Na_(3)V_(2)(PO_(4))_(3)(NVP)has garnered great attentions as a prospective cathode material for sodium-ion batteries(SIBs)by virtue of its decent theoretical capacity,superior ion conductivity and high structural stab...Na_(3)V_(2)(PO_(4))_(3)(NVP)has garnered great attentions as a prospective cathode material for sodium-ion batteries(SIBs)by virtue of its decent theoretical capacity,superior ion conductivity and high structural stability.However,the inherently poor electronic conductivity and sluggish sodium-ion diffusion kinetics of NVP material give rise to inferior rate performance and unsatisfactory energy density,which strictly confine its further application in SIBs.Thus,it is of significance to boost the sodium storage performance of NVP cathode material.Up to now,many methods have been developed to optimize the electrochemical performance of NVP cathode material.In this review,the latest advances in optimization strategies for improving the electrochemical performance of NVP cathode material are well summarized and discussed,including carbon coating or modification,foreign-ion doping or substitution and nanostructure and morphology design.The foreign-ion doping or substitution is highlighted,involving Na,V,and PO_(4)^(3−)sites,which include single-site doping,multiple-site doping,single-ion doping,multiple-ion doping and so on.Furthermore,the challenges and prospects of high-performance NVP cathode material are also put forward.It is believed that this review can provide a useful reference for designing and developing high-performance NVP cathode material toward the large-scale application in SIBs.展开更多
Lithium nickel oxide(Li_(2)NiO_(2)),as a sacrificial cathode prelithiation additive,has been used to compensate for the lithium loss for improving the lifespan of lithium-ion batteries(LIBs).However,high-cost Li_(2)Ni...Lithium nickel oxide(Li_(2)NiO_(2)),as a sacrificial cathode prelithiation additive,has been used to compensate for the lithium loss for improving the lifespan of lithium-ion batteries(LIBs).However,high-cost Li_(2)NiO_(2)suffers from inferior delithiation kinetics during the first cycle.Herein,we investigated the effects of the cost-effective copper substituted Li_(2)Ni_(1-x)Cu_(x)O_(2)(x=0,0.2,0.3,0.5,0.7)synthesized by a high-temperature solid-phase method on the structure,morphology,electrochemical performance of graphite‖LiFePO_(4)battery.The X-ray diffraction(XRD)refinement result demonstrated that Cu substitution strategy could be favorable for eliminating the NiO_(x)impurity phase and weakening Li-O bond.Analysis on density of states(DOS)indicates that Cu substitution is good for enhancing the electronic conductivity,as well as reducing the delithi-ation voltage polarization confirmed by electrochemical characterizations.Therefore,the optimal Li_(2)Ni_(0.7)Cu_(0.3)O_(2)delivered a high delithiation capacity of 437 mAh·g^(-1),around 8%above that of the pristine Li_(2)NiO_(2).Furthermore,a graphite‖LiFePO_(4)pouch cell with a nominal capacity of 3000 mAh demonstrated a notably improved reversible capacity,energy density and cycle life through introducing 2 wt%Li_(2)Ni_(0.7)Cu_(0.3)O_(2)additive,delivering a 6.2 mAh·g^(-1)higher initial discharge capacity and achieving around 5%improvement in capacity retentnion at 0.5P over 1000 cycles.Additionally,the post-mortem analyses testified that the Li_(2)Ni_(0.7)Cu_(0.3)O_(2)additive could suppress solid electrolyte interphase(SEI)decomposition and homogenize the Li distribution,which benefits to stabilizing interface between graphite and electrolyte,and alleviating dendritic Li plating.In conclusion,the Li_(2)Ni_(0.7)Cu_(0.3)O_(2)additive may offer advantages such as lower cost,lower delithiation voltage and higher prelithiation capacity compared with Li_(2)NiO_(2),making it a promising candidate of cathode prelithiation additive for next-generation LIBs.展开更多
Mn-based P2-type oxides are considered as promising cathodes for Na-ion batteries;however,they face significant challenges,including structural degradation when charged at high cutoff voltages and structural changes u...Mn-based P2-type oxides are considered as promising cathodes for Na-ion batteries;however,they face significant challenges,including structural degradation when charged at high cutoff voltages and structural changes upon storing in a humid atmosphere.In response to these issues,we have designed an oxide with co-doping of Cu and Al which can balance both cost and structural stability.The redox reaction of Cu^(2+/3+)can provide certain charge compensation,and the introduction of Al can further suppress the Jahn-Teller effect of Mn,thereby achieving superior long-term cycling performance.The ex-situ XRD testing indicates that Cu/Al co-doping can effectively suppress the phase transition of P2-O2 at high voltage,thereby explaining the improvement in electrochemical performance.DFT calculations reveal a high chemical tolerance to moisture,with lower adsorption energy for H_(2)O compared to pure Na_(0.67)Cu_(0.25)Mn_(0.75)O_(2).A representative Na_(0.67)Cu_(0.20)Al_(0.05)Mn_(0.75)O_(2)cathode demonstrates impressive reversible capacities of 148.7 mAh/g at 0.2 C,along with a remarkable capacity retention of 79.1%(2 C,500 cycles).展开更多
Although manganese-based oxide is regarded as a promising cathode material for zincion hybrid supercapacitors(ZHSCs),its practical application is hindered by slow zinc ion diffusion and the instability of MnO_(2).To o...Although manganese-based oxide is regarded as a promising cathode material for zincion hybrid supercapacitors(ZHSCs),its practical application is hindered by slow zinc ion diffusion and the instability of MnO_(2).To overcome this obstacle,a δ-MnO_(2)/MXene heterostructure was created using a simple one-step process under gentle condition.The ZHSC was assembled using this heterostructure as the cathode,activated carbon(AC)as the anode and 2 mol·L−1 ZnSO_(4) as the electrolyte.The resultingδ-MnO_(2)/MXene//ZnSO4//AC ZHSC shows a maximum specific capacitance of 97.4 F·g^(−1) and an energy density of 32.27 Wh·kg^(−1) at the best cathode-to-anode mass ratio.Ex situ characterizations reveal the reversible energy storage mechanism combing Zn^(2+)insertion/extraction in the cathode,ion adsorption and desorption on the anode surface,and partial reversible formation and dissolution of Zn_(4)SO_(4)(OH)_(6)·5H_(2)O(ZHS)components on both electrodes.Adding of Mn^(2+)to the electrolyte reduced Mn dissolution,improving the ZHSC’s specific capacitance and energy density to 140.4 F·g^(−1) and 49.36 Wh·kg^(−1),respectively,while also enhancing its rate performance and cyclability.The improved electrochemical reaction kinetics was verified through various tests.The results suggest that the δ-MnO_(2)/MXene heterostructure has great potential as a high-performance cathode material for ZHSCs.展开更多
The electrochemical performance of layered O3-type NaCrO_(2)cathode material is significantly affected by the side reactions between NaCrO_(2)and electrolyte during sodium storage.A uniform Cr_(2)O_(3)coating layer wa...The electrochemical performance of layered O3-type NaCrO_(2)cathode material is significantly affected by the side reactions between NaCrO_(2)and electrolyte during sodium storage.A uniform Cr_(2)O_(3)coating layer was in situ constructed on the surface of NaCrO_(2)by controlling the excess ratio of sodium source.The structure,morphology,valence and electrochemical performance of the Cr_(2)O_(3)-coated NaCrO_(2)were characterized.The results indicate that the Cr_(2)O_(3)coating layer does not alter the crystal structure and morphology of NaCrO_(2),but effectively suppresses the side reactions between NaCrO_(2)and electrolyte,and improves the surface/interfacial stability of NaCrO_(2)material.The Cr_(2)O_(3)-coated NaCrO_(2)exhibits improved electrochemical performance with a capacity retention of 66.4%after 500 cycles at 10C.展开更多
LiMn_(2)O_(4)(LMO) represents one of the most prevalent cathode materials utilized in lithium-ion batteries(LIBs), yet its broader application is often hampered by its limited achievable capacity and significant capac...LiMn_(2)O_(4)(LMO) represents one of the most prevalent cathode materials utilized in lithium-ion batteries(LIBs), yet its broader application is often hampered by its limited achievable capacity and significant capacity degradation during cycling. In this work, a novel dual-doping strategy involving Al^(3+) and Zr^(4+) ions has been employed to refine the atomic structure of LMO's spinel framework. The resultant dual-doped material, Li_(1.06)Mn_(1.97)Zr_(0.01)Al_(0.02)O_(4), exhibits enhanced electrochemical properties, boasting a discharge capacity of 124.9 m Ah/g at a rate of 0.1 C. Furthermore, the formation of stronger Al–O and Zr–O bonds contributes to the stabilization of the delithiated LMO structure. Impressively, 97.7%of its initial capacity is retained after 100 cycles at a 5 C rate. Additionally, enhancements in rate performance and hightemperature cycling stability have also been observed. This study underscores the potential of Al^(3+) and Zr^(4+) dual-doping as a promising approach to enhance LMO cathodes, providing a scalable and efficient means of improving the performance of lithium manganese oxide cathode materials through the incorporation of multiple ions.展开更多
Extending the charging voltage of LiCoO_(2)(LCO)is an ongoing and promising approach to increase its energy density.However,the main challenge of the approach lies in the insuperable cathodic interfacial processes at ...Extending the charging voltage of LiCoO_(2)(LCO)is an ongoing and promising approach to increase its energy density.However,the main challenge of the approach lies in the insuperable cathodic interfacial processes at high voltage,which leads to rapid failure both in the performance and structure of the LCO cathode.Herein,a Li_(2)CO_(3)-based additive was prepared by a simple sand-milling method,enabling a low electrochemical decomposition voltage<4.6 V from commonly>4.8 V,stabilizing the interface of the LCO cathode at 4.6 V.The decomposition of Li_(2)CO_(3)provides extra Li^(+)and CO_(2)to supplement the Li consumption required in the initial irreversible interfacial reactions and rapidly form a uniform and stable cathode electrolyte interphase layer(less organic and more inorganic components)on the LCO cathode by reducing CO_(2).Thus,the phase transformation and the emergence of high-valent Co ions on the surface of LCO at 4.6 V high voltage were inhibited.Thanks to this,with 2%Li_(2)CO_(3)-based additive,the capacity retention of commercial LCO at a high voltage of 4.6 V at 0.5 C for 100 cycles was improved from 59.3%to 79.3%.This work improves the high-voltage stability of LCO and provides a new idea for realizing the high-voltage operation of batteries.展开更多
The Li-CO_(2)battery has been highly rated as an intriguing technique for balancing the carbon cycle for years,but it is still significantly challenged by the obstacles such as limited reversibility,sluggish kinetics,...The Li-CO_(2)battery has been highly rated as an intriguing technique for balancing the carbon cycle for years,but it is still significantly challenged by the obstacles such as limited reversibility,sluggish kinetics,and poor energy efficiency.Hence,the design and development of advance catalysts that can enhance the kinetics and reversibility of the CO_(2)electrochemical cycling reactions are considered the imperative tasks.Transition metal-based catalysts are widely considered appealing owing to their unfilled dorbitals,rich and adjustable valences,as well as processibility.In this review,the working mechanism and the key issues of the CO_(2)electrochemical cycling reaction are discussed first.Then the strategies for composition and structure design of different type of transition metal-based catalysts are highlighted,including their benefits,limitations,and the ways to implement these strategies.Finally,based on the pioneering research,the perspectives on the challenges and key points for the future development of cathode catalyst are proposed.展开更多
As a cathode material for thermal batteries,NiS_(2)has a high theoretical capacity but low thermal stability.Besides,the poor formability of NiS_(2)powders also restricts the cathode performance of thermal batteries.I...As a cathode material for thermal batteries,NiS_(2)has a high theoretical capacity but low thermal stability.Besides,the poor formability of NiS_(2)powders also restricts the cathode performance of thermal batteries.In this paper,the novel NiS_(2)/SiO_(2)composite material was developed by high temperature vulcanization to improve the thermal stability formability of NiS_(2).The good filling and lubrication of spherical SiO_(2)can improve the thermal conductivity of NiS_(2)electrode.The discharge test shows that the NiS_(2)/SiO_(2)cathode has a stable discharge voltage at a current density of 200 mA/cm^(2),and the activation time is shortened by nearly 20%compared with the NiS_(2)cathode.In addition,due to the favorable thermal insulation protection of SiO_(2),the initial decomposition temperature of NiS_(2)is increased by 30℃after the addition of SiO_(2).The incorporation of SiO_(2)not only effectively improves the thermal stability and electrochemical properties of NiS_(2),but also improves the cold pressing forming performance of the NiS_(2)powder.Therefore,the novel NiS_(2)/SiO_(2)composite material is more suitable for thermal batteries with high stability and fast response,which is of great significance for improving the maneuverability and quality reliability of weapons and equipment.展开更多
PrBaFe_(2)O_(5+δ)(PBF)is one of the promising cathode materials for intermediate-temperature solid oxide fuel cell(IT-SOFC)technology.However,as the operating temperature decreases,the electrochemical performance of ...PrBaFe_(2)O_(5+δ)(PBF)is one of the promising cathode materials for intermediate-temperature solid oxide fuel cell(IT-SOFC)technology.However,as the operating temperature decreases,the electrochemical performance of this material deteriorates rapidly.To counter this,various doping strategies have been tested and reported in order to improve the electrochemical properties of this material at intermediate-temperatures.In this study,Mg-doping to partially substitute Fe of PBF was investigated.PrBaFe_(2-x)Mg_(x)O_(5+δ)(PBFMgx,x=0.1,0.15,0.2,0.3)materials were successfully synthesized,and their electrochemical performance as IT-SOFC cathode was evaluated.It is shown that Mg-doping enhances the conductivity of PBF between 650 and 800℃,impacts little on the area-specific resistance of oxygen reduction reaction at and above 700℃,and,most significantly,improves the power density of the NiSDC/SDC/PBFMg0.15single cell by 52%compared to the un-doped PBF.This enhanced electrochemical performance is attributed to the improvement in PBF conductivity by Mg-doping.展开更多
To investigate the mechanism by which ZrO_(2)modification affects the electrochemical performance of the NaNi_(1/3)Fe_(1/3)Mn_(1/3)O_(2)(NFM)cathode material for sodium-ion batteries,ZrO_(2)-coated NFM(ZrO_(2)@NFM)was...To investigate the mechanism by which ZrO_(2)modification affects the electrochemical performance of the NaNi_(1/3)Fe_(1/3)Mn_(1/3)O_(2)(NFM)cathode material for sodium-ion batteries,ZrO_(2)-coated NFM(ZrO_(2)@NFM)was prepared via high-temperature calcination.XRD refinement results revealed that ZrO_(2)modification increased the Na-layer spacing in the NFM material.XPS analysis results demonstrated that ZrO_(2)modification adjusted the Mn^(3+)/Mn^(4+)ratio in NFM by reducing the Mn^(3+)content.Electrochemical test results revealed that,compared to NFM,ZrO_(2)@NFM exhibited superior rate capability and cycling stability.It also exhibited significantly enhanced Na^(+)diffusion coefficients and reduced interfacial charge transfer resistance.The ZrO_(2)coating increased Na-layer spacing,reduced electrochemical polarization,and inhibited side reactions.In summary,the synergistic effect of component regulation and surface engineering through ZrO_(2)coating improved Na^(+)diffusion kinetics and enhanced cycling stability.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
Spinel LiNi_(0.5)Mn_(1.5)O_(4)(LNMO)cathode draws significant attention in the field of energy storage due to its unique voltage plateau.To further enhance the long-term electrochemical stability of LNMO,the LNMO cath...Spinel LiNi_(0.5)Mn_(1.5)O_(4)(LNMO)cathode draws significant attention in the field of energy storage due to its unique voltage plateau.To further enhance the long-term electrochemical stability of LNMO,the LNMO cathode covered with an ultrathin ZrO_(2)layer was prepared through atomic layer deposition(ALD).It is found that the LNMO cathode deposited with 20 layers of ZrO_(2)(LNMOZ20)exhibits the best electrochemical performance,achieving a high discharge capacity of 117.1 mA·h/g,with a capacity retention of 87.4%after 600 cycles at a current density of 1C.Furthermore,even at higher current densities of 5C and 10C,the LNMOZ20 electrode still demonstrates excellent stability with discharge capacities reaching 111.7 and 103.6 mA·h/g,and capacity retentions maintaining at 81.0%and 101.4%after 2000 cycles,respectively.This study highlights that the incorporation of an ultrathin ZrO_(2)layer by ALD is an effective strategy for enhancing the long-term cycling stability of LNMO cathodes.展开更多
The insufficient electrocatalytic activity and CO_(2)resistance hinder the application of cathode mate-rial for solid oxide fuel cells(SOFCs).In this study,we introduce a series of Pr-doped perovskite Bi_(0.8-x)Pr_(x)...The insufficient electrocatalytic activity and CO_(2)resistance hinder the application of cathode mate-rial for solid oxide fuel cells(SOFCs).In this study,we introduce a series of Pr-doped perovskite Bi_(0.8-x)Pr_(x)Ca_(0.2)FeO_(3-δ)(BPCF_(x),x=0,0.10,0.15,0.20)as candidate cathode materials,with a focus on its phase structure,oxygen desorption ability,catalytic activity,and electrochemical reduction kinetics.Among all the components,the Bi_(0.6)Pr_(0.2)Ca_(0.2)FeO_(3-δ)(BPCF0.20)catalyst shows impressive oxygen reduc-tion reaction(ORR)activity,with a low polarization resistance of 0.06Ωcm^(2)at 700℃and peak power density of 810 mW cm^(−2)at 800℃.Moreover,the BPCF0.20 cathode shows outstanding CO_(2)resistance in different CO_(2)concentrations(1%-10%)due to the larger average bond energy and higher relative acidity of Bi,Pr,and Fe ions.These findings demonstrate that BPCF_(x)are advanced cathode electrocatalysts for SOFCs.展开更多
Aqueous batteries are an emerging next-generation technology for large-scale energy storage.Among various metal-ion systems,manganese-based batteries have attracted significant interest due to their superior theoretic...Aqueous batteries are an emerging next-generation technology for large-scale energy storage.Among various metal-ion systems,manganese-based batteries have attracted significant interest due to their superior theoretical energy density over zinc-based battery systems.This study demonstrates oxygen vacancy-engineered vanadium oxide(V_(2)O_(4.85))as a high-performance cathode material for aqueous manganese metal batteries.The V_(2)O_(4.85) cathode had a discharge capacity of 212.6 mAh g^(-1) at 0.1 A g^(-1),retaining 89.5%capacity after 500 cycles.Oxygen vacancies enhanced ion diffusion and reduced migration barriers,facilitating both Mn^(2+)and H^(+)ion intercalation.Proton intercalation dominated charge storage,forming Mn(OH)_(2) layers,whereas Mn^(2+)contributed to surface-limited reactions.Furthermore,manganese metal batteries had a significantly higher operating voltage than that of aqueous zinc battery systems.Despite challenges with hydrogen evolution reactions at the Mn metal anode,this study underscores the potential of manganese batteries for future energy storage systems.展开更多
The development of affordable,high-efficiency sodium-ion batteries is primarily dependent on the advancement of cathode materials.These materials need to exhibit a high cell voltage,significant storage capacity,and qu...The development of affordable,high-efficiency sodium-ion batteries is primarily dependent on the advancement of cathode materials.These materials need to exhibit a high cell voltage,significant storage capacity,and quick diffusion of sodium ions to fulfill the requirements for efficient and ecofriendly energy storage systems.In this vein,density functional theory(DFT)calculation has become instrumental in advancing the study of battery materials.This study presents a firstprinciples investigation of P2-type Na_(x)NiO_(2)and Na_(x)Ni_(0.75)M_(0.25)O_(2)(M=Cu,Fe,Mn)cathode materials for sodium-ion batteries(SIBs),focusing on Na content variation and its impact on the battery performance.For NaNiO_(2),we replaced part of the expensive Ni element with lower-cost Cu,Fe,and Mn in hopes of reducing costs and improving material performance.By employing density functional theory(DFT),we explore the relationship between lattice constants,cell volume,enthalpy of formation,and cell voltage,and how these factors influence sodium ion insertion/extraction.We provide insights into the diffusion paths and activation energies for Na ions,and assess the influence of transition metal(TM)substitution on the structural stability and electrochemical properties of the materials.Additionally,the study delves into the electronic structure,highlighting how Cu and Fe integration refines the band gap of the spin-down bands.The findings reveal that certain transition metal substitutions can enhance performance,offering a pathway to optimize sodium-ion battery electrode materials.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
The LiNi_(x)Co_(y)Mn_(1-x-y)O_(2)(NCM)cathode materials have emerged as critical components in lithium-ion batteries due to their high energy and power densities.The co-precipitation method is widely used in laborator...The LiNi_(x)Co_(y)Mn_(1-x-y)O_(2)(NCM)cathode materials have emerged as critical components in lithium-ion batteries due to their high energy and power densities.The co-precipitation method is widely used in laboratory and industry settings to optimize the crystallinity,grain morphology,particle size,and sphericity of precursor materials,directly affecting NCM battery performance.This review addresses the nucleation mechanism and the thermodynamic and kinetic reaction processes of co-precipitation.The comprehensive effects of key parameters on precursor physicochemical properties are also systematically interpreted.展开更多
Ni-rich cathodes(Ni≥70%)with high specific capacities emerge as promising candidates for long-range lithium-ion batteries(LIBs).Nevertheless,their practical application is severely limited by two unresolved challenge...Ni-rich cathodes(Ni≥70%)with high specific capacities emerge as promising candidates for long-range lithium-ion batteries(LIBs).Nevertheless,their practical application is severely limited by two unresolved challenges:structural degradation from uncontrolled Li/Ni mixing and interfacial instability exacerbated by air/electrolyte corrosion.Herein,we propose a dual-modulation strategy to synthesize a stable Ni-rich cathode via carboxylate-based metal-organic frameworks(MOFs)-derived precursors,whereby oxygen vacancies in the precursors induce controlled moderate Li/Ni mixing,while their enhanced specific-surface-area property enables dense amorphous Li_(2)CO_(3)encapsulation.The optimal Li/Ni mixing harnesses the Ni pillar effect to stabilize the structure of cathodes upon cycling.Additionally,amorphous Li_(2)CO_(3)coating serves not only as a thermodynamically stable and air-impermeable protective layer for the cathodes,but as a transformative precursor for an F-rich cathode electrolyte interphase(CEI)which enhances interfacial stability and electrochemical properties.This dual-modulated cathode delivers a high discharge capacity of 215.1 mA h g^(-1)at 0.1 C,retains 84.9% capacity after 200 cycles at 1 C in half cells,and achieves 96.0 mA h g^(-1)at 8 C in full-cell tests.Furthermore,we unravel the potential mechanism of Ni pillar effect from optimal Li/Ni mixing and track the evolution mechanism of Li_(2)CO_(3)coating into F-rich CEI.This work offers advanced perspectives for the controllable cation disordering engineering and rational design of surface residual lithium compounds in Ni-rich cathodes,thereby providing new guiding principles for protecting high-capacity cathodes in energy storage devices.展开更多
Na_(3)V_(2)(PO_(4))_(3)(NVP)is regarded as alternative cathode material for sodium-ion batteries(SIBs)due to its potential high-rate performance and pronounced long-term cycle stability.However,electronic conductivity...Na_(3)V_(2)(PO_(4))_(3)(NVP)is regarded as alternative cathode material for sodium-ion batteries(SIBs)due to its potential high-rate performance and pronounced long-term cycle stability.However,electronic conductivity and tap density are difficult to be balanced.Herein,we report that high-temperature shock(HTS)can prepare“single crystalline like”NVP which combines high-rate capability with high tap density together into one with the assistance of carbon framework and large particle.Thus,high reversible capacity of 110m Ah/g at 0.1 C with 89.9%capacity retention after 1600 cycles at 1 C and specific capacity of 83.5 m Ah/g at 50 C rate has been exhibited.This study provides a novel strategy to guide the production of high tap density,and rate performance polyanionic cathode materials.展开更多
基金partly supported by the National Natural Science Foundation of China(Grant No.52272225).
文摘Na_(3)V_(2)(PO_(4))_(3)(NVP)has garnered great attentions as a prospective cathode material for sodium-ion batteries(SIBs)by virtue of its decent theoretical capacity,superior ion conductivity and high structural stability.However,the inherently poor electronic conductivity and sluggish sodium-ion diffusion kinetics of NVP material give rise to inferior rate performance and unsatisfactory energy density,which strictly confine its further application in SIBs.Thus,it is of significance to boost the sodium storage performance of NVP cathode material.Up to now,many methods have been developed to optimize the electrochemical performance of NVP cathode material.In this review,the latest advances in optimization strategies for improving the electrochemical performance of NVP cathode material are well summarized and discussed,including carbon coating or modification,foreign-ion doping or substitution and nanostructure and morphology design.The foreign-ion doping or substitution is highlighted,involving Na,V,and PO_(4)^(3−)sites,which include single-site doping,multiple-site doping,single-ion doping,multiple-ion doping and so on.Furthermore,the challenges and prospects of high-performance NVP cathode material are also put forward.It is believed that this review can provide a useful reference for designing and developing high-performance NVP cathode material toward the large-scale application in SIBs.
基金supported by the Significant Science and Technology Project in Xiamen(Future Industry Field)(Grant No.3502Z20231057).
文摘Lithium nickel oxide(Li_(2)NiO_(2)),as a sacrificial cathode prelithiation additive,has been used to compensate for the lithium loss for improving the lifespan of lithium-ion batteries(LIBs).However,high-cost Li_(2)NiO_(2)suffers from inferior delithiation kinetics during the first cycle.Herein,we investigated the effects of the cost-effective copper substituted Li_(2)Ni_(1-x)Cu_(x)O_(2)(x=0,0.2,0.3,0.5,0.7)synthesized by a high-temperature solid-phase method on the structure,morphology,electrochemical performance of graphite‖LiFePO_(4)battery.The X-ray diffraction(XRD)refinement result demonstrated that Cu substitution strategy could be favorable for eliminating the NiO_(x)impurity phase and weakening Li-O bond.Analysis on density of states(DOS)indicates that Cu substitution is good for enhancing the electronic conductivity,as well as reducing the delithi-ation voltage polarization confirmed by electrochemical characterizations.Therefore,the optimal Li_(2)Ni_(0.7)Cu_(0.3)O_(2)delivered a high delithiation capacity of 437 mAh·g^(-1),around 8%above that of the pristine Li_(2)NiO_(2).Furthermore,a graphite‖LiFePO_(4)pouch cell with a nominal capacity of 3000 mAh demonstrated a notably improved reversible capacity,energy density and cycle life through introducing 2 wt%Li_(2)Ni_(0.7)Cu_(0.3)O_(2)additive,delivering a 6.2 mAh·g^(-1)higher initial discharge capacity and achieving around 5%improvement in capacity retentnion at 0.5P over 1000 cycles.Additionally,the post-mortem analyses testified that the Li_(2)Ni_(0.7)Cu_(0.3)O_(2)additive could suppress solid electrolyte interphase(SEI)decomposition and homogenize the Li distribution,which benefits to stabilizing interface between graphite and electrolyte,and alleviating dendritic Li plating.In conclusion,the Li_(2)Ni_(0.7)Cu_(0.3)O_(2)additive may offer advantages such as lower cost,lower delithiation voltage and higher prelithiation capacity compared with Li_(2)NiO_(2),making it a promising candidate of cathode prelithiation additive for next-generation LIBs.
基金supported by National Natural Science Youth Foundation of China(No.22308294)National Natural Science Foundation of China(No.22179077)+1 种基金Postgraduate Research&Practice Innovation Program of Jiangsu Province(No.SJCX23_1868)Qing Lan Project of Jiangsu University and the Funding for school-level research projects of Yancheng Institute of Technology.
文摘Mn-based P2-type oxides are considered as promising cathodes for Na-ion batteries;however,they face significant challenges,including structural degradation when charged at high cutoff voltages and structural changes upon storing in a humid atmosphere.In response to these issues,we have designed an oxide with co-doping of Cu and Al which can balance both cost and structural stability.The redox reaction of Cu^(2+/3+)can provide certain charge compensation,and the introduction of Al can further suppress the Jahn-Teller effect of Mn,thereby achieving superior long-term cycling performance.The ex-situ XRD testing indicates that Cu/Al co-doping can effectively suppress the phase transition of P2-O2 at high voltage,thereby explaining the improvement in electrochemical performance.DFT calculations reveal a high chemical tolerance to moisture,with lower adsorption energy for H_(2)O compared to pure Na_(0.67)Cu_(0.25)Mn_(0.75)O_(2).A representative Na_(0.67)Cu_(0.20)Al_(0.05)Mn_(0.75)O_(2)cathode demonstrates impressive reversible capacities of 148.7 mAh/g at 0.2 C,along with a remarkable capacity retention of 79.1%(2 C,500 cycles).
基金supported by Natural Science Foundation of Ningxia Province,China(No.2023AAC05047)Special Project for the Central-Guided Local Science and Technology Development(No.2024FRD05062)+1 种基金Graduate Student Innovation Project of North Minzu University(No.YCX24102)Ningxia Science and Technology Innovation Team for Key Materials and Devices in High-Performance Secondary Batteries(No.2024CXTD003).
文摘Although manganese-based oxide is regarded as a promising cathode material for zincion hybrid supercapacitors(ZHSCs),its practical application is hindered by slow zinc ion diffusion and the instability of MnO_(2).To overcome this obstacle,a δ-MnO_(2)/MXene heterostructure was created using a simple one-step process under gentle condition.The ZHSC was assembled using this heterostructure as the cathode,activated carbon(AC)as the anode and 2 mol·L−1 ZnSO_(4) as the electrolyte.The resultingδ-MnO_(2)/MXene//ZnSO4//AC ZHSC shows a maximum specific capacitance of 97.4 F·g^(−1) and an energy density of 32.27 Wh·kg^(−1) at the best cathode-to-anode mass ratio.Ex situ characterizations reveal the reversible energy storage mechanism combing Zn^(2+)insertion/extraction in the cathode,ion adsorption and desorption on the anode surface,and partial reversible formation and dissolution of Zn_(4)SO_(4)(OH)_(6)·5H_(2)O(ZHS)components on both electrodes.Adding of Mn^(2+)to the electrolyte reduced Mn dissolution,improving the ZHSC’s specific capacitance and energy density to 140.4 F·g^(−1) and 49.36 Wh·kg^(−1),respectively,while also enhancing its rate performance and cyclability.The improved electrochemical reaction kinetics was verified through various tests.The results suggest that the δ-MnO_(2)/MXene heterostructure has great potential as a high-performance cathode material for ZHSCs.
基金supported by the Scientific Research Fund of Hunan Provincial Education Department,China(No.22B0741)。
文摘The electrochemical performance of layered O3-type NaCrO_(2)cathode material is significantly affected by the side reactions between NaCrO_(2)and electrolyte during sodium storage.A uniform Cr_(2)O_(3)coating layer was in situ constructed on the surface of NaCrO_(2)by controlling the excess ratio of sodium source.The structure,morphology,valence and electrochemical performance of the Cr_(2)O_(3)-coated NaCrO_(2)were characterized.The results indicate that the Cr_(2)O_(3)coating layer does not alter the crystal structure and morphology of NaCrO_(2),but effectively suppresses the side reactions between NaCrO_(2)and electrolyte,and improves the surface/interfacial stability of NaCrO_(2)material.The Cr_(2)O_(3)-coated NaCrO_(2)exhibits improved electrochemical performance with a capacity retention of 66.4%after 500 cycles at 10C.
基金Project supported by the National Key Research and Development Program of China (Grant No. 2022YFB2404400)。
文摘LiMn_(2)O_(4)(LMO) represents one of the most prevalent cathode materials utilized in lithium-ion batteries(LIBs), yet its broader application is often hampered by its limited achievable capacity and significant capacity degradation during cycling. In this work, a novel dual-doping strategy involving Al^(3+) and Zr^(4+) ions has been employed to refine the atomic structure of LMO's spinel framework. The resultant dual-doped material, Li_(1.06)Mn_(1.97)Zr_(0.01)Al_(0.02)O_(4), exhibits enhanced electrochemical properties, boasting a discharge capacity of 124.9 m Ah/g at a rate of 0.1 C. Furthermore, the formation of stronger Al–O and Zr–O bonds contributes to the stabilization of the delithiated LMO structure. Impressively, 97.7%of its initial capacity is retained after 100 cycles at a 5 C rate. Additionally, enhancements in rate performance and hightemperature cycling stability have also been observed. This study underscores the potential of Al^(3+) and Zr^(4+) dual-doping as a promising approach to enhance LMO cathodes, providing a scalable and efficient means of improving the performance of lithium manganese oxide cathode materials through the incorporation of multiple ions.
基金supported by the National Key Research and Development Program of China(2022YFB2502103)the Xiamen Science and Technology Project(No.3502Z20231057)+2 种基金the National Natural Science Foundation of China(No.22288102,No.22279107,No.22309153)the Fujian Provincial Natural Science Foundation of China(No.2024J01040)the Fundamental Research Funds for the Central Universities(No.20720230039)。
文摘Extending the charging voltage of LiCoO_(2)(LCO)is an ongoing and promising approach to increase its energy density.However,the main challenge of the approach lies in the insuperable cathodic interfacial processes at high voltage,which leads to rapid failure both in the performance and structure of the LCO cathode.Herein,a Li_(2)CO_(3)-based additive was prepared by a simple sand-milling method,enabling a low electrochemical decomposition voltage<4.6 V from commonly>4.8 V,stabilizing the interface of the LCO cathode at 4.6 V.The decomposition of Li_(2)CO_(3)provides extra Li^(+)and CO_(2)to supplement the Li consumption required in the initial irreversible interfacial reactions and rapidly form a uniform and stable cathode electrolyte interphase layer(less organic and more inorganic components)on the LCO cathode by reducing CO_(2).Thus,the phase transformation and the emergence of high-valent Co ions on the surface of LCO at 4.6 V high voltage were inhibited.Thanks to this,with 2%Li_(2)CO_(3)-based additive,the capacity retention of commercial LCO at a high voltage of 4.6 V at 0.5 C for 100 cycles was improved from 59.3%to 79.3%.This work improves the high-voltage stability of LCO and provides a new idea for realizing the high-voltage operation of batteries.
基金financially supported by the National Natural Science Foundation of China(52201254,52234001,52074177)the National Key Research and Development Program(2022YFC3900905)+3 种基金the Natural Science Foundation of Shandong Province(ZR2020QE012,ZR2020MB090,ZR2023ME155,ZR2023ME085)the Scientific Research Foundation for New Talents in University of Jinan(XRC2406)the project of “20 Items of University”of Jinan(202228046)the Introducing Major Universities and Research Institutions to Jointly Build Innovative Carrier Project of Jining City(2023DYDS022)。
文摘The Li-CO_(2)battery has been highly rated as an intriguing technique for balancing the carbon cycle for years,but it is still significantly challenged by the obstacles such as limited reversibility,sluggish kinetics,and poor energy efficiency.Hence,the design and development of advance catalysts that can enhance the kinetics and reversibility of the CO_(2)electrochemical cycling reactions are considered the imperative tasks.Transition metal-based catalysts are widely considered appealing owing to their unfilled dorbitals,rich and adjustable valences,as well as processibility.In this review,the working mechanism and the key issues of the CO_(2)electrochemical cycling reaction are discussed first.Then the strategies for composition and structure design of different type of transition metal-based catalysts are highlighted,including their benefits,limitations,and the ways to implement these strategies.Finally,based on the pioneering research,the perspectives on the challenges and key points for the future development of cathode catalyst are proposed.
基金Project(23JCYBJC01870)supported by the Natural Science Foundation of Tianjin,ChinaProject(U22A20119)supported by the National Natural Science Foundation of China。
文摘As a cathode material for thermal batteries,NiS_(2)has a high theoretical capacity but low thermal stability.Besides,the poor formability of NiS_(2)powders also restricts the cathode performance of thermal batteries.In this paper,the novel NiS_(2)/SiO_(2)composite material was developed by high temperature vulcanization to improve the thermal stability formability of NiS_(2).The good filling and lubrication of spherical SiO_(2)can improve the thermal conductivity of NiS_(2)electrode.The discharge test shows that the NiS_(2)/SiO_(2)cathode has a stable discharge voltage at a current density of 200 mA/cm^(2),and the activation time is shortened by nearly 20%compared with the NiS_(2)cathode.In addition,due to the favorable thermal insulation protection of SiO_(2),the initial decomposition temperature of NiS_(2)is increased by 30℃after the addition of SiO_(2).The incorporation of SiO_(2)not only effectively improves the thermal stability and electrochemical properties of NiS_(2),but also improves the cold pressing forming performance of the NiS_(2)powder.Therefore,the novel NiS_(2)/SiO_(2)composite material is more suitable for thermal batteries with high stability and fast response,which is of great significance for improving the maneuverability and quality reliability of weapons and equipment.
基金supported by the National Natural Science Foundation of China(51974167)Natural Science Foundation Youth Foundation of Inner Mongolia(2023QN05038)Higher Education Carbon Peak Carbon Neutral Research Project of Inner Mongolia Autonomous Region(STZX202210)。
文摘PrBaFe_(2)O_(5+δ)(PBF)is one of the promising cathode materials for intermediate-temperature solid oxide fuel cell(IT-SOFC)technology.However,as the operating temperature decreases,the electrochemical performance of this material deteriorates rapidly.To counter this,various doping strategies have been tested and reported in order to improve the electrochemical properties of this material at intermediate-temperatures.In this study,Mg-doping to partially substitute Fe of PBF was investigated.PrBaFe_(2-x)Mg_(x)O_(5+δ)(PBFMgx,x=0.1,0.15,0.2,0.3)materials were successfully synthesized,and their electrochemical performance as IT-SOFC cathode was evaluated.It is shown that Mg-doping enhances the conductivity of PBF between 650 and 800℃,impacts little on the area-specific resistance of oxygen reduction reaction at and above 700℃,and,most significantly,improves the power density of the NiSDC/SDC/PBFMg0.15single cell by 52%compared to the un-doped PBF.This enhanced electrochemical performance is attributed to the improvement in PBF conductivity by Mg-doping.
基金supported by the Central South University Innovation-Driven Research Programme,China(No.2023CXQD053)the National Natural Science Foundation of China(No.52274310)financial support from the Government of Chongzuo,Guangxi Zhuang Autonomous Region,China(No.FA20210713).
文摘To investigate the mechanism by which ZrO_(2)modification affects the electrochemical performance of the NaNi_(1/3)Fe_(1/3)Mn_(1/3)O_(2)(NFM)cathode material for sodium-ion batteries,ZrO_(2)-coated NFM(ZrO_(2)@NFM)was prepared via high-temperature calcination.XRD refinement results revealed that ZrO_(2)modification increased the Na-layer spacing in the NFM material.XPS analysis results demonstrated that ZrO_(2)modification adjusted the Mn^(3+)/Mn^(4+)ratio in NFM by reducing the Mn^(3+)content.Electrochemical test results revealed that,compared to NFM,ZrO_(2)@NFM exhibited superior rate capability and cycling stability.It also exhibited significantly enhanced Na^(+)diffusion coefficients and reduced interfacial charge transfer resistance.The ZrO_(2)coating increased Na-layer spacing,reduced electrochemical polarization,and inhibited side reactions.In summary,the synergistic effect of component regulation and surface engineering through ZrO_(2)coating improved Na^(+)diffusion kinetics and enhanced cycling stability.
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 National Natural Science Foundation of China(Nos.51931006,U22A20118).
文摘Spinel LiNi_(0.5)Mn_(1.5)O_(4)(LNMO)cathode draws significant attention in the field of energy storage due to its unique voltage plateau.To further enhance the long-term electrochemical stability of LNMO,the LNMO cathode covered with an ultrathin ZrO_(2)layer was prepared through atomic layer deposition(ALD).It is found that the LNMO cathode deposited with 20 layers of ZrO_(2)(LNMOZ20)exhibits the best electrochemical performance,achieving a high discharge capacity of 117.1 mA·h/g,with a capacity retention of 87.4%after 600 cycles at a current density of 1C.Furthermore,even at higher current densities of 5C and 10C,the LNMOZ20 electrode still demonstrates excellent stability with discharge capacities reaching 111.7 and 103.6 mA·h/g,and capacity retentions maintaining at 81.0%and 101.4%after 2000 cycles,respectively.This study highlights that the incorporation of an ultrathin ZrO_(2)layer by ALD is an effective strategy for enhancing the long-term cycling stability of LNMO cathodes.
基金supported by the Natural Science Foundation of Heilongjiang Province(No.ZD2022E007).
文摘The insufficient electrocatalytic activity and CO_(2)resistance hinder the application of cathode mate-rial for solid oxide fuel cells(SOFCs).In this study,we introduce a series of Pr-doped perovskite Bi_(0.8-x)Pr_(x)Ca_(0.2)FeO_(3-δ)(BPCF_(x),x=0,0.10,0.15,0.20)as candidate cathode materials,with a focus on its phase structure,oxygen desorption ability,catalytic activity,and electrochemical reduction kinetics.Among all the components,the Bi_(0.6)Pr_(0.2)Ca_(0.2)FeO_(3-δ)(BPCF0.20)catalyst shows impressive oxygen reduc-tion reaction(ORR)activity,with a low polarization resistance of 0.06Ωcm^(2)at 700℃and peak power density of 810 mW cm^(−2)at 800℃.Moreover,the BPCF0.20 cathode shows outstanding CO_(2)resistance in different CO_(2)concentrations(1%-10%)due to the larger average bond energy and higher relative acidity of Bi,Pr,and Fe ions.These findings demonstrate that BPCF_(x)are advanced cathode electrocatalysts for SOFCs.
基金supported by the Global Joint Research Program funded by Pukyong National University(202411790001)supported by the Nano&Material Technology Development Program through the National Research Foundation of Korea(NRF),funded by the Ministry of Science and ICT(RS-2024-00446825)by the Technology Innovation Program(RS-2024-00418815)funded by the Ministry of Trade,Industry&Energy(MOTIE,Korea).
文摘Aqueous batteries are an emerging next-generation technology for large-scale energy storage.Among various metal-ion systems,manganese-based batteries have attracted significant interest due to their superior theoretical energy density over zinc-based battery systems.This study demonstrates oxygen vacancy-engineered vanadium oxide(V_(2)O_(4.85))as a high-performance cathode material for aqueous manganese metal batteries.The V_(2)O_(4.85) cathode had a discharge capacity of 212.6 mAh g^(-1) at 0.1 A g^(-1),retaining 89.5%capacity after 500 cycles.Oxygen vacancies enhanced ion diffusion and reduced migration barriers,facilitating both Mn^(2+)and H^(+)ion intercalation.Proton intercalation dominated charge storage,forming Mn(OH)_(2) layers,whereas Mn^(2+)contributed to surface-limited reactions.Furthermore,manganese metal batteries had a significantly higher operating voltage than that of aqueous zinc battery systems.Despite challenges with hydrogen evolution reactions at the Mn metal anode,this study underscores the potential of manganese batteries for future energy storage systems.
基金the financial support from the National Natural Science Foundation of China(No.52072379)the Recruitment Program of Global Experts,and the Fundamental Research Funds for the Central Universities(WK2060000016)。
文摘The development of affordable,high-efficiency sodium-ion batteries is primarily dependent on the advancement of cathode materials.These materials need to exhibit a high cell voltage,significant storage capacity,and quick diffusion of sodium ions to fulfill the requirements for efficient and ecofriendly energy storage systems.In this vein,density functional theory(DFT)calculation has become instrumental in advancing the study of battery materials.This study presents a firstprinciples investigation of P2-type Na_(x)NiO_(2)and Na_(x)Ni_(0.75)M_(0.25)O_(2)(M=Cu,Fe,Mn)cathode materials for sodium-ion batteries(SIBs),focusing on Na content variation and its impact on the battery performance.For NaNiO_(2),we replaced part of the expensive Ni element with lower-cost Cu,Fe,and Mn in hopes of reducing costs and improving material performance.By employing density functional theory(DFT),we explore the relationship between lattice constants,cell volume,enthalpy of formation,and cell voltage,and how these factors influence sodium ion insertion/extraction.We provide insights into the diffusion paths and activation energies for Na ions,and assess the influence of transition metal(TM)substitution on the structural stability and electrochemical properties of the materials.Additionally,the study delves into the electronic structure,highlighting how Cu and Fe integration refines the band gap of the spin-down bands.The findings reveal that certain transition metal substitutions can enhance performance,offering a pathway to optimize sodium-ion battery electrode materials.
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supported by the Major Science and Technology Project of Shenzhen’s Innovation and Entrepreneurship Program(Grant No.KJZD20231023100301004)Foshan Science and Technology Innovation Team Project(1920001004098)the Hydrometal urgy and Battery Materials Laboratory at PT.QMB New Energy Materials(Indonesia)under GEM Co.,Ltd.(China)as a company group。
文摘The LiNi_(x)Co_(y)Mn_(1-x-y)O_(2)(NCM)cathode materials have emerged as critical components in lithium-ion batteries due to their high energy and power densities.The co-precipitation method is widely used in laboratory and industry settings to optimize the crystallinity,grain morphology,particle size,and sphericity of precursor materials,directly affecting NCM battery performance.This review addresses the nucleation mechanism and the thermodynamic and kinetic reaction processes of co-precipitation.The comprehensive effects of key parameters on precursor physicochemical properties are also systematically interpreted.
基金the financial support from the Special Funds for the Cultivation of Guangdong College Students’Scientific and Technological Innovation(“Climbing Program”Special Funds,pdjh2024a109)。
文摘Ni-rich cathodes(Ni≥70%)with high specific capacities emerge as promising candidates for long-range lithium-ion batteries(LIBs).Nevertheless,their practical application is severely limited by two unresolved challenges:structural degradation from uncontrolled Li/Ni mixing and interfacial instability exacerbated by air/electrolyte corrosion.Herein,we propose a dual-modulation strategy to synthesize a stable Ni-rich cathode via carboxylate-based metal-organic frameworks(MOFs)-derived precursors,whereby oxygen vacancies in the precursors induce controlled moderate Li/Ni mixing,while their enhanced specific-surface-area property enables dense amorphous Li_(2)CO_(3)encapsulation.The optimal Li/Ni mixing harnesses the Ni pillar effect to stabilize the structure of cathodes upon cycling.Additionally,amorphous Li_(2)CO_(3)coating serves not only as a thermodynamically stable and air-impermeable protective layer for the cathodes,but as a transformative precursor for an F-rich cathode electrolyte interphase(CEI)which enhances interfacial stability and electrochemical properties.This dual-modulated cathode delivers a high discharge capacity of 215.1 mA h g^(-1)at 0.1 C,retains 84.9% capacity after 200 cycles at 1 C in half cells,and achieves 96.0 mA h g^(-1)at 8 C in full-cell tests.Furthermore,we unravel the potential mechanism of Ni pillar effect from optimal Li/Ni mixing and track the evolution mechanism of Li_(2)CO_(3)coating into F-rich CEI.This work offers advanced perspectives for the controllable cation disordering engineering and rational design of surface residual lithium compounds in Ni-rich cathodes,thereby providing new guiding principles for protecting high-capacity cathodes in energy storage devices.
基金supported by the National Natural Science Foundation of China(No.22109091)Natural Science Foundation of Shandong Province(No.ZR2021QB180)。
文摘Na_(3)V_(2)(PO_(4))_(3)(NVP)is regarded as alternative cathode material for sodium-ion batteries(SIBs)due to its potential high-rate performance and pronounced long-term cycle stability.However,electronic conductivity and tap density are difficult to be balanced.Herein,we report that high-temperature shock(HTS)can prepare“single crystalline like”NVP which combines high-rate capability with high tap density together into one with the assistance of carbon framework and large particle.Thus,high reversible capacity of 110m Ah/g at 0.1 C with 89.9%capacity retention after 1600 cycles at 1 C and specific capacity of 83.5 m Ah/g at 50 C rate has been exhibited.This study provides a novel strategy to guide the production of high tap density,and rate performance polyanionic cathode materials.
