross-sec...Membrane electrode assembly(MEA)is widely considered to be the most promising type of electrolyzer for the practical application of electrochemical CO_(2) reduction reaction(CO_(2)RR).In MEAs,a square-shaped cross-section in the flow channel is normally adopted,the configuration optimization of which could potentially enhance the performance of the electrolyzer.This paper describes the numerical simulation study on the impact of the flow-channel cross-section shapes in the MEA electrolyzer for CO_(2)RR.The results show that wide flow channels with low heights are beneficial to the CO_(2)RR by providing a uniform flow field of CO_(2),especially at high current densities.Moreover,the larger the electrolyzer,the more significant the effect is.This study provides a theoretical basis for the design of high-performance MEA electrolyzers for CO_(2)RR.展开更多
Integrating the CO_(2)capture process with the CO_(2)electrochemical reduction process into a single system can eliminate the need for storage and transportation following CO_(2)capture.This integrated process offers ...Integrating the CO_(2)capture process with the CO_(2)electrochemical reduction process into a single system can eliminate the need for storage and transportation following CO_(2)capture.This integrated process offers several advantages over multi-step cascade processes,including reduced costs and enhanced CO_(2)utilization.However,the integrated CO_(2)capture and electrochemical reduction(CCER)process encounters several challenges,including the low CO_(2)adsorption performance of the gas diffusion electrode(GDE)and catalyst,as well as the poor activity and selectivity of the catalyst for the electrochemical reduction of CO_(2).This review aims to systematically summarize the fundamentals of the CCER process.Based on an in-depth understanding of the CO_(2)mass transfer,adsorption,and electrochemical reduction processes,GDE design strategies based on the modulation of wettability and structure are discussed to enhance the CO_(2)capture capability at the GDE level.At the catalyst level,catalyst design strategies based on the introduction of CO_(2)capture sites and the construction of CO_(2)mass transfer channels were analyzed,and catalyst design strategies for enhanced CO_(2)capture were proposed.This review summarizes the most common catalysts for CO_(2)electrochemical reduction,such as Ni-based,Bi-based,and Cubased catalysts,and analyzes their design strategies based on reaction pathways for generating specific products.Finally,the problems and challenges of the CCER process are summarized and proposed,which provide ideas for the further application of this technology in the future.展开更多
The demand for sustainable and stretchable thin-film printed batteries for bioelectronics,wearables,and e-textiles is rapidly increasing.Recently,we developed a fully 3D-printed soft-matter thin-film Ga-Ag_(2)O batter...The demand for sustainable and stretchable thin-film printed batteries for bioelectronics,wearables,and e-textiles is rapidly increasing.Recently,we developed a fully 3D-printed soft-matter thin-film Ga-Ag_(2)O battery with 3R characteristics:resilient to mechanical strain,repairable after damage,and recyclable.This battery achieved a record-breaking areal capacity of 26.37 mAh cm-2,increasing to 30.32 mAh cm^(-2) after 10 cycles under 100%strain.This performance stems from the synergistic effects of gallium’s liquid metal properties and the styrene-isoprene-styrene polymer in the anode.Gallium’s high specific capacity(1153.2 mAh g^(-1)),deformability,and self-healing abilities,supported by its supercooled liquid phase,significantly enhance the battery’s resilience and efficiency.However,the cathode’s lower theoretical capacity,due to Ag_(2)O(231.31 mAh g^(-1)),remains a limitation.Traditional Ag_(2)O-carbon black-styrene-isoprene-styrene cathodes experience rapid capacity decay as only the surface area of the active materials interacts with the electrolyte.To overcome this,we designed a carbon-filled Ag_(2)O foam electrode using a sacrificial sugar template,increasing the effective surface area.This optimization enhanced ion-exchange efficiency,specific capacity,and cyclability,achieving a specific capacity of 221.16 mAh g^(-1).Consequently,the Ga-Ag_(2)O stretchable battery attained a record areal capacity of 40.91 mAh cm^(-2)—double that of nonfoam electrodes—and exhibited fivefold improved charge-discharge cycles.Using ultrastretchable Ag-EGaIn-styrene-isoprene-styrene and carbon black-styrene-isoprene-styrene current collectors,the battery’s specific capacity increased by 33%under 50%strain.Integrated into a soft-matter smart wristband for temperature monitoring,the battery demonstrated its promise for wearable electronics.展开更多
Due to the microstructural degradation of fuel electrodes,high cycling stability and catalytic activity remain a significant barrier for solid oxide electrolysis cells(SOEC).Perovskite materials exhibit favorable mixe...Due to the microstructural degradation of fuel electrodes,high cycling stability and catalytic activity remain a significant barrier for solid oxide electrolysis cells(SOEC).Perovskite materials exhibit favorable mixed conductivity and redox stability as cathode materials,but their catalytic activity is not ideal.This study systematically investigates the structural,morphological,and electrochemical properties of cobalt doping in the Pr_(0.4)Sr_(0.6)Co_(xF)e_(1-x)O_(3-δ)(PSC_(x)F)system,characterized using scanning electron microscopy,transmission electron microscopy,X-ray photoelectron spectroscopy,CO_(2)-temperature-programmed desorption,and Raman spectroscopy.The effect of cobalt-doping concentration on the electrochemical properties was further investigated.The electrochemical performance evaluation demonstrates that the optimal is achieved with a cob alt-doping ratio of 0.1.At 800℃and 1.5 V,the CO_(2)electrolysis current density of the PSC_(0.1)F-Gd_(0.1)Ce_(0.9)O_(2-δ)(GDC)IGDCISc_(0.1)Zr_(0.9)O_(2-δ)|IGDCILa_(0.6)Sr_(0.4)Co_(0.2)Fe_(0.8)O_(3+δ)full cell reaches 1.37 A·cm^(-2),approximately 34.3%higher than that of electrodes without cobalt doping.Furthermore,the electrode maintains stability for over 100 h at 800℃and 1.3 V.This work offers new insights into how metal doping can be applied to regulate electrode structures,thereby providing enhanced performance and stability for perovskite-based fuel electrodes.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
The pore size distribution is often an important parameter for transport processes in porous media.Cryoporometry experiments can provide such data in the meso and macropore size up to 1 mm providing the sample tempera...The pore size distribution is often an important parameter for transport processes in porous media.Cryoporometry experiments can provide such data in the meso and macropore size up to 1 mm providing the sample temperature is finely controlled.We use a Peltier based system inserted directly into the NMR probe to control the temperature within 0.05℃and impose temperature ramps down to 0.002℃/min,necessary to characterize the largest pore sizes.The pore size information in the macropore range cannot be obtained from gas adsorption techniques while mercury injection is questionable for the material considered here.For porous materials made of paramagnetic minerals such as lithium-iron phosphate(LiFePO_(4),LFP)or nickel-manganese-cobalt oxides(NMC)and saturated with octamethylcyclotetrasiloxane(OMCTS),the T_(2)relaxation times are very short such as protons from the liquid and frozen phases cannot be separated.Hence the usual cryoporometry experiment cannot be performed.Instead,we propose to use the T_(1)contrast to separate these phases.The method is studied in detail along with some temperature effects linked with the T_(1)variation of the bulk frozen OMCTS.We show an example on two cathode materials part of industrial battery product.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
Surgical electrodes are frequently associated with disadvantages such as high surface adhesion and severe thermal damage to adjacent normal tissues,which threaten operation quality and patient safety.In this study,by ...Surgical electrodes are frequently associated with disadvantages such as high surface adhesion and severe thermal damage to adjacent normal tissues,which threaten operation quality and patient safety.In this study,by mimicking the micromorphology and bio-anti-adhesion of shark skin,we proposed a strategy that utilized nanoscale aluminium oxide(Al_(2)O_(3))films deposited on bioinspired shark skin(BSS)microstructures to design a composite surface(Al_(2)O_(3)@BSS)and integrated it into both flat sides of the surgical electrodes.Micro/nano-manufacturing of the Al_(2)O_(3)@BSS surface was sequentially accomplished using nanosecond laser texturing,atomic layer deposition,and low-temperature annealing,endowing it with excellent blood-repellent properties.Visualisation experiments revealed that the tensile stress gradient of the blood coagulum with increasing thickness under a thermal field prompted it to separate from the Al_(2)O_(3)@BSS surface,resulting in anti-adhesion.Furthermore,it was observed for the first time that Al_(2)O_(3) films could transiently excite discharge along a dielectric surface(DADS)to ablate tissues while suppressing Joule heat,thereby minimising thermal damage.A combination of ex vivo tissue and living mouse experiments demonstrated that the Al_(2)O_(3)@BSS electrodes exhibited optimal comprehensive performance in terms of anti-adhesion,damage minimisation,and drag reduction.In addition,the Al_(2)O_(3)@BSS electrodes possessed remarkable antibacterial efficacy against E.coli and S.aureus.The proposed strategy can meet the extreme application requirements of surgical electrodes to improve operation quality and offer valuable insights for future studies.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
The low specific capacitances(SCs)of traditional carbonaceous negative electrodes significantly limit the enhancement in energy density of aqueous hybrid supercapacitors(AHCs).It is still hugely challengeable to explo...The low specific capacitances(SCs)of traditional carbonaceous negative electrodes significantly limit the enhancement in energy density of aqueous hybrid supercapacitors(AHCs).It is still hugely challengeable to explore a candidate with large SCs,which can stably operate in the negative potential region mean-while.For this propose,we design and fabricate solid-solution Ru_(x)Cu_(1-x)O_(2) nanocrystals(NCs),which exhibit competitive SCs and electrochemical stability within the potential range from-0.9 V to 0.0 V in the aqueous KOH electrolyte.The incorporation of Cu enhances the electrochemical utilization of RuO_(2),reaction kinetics,electronic conductivity,and hydrogen evolution overpotentials,which are all highly dependent upon the added contents of Cu species.The optimized Ru_(0.8)Cu_(0.2)O_(2)(RuCu82)electrode of a high mass loading of 5 mg cm^(-2) reveals the best electrochemical capacitances in terms of reversible SCs and capacitance degradation at room temperature and-20℃.Furthermore,the reversible K^(+)-(de)intercalation induced pseudocapacitance is proposed for electrochemical charge storage process of RuCu82.In particu-lar,remarkable specific energy of 59.1 Wh kg-1 at 400 W kg-1 and excellent cycling stability are achieved in the assembled NiCoO_(2)//RuCu82 AHCs.Our contribution here presents a new promising negative elec-trode platform with high SCs and electrochemical stability for next-generation AHCs.展开更多
Even in small concentrations,toxic metals like lead,cadmium,and mercury are dangerous to the environment and human health.Environmental monitoring depends on precisely identifying these heavy metals,particularly cadmi...Even in small concentrations,toxic metals like lead,cadmium,and mercury are dangerous to the environment and human health.Environmental monitoring depends on precisely identifying these heavy metals,particularly cadmium ions(Cd(Ⅱ)).In this study,we present a novel screen-printed carbon electrode(SPCE)modified with single crystallineα-Fe_(2)O_(3)nano-hexagons that functions as a sensor for detecting Cd(Ⅱ).The performance of the fabricated sensor was thoroughly assessed and compared with unmodified SPCE using the voltammetric method.The crystalline structure of the synthesizedα-Fe_(2)O_(3)nano-hexagons was confirmed through XRD,and surface analysis revealed an average diameter and thickness of 86 nm and 9 nm,respectively.Theα-Fe_(2)O_(3)modified SPCE yields a 7-fold enhanced response(at pH 5.0 vs.Ag/AgCl)to Cd(Ⅱ)than bare SPCE.The modified electrode effectively detects Cd(Ⅱ)with a linear response range of up to 333.0μmol/L and a detection limit of 0.65 nmol/L under ideal circumstances.This newly fabricated sensor offers significant potential for environmental monitoring applications by providing outstanding practicality,anti-interference ability,and repeatability for detecting Cd(Ⅱ)in water samples.展开更多
In order to ameliorate the electrochemical hydrogen storage performance of La-Mg-Ni system A2B7-type electrode alloys, a small amount of Si was added. The La0.8Mg0.2Ni3.3Co0.2Six （x=0-0.2） electrode alloys were prep...In order to ameliorate the electrochemical hydrogen storage performance of La-Mg-Ni system A2B7-type electrode alloys, a small amount of Si was added. The La0.8Mg0.2Ni3.3Co0.2Six （x=0-0.2） electrode alloys were prepared by casting and annealing. The effects of adding Si on the structure and electrochemical hydrogen storage characteristics of the alloys were investigated systematically. The results indicate that the as-cast and annealed alloys hold multiple structures, involving two major phases of （La, Mg）2Ni7 with a Ce2Ni7-type hexagonal structure and LaNi5 with a CaCu5-type hexagonal structure as well as one residual phase LaNi3. The addition of Si results in a decrease in （La, Mg）2Ni7 phase and an increase in LaNi5 phase without changing the phase structure of the alloys. What is more, it brings on an obvious effect on electrochemical hydrogen storage characteristics of the alloys. The discharge capacities of the as-cast and annealed alloys decline with the increase of Si content, but their cycle stabilities clearly grow under the same condition. Furthermore, the measurements of the high rate discharge ability, the limiting current density, hydrogen diffusion coefficient as well as electrochemical impedance spectra all indicate that the electrochemical kinetic properties of the electrode alloys first increase and then decrease with the rising of Si content.展开更多
Electrochemical oxidation of aniline in aqueous solution was investigated over a novel Ti/TiOxHy/Sb-SnO2 electrode prepared by the electrodeposition method.Scanning electron microscopy,X-ray diffraction,and electroche...Electrochemical oxidation of aniline in aqueous solution was investigated over a novel Ti/TiOxHy/Sb-SnO2 electrode prepared by the electrodeposition method.Scanning electron microscopy,X-ray diffraction,and electrochemical measurements were used to characterize its morphology,crystal structure,and electrochemical properties.Removal of aniline by the Ti/TiOxHy/Sb-SnO2electrode was investigated by ultraviolet-Visible spectroscopy and chemical oxygen demand（COD）analysis under different conditions,including current densities,initial concentrations of aniline,pH values,concentrations of chloride ions,and types of reactor.It was found that a higher current density,a lower initial concentration of aniline,an acidic solution,the presence of chloride ions（0.2wt%NaCl）,and a three-dimensional（3D） reactor promoted the removal efficiency of aniline.Electrochemical degradation of aniline followed pseudo-first-order kinetics.The aniline（200 mL of 100mg·L-（-1）） and COD removal efficiencies reached 100%and 73.5%,respectively,at a current density of 20 mA·cm-（-2）,pH of 7.0,and supporting electrolyte of 0.5 wt%Na2SO4 after 2 h electrolysis in a 3D reactor.These results show that aniline can be significantly removed on the Ti/TiOxHy/Sb-SnO2electrode,which provides an efficient way for elimination of aniline from aqueous solution.展开更多
基金supported by a GRF grant (No.CUHK477610) of the Research Grants Council of Hong Kong SAR Governmentthe National Natural Science Foundation of China (No. 50708037)
文摘β-PbO2 electrodes were prepared by electro-deposition and characterized by scanning electron microscopy,X-ray diffraction,X-ray photoelectron spectroscopy,and linear sweep voltammetry.We confirmed pure β-PbO2 crystals were on the electrode and it had a high oxygen evolution potential.The photoactivity and photoelectrochemical（PEC） properties of the β-PbO2 electrode were investigated under visible light irradiation（λ 〉 420 nm） for the decolorization of Methylene Blue.Pseudo first-order kinetics parameter（Kapp） for dye decolorization using the β-PbO2 electrode achieved 6.71×10-4 min-1 under visible light irradiation,which indicated its excellent visible light-induced photoactivity.The Kapp of the PEC process was as much as 1.41×10-3 min-1 and was 1.71 times that of visible light irradiation or electrolysis even in the presence of the β-PbO2 electrode.A significant synergetic effect was observed in the PEC system.We also employed TiO2 modified β-PbO2 electrodes in this test,which revealed that the TiO2 immobilized on the β-PbO2 electrode inhibited the visible light-induced PEC efficiency despite the amount of TiO2 used for electrode preparation.The β-PbO2 electrode was also superior to the dimensionally stable anode（Ti/Ru0.3Ti0.7O2） in visible light-induced photoactivity and PEC efficiency.
基金the National Natural Science Foundation of China (20476070,20771080)Natural Science Foundation of Shanxi Province (20031024 ,20041020)
文摘The acid-proof anode Ti/SnO2+Mn2O3/PbO2 doped with Ce was prepared by thermal decomposition and electrodeposition combination technology, the effect of Ce on the morphology and structure of anode was also studied in this paper. The results obtained by cyclic voltammetry (CV), electrochemical impedance spectroscopic (EIS), X-ray Diffraction (XRD) and scanning electron microscopy (SEM) indicated that PbO2 crystal grains presented honeycomb structure were formed on the electrode surface by doping with Ce. The specific surface areas and catalytic active sites of the Ce-PbO2 doped electrode were increased and the catalytic activity was evidently greater than the undoped one. However, when Ce was doped into the intermediate layer (SnO2+Mn2O3), a more cracked surface structure formed, thus leading electrode deactivation by passivation of the Ti-substrate. So the anodic stability was decreased according to the accelerated life tests.
基金Project(50964008)supported by the National Natural Science Foundation of ChinaProject(2010287)supported by Analysis and Testing Foundation of Kunming University of Science and Technology,China
文摘Al/α-PbO2/β-PbO2 composite electrodes doped with rare earth oxide （CeO2） were prepared by anodic oxidation method investigate the influence of nano-CeO2 dopants on the properties of Al/α-PbO2/β-PbO2-CeO2 electrodes and the impact of α-PbO2 as the intermediate layer. The results show that using α-PbO2 as the intermediate layer will benefit the crystallization of β-PbO2 and β-PbO2 is more suitable as the surface layer than α-PbO2. CeO2 dopants change the crystallite size and crystal structure, enhance the catalytic activity, and even change the deposition mechanism of PbO2. The doping of CeO2 in the PbO2 electrodes can enhance the electro-catalytic activity, which is helpful for oxygen evolution, and therefore reduce the cell voltage.
基金Projects(51004056,51004057)supported by the National Natural Science Foundation of ChinaProject(KKZ6201152009)supported by the Opening Foundation of Key Laboratory of Inorganic Coating Materials,Chinese Academy of Sciences+2 种基金Project(2010ZC052)supported by the Applied Basic Research Foundation of Yunnan Province,ChinaProject(20125314110011)supported by the Specialized Research Fund for the Doctoral Program of Higher Education,ChinaProject(2010247)supported by Analysis&Testing Foundation of Kunming University of Science and Technology,China
文摘Al/conductive coating/α-Pb O2-Ce O2-Ti O2/β-PbO 2-MnO 2-WC-Zr O2 composite electrode material was prepared on Al/conductive coating/α-PbO 2-Ce O2-Ti O2 substrate by electrochemical oxidation co-deposition technique. The effects of current density on the chemical composition, electrocatalytic activity, and stability of the composite anode material were investigated by energy dispersive X-ray spectroscopy（EDXS）, anode polarization curves, quasi-stationary polarization（Tafel） curves, electrochemical impedance spectroscopy（EIS）, scanning electron microscopy（SEM）, and X-ray diffraction（XRD）. Results reveal that the composite electrode obtained at 1 A/dm2 possesses the lowest overpotential（0.610 V at 500 A/m2） for oxygen evolution, the best electrocatalytic activity, the longest service life（360 h at 40 °C in 150 g/L H2SO4 solution under 2 A/cm2）, and the lowest cell voltage（2.75 V at 500 A/m2）. Furthermore, with increasing current density, the coating exhibits grain growth and the decrease of content of Mn O2. Only a slight effect on crystalline structure is observed.
基金We are greateful to the National Narural Science Foundation of China(No.20455017)Science and Technology Committee of Shanghai Municipal(No.0452nm084).
文摘A novel nano crystalline Ag2O2-PbO2 film chemically modified electrode (CME) was prepared and the CME was characterized by X-ray diffractometer (XRD) and atomic force microscope (AFM). By chronoamperometry, the nano Ag2O2-PbO2 CME was used as bioelectro- chemical sensor to determine the population of Escherichia coli (E. coli) in water. Compared with conventional methods, it is found that the technique we used is fast and convenient in counting E. coli.
基金the National Key R&D Program of China(No.2021YFA1501503)the National Natural Science Foundation of China(Nos.22250008,22121004,22108197)+3 种基金the Haihe Laboratory of Sustainable Chemical Transformations(No.CYZC202107)the Natural Science Foundation of Tianjin City(No.21JCZXJC00060)the Program of Introducing Talents of Discipline to Universities(No.BP0618007)the Xplorer Prize for financial support。
文摘Membrane electrode assembly(MEA)is widely considered to be the most promising type of electrolyzer for the practical application of electrochemical CO_(2) reduction reaction(CO_(2)RR).In MEAs,a square-shaped cross-section in the flow channel is normally adopted,the configuration optimization of which could potentially enhance the performance of the electrolyzer.This paper describes the numerical simulation study on the impact of the flow-channel cross-section shapes in the MEA electrolyzer for CO_(2)RR.The results show that wide flow channels with low heights are beneficial to the CO_(2)RR by providing a uniform flow field of CO_(2),especially at high current densities.Moreover,the larger the electrolyzer,the more significant the effect is.This study provides a theoretical basis for the design of high-performance MEA electrolyzers for CO_(2)RR.
基金supported by the National Natural Science Foundation of China(U23A20573,U23A20140)the Hebei Natural Science Foundation(B202420809,B2024208088)+2 种基金S&T Program of Hebei(242Q4301Z,22373709D)Project of Basic Research at Universities in Shijiazhuang(241790977A)Huang jin tai plan project of Hebei provincial department of education(HJZD202512)。
文摘Integrating the CO_(2)capture process with the CO_(2)electrochemical reduction process into a single system can eliminate the need for storage and transportation following CO_(2)capture.This integrated process offers several advantages over multi-step cascade processes,including reduced costs and enhanced CO_(2)utilization.However,the integrated CO_(2)capture and electrochemical reduction(CCER)process encounters several challenges,including the low CO_(2)adsorption performance of the gas diffusion electrode(GDE)and catalyst,as well as the poor activity and selectivity of the catalyst for the electrochemical reduction of CO_(2).This review aims to systematically summarize the fundamentals of the CCER process.Based on an in-depth understanding of the CO_(2)mass transfer,adsorption,and electrochemical reduction processes,GDE design strategies based on the modulation of wettability and structure are discussed to enhance the CO_(2)capture capability at the GDE level.At the catalyst level,catalyst design strategies based on the introduction of CO_(2)capture sites and the construction of CO_(2)mass transfer channels were analyzed,and catalyst design strategies for enhanced CO_(2)capture were proposed.This review summarizes the most common catalysts for CO_(2)electrochemical reduction,such as Ni-based,Bi-based,and Cubased catalysts,and analyzes their design strategies based on reaction pathways for generating specific products.Finally,the problems and challenges of the CCER process are summarized and proposed,which provide ideas for the further application of this technology in the future.
基金supported by the European Research Council,ERC project Liquid3D,grant number 101045072supported by the Foundation of Science and Technology(FCT)of Portugal through the CMU-Portugal project WoW(Reference No:45913).
文摘The demand for sustainable and stretchable thin-film printed batteries for bioelectronics,wearables,and e-textiles is rapidly increasing.Recently,we developed a fully 3D-printed soft-matter thin-film Ga-Ag_(2)O battery with 3R characteristics:resilient to mechanical strain,repairable after damage,and recyclable.This battery achieved a record-breaking areal capacity of 26.37 mAh cm-2,increasing to 30.32 mAh cm^(-2) after 10 cycles under 100%strain.This performance stems from the synergistic effects of gallium’s liquid metal properties and the styrene-isoprene-styrene polymer in the anode.Gallium’s high specific capacity(1153.2 mAh g^(-1)),deformability,and self-healing abilities,supported by its supercooled liquid phase,significantly enhance the battery’s resilience and efficiency.However,the cathode’s lower theoretical capacity,due to Ag_(2)O(231.31 mAh g^(-1)),remains a limitation.Traditional Ag_(2)O-carbon black-styrene-isoprene-styrene cathodes experience rapid capacity decay as only the surface area of the active materials interacts with the electrolyte.To overcome this,we designed a carbon-filled Ag_(2)O foam electrode using a sacrificial sugar template,increasing the effective surface area.This optimization enhanced ion-exchange efficiency,specific capacity,and cyclability,achieving a specific capacity of 221.16 mAh g^(-1).Consequently,the Ga-Ag_(2)O stretchable battery attained a record areal capacity of 40.91 mAh cm^(-2)—double that of nonfoam electrodes—and exhibited fivefold improved charge-discharge cycles.Using ultrastretchable Ag-EGaIn-styrene-isoprene-styrene and carbon black-styrene-isoprene-styrene current collectors,the battery’s specific capacity increased by 33%under 50%strain.Integrated into a soft-matter smart wristband for temperature monitoring,the battery demonstrated its promise for wearable electronics.
基金supported by the Strategic Priority Research Program of the Chinese Academy of Sciences(No.XDA0400000)Shanghai Municipal Science and Technology Program(No.21DZ1207700)+4 种基金the National Key R&D Program of China(Nos.2024YFF0506300,2024YFB4106400)the National Natural Science Foundation of China(No.22209200)Shanghai Sailing Program(No.22YF1457700)the Major Science and Technology Projects of China National Offshore Oil Corporation Limited during the 14th Five Year Plan(No.KJGG-2022-12-CCUS-030500)the Industrial Fund of Shanghai Institute of Applied Physics,Chinese Academy of Sciences(No.1124100602)。
文摘Due to the microstructural degradation of fuel electrodes,high cycling stability and catalytic activity remain a significant barrier for solid oxide electrolysis cells(SOEC).Perovskite materials exhibit favorable mixed conductivity and redox stability as cathode materials,but their catalytic activity is not ideal.This study systematically investigates the structural,morphological,and electrochemical properties of cobalt doping in the Pr_(0.4)Sr_(0.6)Co_(xF)e_(1-x)O_(3-δ)(PSC_(x)F)system,characterized using scanning electron microscopy,transmission electron microscopy,X-ray photoelectron spectroscopy,CO_(2)-temperature-programmed desorption,and Raman spectroscopy.The effect of cobalt-doping concentration on the electrochemical properties was further investigated.The electrochemical performance evaluation demonstrates that the optimal is achieved with a cob alt-doping ratio of 0.1.At 800℃and 1.5 V,the CO_(2)electrolysis current density of the PSC_(0.1)F-Gd_(0.1)Ce_(0.9)O_(2-δ)(GDC)IGDCISc_(0.1)Zr_(0.9)O_(2-δ)|IGDCILa_(0.6)Sr_(0.4)Co_(0.2)Fe_(0.8)O_(3+δ)full cell reaches 1.37 A·cm^(-2),approximately 34.3%higher than that of electrodes without cobalt doping.Furthermore,the electrode maintains stability for over 100 h at 800℃and 1.3 V.This work offers new insights into how metal doping can be applied to regulate electrode structures,thereby providing enhanced performance and stability for perovskite-based fuel electrodes.
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℃.
文摘The pore size distribution is often an important parameter for transport processes in porous media.Cryoporometry experiments can provide such data in the meso and macropore size up to 1 mm providing the sample temperature is finely controlled.We use a Peltier based system inserted directly into the NMR probe to control the temperature within 0.05℃and impose temperature ramps down to 0.002℃/min,necessary to characterize the largest pore sizes.The pore size information in the macropore range cannot be obtained from gas adsorption techniques while mercury injection is questionable for the material considered here.For porous materials made of paramagnetic minerals such as lithium-iron phosphate(LiFePO_(4),LFP)or nickel-manganese-cobalt oxides(NMC)and saturated with octamethylcyclotetrasiloxane(OMCTS),the T_(2)relaxation times are very short such as protons from the liquid and frozen phases cannot be separated.Hence the usual cryoporometry experiment cannot be performed.Instead,we propose to use the T_(1)contrast to separate these phases.The method is studied in detail along with some temperature effects linked with the T_(1)variation of the bulk frozen OMCTS.We show an example on two cathode materials part of industrial battery product.
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financially supported by the National Natural Science Foundation of China(Grant Nos.52275425,52405473,and 52405472)the Natural Science Foundation of Guangdong Province(Grant No.2024A1515010993)。
文摘Surgical electrodes are frequently associated with disadvantages such as high surface adhesion and severe thermal damage to adjacent normal tissues,which threaten operation quality and patient safety.In this study,by mimicking the micromorphology and bio-anti-adhesion of shark skin,we proposed a strategy that utilized nanoscale aluminium oxide(Al_(2)O_(3))films deposited on bioinspired shark skin(BSS)microstructures to design a composite surface(Al_(2)O_(3)@BSS)and integrated it into both flat sides of the surgical electrodes.Micro/nano-manufacturing of the Al_(2)O_(3)@BSS surface was sequentially accomplished using nanosecond laser texturing,atomic layer deposition,and low-temperature annealing,endowing it with excellent blood-repellent properties.Visualisation experiments revealed that the tensile stress gradient of the blood coagulum with increasing thickness under a thermal field prompted it to separate from the Al_(2)O_(3)@BSS surface,resulting in anti-adhesion.Furthermore,it was observed for the first time that Al_(2)O_(3) films could transiently excite discharge along a dielectric surface(DADS)to ablate tissues while suppressing Joule heat,thereby minimising thermal damage.A combination of ex vivo tissue and living mouse experiments demonstrated that the Al_(2)O_(3)@BSS electrodes exhibited optimal comprehensive performance in terms of anti-adhesion,damage minimisation,and drag reduction.In addition,the Al_(2)O_(3)@BSS electrodes possessed remarkable antibacterial efficacy against E.coli and S.aureus.The proposed strategy can meet the extreme application requirements of surgical electrodes to improve operation quality and offer valuable insights for future studies.
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supported by the National Natural Science Foundation of China(Nos.U22A20145,51904115,52072151,52171211,and 52271218)Jinan Independent Innovative Team(No.2020GXRC015)the Major Program of Shandong Province Natural Science Foundation(Nos.ZR2023ZD43 and ZR2021ZD05).
文摘The low specific capacitances(SCs)of traditional carbonaceous negative electrodes significantly limit the enhancement in energy density of aqueous hybrid supercapacitors(AHCs).It is still hugely challengeable to explore a candidate with large SCs,which can stably operate in the negative potential region mean-while.For this propose,we design and fabricate solid-solution Ru_(x)Cu_(1-x)O_(2) nanocrystals(NCs),which exhibit competitive SCs and electrochemical stability within the potential range from-0.9 V to 0.0 V in the aqueous KOH electrolyte.The incorporation of Cu enhances the electrochemical utilization of RuO_(2),reaction kinetics,electronic conductivity,and hydrogen evolution overpotentials,which are all highly dependent upon the added contents of Cu species.The optimized Ru_(0.8)Cu_(0.2)O_(2)(RuCu82)electrode of a high mass loading of 5 mg cm^(-2) reveals the best electrochemical capacitances in terms of reversible SCs and capacitance degradation at room temperature and-20℃.Furthermore,the reversible K^(+)-(de)intercalation induced pseudocapacitance is proposed for electrochemical charge storage process of RuCu82.In particu-lar,remarkable specific energy of 59.1 Wh kg-1 at 400 W kg-1 and excellent cycling stability are achieved in the assembled NiCoO_(2)//RuCu82 AHCs.Our contribution here presents a new promising negative elec-trode platform with high SCs and electrochemical stability for next-generation AHCs.
文摘Even in small concentrations,toxic metals like lead,cadmium,and mercury are dangerous to the environment and human health.Environmental monitoring depends on precisely identifying these heavy metals,particularly cadmium ions(Cd(Ⅱ)).In this study,we present a novel screen-printed carbon electrode(SPCE)modified with single crystallineα-Fe_(2)O_(3)nano-hexagons that functions as a sensor for detecting Cd(Ⅱ).The performance of the fabricated sensor was thoroughly assessed and compared with unmodified SPCE using the voltammetric method.The crystalline structure of the synthesizedα-Fe_(2)O_(3)nano-hexagons was confirmed through XRD,and surface analysis revealed an average diameter and thickness of 86 nm and 9 nm,respectively.Theα-Fe_(2)O_(3)modified SPCE yields a 7-fold enhanced response(at pH 5.0 vs.Ag/AgCl)to Cd(Ⅱ)than bare SPCE.The modified electrode effectively detects Cd(Ⅱ)with a linear response range of up to 333.0μmol/L and a detection limit of 0.65 nmol/L under ideal circumstances.This newly fabricated sensor offers significant potential for environmental monitoring applications by providing outstanding practicality,anti-interference ability,and repeatability for detecting Cd(Ⅱ)in water samples.
基金Projects(50961009,51161015)supported by the National Natural Science Foundation of ChinaProject(2011AA03A408)supported by the High-tech Research and Development Program of ChinaProjects(2011ZD10,2010ZD05)supported by the Natural Science Foundation of Inner Mongolia,China
文摘In order to ameliorate the electrochemical hydrogen storage performance of La-Mg-Ni system A2B7-type electrode alloys, a small amount of Si was added. The La0.8Mg0.2Ni3.3Co0.2Six （x=0-0.2） electrode alloys were prepared by casting and annealing. The effects of adding Si on the structure and electrochemical hydrogen storage characteristics of the alloys were investigated systematically. The results indicate that the as-cast and annealed alloys hold multiple structures, involving two major phases of （La, Mg）2Ni7 with a Ce2Ni7-type hexagonal structure and LaNi5 with a CaCu5-type hexagonal structure as well as one residual phase LaNi3. The addition of Si results in a decrease in （La, Mg）2Ni7 phase and an increase in LaNi5 phase without changing the phase structure of the alloys. What is more, it brings on an obvious effect on electrochemical hydrogen storage characteristics of the alloys. The discharge capacities of the as-cast and annealed alloys decline with the increase of Si content, but their cycle stabilities clearly grow under the same condition. Furthermore, the measurements of the high rate discharge ability, the limiting current density, hydrogen diffusion coefficient as well as electrochemical impedance spectra all indicate that the electrochemical kinetic properties of the electrode alloys first increase and then decrease with the rising of Si content.
基金supported by the National Natural Science Foundation of China(21507104)the Fundamental Research Funds for the Central Universities of China
文摘Electrochemical oxidation of aniline in aqueous solution was investigated over a novel Ti/TiOxHy/Sb-SnO2 electrode prepared by the electrodeposition method.Scanning electron microscopy,X-ray diffraction,and electrochemical measurements were used to characterize its morphology,crystal structure,and electrochemical properties.Removal of aniline by the Ti/TiOxHy/Sb-SnO2electrode was investigated by ultraviolet-Visible spectroscopy and chemical oxygen demand（COD）analysis under different conditions,including current densities,initial concentrations of aniline,pH values,concentrations of chloride ions,and types of reactor.It was found that a higher current density,a lower initial concentration of aniline,an acidic solution,the presence of chloride ions（0.2wt%NaCl）,and a three-dimensional（3D） reactor promoted the removal efficiency of aniline.Electrochemical degradation of aniline followed pseudo-first-order kinetics.The aniline（200 mL of 100mg·L-（-1）） and COD removal efficiencies reached 100%and 73.5%,respectively,at a current density of 20 mA·cm-（-2）,pH of 7.0,and supporting electrolyte of 0.5 wt%Na2SO4 after 2 h electrolysis in a 3D reactor.These results show that aniline can be significantly removed on the Ti/TiOxHy/Sb-SnO2electrode,which provides an efficient way for elimination of aniline from aqueous solution.
