Pulsed dynamic electrolysis(PDE),driven by renewable energy,has emerged as an innovative electrocatalytic conversion method,demonstrating significant potential in addressing global energy challenges and promoting sust...Pulsed dynamic electrolysis(PDE),driven by renewable energy,has emerged as an innovative electrocatalytic conversion method,demonstrating significant potential in addressing global energy challenges and promoting sustainable development.Despite significant progress in various electrochemical systems,the regulatory mechanisms of PDE in energy and mass transfer and the lifespan extension of electrolysis systems,particularly in water electrolysis(WE)for hydrogen production,remain insufficiently explored.Therefore,there is an urgent need for a deeper understanding of the unique contributions of PDE in mass transfer enhancement,microenvironment regulation,and hydrogen production optimization,aiming to achieve low-energy consumption,high catalytic activity,and long-term stability in the generation of target products.Here,this review critically examines the microenvironmental effects of PDE on energy and mass transfer,the electrode degradation mechanisms in the lifespan extension of electrolysis systems,and the key factors in enhancing WE for hydrogen production,providing a comprehensive summary of current research progress.The review focuses on the complex regulatory mechanisms of frequency,duty cycle,amplitude,and other factors in hydrogen evolution reaction(HER)performance within PDE strategies,revealing the interrelationships among them.Finally,the potential future directions and challenges for transitioning from laboratory studies to industrial applications are proposed.展开更多
Titanium exhibits outstanding properties,particularly,high specific strength and resistance to both high and low temperatures,earning it a reputation as the metal of the future.However,because of the highly reactive n...Titanium exhibits outstanding properties,particularly,high specific strength and resistance to both high and low temperatures,earning it a reputation as the metal of the future.However,because of the highly reactive nature of titanium,metallic titanium production involves extensive procedures and high costs.Considering its advantages and limitations,the European Union has classified titanium metal as a critical raw material(CRM)of low category.The Kroll process is predominantly used to produce titanium;however,molten salt electrolysis(MSE)is currently being explored for producing metallic titanium at a low cost.Since 2000,electrolytic titanium production has undergone a wave of technological advancements.However,because of the intermediate and disproportionation reactions in the electrolytic titanium production process,the process efficiency and titanium purity according to industrial standards could not be achieved.Consequently,metallic titanium production has gradually diversified into employing technologies such as thermal reduction,MSE,and titanium alloy preparation.This study provides a comprehensive review of research advances in titanium metal preparation technologies over the past two decades,highlighting the challenges faced by the existing methods and proposing potential solutions.It offers useful insights into the development of low-cost titanium preparation technologies.展开更多
Protonic solid oxide electrolysis cells(P-SOECs)are a promising technology for water electrolysis to produce green hydrogen.However,there are still challenges related key materials and anode/electrolyte interface.P-SO...Protonic solid oxide electrolysis cells(P-SOECs)are a promising technology for water electrolysis to produce green hydrogen.However,there are still challenges related key materials and anode/electrolyte interface.P-SOECs with Zr-rich electrolyte,called Zr-rich side P-SOECs,possess high thermodynamically stability under high steam concentrations but the large reaction resistances and the current leakage,thus the inferior performances.In this study,an efficient functional interlayer Ba_(0.95)La_(0.05)Fe_(0.8)Zn_(0.2)O_(3-δ)(BLFZ)in-between the anode and the electrolyte is developed.The electrochemical performances of P-SOECs are greatly enhanced because the BLFZ can greatly increase the interface contact,boost anode reaction kinetics,and increase proton injection into electrolyte.As a result,the P-SOEC yields high current density of 0.83 A cm^(-2) at 600℃ in 1.3 Vamong all the reported Zr-rich side cells.This work not only offers an efficient functional interlayer for P-SOECs but also holds the potential to achieve P-SOECs with high performances and long-term stability.展开更多
Solid oxide electrolysis cells(SOECs)can effectively convert CO_(2)into high value-added CO fuel.In this paper,Sc-doped Sr_(2)Fe_(1.5)Mo_(0.3)Sc_(0.2)O_(6−δ)(SFMSc)perovskite oxide material is synthesized via solid-p...Solid oxide electrolysis cells(SOECs)can effectively convert CO_(2)into high value-added CO fuel.In this paper,Sc-doped Sr_(2)Fe_(1.5)Mo_(0.3)Sc_(0.2)O_(6−δ)(SFMSc)perovskite oxide material is synthesized via solid-phase method as the cathode for CO_(2)electrolysis by SOECs.XRD confirms that SFMSc exhibits a stable cubic phase crystal structure.The experimental results of TPD,TG,EPR,CO_(2)-TPD further demonstrate that Sc-doping increases the concentration of oxygen vacancy in the material and the chemical adsorption capacity of CO_(2)molecules.Electrochemical tests reveal that SFMSc single cell achieves a current density of 2.26 A/cm^(2) and a lower polarization impedance of 0.32Ω·cm^(2) at 800°C under the applied voltage of 1.8 V.And no significant performance attenuation or carbon deposition is observed after 80 h continuous long-term stability test.This study provides a favorable support for the development of SOEC cathode materials with good electro-catalytic performance and stability.展开更多
The transition of hydrogen sourcing from carbon-intensive to water-based methodologies is underway,with renewable energy-powered proton exchange membrane water electrolysis(PEMWE)emerging as the preeminent pathway for...The transition of hydrogen sourcing from carbon-intensive to water-based methodologies is underway,with renewable energy-powered proton exchange membrane water electrolysis(PEMWE)emerging as the preeminent pathway for hydrogen production.Despite remarkable advancements in this field,confronting the sluggish electrochemical kinetics and inherent high-energy consumption arising from deteriorated mass transport within PEMWE systems remains a formidable obstacle.This impediment stems primarily from the hindered protons mass transfer and the untimely hydrogen bubbles detachment.To address these challenges,we harness the inherent variability of electrical energy and introduce an innovative pulsed dynamic water electrolysis system.Compared to constant voltage electrolysis(hydrogen production rate:51.6 m L h^(-1),energy consumption:5.37 kWh Nm-^(3)H_(2)),this strategy(hydrogen production rate:66 m L h^(-1),energy consumption:3.83 kWh Nm-^(3)H_(2))increases the hydrogen production rate by approximately 27%and reduces the energy consumption by about 28%.Furthermore,we demonstrate the practicality of this system by integrating it with an off-grid photovoltaic(PV)system designed for outdoor operation,successfully driving a hydrogen production current of up to 500 mA under an average voltage of approximately 2 V.The combined results of in-situ characterization and finite element analysis reveal the performance enhancement mechanism:pulsed dynamic electrolysis(PDE)dramatically accelerates the enrichment of protons at the electrode/solution interface and facilitates the release of bubbles on the electrode surface.As such,PDE-enhanced PEMWE represents a synergistic advancement,concurrently enhancing both the hydrogen generation reaction and associated transport processes.This promising technology not only redefines the landscape of electrolysis-based hydrogen production but also holds immense potential for broadening its application across a diverse spectrum of electrocatalytic endeavors.展开更多
Sodium(Na)and magnesium(Mg)are becoming important for making energy-storage batteries and structural materials.Herein,we develop a liquid-metal-electrode-assisted electrolysis route to producing Na and Mg with low-car...Sodium(Na)and magnesium(Mg)are becoming important for making energy-storage batteries and structural materials.Herein,we develop a liquid-metal-electrode-assisted electrolysis route to producing Na and Mg with low-carbon emissions and no chlorine gas evolution.The clean production stems from the choice of a molten NaCl-Na_(2)CO_(3) electrolyte to prevent chlorine gas evolution,an inert nickel-based anode to produce oxygen,and a liquid metal cathode to make the cathodic product sit at the bottom of the electrolytic cell.We achieve a current efficiency of>90%for the electrolytic production of liquid Na-Sn alloy.Later,Mg-Sn alloy is prepared using the obtained Na-Sn alloy to displace Mg from molten NaCl-MgCl_(2) with a displacement efficiency of>96%.Further,Na and Mg are separated from the electrolytic Na-Sn and displaced Mg-Sn alloys by vacuum distillation with a recovery rate of>92%and Sn can be reused.Using this electrolysisdisplacement-distillation(EDD)approach,we prepare Mg from seawater.The CO_(2)emission of the EDD approach is~20.6 kg CO_(2)per kg Mg,which is less than that of the Australian Magnesium(AM)electrolysis process(~25.0 kg CO_(2)per kg Mg)and less than half that of the Pidgeon process(~45.2 kg CO_(2)per kg Mg).展开更多
Developing heterojunction catalysts with diverse adsorption sites presents significant opportunities to enhance the performance of urea-assisted water electrolysis.Herein,we highlighted a NiTe/Mo_(6)Te_(8)heterojuncti...Developing heterojunction catalysts with diverse adsorption sites presents significant opportunities to enhance the performance of urea-assisted water electrolysis.Herein,we highlighted a NiTe/Mo_(6)Te_(8)heterojunction catalyst confined in carbon nanofiber with spontaneous charge redistribution driven by high valent metal,which promotes the adsorption and transformation of intermediates and greatly reduces the reaction energy barrier for urea oxidation.The heterojunction catalyst promotes the formation of Ni^(3+)active species and accelerates the fracture of the C-N bond by enhancing selective adsorption of-NH_(2)and C=O groups in binding urea molecules driven by the spontaneous formation of nucleophilic and electrophilic sites.The catalyst achieves a low kinetic current density of 10 mA cm^(-2)at 1.35 V with a cell voltage for urea electrolysis of just 1.47 V and good durability over 60 h.Density-functional theory and in-situ spectral observation reveal that the high valent Mo promoted the 3d orbit of Ni approaching the Fermi level by adjusting the electronic structure,which enhanced spontaneous urea dehydrogenation and reduced the energy barrier for^(*)COO desorption.This study highlights the effectiveness of modulating the interfacial electronic structure to improve energy conversion efficiency.展开更多
This work investigates the transient performance and stability of CO_(2)/H_(2)O co-electrolysis in an air-free environment using a flat-tube solid oxide electrolysis cell(SOEC)stack.The results showed that the transie...This work investigates the transient performance and stability of CO_(2)/H_(2)O co-electrolysis in an air-free environment using a flat-tube solid oxide electrolysis cell(SOEC)stack.The results showed that the transient behavior of the stack with and without blowing gas into the air electrode is almost the same.With a current density of 0.67 A·cm^(-2)@750℃,the stack operated for over 200 h under co-electrolysis conditions without air blowing,and the voltage drop rate of the stack was approximately 0.203%/100 hours.Microstructure analysis revealed a significant loss of nickel particles and an apparent for-mation of an insulating phase strontium chromate(SrCrO4)on the surface of the current collection layer of the air electrode,which are identified as key factors contributing to the performance degradation of the stack.This study provides a reference for development of efficient fuel preparation technology based on SOEC stack in airless environments.展开更多
Atomically dispersed metal site(ADMS)materials have emerged as a promising class of materials for electrocatalysis reactions in the field of energy conversion.Characterized by individual metal atoms dispersed on suita...Atomically dispersed metal site(ADMS)materials have emerged as a promising class of materials for electrocatalysis reactions in the field of energy conversion.Characterized by individual metal atoms dispersed on suitable supports,ADMS materials provide unique catalytic sites with highly tunable electronic structures.This review summarizes recent advancements in the field,with a focus on the critical roles of support materials,coordination environments,and the mechanisms underlying catalytic activity at the atomic level.First,commonly used density functional theory(DFT)simulations are reviewed,emphasizing their pivotal role in elucidating reaction mechanisms and predicting the behavior of ADMS in electrochemical reactions for hydrogen energy utilization.Then,advancements in ADMS for half-cell electrochemical reactions,including oxygen evolution reaction,hydrogen evolution reaction,and oxygen reduction reaction,as well as their applications in fuel cells and water splitting,are summarized.Finally,the challenges and future prospects of ADMS are discussed.This review underscores the transformative potential of ADMS in electrocatalysis,paving the way for innovative and sustainable energy conversion technologies.展开更多
Electrocatalytic carbon dioxide reduction is a promising technology for addressing global energy and environmental crises. However, its practical application faces two critical challenges: the complex and energy-inten...Electrocatalytic carbon dioxide reduction is a promising technology for addressing global energy and environmental crises. However, its practical application faces two critical challenges: the complex and energy-intensive process of separat-ing mixed reduction products and the economic viability of the carbon sources (reactants) used. To tackle these challenges simultaneously, solid-state electrolyte (SSE) reactors are emerging as a promising solution. In this review, we focus on the feasibility of applying SSE for tandem electrochemical CO_(2) capture and conversion. The configurations and fundamental principles of SSE reactors are first discussed, followed by an introduction to its applications in these two specific areas, along with case studies on the implementation of tandem electrolysis. In comparison to conventional H-type cell, flow cell and membrane electrode assembly cell reactors, SSE reactors incorporate gas diffusion electrodes and utilize a solid electro-lyte layer positioned between an anion exchange membrane (AEM) and a cation exchange membrane (CEM). A key inno-vation of this design is the sandwiched SSE layer, which enhances efficient ion transport and facilitates continuous product extraction through a stream of deionized water or humidified nitrogen, effectively separating ion conduction from product collection. During electrolysis, driven by an electric field and concentration gradient, electrochemically generated ions (e.g., HCOO- and CH3COO-) migrate through the AEM into the SSE layer, while protons produced from water oxidation at the anode traverse the CEM into the central chamber to maintain charge balance. Targeted products like HCOOH can form in the middle layer through ionic recombination and are efficiently carried away by the flowing medium through the porous SSE layer, in the absence of electrolyte salt impurities. As CO_(2)RR can generate a series of liquid products, advancements in catalyst discovery over the past several years have facilitated the industrial application of SSE for more efficient chemicals production. Also noteworthy, the cathode reduction reaction can readily consume protons from water, creating a highly al-kaline local environment. SSE reactors are thereby employed to capture acidic CO_(2), forming CO_(3)^(2-) from various gas sources including flue gases. Driven by the electric field, the formed CO_(3)^(2-) can traverse through the AEM and react with protons originating from the anode, thereby regenerating CO_(2). This CO_(2) can then be collected and utilized as a low-cost feedstock for downstream CO_(2) electrolysis. Based on this principle, several cell configurations have been proposed to enhance CO_(2) capture from diverse gas sources. Through the collaboration of two SSE units, tandem electrochemical CO_(2) capture and con-version has been successfully implemented. Finally, we offer insights into the future development of SSE reactors for prac-tical applications aimed at achieving carbon neutrality. We recommend that greater attention be focused on specific aspects, including the fundamental physicochemical properties of the SSE layer, the electrochemical engineering perspective related to ion and species fluxes and selectivity, and the systematic pairing of consecutive CO_(2) capture and conversion units. These efforts aim to further enhance the practical application of SSE reactors within the broader electrochemistry community.展开更多
The performance of solid oxide electrolysis cells(SOECs)for CO_(2) electrolysis is significantly impeded by the limited electrochemical activity and insufficient durability of the cathode.This study introduces a novel...The performance of solid oxide electrolysis cells(SOECs)for CO_(2) electrolysis is significantly impeded by the limited electrochemical activity and insufficient durability of the cathode.This study introduces a novel(LaSrPrBaCaGd)_(2)Fe_(1.5)Mo_(0.5)O_(6-δ)(LSPBCGFM)perovskite via A-site entropy engineering,to improve both activity and durability.Experimental results reveal that LSPBCGFM cathode-based SOEC achieves a current density of 1.34 A·cm^(−2) at 1.5 V and 800℃,maintaining stable operation for more than 400 h at 1.2 V with negligible degradation.Theoretical calculations suggest that the high-entropy strategy shifts the transition metal d-band center and O-2p-band center closer to the Fermi energy level simultaneously,thereby initiating more favorable CO_(2) adsorption and activation.In addition,a higher O-2p-band center promotes the formation and diffusion of oxygen vacancies.The findings of this study provide crucial insights into the role of conformational entropy strategies in CO_(2) electrolysis and offer potential pathways for the development of highly efficient and stable catalysts.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
Seawater electrolysis offers a promising pathway to generate green hydrogen,which is crucial for the net-zero emission targets.Indirect seawater electrolysis is severely limited by high energy demands and system compl...Seawater electrolysis offers a promising pathway to generate green hydrogen,which is crucial for the net-zero emission targets.Indirect seawater electrolysis is severely limited by high energy demands and system complexity,while the direct seawater electrolysis bypasses pre-treatment,offering a simpler and more cost-effective solution.However,the chlorine evolution reaction and impurities in the seawater lead to severe corrosion and hinder electrolysis’s efficiency.Herein,we review recent advances in the rational design of chlorine-suppressive catalysts and integrated electrolysis systems architectures for chloride-induced corrosion,with simultaneous enhancement of Faradaic efficiency and reduction of electrolysis’s cost.Furthermore,promising directions are proposed for durable and efficient seawater electrolysis systems.This review provides perspectives for seawater electrolysis toward sustainable energy conversion and environmental protection.展开更多
CO_(2)electrolysis using solid oxide electrolysis cells is a promising technology for CO_(2)utilization and conversion,which has attracted more and more attention in recent years because of its extremely high efficien...CO_(2)electrolysis using solid oxide electrolysis cells is a promising technology for CO_(2)utilization and conversion,which has attracted more and more attention in recent years because of its extremely high efficiency.However,traditional Ni-yttria-stabilized zirconia(Ni-YSZ)or Ni-Gd_(0.1)Ce_(0.9)O_(2-δ)(Ni-GDC)metal-ceramic cathode faces many problems such as Ni agglomeration and carbon deposition during long-time operation.Herein,a perovskite oxide La_(0.43-x)Ca_(0.37)Ti_(0.9)Ni_(0.1)O_(3-δ)(LCTN,x=0,0.05,0.1)with nanophase-LaVO_(4)exsolution was investigated as the novel cathode of solid oxide electrolysis cell(SOEC)for efficient CO_(2)electrolysis.The results confirm that the exsolution nanophase on LCTN surface can significantly improve the CO_(2)adsorption and conversion performance.For CO_(2)electrolysis at 1.8 V,an electrolysis current density of 1.24 A/cm2at 800℃can be obtained on SOEC with La_(0.43-x)Ca_(0.37)Ti_(0.9)Ni_(0.1)O_(3-δ)decorated with LaVO_(4)(LCTN-V0.05)cathode.Furthermore,the corresponding cell can maintain stable operation up to 100 h without apparent performance degradation.These results demonstrate that doping-induced second nanophase exsolution is a promising way to design high-performance SOEC cathodes for CO_(2)electrolysis.展开更多
Using abundant saline water for electrolysis,rather than limited freshwater,presents a promising technique for generating clean hydrogen energy.However,high concentration of corrosive chloride ions in saline water pos...Using abundant saline water for electrolysis,rather than limited freshwater,presents a promising technique for generating clean hydrogen energy.However,high concentration of corrosive chloride ions in saline water poses a great challenge in the stability of anode.In this study,we present a straightforward strategy to protect the anode from corrosion by patching the catalyst layer through a treatment of the anode with a sodium sulfide(Na2S) solution followed by electrochemical activation.The rapid sulfurization of the Ni electrode in Na2S results in the formation of a Na2S layer,which can subsequently be converted to NiOOH upon electrochemical activation,thereby shielding the inner Ni electrode from corrosion.The as-prepared electrode (P-NiFe-LDH/Ni) based on the strategy demonstrated stability over 3,500 h at an industrial current density of 0.5 A cm^(-2)in a 0.5 M NaCl and 1 M KOH solution.This study presents an effective strategy to significantly enhance the stability of anodes for saline water electrolysis by effectively patching the cracks in the catalyst layer.展开更多
Traditional pyrometallurgical and hydrometallurgical methods to extract bismuth from sulfide ores face problems such as high cost,low-concentration SO_(2)generation,and long process time.In this study,the cyclone tech...Traditional pyrometallurgical and hydrometallurgical methods to extract bismuth from sulfide ores face problems such as high cost,low-concentration SO_(2)generation,and long process time.In this study,the cyclone technology and slurry electrolysis method were combined.The bismuth sulfide ore was dissolved directly at the anode,while the high purity bismuth was deposited efficiently at the cathode under the advantages of the two methods.The short process and high-efficiency extraction of bismuth sulfide ore were realized,and the pollution of low-concentration SO_(2)was avoided.Then,the effects of several crucial experimental conditions(current density,reaction time,temperature,pH,liquid-solid ratio,and circulation flow rate)on the leaching efficiency and recovery efficiency of bismuth were investigated.The leaching and electrowinning mechanisms during the recovery process were also analyzed according to the research results of this paper to better understand the cyclone slurry electrolysis process.The experimental results showed that 95.19%bismuth was leached into the acid solution in the anode area under optimal conditions,and the recovery efficiency and purity of bismuth on the cathode reached 91.13%and 99.26%,respectively,which were better than those by the traditional hydrometallurgy recovery process.展开更多
The effect of iron concentration on the microstructural and structural properties of ZnO for electrolysis and photodetector applications was investigated.The thin layers of un-doped and doped ZnO with different percen...The effect of iron concentration on the microstructural and structural properties of ZnO for electrolysis and photodetector applications was investigated.The thin layers of un-doped and doped ZnO with different percentages of Fe(2,4,and 6 wt.%)were deposited by spin-coating on glass substrates.Sample characterization was done by X-ray diffraction(XRD),atomic force microscopy(AFM),scanning electron microscopy(SEM),energy-dispersive X-ray spectroscopy(EDS),UV−Vis absorption spectra and X-ray photoelectron spectroscopy(XPS).Structural measurements by XRD showed that all the layers were composed of polycrystallines with a hexagonal Wurtzite structure.Two new peaks were also discovered after the doping process belonging to the Fe_(2)O_(4)(400)and(440)crystal phase.Morphological analysis showed that the surface roughness values of ZnO layers ranged between 8 and 45 nm.XPS studies confirmed the presence of Fe in 3+states in ZnO layers.An average transmittance of 90%was measured by UV−Vis in the wavelength range of 200−900 nm.The values of the energy gap(Eg)decreased with an increase in the concentration of Fe.AFM topography results confirmed that ZnO-based thin layers had a relatively uniform surface.The efficiency of these samples has been confirmed for their use in many electrical applications,including photodetectors and electrolysis of contaminated solutions.展开更多
Integrating electrochemical upgrading of glycerol and water electrolysis is regarded as a promising and energy-saving approach for the co-production of chemicals and hydrogen.However,developing efficient electrocataly...Integrating electrochemical upgrading of glycerol and water electrolysis is regarded as a promising and energy-saving approach for the co-production of chemicals and hydrogen.However,developing efficient electrocatalyst towards this technology remains challenging.Herein,a metallic cobalt mediated molybdenum nitride heterostructural material has been exploited on nickel foam(Co@Mo_(2)N/NF)for the glycerol oxidation reaction(GOR)and hydrogen evolution reaction(HER).Remarkably,the obtained Co@Mo_(2)N/NF realizes eminent performance with low overpotential of 49 mV at 50 mA/cm^(2)for HER and high Faradaic efficiency of formate of 95.03%at 1.35 V vs.RHE for GOR,respectively.The systematic in-situ experiments reveal that the Co@Mo_(2)N heterostructure promotes the cleavage of C-C bond in glycerol by active CoOOH species and boosts the conversion of glycerol to aldehyde intermediates to formate product.Moreover,the density functional theory(DFT)calculations confirm the strong interaction at Co@Mo_(2)N interface,which contributes to the optimized water dissociation and the transformation of H^(*)to H^(2).Benefiting from those advantages,the built HER||GOR electrolyzer delivers a low voltage of 1.61 V at 50 mA/cm^(2),high Faradaic efficiency,and robust stability over 120 h for sustained and stable electrolysis.展开更多
Seawater electrolysis provides a sustainable pathway for large-scale hydrogen production without reliance on freshwater resources.However,its practical implementation is hindered by the short lifespan of anodes,primar...Seawater electrolysis provides a sustainable pathway for large-scale hydrogen production without reliance on freshwater resources.However,its practical implementation is hindered by the short lifespan of anodes,primarily caused by chlorine-induced corrosion in seawater.Herein,we present a self-sustaining anode protection strategy that remarkably enhances the durability of seawater electrolysis for efficient hydrogen production.This OH^(–)-trapping anode is designed by trapping OH^(–)within in-situ generated Lewis acid sites and structural vacancies formed via alkaline corrosion of amorphous NiMoSx.This design creates an anion-rich electrode interface with spontaneous accumulation and continuous replenishment of OH^(–)from the bulk electrolyte,ensuring long-lasting anode protection against corrosion through the electrostatic repulsion of chloride ions during operation.Simultaneously,it directs the anodic reaction along a stable adsorbate evolution mechanism with minimal metal leaching.Consequently,alkaline seawater electrolysis avoiding chlorine-induced corrosion achieves an exceptional lifespan exceeding 3,000 h under industrial current densities.By directly utilizing OH^(–)from the alkaline electrolyte for long-term anode protection,the operational complexity and cost of seawater electrolysis are significantly reduced,making it highly appealing for practical use.展开更多
Upgrading carbon dioxide(CO_(2))into value-added bulk chemicals offers a dual-benefit strategy for the carbon neutrality and circular carbon economy.Herein,we develop an integrated CO_(2) valorization strategy that sy...Upgrading carbon dioxide(CO_(2))into value-added bulk chemicals offers a dual-benefit strategy for the carbon neutrality and circular carbon economy.Herein,we develop an integrated CO_(2) valorization strategy that synergizes CO_(2)-H_(2)O co-electrolysis(producing CO/O_(2) feeds)with oxidative double carbonylation of ethylene/acetylene to synthesize CO_(2)-derived C_(4) diesters(dimethyl succinate,fumarate,and maleate).A group of versatile building blocks for manufacturing plasticizers,biodegradable polymers,and pharmaceutical intermediates.Remarkably,CO_(2) exhibits dual functionality:serving simultaneously as a CO/O_(2) source and an explosion suppressant during the oxidative carbonylation process.We systematically investigated the explosion-suppressing efficacy of CO_(2) in flammable gas mixtures(CO/O_(2),C_(2)H_(4)/CO/O_(2),and C_(2)H_(2)/CO/O_(2))across varying concentrations.Notably,the mixed gas stream from CO_(2)/H_(2)O co-electrolysis at an industrial-scale current densities of 400 mA/cm^(2),enabling direct utilization in oxidative double carbonylation reactions with exceptional compatibility and inherent safety.Extended applications were demonstrated through substrate scope expansion and gram-scale synthesis.This study establishes not only a safe protocol for oxidative carbonylation processes,but also opens an innovative pathway for sustainable CO_(2) valorization,including CO surrogate and explosion suppressant.展开更多
基金financially supported by the Key Research and Development Program of Heilongjiang Province(No.2024ZXJ03C06)National Natural Science Foundation of China(No.52476192,No.52106237)+1 种基金Natural Science Foundation of Heilongjiang Province(No.YQ2022E027)Technology Project of China Datang Technology Innovation Co.,Ltd(No.DTKC-2024-20610).
文摘Pulsed dynamic electrolysis(PDE),driven by renewable energy,has emerged as an innovative electrocatalytic conversion method,demonstrating significant potential in addressing global energy challenges and promoting sustainable development.Despite significant progress in various electrochemical systems,the regulatory mechanisms of PDE in energy and mass transfer and the lifespan extension of electrolysis systems,particularly in water electrolysis(WE)for hydrogen production,remain insufficiently explored.Therefore,there is an urgent need for a deeper understanding of the unique contributions of PDE in mass transfer enhancement,microenvironment regulation,and hydrogen production optimization,aiming to achieve low-energy consumption,high catalytic activity,and long-term stability in the generation of target products.Here,this review critically examines the microenvironmental effects of PDE on energy and mass transfer,the electrode degradation mechanisms in the lifespan extension of electrolysis systems,and the key factors in enhancing WE for hydrogen production,providing a comprehensive summary of current research progress.The review focuses on the complex regulatory mechanisms of frequency,duty cycle,amplitude,and other factors in hydrogen evolution reaction(HER)performance within PDE strategies,revealing the interrelationships among them.Finally,the potential future directions and challenges for transitioning from laboratory studies to industrial applications are proposed.
基金financial support from the Yunnan Province Key Industries Science and Technology Special Project for Colleges and UniversitiesChina(No.FWCY-QYCT2024006)+6 种基金National Natural Science Foundation of China(Nos.52104351 and 52364051)Science and Technology Major Project of Yunnan Province,China(No.202202AG050007)the Yunnan Fundamental Research ProjectsChina(No.202401AT070314)the Key Technology Research and Development Program of Shandong Province,China(No.2023CXGC010903)Central Guidance Local Scientific and Technological Development Funds,China(No.202407AB110022)Yunnan Province Xingdian Talent Support Plan Project,China。
文摘Titanium exhibits outstanding properties,particularly,high specific strength and resistance to both high and low temperatures,earning it a reputation as the metal of the future.However,because of the highly reactive nature of titanium,metallic titanium production involves extensive procedures and high costs.Considering its advantages and limitations,the European Union has classified titanium metal as a critical raw material(CRM)of low category.The Kroll process is predominantly used to produce titanium;however,molten salt electrolysis(MSE)is currently being explored for producing metallic titanium at a low cost.Since 2000,electrolytic titanium production has undergone a wave of technological advancements.However,because of the intermediate and disproportionation reactions in the electrolytic titanium production process,the process efficiency and titanium purity according to industrial standards could not be achieved.Consequently,metallic titanium production has gradually diversified into employing technologies such as thermal reduction,MSE,and titanium alloy preparation.This study provides a comprehensive review of research advances in titanium metal preparation technologies over the past two decades,highlighting the challenges faced by the existing methods and proposing potential solutions.It offers useful insights into the development of low-cost titanium preparation technologies.
基金financial support from the JSPS KAKENHI Grant-in-Aid for Scientific Research(B),No.21H02035KAKENHI Grant-in-Aid for Challenging Research(Exploratory),No.21K19017+2 种基金KAKENHI Grant-in-Aid for Transformative Research Areas(B),No.21H05100National Natural Science Foundation of China,No.22409033 and No.22409035Basic and Applied Basic Research Foundation of Guangdong Province,No.2022A1515110470.
文摘Protonic solid oxide electrolysis cells(P-SOECs)are a promising technology for water electrolysis to produce green hydrogen.However,there are still challenges related key materials and anode/electrolyte interface.P-SOECs with Zr-rich electrolyte,called Zr-rich side P-SOECs,possess high thermodynamically stability under high steam concentrations but the large reaction resistances and the current leakage,thus the inferior performances.In this study,an efficient functional interlayer Ba_(0.95)La_(0.05)Fe_(0.8)Zn_(0.2)O_(3-δ)(BLFZ)in-between the anode and the electrolyte is developed.The electrochemical performances of P-SOECs are greatly enhanced because the BLFZ can greatly increase the interface contact,boost anode reaction kinetics,and increase proton injection into electrolyte.As a result,the P-SOEC yields high current density of 0.83 A cm^(-2) at 600℃ in 1.3 Vamong all the reported Zr-rich side cells.This work not only offers an efficient functional interlayer for P-SOECs but also holds the potential to achieve P-SOECs with high performances and long-term stability.
基金supported by National Key R&D Program of China(2021YFB4001401)National Natural Science Foundation of China(52272190,22178023).
文摘Solid oxide electrolysis cells(SOECs)can effectively convert CO_(2)into high value-added CO fuel.In this paper,Sc-doped Sr_(2)Fe_(1.5)Mo_(0.3)Sc_(0.2)O_(6−δ)(SFMSc)perovskite oxide material is synthesized via solid-phase method as the cathode for CO_(2)electrolysis by SOECs.XRD confirms that SFMSc exhibits a stable cubic phase crystal structure.The experimental results of TPD,TG,EPR,CO_(2)-TPD further demonstrate that Sc-doping increases the concentration of oxygen vacancy in the material and the chemical adsorption capacity of CO_(2)molecules.Electrochemical tests reveal that SFMSc single cell achieves a current density of 2.26 A/cm^(2) and a lower polarization impedance of 0.32Ω·cm^(2) at 800°C under the applied voltage of 1.8 V.And no significant performance attenuation or carbon deposition is observed after 80 h continuous long-term stability test.This study provides a favorable support for the development of SOEC cathode materials with good electro-catalytic performance and stability.
基金National Natural Science Foundation of China(No.52476192,No.52106237)Natural Science Foundation of Heilongjiang Province(No.YQ2022E027)。
文摘The transition of hydrogen sourcing from carbon-intensive to water-based methodologies is underway,with renewable energy-powered proton exchange membrane water electrolysis(PEMWE)emerging as the preeminent pathway for hydrogen production.Despite remarkable advancements in this field,confronting the sluggish electrochemical kinetics and inherent high-energy consumption arising from deteriorated mass transport within PEMWE systems remains a formidable obstacle.This impediment stems primarily from the hindered protons mass transfer and the untimely hydrogen bubbles detachment.To address these challenges,we harness the inherent variability of electrical energy and introduce an innovative pulsed dynamic water electrolysis system.Compared to constant voltage electrolysis(hydrogen production rate:51.6 m L h^(-1),energy consumption:5.37 kWh Nm-^(3)H_(2)),this strategy(hydrogen production rate:66 m L h^(-1),energy consumption:3.83 kWh Nm-^(3)H_(2))increases the hydrogen production rate by approximately 27%and reduces the energy consumption by about 28%.Furthermore,we demonstrate the practicality of this system by integrating it with an off-grid photovoltaic(PV)system designed for outdoor operation,successfully driving a hydrogen production current of up to 500 mA under an average voltage of approximately 2 V.The combined results of in-situ characterization and finite element analysis reveal the performance enhancement mechanism:pulsed dynamic electrolysis(PDE)dramatically accelerates the enrichment of protons at the electrode/solution interface and facilitates the release of bubbles on the electrode surface.As such,PDE-enhanced PEMWE represents a synergistic advancement,concurrently enhancing both the hydrogen generation reaction and associated transport processes.This promising technology not only redefines the landscape of electrolysis-based hydrogen production but also holds immense potential for broadening its application across a diverse spectrum of electrocatalytic endeavors.
基金support from the National Natural Science Foundation of China(No’s.U22B2071,51874211,52031008)the Chilwee Group(CWDY-ZH-YJY-202101-001).
文摘Sodium(Na)and magnesium(Mg)are becoming important for making energy-storage batteries and structural materials.Herein,we develop a liquid-metal-electrode-assisted electrolysis route to producing Na and Mg with low-carbon emissions and no chlorine gas evolution.The clean production stems from the choice of a molten NaCl-Na_(2)CO_(3) electrolyte to prevent chlorine gas evolution,an inert nickel-based anode to produce oxygen,and a liquid metal cathode to make the cathodic product sit at the bottom of the electrolytic cell.We achieve a current efficiency of>90%for the electrolytic production of liquid Na-Sn alloy.Later,Mg-Sn alloy is prepared using the obtained Na-Sn alloy to displace Mg from molten NaCl-MgCl_(2) with a displacement efficiency of>96%.Further,Na and Mg are separated from the electrolytic Na-Sn and displaced Mg-Sn alloys by vacuum distillation with a recovery rate of>92%and Sn can be reused.Using this electrolysisdisplacement-distillation(EDD)approach,we prepare Mg from seawater.The CO_(2)emission of the EDD approach is~20.6 kg CO_(2)per kg Mg,which is less than that of the Australian Magnesium(AM)electrolysis process(~25.0 kg CO_(2)per kg Mg)and less than half that of the Pidgeon process(~45.2 kg CO_(2)per kg Mg).
基金supported by the National Natural Science Foundation of China(22272148,22202172)financial support from the China Postdoctoral Science Foundation(2023M742947)support of the Postgraduate Research&Practice Innovation Program of Jiangsu Province(Yangzhou University)(KYCX24_3720)。
文摘Developing heterojunction catalysts with diverse adsorption sites presents significant opportunities to enhance the performance of urea-assisted water electrolysis.Herein,we highlighted a NiTe/Mo_(6)Te_(8)heterojunction catalyst confined in carbon nanofiber with spontaneous charge redistribution driven by high valent metal,which promotes the adsorption and transformation of intermediates and greatly reduces the reaction energy barrier for urea oxidation.The heterojunction catalyst promotes the formation of Ni^(3+)active species and accelerates the fracture of the C-N bond by enhancing selective adsorption of-NH_(2)and C=O groups in binding urea molecules driven by the spontaneous formation of nucleophilic and electrophilic sites.The catalyst achieves a low kinetic current density of 10 mA cm^(-2)at 1.35 V with a cell voltage for urea electrolysis of just 1.47 V and good durability over 60 h.Density-functional theory and in-situ spectral observation reveal that the high valent Mo promoted the 3d orbit of Ni approaching the Fermi level by adjusting the electronic structure,which enhanced spontaneous urea dehydrogenation and reduced the energy barrier for^(*)COO desorption.This study highlights the effectiveness of modulating the interfacial electronic structure to improve energy conversion efficiency.
基金co-supported by the National Key R&D Program of China(No.2022YFB4002203)Baima Lake Laboratory Joint Funds of the Zhejiang Provincial Natural Science Foundation of China(No.LBMHY24B060003)Ningbo Key R&D Project(No.2023Z155).
文摘This work investigates the transient performance and stability of CO_(2)/H_(2)O co-electrolysis in an air-free environment using a flat-tube solid oxide electrolysis cell(SOEC)stack.The results showed that the transient behavior of the stack with and without blowing gas into the air electrode is almost the same.With a current density of 0.67 A·cm^(-2)@750℃,the stack operated for over 200 h under co-electrolysis conditions without air blowing,and the voltage drop rate of the stack was approximately 0.203%/100 hours.Microstructure analysis revealed a significant loss of nickel particles and an apparent for-mation of an insulating phase strontium chromate(SrCrO4)on the surface of the current collection layer of the air electrode,which are identified as key factors contributing to the performance degradation of the stack.This study provides a reference for development of efficient fuel preparation technology based on SOEC stack in airless environments.
基金supported by the National Natural Science Foundation of China(22005072,21965006)Guizhou Provincial Key Technology R&D Program(Qian Ke He support(2023)General 122)+3 种基金Guiyang Guian Science and Technology Personnel Training Project([2024]2-13)Youth Science and Technology Talent Development Project from Guizhou Provincial Department of Education(KY[2022]163)Guizhou Provincial Science and Technology Foundation(KYJZ[2024]029)the ETS Marcelle-Gauvreau Engineering Research Chair program.
文摘Atomically dispersed metal site(ADMS)materials have emerged as a promising class of materials for electrocatalysis reactions in the field of energy conversion.Characterized by individual metal atoms dispersed on suitable supports,ADMS materials provide unique catalytic sites with highly tunable electronic structures.This review summarizes recent advancements in the field,with a focus on the critical roles of support materials,coordination environments,and the mechanisms underlying catalytic activity at the atomic level.First,commonly used density functional theory(DFT)simulations are reviewed,emphasizing their pivotal role in elucidating reaction mechanisms and predicting the behavior of ADMS in electrochemical reactions for hydrogen energy utilization.Then,advancements in ADMS for half-cell electrochemical reactions,including oxygen evolution reaction,hydrogen evolution reaction,and oxygen reduction reaction,as well as their applications in fuel cells and water splitting,are summarized.Finally,the challenges and future prospects of ADMS are discussed.This review underscores the transformative potential of ADMS in electrocatalysis,paving the way for innovative and sustainable energy conversion technologies.
基金This work was supported by the National Key R&D Program of China(2022YFB4102000 and 2022YFA1505100)the NSFC(22472038)the Shanghai Science and Technology Innovation Action Plan(22dz1205500).
文摘Electrocatalytic carbon dioxide reduction is a promising technology for addressing global energy and environmental crises. However, its practical application faces two critical challenges: the complex and energy-intensive process of separat-ing mixed reduction products and the economic viability of the carbon sources (reactants) used. To tackle these challenges simultaneously, solid-state electrolyte (SSE) reactors are emerging as a promising solution. In this review, we focus on the feasibility of applying SSE for tandem electrochemical CO_(2) capture and conversion. The configurations and fundamental principles of SSE reactors are first discussed, followed by an introduction to its applications in these two specific areas, along with case studies on the implementation of tandem electrolysis. In comparison to conventional H-type cell, flow cell and membrane electrode assembly cell reactors, SSE reactors incorporate gas diffusion electrodes and utilize a solid electro-lyte layer positioned between an anion exchange membrane (AEM) and a cation exchange membrane (CEM). A key inno-vation of this design is the sandwiched SSE layer, which enhances efficient ion transport and facilitates continuous product extraction through a stream of deionized water or humidified nitrogen, effectively separating ion conduction from product collection. During electrolysis, driven by an electric field and concentration gradient, electrochemically generated ions (e.g., HCOO- and CH3COO-) migrate through the AEM into the SSE layer, while protons produced from water oxidation at the anode traverse the CEM into the central chamber to maintain charge balance. Targeted products like HCOOH can form in the middle layer through ionic recombination and are efficiently carried away by the flowing medium through the porous SSE layer, in the absence of electrolyte salt impurities. As CO_(2)RR can generate a series of liquid products, advancements in catalyst discovery over the past several years have facilitated the industrial application of SSE for more efficient chemicals production. Also noteworthy, the cathode reduction reaction can readily consume protons from water, creating a highly al-kaline local environment. SSE reactors are thereby employed to capture acidic CO_(2), forming CO_(3)^(2-) from various gas sources including flue gases. Driven by the electric field, the formed CO_(3)^(2-) can traverse through the AEM and react with protons originating from the anode, thereby regenerating CO_(2). This CO_(2) can then be collected and utilized as a low-cost feedstock for downstream CO_(2) electrolysis. Based on this principle, several cell configurations have been proposed to enhance CO_(2) capture from diverse gas sources. Through the collaboration of two SSE units, tandem electrochemical CO_(2) capture and con-version has been successfully implemented. Finally, we offer insights into the future development of SSE reactors for prac-tical applications aimed at achieving carbon neutrality. We recommend that greater attention be focused on specific aspects, including the fundamental physicochemical properties of the SSE layer, the electrochemical engineering perspective related to ion and species fluxes and selectivity, and the systematic pairing of consecutive CO_(2) capture and conversion units. These efforts aim to further enhance the practical application of SSE reactors within the broader electrochemistry community.
基金supported by the National Natural Science Foundation of China(Nos.22379133,22075256,and 52072350)the Natural Science Foundation of Guangdong Province(No.2024A1515012235).
文摘The performance of solid oxide electrolysis cells(SOECs)for CO_(2) electrolysis is significantly impeded by the limited electrochemical activity and insufficient durability of the cathode.This study introduces a novel(LaSrPrBaCaGd)_(2)Fe_(1.5)Mo_(0.5)O_(6-δ)(LSPBCGFM)perovskite via A-site entropy engineering,to improve both activity and durability.Experimental results reveal that LSPBCGFM cathode-based SOEC achieves a current density of 1.34 A·cm^(−2) at 1.5 V and 800℃,maintaining stable operation for more than 400 h at 1.2 V with negligible degradation.Theoretical calculations suggest that the high-entropy strategy shifts the transition metal d-band center and O-2p-band center closer to the Fermi energy level simultaneously,thereby initiating more favorable CO_(2) adsorption and activation.In addition,a higher O-2p-band center promotes the formation and diffusion of oxygen vacancies.The findings of this study provide crucial insights into the role of conformational entropy strategies in CO_(2) electrolysis and offer potential pathways for the development of highly efficient and stable catalysts.
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 Natural Science Foundation of China(Nos.22208376,UA22A20429)Shandong Provincial Natural Science Foundation(Nos.ZR2024QB175,ZR2023LFG005)+1 种基金Qingdao New Energy Shandong Laboratory Open Project(QNESL OP 202303)Ministry of Education University-Industry Collaborative Education Program(No.230804132140429).
文摘Seawater electrolysis offers a promising pathway to generate green hydrogen,which is crucial for the net-zero emission targets.Indirect seawater electrolysis is severely limited by high energy demands and system complexity,while the direct seawater electrolysis bypasses pre-treatment,offering a simpler and more cost-effective solution.However,the chlorine evolution reaction and impurities in the seawater lead to severe corrosion and hinder electrolysis’s efficiency.Herein,we review recent advances in the rational design of chlorine-suppressive catalysts and integrated electrolysis systems architectures for chloride-induced corrosion,with simultaneous enhancement of Faradaic efficiency and reduction of electrolysis’s cost.Furthermore,promising directions are proposed for durable and efficient seawater electrolysis systems.This review provides perspectives for seawater electrolysis toward sustainable energy conversion and environmental protection.
基金Project supported by the National Key Research&Development Project(2023YFB4006001)National Natural Science Foundation of China(52172199)。
文摘CO_(2)electrolysis using solid oxide electrolysis cells is a promising technology for CO_(2)utilization and conversion,which has attracted more and more attention in recent years because of its extremely high efficiency.However,traditional Ni-yttria-stabilized zirconia(Ni-YSZ)or Ni-Gd_(0.1)Ce_(0.9)O_(2-δ)(Ni-GDC)metal-ceramic cathode faces many problems such as Ni agglomeration and carbon deposition during long-time operation.Herein,a perovskite oxide La_(0.43-x)Ca_(0.37)Ti_(0.9)Ni_(0.1)O_(3-δ)(LCTN,x=0,0.05,0.1)with nanophase-LaVO_(4)exsolution was investigated as the novel cathode of solid oxide electrolysis cell(SOEC)for efficient CO_(2)electrolysis.The results confirm that the exsolution nanophase on LCTN surface can significantly improve the CO_(2)adsorption and conversion performance.For CO_(2)electrolysis at 1.8 V,an electrolysis current density of 1.24 A/cm2at 800℃can be obtained on SOEC with La_(0.43-x)Ca_(0.37)Ti_(0.9)Ni_(0.1)O_(3-δ)decorated with LaVO_(4)(LCTN-V0.05)cathode.Furthermore,the corresponding cell can maintain stable operation up to 100 h without apparent performance degradation.These results demonstrate that doping-induced second nanophase exsolution is a promising way to design high-performance SOEC cathodes for CO_(2)electrolysis.
基金financially supported by the National Key Research and Development Program(No.2023YFB4006100)the National Natural Science Foundation of China(No.52271232)+3 种基金Ningbo Youth Science and Technology Leading Talents Project(No.2023QL026)the Youth Innovation Promotion Association,CAS(No.2020300)the Natural Science Foundation of Zhejiang Province(Nos.LY21E020008 and LD21E020001)the“From 0 to 1”Innovative Program of CAS(No.ZDBS-LY-JSC021)
文摘Using abundant saline water for electrolysis,rather than limited freshwater,presents a promising technique for generating clean hydrogen energy.However,high concentration of corrosive chloride ions in saline water poses a great challenge in the stability of anode.In this study,we present a straightforward strategy to protect the anode from corrosion by patching the catalyst layer through a treatment of the anode with a sodium sulfide(Na2S) solution followed by electrochemical activation.The rapid sulfurization of the Ni electrode in Na2S results in the formation of a Na2S layer,which can subsequently be converted to NiOOH upon electrochemical activation,thereby shielding the inner Ni electrode from corrosion.The as-prepared electrode (P-NiFe-LDH/Ni) based on the strategy demonstrated stability over 3,500 h at an industrial current density of 0.5 A cm^(-2)in a 0.5 M NaCl and 1 M KOH solution.This study presents an effective strategy to significantly enhance the stability of anodes for saline water electrolysis by effectively patching the cracks in the catalyst layer.
基金Projects(52104355,52074363,52374364)supported by the National Natural Science Foundation of ChinaProject(2023YFC2907904)supported by the National Key R&D Program of China。
文摘Traditional pyrometallurgical and hydrometallurgical methods to extract bismuth from sulfide ores face problems such as high cost,low-concentration SO_(2)generation,and long process time.In this study,the cyclone technology and slurry electrolysis method were combined.The bismuth sulfide ore was dissolved directly at the anode,while the high purity bismuth was deposited efficiently at the cathode under the advantages of the two methods.The short process and high-efficiency extraction of bismuth sulfide ore were realized,and the pollution of low-concentration SO_(2)was avoided.Then,the effects of several crucial experimental conditions(current density,reaction time,temperature,pH,liquid-solid ratio,and circulation flow rate)on the leaching efficiency and recovery efficiency of bismuth were investigated.The leaching and electrowinning mechanisms during the recovery process were also analyzed according to the research results of this paper to better understand the cyclone slurry electrolysis process.The experimental results showed that 95.19%bismuth was leached into the acid solution in the anode area under optimal conditions,and the recovery efficiency and purity of bismuth on the cathode reached 91.13%and 99.26%,respectively,which were better than those by the traditional hydrometallurgy recovery process.
基金the support received from the Researchers Supporting Project(No.RSP2024R404),King Saud University,Riyadh,Saudi Arabia。
文摘The effect of iron concentration on the microstructural and structural properties of ZnO for electrolysis and photodetector applications was investigated.The thin layers of un-doped and doped ZnO with different percentages of Fe(2,4,and 6 wt.%)were deposited by spin-coating on glass substrates.Sample characterization was done by X-ray diffraction(XRD),atomic force microscopy(AFM),scanning electron microscopy(SEM),energy-dispersive X-ray spectroscopy(EDS),UV−Vis absorption spectra and X-ray photoelectron spectroscopy(XPS).Structural measurements by XRD showed that all the layers were composed of polycrystallines with a hexagonal Wurtzite structure.Two new peaks were also discovered after the doping process belonging to the Fe_(2)O_(4)(400)and(440)crystal phase.Morphological analysis showed that the surface roughness values of ZnO layers ranged between 8 and 45 nm.XPS studies confirmed the presence of Fe in 3+states in ZnO layers.An average transmittance of 90%was measured by UV−Vis in the wavelength range of 200−900 nm.The values of the energy gap(Eg)decreased with an increase in the concentration of Fe.AFM topography results confirmed that ZnO-based thin layers had a relatively uniform surface.The efficiency of these samples has been confirmed for their use in many electrical applications,including photodetectors and electrolysis of contaminated solutions.
基金financially supported by the National Natural Science Foundation of China(No.22205205)the Natural Science Foundation of Zhejiang Province(No.LQ24E040002)the Science Foundation of Zhejiang Sci-Tech University(ZSTU)(Nos.21062337Y,LW-YP2024076)。
文摘Integrating electrochemical upgrading of glycerol and water electrolysis is regarded as a promising and energy-saving approach for the co-production of chemicals and hydrogen.However,developing efficient electrocatalyst towards this technology remains challenging.Herein,a metallic cobalt mediated molybdenum nitride heterostructural material has been exploited on nickel foam(Co@Mo_(2)N/NF)for the glycerol oxidation reaction(GOR)and hydrogen evolution reaction(HER).Remarkably,the obtained Co@Mo_(2)N/NF realizes eminent performance with low overpotential of 49 mV at 50 mA/cm^(2)for HER and high Faradaic efficiency of formate of 95.03%at 1.35 V vs.RHE for GOR,respectively.The systematic in-situ experiments reveal that the Co@Mo_(2)N heterostructure promotes the cleavage of C-C bond in glycerol by active CoOOH species and boosts the conversion of glycerol to aldehyde intermediates to formate product.Moreover,the density functional theory(DFT)calculations confirm the strong interaction at Co@Mo_(2)N interface,which contributes to the optimized water dissociation and the transformation of H^(*)to H^(2).Benefiting from those advantages,the built HER||GOR electrolyzer delivers a low voltage of 1.61 V at 50 mA/cm^(2),high Faradaic efficiency,and robust stability over 120 h for sustained and stable electrolysis.
基金supported by the National Natural Science Foundation of China(No.52372175)the General Program of Science and Technology of Liaoning(2024-MSBA-20)+1 种基金the Innovation and Technology Fund of Dalian(2023JJ12GX020)the Fundamental Research Funds for the Central Universities(DUT24ZD406)。
文摘Seawater electrolysis provides a sustainable pathway for large-scale hydrogen production without reliance on freshwater resources.However,its practical implementation is hindered by the short lifespan of anodes,primarily caused by chlorine-induced corrosion in seawater.Herein,we present a self-sustaining anode protection strategy that remarkably enhances the durability of seawater electrolysis for efficient hydrogen production.This OH^(–)-trapping anode is designed by trapping OH^(–)within in-situ generated Lewis acid sites and structural vacancies formed via alkaline corrosion of amorphous NiMoSx.This design creates an anion-rich electrode interface with spontaneous accumulation and continuous replenishment of OH^(–)from the bulk electrolyte,ensuring long-lasting anode protection against corrosion through the electrostatic repulsion of chloride ions during operation.Simultaneously,it directs the anodic reaction along a stable adsorbate evolution mechanism with minimal metal leaching.Consequently,alkaline seawater electrolysis avoiding chlorine-induced corrosion achieves an exceptional lifespan exceeding 3,000 h under industrial current densities.By directly utilizing OH^(–)from the alkaline electrolyte for long-term anode protection,the operational complexity and cost of seawater electrolysis are significantly reduced,making it highly appealing for practical use.
文摘Upgrading carbon dioxide(CO_(2))into value-added bulk chemicals offers a dual-benefit strategy for the carbon neutrality and circular carbon economy.Herein,we develop an integrated CO_(2) valorization strategy that synergizes CO_(2)-H_(2)O co-electrolysis(producing CO/O_(2) feeds)with oxidative double carbonylation of ethylene/acetylene to synthesize CO_(2)-derived C_(4) diesters(dimethyl succinate,fumarate,and maleate).A group of versatile building blocks for manufacturing plasticizers,biodegradable polymers,and pharmaceutical intermediates.Remarkably,CO_(2) exhibits dual functionality:serving simultaneously as a CO/O_(2) source and an explosion suppressant during the oxidative carbonylation process.We systematically investigated the explosion-suppressing efficacy of CO_(2) in flammable gas mixtures(CO/O_(2),C_(2)H_(4)/CO/O_(2),and C_(2)H_(2)/CO/O_(2))across varying concentrations.Notably,the mixed gas stream from CO_(2)/H_(2)O co-electrolysis at an industrial-scale current densities of 400 mA/cm^(2),enabling direct utilization in oxidative double carbonylation reactions with exceptional compatibility and inherent safety.Extended applications were demonstrated through substrate scope expansion and gram-scale synthesis.This study establishes not only a safe protocol for oxidative carbonylation processes,but also opens an innovative pathway for sustainable CO_(2) valorization,including CO surrogate and explosion suppressant.
