Biomass-derived heteroatom self-doped cathode catalysts has attracted considerable interest for electrochemical advanced oxidation processes(EAOPs)due to its high performance and sustainable synthesis.Herein,we illust...Biomass-derived heteroatom self-doped cathode catalysts has attracted considerable interest for electrochemical advanced oxidation processes(EAOPs)due to its high performance and sustainable synthesis.Herein,we illustrated the morphological fates of waste leaf-derived graphitic carbon(WLGC)produced from waste ginkgo leaves via pyrolysis temperature regulation and used as bifunctional cathode catalyst for simultaneous H_(2)O_(2) electrochemical generation and organic pollutant degradation,discovering S/N-self-doping shown to facilitate a synergistic effect on reactive oxygen species(ROS)generation.Under the optimum temperature of 800℃,the WLGC exhibited a H_(2)O_(2) selectivity of 94.2%and tetracycline removal of 99.3%within 60 min.Density functional theory calculations and in-situ Fourier transformed infrared spectroscopy verified that graphitic N was the critical site for H_(2)O_(2) generation.While pyridinic N and thiophene S were the main active sites responsible for OH generation,N vacancies were the active sites to produce ^(1)O_(2) from O_(2).The performance of the novel cathode for tetracycline degradation remains well under a wide pH range(3–11),maintaining excellent stability in 10 cycles.It is also industrially applicable,achieving satisfactory performance treating in real water matrices.This system facilitates both radical and non-radical degradation,offering valuable advances in the preparation of cost-effective and sustainable electrocatalysts and hold strong potentials in metal-free EAOPs for organic pollutant degradation.展开更多
For the efficient electrolytic extraction of Er from spent nuclear fuel,a series of electrochemical methods was used to research the electrochemical behavior of Er(Ⅲ)in the LiCl—KCl system on inert(Mo)electrode and ...For the efficient electrolytic extraction of Er from spent nuclear fuel,a series of electrochemical methods was used to research the electrochemical behavior of Er(Ⅲ)in the LiCl—KCl system on inert(Mo)electrode and on reactive(Ni)electrodes.On the inert Mo electrode,the reduction of Er(Ⅲ)to Er(0)is a onestep with three-electron and quasi-reversible reaction process.Meanwhile,the apparent generation Gibbs free energy and activity coefficients of Er(Ⅲ)on the inert electrode were determined.Thereafter,the electrochemical reduction of Er(Ⅲ)on the Ni electrode was emphatically investigated.Er(Ⅲ)is reduced at a corrected potential owing to the formation of Ni-Er alloys.In addition,thermodynamic parameters such as partial excess Gibbs free energy change of Er in Ni,activity and apparent generation Gibbs free energy of the Ni-Er alloys were determined by the electromotive force method.Finally,different Ni-Er alloys were produced using potentiostatic electrolysis on the Ni cathode by controlling different potentials,Moreover,electrolytic extraction was carried out on the Ni cathode at the potential of-2.0 V,and the separation efficiency of Er reaches 99.72%,which proves the practicability of separating Er from LiCl-KCl eutectic on the reactive Ni cathode.展开更多
Effects of citrate concentration and pH on the electrochemical reduction process of Co（Ⅱ） were investigated by cyclic voltammetry（CV） and electrochemical impedance spectroscopy（EIS）. The results show that Co（...Effects of citrate concentration and pH on the electrochemical reduction process of Co（Ⅱ） were investigated by cyclic voltammetry（CV） and electrochemical impedance spectroscopy（EIS）. The results show that Co（Ⅱ） is reduced into two species which are free Co2＋ and [Co（C6H607）] in the solution composed of 0.05 mol/L CoS04·5H2O, 0.20 mol/L Na2SO4 and 0-0.40 mol/L C6H5O7Na3·2H2O in the pH range of 3-9. The reduction behavior depends on the pH of the solution. Co（H） is mainly reduced into the form of free Co^2＋ at pH 3 and into the form of [Co（C6H6O7）] at the pH range of 4-6 in citrate solution. The [Co（C6H6O7）] is first reduced to an intermediate state and then to Co°. Adsorption of the intermediate state exists on the surface of the electrode. Co（Ⅱ） is difficult to be reduced in the solution with the pH above 7, because the existing Co（Ⅱ）-citrate complex species [Co（C6H5O7）]- and [Co（C6H4O7）]2- are more difficult to be reduced than the hydrogen ion.展开更多
Achieving high-energy density remains a key objective for advanced energy storage systems.However,challenges,such as poor cathode conductivity,anode dendrite formation,polysulfide shuttling,and electrolyte degradation...Achieving high-energy density remains a key objective for advanced energy storage systems.However,challenges,such as poor cathode conductivity,anode dendrite formation,polysulfide shuttling,and electrolyte degradation,continue to limit performance and stability.Molecular and ionic dipole interactions have emerged as an effective strategy to address these issues by regulating ionic transport,modulating solvation structures,optimizing interfacial chemistry,and enhancing charge transfer kinetics.These interactions also stabilize electrode interfaces,suppress side reactions,and mitigate anode corrosion,collectively improving the durability of high-energy batteries.A deeper understanding of these mechanisms is essential to guide the design of next-generation battery materials.Herein,this review summarizes the development,classification,and advantages of dipole interactions in high-energy batteries.The roles of dipoles,including facilitating ion transport,controlling solvation dynamics,stabilizing the electric double layer,optimizing solid electrolyte interphase and cathode–electrolyte interface layers,and inhibiting parasitic reactions—are comprehensively discussed.Finally,perspectives on future research directions are proposed to advance dipole-enabled strategies for high-performance energy storage.This review aims to provide insights into the rational design of dipole-interactive systems and promote the progress of electrochemical energy storage technologies.展开更多
Stress corrosion cracking （SCC） of X70 pipeline steel in simulated solution of the acidic soil in Yingtan in China was investigated using slow strain rate test （SSRT）, SEM and potentiodynamic polarization techniqu...Stress corrosion cracking （SCC） of X70 pipeline steel in simulated solution of the acidic soil in Yingtan in China was investigated using slow strain rate test （SSRT）, SEM and potentiodynamic polarization technique. Experiment results indicate that X70 steel is highly susceptible to SCC as applied potential reduces, which is manifested in loss of toughness and brittle fracture. Constaat polarization current can detect the occurrence of SCC. The lower the polarization current is the sooner stress corrosion cracking occurs. The SCC mechanisms are different at varying potentials. When potential is higher than open circuit potential, anodic process controls SCC, whereas when potential is far lower than open circuit potential, cathodic process controls SCC, and between these two potential regions, a combined electrochemical process controls the SCC. Stress or strain has a synergistic effect with electrochemical reactions to accelerate the cathodic hydrogen evolution process, which makes the X70 pipeline steel to be more susceptible to SCC.展开更多
Graphite materials are widely used as electrode materials for electrochemical energy storage.N-doping is an effective method for enhancing the electrochemical properties of graphite.A novel one-step N-doping method fo...Graphite materials are widely used as electrode materials for electrochemical energy storage.N-doping is an effective method for enhancing the electrochemical properties of graphite.A novel one-step N-doping method for complete and compact carbon paper was proposed for molten salt electrolysis in the Li Cl-KCl-Li3 N system.The results show that the degree of graphitization of carbon paper can be improved by the electrolysis of molten salts,especially at 2.0 V.Nitrogen gas was produced at the anode and nitrogen atoms can substitute carbon atoms of carbon paper at different sites to create nitrogen doping during the electrolysis process.The doping content of N in carbon paper is up to 13.0 wt%.There were three groups of nitrogen atoms,i.e.quaternary N(N-Q),pyrrolic N(N-5),and pyridinic N(N-6)in N-doping carbon paper.N-doping carbon paper as an Al-ion battery cathode shows strong charge-recharge properties.展开更多
A novel electrochemical setup for wastewater treatment-rotating electrochemical disc process(RECDP)was developed in this article. The anode and cathode are distributed alternatively and evenly on a flat round disc,whi...A novel electrochemical setup for wastewater treatment-rotating electrochemical disc process(RECDP)was developed in this article. The anode and cathode are distributed alternatively and evenly on a flat round disc,which was designed to improve mass transfer of organics from bulk solution to electrode surface,while at the same time increasing oxygen transfer from air to the liquid to benefit the organics oxidization.The color removal of dye Reactive Brilliant Orange X-GN(RBO)was experimentally investigated u...展开更多
Electrochemical oxidation of aqueous tris(1,3-dichloro-2-propyl)phosphate(TDCPP)by using Ti/SnO_(2)-Sb/La-PbO_(2)as anode was investigated for the first time,and the degradation mechanisms and toxicity changes of the ...Electrochemical oxidation of aqueous tris(1,3-dichloro-2-propyl)phosphate(TDCPP)by using Ti/SnO_(2)-Sb/La-PbO_(2)as anode was investigated for the first time,and the degradation mechanisms and toxicity changes of the degradation intermediates were further determined.Results suggested that electrochemical degradation of TDCPP followed pseudo-first-order kinetics,and the reaction rate constant(k)was 0.0332 min^(−1)at the applied current density of 10 mA/cm^(2)and Na_(2)SO_(4)concentration of 10 mmol/L.There was better TDCPP degradation performance at higher current density.Free hydroxy radical(•OH)was proved to play dominant role in TDCPP oxidation via quenching experiment,with a relative contribution rate of 60.1%.A total of five intermediates(M1,C_(6)H_(11)Cl_(4)O_(4)P;M2,C_(3)H_(7)Cl_(2)O_(4)P;M3,C_(9)H_(16)Cl_(5)O_(5)P;M4,C_(9)H_(14)Cl_(5)O_(6)P;M5,C_(6)H_(10)Cl_(3)O_(6)P)were identified,and the intermediates were further degraded prolonging with the reaction time.Flow cytometer results suggested that the toxicity of TDCPP and degradation intermediates significantly reduced,and the detoxification efficiency was achieved at 78.1%at 180 min.ECOSAR predictive model was used to assess the relative toxicity of TDCPP and the degradation intermediates.The EC_(50)to green algae was 3.59 mg/L for TDCPP,and the values raised to 84,574,54.6,391,and 8920 mg/L for M1,M2,M3,M4,and M5,respectively,indicating that the degradation intermediates are less toxic or not toxic.Electrochemical advanced oxidation process is a valid technology to degrade TDCPP and pose a good detoxification effect.展开更多
Colorless‐to‐black switching has attracted widespread attention for smart windows and multifunctional displays because they are more useful to control solar energy.However,it still remains a challenge owing to the t...Colorless‐to‐black switching has attracted widespread attention for smart windows and multifunctional displays because they are more useful to control solar energy.However,it still remains a challenge owing to the tremendous difficulties in the design of completely reverse absorptions in transmissive and colored states.Herein,we report on an electrochemical device that can switch between colorless and black by using the electrochemical process of hybrid organic–inorganic perovskite MAPbBr_(3),which shows a high integrated contrast ratio of up to 73%from 400 to 800 nm.The perovskite solution can be used as the active layer to assemble the device,showing superior transmittance over the entire visible region in neutral states.By applying an appropriate voltage,the device undergoes reversible switching between colorless and black,which is attributed to the formation of lead and Br_(2)in the redox reaction induced by the electron transfer process in MAPbBr_(3).In addition,the contrast ratio can be modulated over the entire visible region by changing the concentration and the applied voltage.These results contribute toward gaining an insightful understanding of the electrochemical process of perovskites and greatly promoting the development of switchable devices.展开更多
This review focuses on the application of process engineering in electrochemical energy conversion and storage devices innovation. For polymer electrolyte based devices, it highlights that a strategic simple switch fr...This review focuses on the application of process engineering in electrochemical energy conversion and storage devices innovation. For polymer electrolyte based devices, it highlights that a strategic simple switch from proton exchange membranes(PEMs) to hydroxide exchange membranes(HEMs) may lead to a new-generation of affordable electrochemical energy devices including fuel cells, electrolyzers, and solar hydrogen generators. For lithium-ion batteries, a series of advancements in design and chemistry are required for electric vehicle and energy storage applications. Manufacturing process development and optimization of the LiF eP O_4/C cathode materials and several emerging novel anode materials are also discussed using the authors' work as examples.Design and manufacturing process of lithium-ion battery electrodes are introduced in detail, and modeling and optimization of large-scale lithium-ion batteries are also presented. Electrochemical energy materials and device innovations can be further prompted by better understanding of the fundamental transport phenomena involved in unit operations.展开更多
Superhydrophilic surfaces were fabricated on copper substrates by an electrochemical deposition and sintering process. Superhydrophobic surfaces were prepared by constructing micro/nano-structure on copper substrates ...Superhydrophilic surfaces were fabricated on copper substrates by an electrochemical deposition and sintering process. Superhydrophobic surfaces were prepared by constructing micro/nano-structure on copper substrates through an electrochemical deposition method. Conversion from superhydrophobic to superhydrophilic was obtained via a suitable sintering process. After reduction sintering, the contact angle of the superhydrophilic surfaces changed from 155° to 0°. The scanning electron microscope （SEM） images show that the morphology of superhydrophobic and superhydrophilic surfaces looks like corals and cells respectively. The chemical composition and crystal structure of these surfaces were examined using energy dispersive spectrometry （EDS） and X-ray diffraction （XRD）. The results show that the main components on superhydrophobic surfaces are Cu, Cu2O and CuO, while the superhydrophilic surfaces are composed of Cu merely. The crystal structure is more inerratic and the grain size becomes bigger after the sintering. The interracial strength of the superhydrophilic surfaces was investigated, showing that the interfacial strength between superhydrophilic layer and copper substrate is considerably high.展开更多
A series of nanostructured Zr-doped anatase TiO_2 tubes with the Zr/Ti molar ratio of 0.01, 0.02, 0.03, and0.09 were prepared by a sol–gel technology on a carbon fiber template. The electrochemical performance of Zr-...A series of nanostructured Zr-doped anatase TiO_2 tubes with the Zr/Ti molar ratio of 0.01, 0.02, 0.03, and0.09 were prepared by a sol–gel technology on a carbon fiber template. The electrochemical performance of Zr-doped anatase TiO_2 as anodes for rechargeable lithium batteries was investigated and compared with undoped titania. Tests represented that after 35-fold charge/discharge cycling at C/10 the reversible capacity of Zr-doped titania（Zr/Ti = 0.03） reaches 135 m A h g^（-1）, while the capacity of undoped titania（Zr/Ti = 0） yielded only 50 m A h g^（-1）. Based on the results of the physicochemical investigation, three reasons of improving electrochemical performance of Zr-doped titania were suggested. According to the scanning electron microscopy and transmission electron microscopy, Zr^（4＋） doping induces a decrease in nanoparticle size, which facilitates the Li＋diffusion. The Raman investigations show the more open structure of Zr-doped TiO_2 as compared to undoped titania due to changing of the unit cell parameters, that significantly affects on the reversibility of the insertion/extraction process. The electrochemical impedance spectroscopy results indicate that substitution of Zr^（4＋） for Ti^（4＋） into anatase TiO_2 has favorable effects on the conductivity.展开更多
The Mg-based hydrogen storage alloys Mg2Ni, Mg2Ni0.7Fe0.3 and Mgl.7Alo.3Ni were successfully synthesized by a two-step process （sintering and ball milling）. The crystal structure and microstructure were examined by ...The Mg-based hydrogen storage alloys Mg2Ni, Mg2Ni0.7Fe0.3 and Mgl.7Alo.3Ni were successfully synthesized by a two-step process （sintering and ball milling）. The crystal structure and microstructure were examined by X-ray diffraction, Scanning Electron Microscope and Malvern particle size analyzer. New phase appears in the tripe alloys doped with A1 and Fe, and the particle size ranges from 3μm to 5 μm. The electrochemical performance studies indicate that the partial substitution of AI for Mg, and Fe for Ni significantly improve the cycle life, reversibility of hydrogen absorption and desorption. The diffusion process is the control step in the electrode reaction of hydrogen storage alloys.展开更多
Objective:The purpose of this study was to investigate the effects of a zinc-substituted nano-hydroxyapatite(Zn-HA) coating,applied by an electrochemical process,on implant osseointegraton in a rabbit model.Methods:A ...Objective:The purpose of this study was to investigate the effects of a zinc-substituted nano-hydroxyapatite(Zn-HA) coating,applied by an electrochemical process,on implant osseointegraton in a rabbit model.Methods:A Zn-HA coating or an HA coating was deposited using an electrochemical process.Surface morphology was examined using field-emission scanning electron microscopy.The crystal structure and chemical composition of the coatings were examined using an X-ray diffractometer(XRD) and Fourier transform infrared spectroscopy(FTIR).A total of 78 implants were inserted into femurs and tibias of rabbits.After two,four,and eight weeks,femurs and tibias were retrieved and prepared for histomorphometric evaluation and removal torque(RTQ) tests.Results:Rod-like HA crystals appeared on both implant surfaces.The dimensions of the Zn-HA crystals seemed to be smaller than those of HA.XRD patterns showed that the peaks of both coatings matched well with standard HA patterns.FTIR spectra showed that both coatings consisted of HA crystals.The Zn-HA coating significantly improved the bone area within all threads after four and eight weeks(P<0.05),the bone to implant contact(BIC) at four weeks(P<0.05),and RTQ values after four and eight weeks(P<0.05).Conclusions:The study showed that an electrochemically deposited Zn-HA coating has potential for improving bone integration with an implant surface.展开更多
Surface chemistry focuses on the investigation of the adsorption,migration,assembly,activation,reaction,and desorption of atoms and molecules at surfaces.Surface chemistry plays the pivotal roles in both fundamental s...Surface chemistry focuses on the investigation of the adsorption,migration,assembly,activation,reaction,and desorption of atoms and molecules at surfaces.Surface chemistry plays the pivotal roles in both fundamental science and applied technology.This review will summarize the recent progresses on surface assembly,synthesis and catalysis investigated mainly by scanning tunneling microscopy and atomic force microscopy.Surface assemblies of water and small biomolecules,construction of Sierpin′ski triangles and surface chirality are summarized.On-surface synthesis of conjugated carbo-and heterocycles and other kinds of carbon nanostructures are surveyed.Surface model catalysis,including single-atom catalysis and electrochemical catalysis,are discussed at the single-atom level.展开更多
In this article,we looked at metallenes,a novel class of two-dimensional(2D)metals that are attracting interest in the energy and catalysis sectors.Catalysis is one area where their exceptional physicochemical and ele...In this article,we looked at metallenes,a novel class of two-dimensional(2D)metals that are attracting interest in the energy and catalysis sectors.Catalysis is one area where their exceptional physicochemical and electrical characteristics might be useful.Metallenes are unique because they include several metal atoms that are not in a coordinated bond.This makes them more active and improves their atomic uti-lization,which in turn increases their catalytic potential.This article delves into the potential of two-dimensional metals as electrocatalysts for carbon dioxide reduction,fuel oxidation,oxygen evolution,and oxygen reduction reactions in the context of sustainable energy conversion.Owing to the exception-ally high surface-to-volume ratio,large surface area as well as their optimized atomic use efficiency,2D materials defined by atomic layers are crucial for surface-related sustainable energy applications.Due to its exceptional properties,such as high conductivity and the ability to enhance the exposure of active metal sites,2D metallenes have recently attracted a lot of interest for use in catalysis,electronics,and energy-related applications.With their highly mobility,adjustable surface states,and electrical struc-tures that can be fine-tuned,2D metallenes are promising nanostructure materials for use in energy con-version with the sustainable applications.展开更多
TiO_(2)has demonstrated outstanding performance in electrochemical advanced oxidation processes(EAOPs)due to its structural stability and high oxygen overpotential.However,there is still much room for improving its el...TiO_(2)has demonstrated outstanding performance in electrochemical advanced oxidation processes(EAOPs)due to its structural stability and high oxygen overpotential.However,there is still much room for improving its electrochemical activity.Herein,narrow bandgap manganese oxide(MnO_(x))was composited with TiO_(2)nanotube arrays(TiO_(2)NTAs)that in-situ oxidized on porous Ti sponge,forming the MnO_(x)-TiO_(2)NTAs anode.XANES and XPS analysis further proved that the composition of MnO_(x)is Mn2O3.Electrochemical characterizations revealed that increasing the composited concentration of MnO_(x)can improve the conductivity and reduce oxygen evolution potential so as to improve the electrochemical activity of the composited MnO_(x)-TiO_(2)NTAs anode.Meanwhile,the optimal degradation rate of benzoic acid(BA)was achieved using MnO_(x)-TiO_(2)NTAs with a MnO_(x)concentration of 0.1 mmol L^(-1),and the role of MnO_(x)was proposed based on DFT calculation.Additionally,the required electrical energy(EE/O)to destroy BA was optimized by varying the composited concentration of MnO_(x)and the degradation voltage.These quantitative results are of great significance for the design and application of high-performance materials for EAOPs.展开更多
The electrochemical process of Ti-Ni alloy electrode was studied by using cyclic voltammetry. The hydrogen-absorbing electrode could be approximately regarded as a reversible hydrogen elecrede. The con- trolling steps...The electrochemical process of Ti-Ni alloy electrode was studied by using cyclic voltammetry. The hydrogen-absorbing electrode could be approximately regarded as a reversible hydrogen elecrede. The con- trolling steps of the discharging process varying with the anodic overpotentials were investigated and the effect ofelecrode constituent modification or Zr adulteation on the electrochemical behavior was also studied.展开更多
Integrating titanium-based implants with the surrounding bone tissue remains challenging.This study aims to explore the impact of different anodization voltages(20−80 V)on the surface topography of two-phase(α/β)Ti ...Integrating titanium-based implants with the surrounding bone tissue remains challenging.This study aims to explore the impact of different anodization voltages(20−80 V)on the surface topography of two-phase(α/β)Ti alloys and to produce TiO_(2) films with enhanced bone formation abilities.Scanning electron microscopy coupled with energy dispersive spectroscopy(SEM−EDS)and atomic force microscopy(AFM)were applied to investigate the morphological,chemical,and surface topography of the prepared alloys and to confirm the growth of hydroxyapatite(HA)on their surfaces.Results disclosed that the surface roughness of TiO_(2) films formed on Ti−6Al−7Nb alloys was superior to that of Ti−6Al−4V alloys.Ti−6Al−7Nb alloy anodized at 80 V had the highest yields of HA after immersion in simulated body fluid with enhanced HA surface coverage.The developed HA layer had a mean thickness of(128.38±18.13)μm,suggesting its potential use as an orthopedic implantable material due to its promising bone integration and,hence,remarkable stability inside the human body.展开更多
The development of differential electrochemical mass spectrometry (DEMS) originated in the late 20th century[1–4],with its core objective being the integration of electrochemical processes with mass spectrometric det...The development of differential electrochemical mass spectrometry (DEMS) originated in the late 20th century[1–4],with its core objective being the integration of electrochemical processes with mass spectrometric detection to enable real-time tracking of reaction intermediates and products at the electrodes [5,6].DEMS was initially employed to study electrochemical processes in aqueous solutions,such as methanol oxidation [7].Recently,with the rapid development of new energy technologies,DEMS has been widely applied in the research and development of electrocatalysis,lithium-ion,sodium-ion,and metal-air batteries[8–16].展开更多
基金financially supported by National Key R&D Program International Cooperation Project(2023YFE0108100)Natural Science Foundation of China(No.52170085)+2 种基金Key Project of Natural Science Foundation of Tianjin(No.21JCZDJC00320)Tianjin Post-graduate Students Research and Innovation Project(2021YJSB013)Fundamental Research Funds for the Central Universities,Nankai University.
文摘Biomass-derived heteroatom self-doped cathode catalysts has attracted considerable interest for electrochemical advanced oxidation processes(EAOPs)due to its high performance and sustainable synthesis.Herein,we illustrated the morphological fates of waste leaf-derived graphitic carbon(WLGC)produced from waste ginkgo leaves via pyrolysis temperature regulation and used as bifunctional cathode catalyst for simultaneous H_(2)O_(2) electrochemical generation and organic pollutant degradation,discovering S/N-self-doping shown to facilitate a synergistic effect on reactive oxygen species(ROS)generation.Under the optimum temperature of 800℃,the WLGC exhibited a H_(2)O_(2) selectivity of 94.2%and tetracycline removal of 99.3%within 60 min.Density functional theory calculations and in-situ Fourier transformed infrared spectroscopy verified that graphitic N was the critical site for H_(2)O_(2) generation.While pyridinic N and thiophene S were the main active sites responsible for OH generation,N vacancies were the active sites to produce ^(1)O_(2) from O_(2).The performance of the novel cathode for tetracycline degradation remains well under a wide pH range(3–11),maintaining excellent stability in 10 cycles.It is also industrially applicable,achieving satisfactory performance treating in real water matrices.This system facilitates both radical and non-radical degradation,offering valuable advances in the preparation of cost-effective and sustainable electrocatalysts and hold strong potentials in metal-free EAOPs for organic pollutant degradation.
基金Project supported by Ph.D.Student Research and Innovation Fund of the Fundamental Research Funds for the Central Universities(3072023GIP1005)。
文摘For the efficient electrolytic extraction of Er from spent nuclear fuel,a series of electrochemical methods was used to research the electrochemical behavior of Er(Ⅲ)in the LiCl—KCl system on inert(Mo)electrode and on reactive(Ni)electrodes.On the inert Mo electrode,the reduction of Er(Ⅲ)to Er(0)is a onestep with three-electron and quasi-reversible reaction process.Meanwhile,the apparent generation Gibbs free energy and activity coefficients of Er(Ⅲ)on the inert electrode were determined.Thereafter,the electrochemical reduction of Er(Ⅲ)on the Ni electrode was emphatically investigated.Er(Ⅲ)is reduced at a corrected potential owing to the formation of Ni-Er alloys.In addition,thermodynamic parameters such as partial excess Gibbs free energy change of Er in Ni,activity and apparent generation Gibbs free energy of the Ni-Er alloys were determined by the electromotive force method.Finally,different Ni-Er alloys were produced using potentiostatic electrolysis on the Ni cathode by controlling different potentials,Moreover,electrolytic extraction was carried out on the Ni cathode at the potential of-2.0 V,and the separation efficiency of Er reaches 99.72%,which proves the practicability of separating Er from LiCl-KCl eutectic on the reactive Ni cathode.
基金Project(200800560002)supported by the Ph.D.Programs Foundation of Ministry of Education of China
文摘Effects of citrate concentration and pH on the electrochemical reduction process of Co（Ⅱ） were investigated by cyclic voltammetry（CV） and electrochemical impedance spectroscopy（EIS）. The results show that Co（Ⅱ） is reduced into two species which are free Co2＋ and [Co（C6H607）] in the solution composed of 0.05 mol/L CoS04·5H2O, 0.20 mol/L Na2SO4 and 0-0.40 mol/L C6H5O7Na3·2H2O in the pH range of 3-9. The reduction behavior depends on the pH of the solution. Co（H） is mainly reduced into the form of free Co^2＋ at pH 3 and into the form of [Co（C6H6O7）] at the pH range of 4-6 in citrate solution. The [Co（C6H6O7）] is first reduced to an intermediate state and then to Co°. Adsorption of the intermediate state exists on the surface of the electrode. Co（Ⅱ） is difficult to be reduced in the solution with the pH above 7, because the existing Co（Ⅱ）-citrate complex species [Co（C6H5O7）]- and [Co（C6H4O7）]2- are more difficult to be reduced than the hydrogen ion.
基金supported by the introduction of Talent Research Fund in Nanjing Institute of Technology(YKJ202204)the National Natural Science Foundation of China(52401282 and 52300206)the Natural Science Foundation of Jiangsu Province(BK20230701 and BK20230705).
文摘Achieving high-energy density remains a key objective for advanced energy storage systems.However,challenges,such as poor cathode conductivity,anode dendrite formation,polysulfide shuttling,and electrolyte degradation,continue to limit performance and stability.Molecular and ionic dipole interactions have emerged as an effective strategy to address these issues by regulating ionic transport,modulating solvation structures,optimizing interfacial chemistry,and enhancing charge transfer kinetics.These interactions also stabilize electrode interfaces,suppress side reactions,and mitigate anode corrosion,collectively improving the durability of high-energy batteries.A deeper understanding of these mechanisms is essential to guide the design of next-generation battery materials.Herein,this review summarizes the development,classification,and advantages of dipole interactions in high-energy batteries.The roles of dipoles,including facilitating ion transport,controlling solvation dynamics,stabilizing the electric double layer,optimizing solid electrolyte interphase and cathode–electrolyte interface layers,and inhibiting parasitic reactions—are comprehensively discussed.Finally,perspectives on future research directions are proposed to advance dipole-enabled strategies for high-performance energy storage.This review aims to provide insights into the rational design of dipole-interactive systems and promote the progress of electrochemical energy storage technologies.
基金supported by Chinese National Science and Technology Infrastructure Platforms Construction Project (No.2005DKA10400)Major Foundation in the Tenth Five-Year Development Plan of China (No.50499333-08)
文摘Stress corrosion cracking （SCC） of X70 pipeline steel in simulated solution of the acidic soil in Yingtan in China was investigated using slow strain rate test （SSRT）, SEM and potentiodynamic polarization technique. Experiment results indicate that X70 steel is highly susceptible to SCC as applied potential reduces, which is manifested in loss of toughness and brittle fracture. Constaat polarization current can detect the occurrence of SCC. The lower the polarization current is the sooner stress corrosion cracking occurs. The SCC mechanisms are different at varying potentials. When potential is higher than open circuit potential, anodic process controls SCC, whereas when potential is far lower than open circuit potential, cathodic process controls SCC, and between these two potential regions, a combined electrochemical process controls the SCC. Stress or strain has a synergistic effect with electrochemical reactions to accelerate the cathodic hydrogen evolution process, which makes the X70 pipeline steel to be more susceptible to SCC.
基金the National Natural Science Foundation of China(No.51725401)the Fundamental Research Funds for the Central Universities(No.FRT-TP-18-003C2)。
文摘Graphite materials are widely used as electrode materials for electrochemical energy storage.N-doping is an effective method for enhancing the electrochemical properties of graphite.A novel one-step N-doping method for complete and compact carbon paper was proposed for molten salt electrolysis in the Li Cl-KCl-Li3 N system.The results show that the degree of graphitization of carbon paper can be improved by the electrolysis of molten salts,especially at 2.0 V.Nitrogen gas was produced at the anode and nitrogen atoms can substitute carbon atoms of carbon paper at different sites to create nitrogen doping during the electrolysis process.The doping content of N in carbon paper is up to 13.0 wt%.There were three groups of nitrogen atoms,i.e.quaternary N(N-Q),pyrrolic N(N-5),and pyridinic N(N-6)in N-doping carbon paper.N-doping carbon paper as an Al-ion battery cathode shows strong charge-recharge properties.
文摘A novel electrochemical setup for wastewater treatment-rotating electrochemical disc process(RECDP)was developed in this article. The anode and cathode are distributed alternatively and evenly on a flat round disc,which was designed to improve mass transfer of organics from bulk solution to electrode surface,while at the same time increasing oxygen transfer from air to the liquid to benefit the organics oxidization.The color removal of dye Reactive Brilliant Orange X-GN(RBO)was experimentally investigated u...
基金This study was financially supported by National Science Foundation(Nos.41907294,52000028 and 51878169)the Guangdong Innovation Team Project for Colleges and Universities(No.2016KCXTD023).
文摘Electrochemical oxidation of aqueous tris(1,3-dichloro-2-propyl)phosphate(TDCPP)by using Ti/SnO_(2)-Sb/La-PbO_(2)as anode was investigated for the first time,and the degradation mechanisms and toxicity changes of the degradation intermediates were further determined.Results suggested that electrochemical degradation of TDCPP followed pseudo-first-order kinetics,and the reaction rate constant(k)was 0.0332 min^(−1)at the applied current density of 10 mA/cm^(2)and Na_(2)SO_(4)concentration of 10 mmol/L.There was better TDCPP degradation performance at higher current density.Free hydroxy radical(•OH)was proved to play dominant role in TDCPP oxidation via quenching experiment,with a relative contribution rate of 60.1%.A total of five intermediates(M1,C_(6)H_(11)Cl_(4)O_(4)P;M2,C_(3)H_(7)Cl_(2)O_(4)P;M3,C_(9)H_(16)Cl_(5)O_(5)P;M4,C_(9)H_(14)Cl_(5)O_(6)P;M5,C_(6)H_(10)Cl_(3)O_(6)P)were identified,and the intermediates were further degraded prolonging with the reaction time.Flow cytometer results suggested that the toxicity of TDCPP and degradation intermediates significantly reduced,and the detoxification efficiency was achieved at 78.1%at 180 min.ECOSAR predictive model was used to assess the relative toxicity of TDCPP and the degradation intermediates.The EC_(50)to green algae was 3.59 mg/L for TDCPP,and the values raised to 84,574,54.6,391,and 8920 mg/L for M1,M2,M3,M4,and M5,respectively,indicating that the degradation intermediates are less toxic or not toxic.Electrochemical advanced oxidation process is a valid technology to degrade TDCPP and pose a good detoxification effect.
基金Natural Science Foundation of Hebei Province(China),Grant/Award Numbers:B2020203013,B2021203016Science and Technology Project of Hebei Education Department(China),Grant/Award Number:QN2020137+3 种基金Cultivation Project for Basic Research Innovation of Yanshan University(China),Grant/Award Number:2021LGZD015Subsidy for Hebei Key Laboratory of Applied Chemistry after Operation Performance(China),Grant/Award Number:22567616HNatural Science Foundation of Heilongjiang Province(China),Grant/Award Number:LH2022B025Fundamental Research Funds for the Provincial Universities of Heilongjiang Province(China),Grant/Award Number:KYYWF10236190104。
文摘Colorless‐to‐black switching has attracted widespread attention for smart windows and multifunctional displays because they are more useful to control solar energy.However,it still remains a challenge owing to the tremendous difficulties in the design of completely reverse absorptions in transmissive and colored states.Herein,we report on an electrochemical device that can switch between colorless and black by using the electrochemical process of hybrid organic–inorganic perovskite MAPbBr_(3),which shows a high integrated contrast ratio of up to 73%from 400 to 800 nm.The perovskite solution can be used as the active layer to assemble the device,showing superior transmittance over the entire visible region in neutral states.By applying an appropriate voltage,the device undergoes reversible switching between colorless and black,which is attributed to the formation of lead and Br_(2)in the redox reaction induced by the electron transfer process in MAPbBr_(3).In addition,the contrast ratio can be modulated over the entire visible region by changing the concentration and the applied voltage.These results contribute toward gaining an insightful understanding of the electrochemical process of perovskites and greatly promoting the development of switchable devices.
基金Supported by the National Basic Research Program of China(2014CB239703)the National Natural Science Foundation of China(21336003)the Science and Technology Commission of Shanghai Municipality(14DZ2250800)
文摘This review focuses on the application of process engineering in electrochemical energy conversion and storage devices innovation. For polymer electrolyte based devices, it highlights that a strategic simple switch from proton exchange membranes(PEMs) to hydroxide exchange membranes(HEMs) may lead to a new-generation of affordable electrochemical energy devices including fuel cells, electrolyzers, and solar hydrogen generators. For lithium-ion batteries, a series of advancements in design and chemistry are required for electric vehicle and energy storage applications. Manufacturing process development and optimization of the LiF eP O_4/C cathode materials and several emerging novel anode materials are also discussed using the authors' work as examples.Design and manufacturing process of lithium-ion battery electrodes are introduced in detail, and modeling and optimization of large-scale lithium-ion batteries are also presented. Electrochemical energy materials and device innovations can be further prompted by better understanding of the fundamental transport phenomena involved in unit operations.
基金Supported by the National Natural Science Foundation of China(51275180)the Fundamental Research Funds for the Central Universities(2013ZM0003)the Doctorate Dissertation Funds of Guangdong Province(sybzzxm 201213)
文摘Superhydrophilic surfaces were fabricated on copper substrates by an electrochemical deposition and sintering process. Superhydrophobic surfaces were prepared by constructing micro/nano-structure on copper substrates through an electrochemical deposition method. Conversion from superhydrophobic to superhydrophilic was obtained via a suitable sintering process. After reduction sintering, the contact angle of the superhydrophilic surfaces changed from 155° to 0°. The scanning electron microscope （SEM） images show that the morphology of superhydrophobic and superhydrophilic surfaces looks like corals and cells respectively. The chemical composition and crystal structure of these surfaces were examined using energy dispersive spectrometry （EDS） and X-ray diffraction （XRD）. The results show that the main components on superhydrophobic surfaces are Cu, Cu2O and CuO, while the superhydrophilic surfaces are composed of Cu merely. The crystal structure is more inerratic and the grain size becomes bigger after the sintering. The interracial strength of the superhydrophilic surfaces was investigated, showing that the interfacial strength between superhydrophilic layer and copper substrate is considerably high.
基金the program of fundamental scientific researches of the Russian Academy of Sciences (project No. 0265-2014-0001)the support of the Russian Science Foundation (project No. 14-33-00009)+1 种基金the Government of the Russian Federation (the Federal Agency of Scientific Organizations)supported by the BP grant (A.A. Sokolov is superviser, competition for 2016–2017 years) for young researchers, postgraduates, and students
文摘A series of nanostructured Zr-doped anatase TiO_2 tubes with the Zr/Ti molar ratio of 0.01, 0.02, 0.03, and0.09 were prepared by a sol–gel technology on a carbon fiber template. The electrochemical performance of Zr-doped anatase TiO_2 as anodes for rechargeable lithium batteries was investigated and compared with undoped titania. Tests represented that after 35-fold charge/discharge cycling at C/10 the reversible capacity of Zr-doped titania（Zr/Ti = 0.03） reaches 135 m A h g^（-1）, while the capacity of undoped titania（Zr/Ti = 0） yielded only 50 m A h g^（-1）. Based on the results of the physicochemical investigation, three reasons of improving electrochemical performance of Zr-doped titania were suggested. According to the scanning electron microscopy and transmission electron microscopy, Zr^（4＋） doping induces a decrease in nanoparticle size, which facilitates the Li＋diffusion. The Raman investigations show the more open structure of Zr-doped TiO_2 as compared to undoped titania due to changing of the unit cell parameters, that significantly affects on the reversibility of the insertion/extraction process. The electrochemical impedance spectroscopy results indicate that substitution of Zr^（4＋） for Ti^（4＋） into anatase TiO_2 has favorable effects on the conductivity.
基金Funded by the National High Technology Research and Development Program of China (Key Project) (2001AA 331050) and the Chongqing Applied Fundamental Research (7941-2).
文摘The Mg-based hydrogen storage alloys Mg2Ni, Mg2Ni0.7Fe0.3 and Mgl.7Alo.3Ni were successfully synthesized by a two-step process （sintering and ball milling）. The crystal structure and microstructure were examined by X-ray diffraction, Scanning Electron Microscope and Malvern particle size analyzer. New phase appears in the tripe alloys doped with A1 and Fe, and the particle size ranges from 3μm to 5 μm. The electrochemical performance studies indicate that the partial substitution of AI for Mg, and Fe for Ni significantly improve the cycle life, reversibility of hydrogen absorption and desorption. The diffusion process is the control step in the electrode reaction of hydrogen storage alloys.
基金Project supported by the National Natural Science Foundation of China (No. 81000462)the Zhejiang Provincial Natural Science Foundation (No. R2110374),China
文摘Objective:The purpose of this study was to investigate the effects of a zinc-substituted nano-hydroxyapatite(Zn-HA) coating,applied by an electrochemical process,on implant osseointegraton in a rabbit model.Methods:A Zn-HA coating or an HA coating was deposited using an electrochemical process.Surface morphology was examined using field-emission scanning electron microscopy.The crystal structure and chemical composition of the coatings were examined using an X-ray diffractometer(XRD) and Fourier transform infrared spectroscopy(FTIR).A total of 78 implants were inserted into femurs and tibias of rabbits.After two,four,and eight weeks,femurs and tibias were retrieved and prepared for histomorphometric evaluation and removal torque(RTQ) tests.Results:Rod-like HA crystals appeared on both implant surfaces.The dimensions of the Zn-HA crystals seemed to be smaller than those of HA.XRD patterns showed that the peaks of both coatings matched well with standard HA patterns.FTIR spectra showed that both coatings consisted of HA crystals.The Zn-HA coating significantly improved the bone area within all threads after four and eight weeks(P<0.05),the bone to implant contact(BIC) at four weeks(P<0.05),and RTQ values after four and eight weeks(P<0.05).Conclusions:The study showed that an electrochemically deposited Zn-HA coating has potential for improving bone integration with an implant surface.
基金supported by the National Natural Science Foundation of China(Nos.22225202,92356309,22132007,21991132,22172002)。
文摘Surface chemistry focuses on the investigation of the adsorption,migration,assembly,activation,reaction,and desorption of atoms and molecules at surfaces.Surface chemistry plays the pivotal roles in both fundamental science and applied technology.This review will summarize the recent progresses on surface assembly,synthesis and catalysis investigated mainly by scanning tunneling microscopy and atomic force microscopy.Surface assemblies of water and small biomolecules,construction of Sierpin′ski triangles and surface chirality are summarized.On-surface synthesis of conjugated carbo-and heterocycles and other kinds of carbon nanostructures are surveyed.Surface model catalysis,including single-atom catalysis and electrochemical catalysis,are discussed at the single-atom level.
基金funded by the Princess Nourah bint Abdulrahman University Researchers Supporting Project number(PNURSP2024R24),Princess Nourah bint Abdulrahman University,Riyadh,Saudi Arabiafunding from the Prince Sattam bin Abdulaziz University project number(PSAU/2023/R/1444).
文摘In this article,we looked at metallenes,a novel class of two-dimensional(2D)metals that are attracting interest in the energy and catalysis sectors.Catalysis is one area where their exceptional physicochemical and electrical characteristics might be useful.Metallenes are unique because they include several metal atoms that are not in a coordinated bond.This makes them more active and improves their atomic uti-lization,which in turn increases their catalytic potential.This article delves into the potential of two-dimensional metals as electrocatalysts for carbon dioxide reduction,fuel oxidation,oxygen evolution,and oxygen reduction reactions in the context of sustainable energy conversion.Owing to the exception-ally high surface-to-volume ratio,large surface area as well as their optimized atomic use efficiency,2D materials defined by atomic layers are crucial for surface-related sustainable energy applications.Due to its exceptional properties,such as high conductivity and the ability to enhance the exposure of active metal sites,2D metallenes have recently attracted a lot of interest for use in catalysis,electronics,and energy-related applications.With their highly mobility,adjustable surface states,and electrical struc-tures that can be fine-tuned,2D metallenes are promising nanostructure materials for use in energy con-version with the sustainable applications.
基金the support from the Brook Byers Institute for Sustainable Systems,Hightower ChairGeorgia Research Alliance at the Georgia Institute of Technology。
文摘TiO_(2)has demonstrated outstanding performance in electrochemical advanced oxidation processes(EAOPs)due to its structural stability and high oxygen overpotential.However,there is still much room for improving its electrochemical activity.Herein,narrow bandgap manganese oxide(MnO_(x))was composited with TiO_(2)nanotube arrays(TiO_(2)NTAs)that in-situ oxidized on porous Ti sponge,forming the MnO_(x)-TiO_(2)NTAs anode.XANES and XPS analysis further proved that the composition of MnO_(x)is Mn2O3.Electrochemical characterizations revealed that increasing the composited concentration of MnO_(x)can improve the conductivity and reduce oxygen evolution potential so as to improve the electrochemical activity of the composited MnO_(x)-TiO_(2)NTAs anode.Meanwhile,the optimal degradation rate of benzoic acid(BA)was achieved using MnO_(x)-TiO_(2)NTAs with a MnO_(x)concentration of 0.1 mmol L^(-1),and the role of MnO_(x)was proposed based on DFT calculation.Additionally,the required electrical energy(EE/O)to destroy BA was optimized by varying the composited concentration of MnO_(x)and the degradation voltage.These quantitative results are of great significance for the design and application of high-performance materials for EAOPs.
文摘The electrochemical process of Ti-Ni alloy electrode was studied by using cyclic voltammetry. The hydrogen-absorbing electrode could be approximately regarded as a reversible hydrogen elecrede. The con- trolling steps of the discharging process varying with the anodic overpotentials were investigated and the effect ofelecrode constituent modification or Zr adulteation on the electrochemical behavior was also studied.
基金financial support from the Science and Technology Development Fund of Egypt (No.5540)。
文摘Integrating titanium-based implants with the surrounding bone tissue remains challenging.This study aims to explore the impact of different anodization voltages(20−80 V)on the surface topography of two-phase(α/β)Ti alloys and to produce TiO_(2) films with enhanced bone formation abilities.Scanning electron microscopy coupled with energy dispersive spectroscopy(SEM−EDS)and atomic force microscopy(AFM)were applied to investigate the morphological,chemical,and surface topography of the prepared alloys and to confirm the growth of hydroxyapatite(HA)on their surfaces.Results disclosed that the surface roughness of TiO_(2) films formed on Ti−6Al−7Nb alloys was superior to that of Ti−6Al−4V alloys.Ti−6Al−7Nb alloy anodized at 80 V had the highest yields of HA after immersion in simulated body fluid with enhanced HA surface coverage.The developed HA layer had a mean thickness of(128.38±18.13)μm,suggesting its potential use as an orthopedic implantable material due to its promising bone integration and,hence,remarkable stability inside the human body.
基金supported by the Jiangsu Province Carbon Peak and Neutrality Innovation Program (Industry Tackling on Prospect and Key Technology)(BE2022031-4,BE2022002-3)the National Natural Science Foundation of China (52173173,22572087)the State Key Laboratory of Materials-Oriented Chemical Engineering (SKL-MCE-24A16)。
文摘The development of differential electrochemical mass spectrometry (DEMS) originated in the late 20th century[1–4],with its core objective being the integration of electrochemical processes with mass spectrometric detection to enable real-time tracking of reaction intermediates and products at the electrodes [5,6].DEMS was initially employed to study electrochemical processes in aqueous solutions,such as methanol oxidation [7].Recently,with the rapid development of new energy technologies,DEMS has been widely applied in the research and development of electrocatalysis,lithium-ion,sodium-ion,and metal-air batteries[8–16].
