The poor reversibility and stability of Zn anodes greatly restrict the practical application of aqueous Zn-ion batteries(AZIBs),resulting from the uncontrollable dendrite growth and H_(2)O-induced side reactions durin...The poor reversibility and stability of Zn anodes greatly restrict the practical application of aqueous Zn-ion batteries(AZIBs),resulting from the uncontrollable dendrite growth and H_(2)O-induced side reactions during cycling.Electrolyte additive modification is considered one of the most effective and simplest methods for solving the aforementioned problems.Herein,the pyridine derivatives(PD)including 2,4-dihydroxypyridine(2,4-DHP),2,3-dihydroxypyridine(2,3-DHP),and 2-hydroxypyrdine(2-DHP),were em-ployed as novel electrolyte additives in ZnSO_(4)electrolyte.Both density functional theory calculation and experimental findings demonstrated that the incorporation of PD additives into the electrolyte effectively modulates the solvation structure of hydrated Zn ions,thereby suppressing side reactions in AZIBs.Ad-ditionally,the adsorption of PD molecules on the zinc anode surface contributed to uniform Zn deposi-tion and dendrite growth inhibition.Consequently,a 2,4-DHP-modified Zn/Zn symmetrical cell achieved an extremely long cyclic stability up to 5650 h at 1 mA cm^(-2).Furthermore,the Zn/NH_(4)V_(4)O_(10)full cell with 2,4-DHP-containing electrolyte exhibited an outstanding initial capacity of 204 mAh g^(-1),with a no-table capacity retention of 79%after 1000 cycles at 5 A g^(-1).Hence,this study expands the selection of electrolyte additives for AZIBs,and the working mechanism of PD additives provides new insights for electrolyte modification enabling highly reversible zinc anode.展开更多
All-solid-state sodium(Na)-metal batteries(ASSSMBs)are considered promising candidates for large-scale energy storage systems due to their abundant sodium resources,unparalleled safety performance,and impressive energ...All-solid-state sodium(Na)-metal batteries(ASSSMBs)are considered promising candidates for large-scale energy storage systems due to their abundant sodium resources,unparalleled safety performance,and impressive energy density.Na superionic conductors(NASICONs)are among the best enablers of ASSSMBs in view of their high ionic conductivity,ease of synthesis,and excellent thermal stability and good electrochemical/chemical compatibility with common electrodes.However,challenges surrounding the NASICON/electrode interface,such as high interfacial resistance and dendrite formation,have hindered the development of practical ASSSMBs based on NASICONs.This review starts with an explicit summary of the interface problems between the metallic Na anode and NASICON arising from mechanical,chemical,and electrochemical aspects(i.e.,poor interface contact,insulating side-reaction products,and irregular dendrite growth).Subsequently,we systematically analyze and logically categorize modification strategies for addressing anode interface problems and provide a comprehensive discussion on the underlying enhancement mechanisms.As such,we identify underlying and universal interface enhancement mechanisms by comparatively studying various modification strategies.Furthermore,we briefly summarize the challenges in the cathode/electrolyte interface and early-stage research efforts in constructing stable cathode/electrolyte interface and fabricating high-performance composite cathodes.Finally,key suggestions and future prospectives for the advancement of NASICON-based ASSSMBs are outlined.展开更多
The interfacial contacts between the electron transporting layers(ETLs)and the photoactive layers are crucial to device performance and stability for OSCs with inverted architecture.Herein,atomic layer deposition(ALD)...The interfacial contacts between the electron transporting layers(ETLs)and the photoactive layers are crucial to device performance and stability for OSCs with inverted architecture.Herein,atomic layer deposition(ALD)fabricated ultrathin Al_(2)O_(3)layers are applied to modify the ETLs/active blends(PM6:BTP-BO-4F)interfaces of OSCs,thus improving device performance.The ALD-Al_(2)O_(3)thin layers on ZnO significantly improved its surface morphology,which led to the decreased work function of ZnO and reduced recombination losses in devices.The simultaneous increase in open-circuit voltage(V_(OC)),short-circuit current density(J_(SC))and fill factor(FF)were achieved for the OSCs incorporated with ALD-Al_(2)O_(3)interlayers of a certain thickness,which produced a maximum PCE of 16.61%.Moreover,the ALD-Al_(2)O_(3)interlayers had significantly enhanced device stability by suppressing degradation of the photoactive layers induced by the photocatalytic activity of ZnO and passivating surface defects of ZnO that may play the role of active sites for the adsorption of oxygen and moisture.展开更多
Carbon-based perovskite solar cells have attracted much attention,due to their low cost,simple preparation process and high chemical stability.However,the devices exhibit low photoelectric conversion efficiency,owing ...Carbon-based perovskite solar cells have attracted much attention,due to their low cost,simple preparation process and high chemical stability.However,the devices exhibit low photoelectric conversion efficiency,owing to the presence of defects and interface impedance between the perovskite active layer and the contact interface.In order to minimize the interfacial defects and improve the charge transfer performance between the perovskite layer and the contact interface,cetyltrimethylammonium chloride(CTAC)was introduced into the lower interface of HTL-free carbon-based perovskite solar cells,because CTAC can be used as interface modification material to passivate the buried interface of perovskite and promote grain growth.It was found that CTAC can not only passivate the interface defects of perovskite,but also improve the crystalline quality of perovskite.As a result,the photovoltaic conversion efficiency of reaches 17.18%,which is 12.5%higher than that of the control group.After 20 days in air with 60%RH humidity,the cell can still maintain more than 90%of the initial efficiency,which provides a new strategy for interfacial passivation of perovskite solar cells.展开更多
For nano-collision, regulating the interaction between nanoparticles(NPs) and electrode interfaces is crucial for the precise analysis of individual NPs. However, existing ultramicroelectrodes(UMEs) suffer from narrow...For nano-collision, regulating the interaction between nanoparticles(NPs) and electrode interfaces is crucial for the precise analysis of individual NPs. However, existing ultramicroelectrodes(UMEs) suffer from narrow electrochemical window and poor electrode interface adhesion, severely hindering the application of precise single NP analysis. Here, we propose a simple and effective interface modification strategy. By electrochemically self-assembling poly(diallyldimethylammonium chloride)(PC) on the surface of carbon nanocone electrodes(CNCEs), we successfully prepared PC-modified CNCEs(PC–CNCEs). These electrodes not only possess sufficiently wide electrochemical window but also exhibit strong adhesion to negatively charged Ag NPs on their surfaces. Surface physical analysis and electrochemical molecule detection validated the high-density loading of PC on the modified electrodes. Furthermore, the working principle of PC–CNCEs for single Ag NP collision detection was further verified through the techniques of nanocollision and double-potential steps. Leveraging these significant advantages, PC–CNCEs not only achieved precise measurements of single or mixed-sized Ag NPs but also detected Ag NP solutions at concentrations as low as fmol/L levels. This advancement offers a new strategy for the rapid and precise analysis of NP colloids.展开更多
Aluminum(Al)exhibits excellent electrical conductivity,mechanical ductility,and good chemical compatibility with high-ionic-conductivity electrolytes.This makes it more suitable as an anode material for all-solid-stat...Aluminum(Al)exhibits excellent electrical conductivity,mechanical ductility,and good chemical compatibility with high-ionic-conductivity electrolytes.This makes it more suitable as an anode material for all-solid-state lithium batteries(ASSLBs)compared to the overly reactive metallic lithium anode and the mechanically weak silicon anode.This study finds that the pre-lithiated Al anode demonstrates outstanding interfacial stability with the Li_6PS_5Cl(LPSCl)electrolyte,maintaining stable cycling for over 1200 h under conditions of deep charge-discharge.This paper combines the pre-lithiated Al anode with a high-nickel cathode,LiNi_(0.8)Co_(0.1)Mn_(0.1)O_(2),paired with the highly ionic conductive LPSCl electrolyte,to design an ASSLB with high energy density and stability.Using anode pre-lithiation techniques,along with dual-reinforcement technology between the electrolyte and the cathode active material,the ASSLB achieves stable cycling for 1000 cycles at a 0.2C rate,with a capacity retention rate of up to 82.2%.At a critical negative-to-positive ratio of 1.1,the battery's specific energy reaches up to 375 Wh kg^(-1),and it maintains over 85.9%of its capacity after 100 charge-discharge cycles.This work provides a new approach and an excellent solution for developing low-cost,high-stability all-solid-state batteries.展开更多
A comprehensive understanding of the relevance between molecular structure and passivation ability to screen efficient modifiers is essential for enhancing the performance of perovskite solar cells(PSCs).Here,three si...A comprehensive understanding of the relevance between molecular structure and passivation ability to screen efficient modifiers is essential for enhancing the performance of perovskite solar cells(PSCs).Here,three similarπ-πstacking molecules namely benzophenone(BPN),diphenyl sulfone(DPS),and diphenyl sulfoxide(DPSO)are used as back-interface modifiers in carbon-based CsPbBr_(3)PSCs.After investigation,the results demonstrate the positive effect of the p-πconjugation characteristic inπ-πstacking molecules on maximizing their passivation ability.The p-πco njugation of DPSO enables a higher coordinative activity of oxygen atom in its S=O group than that in 0=S=O group of DPS and C=O group of BPN,which gives a superior passivation effect of DPSO on defects of perovskite films.The modification of DPSO also significantly improves the p-type behavior of perovskite films and the back-interfacial energetics matching,inducing an increase of hole extraction and a decrease of energy loss.Finally,the unencapsulated carbon-based CsPbBr_(3)PSCs with DPSO achieve a maximum power conversion efficiency of 10.60%and outstanding long-term stability in high-temperature,high-humidity(85℃,85%relative humidity)air environment.This work provides insights into the influence of the structure ofπ-πstacking molecules on their ability to improve the perovskite films quality and therefore the PSCs performance.展开更多
Carbonized melamine foam has been recognized as a promising material for microwave absorption due to its exceptional thermal stability,lightweight,and remarkable dielectric properties.In this study,we investigated the...Carbonized melamine foam has been recognized as a promising material for microwave absorption due to its exceptional thermal stability,lightweight,and remarkable dielectric properties.In this study,we investigated the impact of nitric acid oxidation on the surface of carbonized melamine foam and its microwave absorption properties.The treated foam exhibits optimal reflection loss of−21.51 dB at 13.20 GHz,with an effective absorption bandwidth of 7.04 GHz.The enhanced absorption properties are primarily attributed to the strengthened dielectric loss,improved impedance matching,and increased polarization losses resulting from the oxidized surfaces.This research demonstrates a promising new approach for research into surface treatments to improve the performances of microwave absorbers.展开更多
Diamond/metal composites are widely used in aerospace and electronic packaging fields due to their outstanding high thermal conductivity and low expansion.However,the difference in chemical properties leads to interfa...Diamond/metal composites are widely used in aerospace and electronic packaging fields due to their outstanding high thermal conductivity and low expansion.However,the difference in chemical properties leads to interface incompatibility between diamond and metal,which has a considerable impact on the performance of the composites.To improve the interface compatibility between diamond and metal,it is necessary to modify the interface of composites.This paper reviews the experimental research on interface modification and the application of computational simulation in diamond/metal composites.Combining computational simulation with experimental methods is a promising way to promote diamond/metal composite interface modification research.展开更多
Sulfide solid electrolytes are promising for high energy density and safety in all-solid-state batteries due to their high ionic conductivity and good mechanical properties.However,the application of sulfide solid ele...Sulfide solid electrolytes are promising for high energy density and safety in all-solid-state batteries due to their high ionic conductivity and good mechanical properties.However,the application of sulfide solid electrolytes in all-solid-state batteries with lithium anode is restricted by the side reactions at lithium/electrolytes interfaces and the growth of lithium dendrite caused by nonuniform lithium deposition.Herein,a homogeneous LiF-Li_(3)N composite protective layer is in situ formed via a manipulated reaction of pentafluorobenzamide with Li metal.The LiF-Li_(3)N layer with both high interfacial energy and interfacial adhesion energy can synergistically suppress side reactions and inhibit the growth of lithium dendrite,achieving uniform deposition of lithium.The critical current densities of Li_(10)GeP_(2)S_(12)and Li_(6)PS_(5)Cl are increased to 3.25 and 1.25 mA cm^(-2)with Li@LiF-Li_(3)N layer,which are almost triple and twice as those of Li-symmetric cells in the absence of protection layer,respectively.Moreover,the Li@LiF-Li_(3)N/Li10GeP2S12/Li@LiF-Li_(3)N cell can stably cycle for 9000 h at 0.1 mA cm^(-2)under 0.1 mA h cm^(-2),and Li@LiF-Li_(3)N/Li_(6)PS_(5)Cl/Li@LiF-Li_(3)N cell achieves stable Li plating/stripping for 8000 h at 0.1 mA cm^(-2)under10 m A h cm^(-2).The improved dynamic stability of lithium plating/stripping in Li@LiF-Li_(3)N/Li_(10)GeP_(2)S_(12)or Li_(6)PS_(5)Cl interfaces is proved by three-electrode cells.As a result,LiCoO_(2)/electrolytes/Li@LiF-Li_(3)N batteries with Li_(10)GeP_(2)S_(12)and Li_(6)PS_(5)Cl exhibit remarkable cycling stability of 500 cycles with capacity retentions of 93.5%and 89.2%at 1 C,respectively.展开更多
Since the electrode/electrolyte interface(EEI)is the main redox center of electrochemical processes,proper manipulation of the EEI microenvironment is crucial to stabilize interfacial behaviors.Here,a finger-paint met...Since the electrode/electrolyte interface(EEI)is the main redox center of electrochemical processes,proper manipulation of the EEI microenvironment is crucial to stabilize interfacial behaviors.Here,a finger-paint method is proposed to enable quick physical modification of glass-fiber separator without complicated chemical technology to modulate EEI of bilateral electrodes for aqueous zinc-ion batteries(ZIBs).An elaborate biochar derived from Aspergillus Niger is exploited as the modification agent of EEI,in which the multi-functional groups assist to accelerate Zn^(2+)desolvation and create a hydrophobic environment to homogenize the deposition behavior of Zn anode.Importantly,the finger-paint interface on separator can effectively protect cathodes from abnormal capacity fluctuation and/or rapid attenuation induced by H_(2)O molecular on the interface,which is demonstrated in modified MnO_(2),V_(2)O_(5),and KMn HCF-based cells.The as-proposed finger-paint method opens a new idea of bilateral interface engineering to facilitate the access to the practical application of the stable zinc electrochemistry.展开更多
Despite the advanced efficiency of perovskite solar cells(PSCs),electron transportation is still a pending issue.Here the polymer polyvinylpyrrolidone(PVP)is used to enhance the electron injection,which is thanks to t...Despite the advanced efficiency of perovskite solar cells(PSCs),electron transportation is still a pending issue.Here the polymer polyvinylpyrrolidone(PVP)is used to enhance the electron injection,which is thanks to the passivation of the defects at the interface between the ZnO electron transporting layer(ETL)and the perovskite.The application of the PVP layer inhibits the device degradation,and 80%of the primary efficiency is kept after 30 d storage in air condition.Additionally,the efficiency of the device is further enhanced by improving the conductivity and crystallinity of the ZnO ETL via Magnesium(Mg)doping in the ZnO nanorods(ZnO NRs).Moreover,the preparation parameters of the ZnO NRs are optimized.By employing the high-crystallinity ZnO ETL and the PVP layer,the power conversion efficiency(PCE)of the champion device is increased from 16.29%to 19.63%.These results demonstrate the advantages of combining mesoscale manipulation with interface modification and doping together.展开更多
Improved hybrid solar cells consisting of vertical aligned cadmium sulfide （CdS） nanorod arrays and interpenetrating polythiophene （P3HT） have been achieved via modification of CdS nanorod surface by using conjuga...Improved hybrid solar cells consisting of vertical aligned cadmium sulfide （CdS） nanorod arrays and interpenetrating polythiophene （P3HT） have been achieved via modification of CdS nanorod surface by using conjugated N719 dye. The complete infiltration of P3HT between CdS nanorods interspacing was verified by scanning electron microscopy. By employing absorption and photoluminescence spectra, and current-voltage characterization the interaction between N719 molecules and CdS nanorods/P3HT interface was explored, and the role of N719 dye on the improvement of device performance was discussed.展开更多
Perovskite solar cells(PSCs)have witnessed great achievement in the past decade.Most of previous researches focus on the n-i-p structure of PSCs with ultra-high efficiency.While the n-i-p devices usually used the unst...Perovskite solar cells(PSCs)have witnessed great achievement in the past decade.Most of previous researches focus on the n-i-p structure of PSCs with ultra-high efficiency.While the n-i-p devices usually used the unstable charge transport layers,such as the hygroscopic doped spiro-OMe TAD,which affect the long-term stability.The inverted device with the p-i-n structure owns better stability when using stable undoped organic molecular or metal oxide materials.There are significant progresses in inverted PSCs,most of them related to charge transport or interface engineering.In this review,we will mainly summarize the inverted PSCs progresses related to the interface engineering.After that,we prospect the future direction on inverted PSCs.展开更多
Two-dimensional materials have been widely used to tune the growth and energy-level alignment of perovskites.However,their incomplete passivation and chaotic usage amounts are not conducive to the preparation of highq...Two-dimensional materials have been widely used to tune the growth and energy-level alignment of perovskites.However,their incomplete passivation and chaotic usage amounts are not conducive to the preparation of highquality perovskite films.Herein,we succeeded in obtaining higher-quality CsPbBr_(3)films by introducing large-area monolayer graphene as a stable physical overlay on top of TiO_(2)substrates.Benefiting from the inert and atomic smooth graphene surface,the CsPbBr_(3)film grown on top by the van der Waal epitaxy has higher crystallinity,improved(100)orientation,and an average domain size of up to 1.22μm.Meanwhile,a strong downward band bending is observed at the graphene/perovskite interface,improving the electron extraction to the electron transport layers(ETL).As a result,perovskite film grown on graphene has lower photoluminescence(PL)intensity,shorter carrier lifetime,and fewer defects.Finally,a photovoltaic device based on epitaxy CsPbBr_(3)film is fabricated,exhibiting power conversion efficiency(PCE)of up to 10.64%and stability over 2000 h in the air.展开更多
The vertical phase distribution of the activelayer and the effective interface contact between the activelayer and transport layer are crucial for the photovoltaic per-formance of organic solar cells (OSCs). We synthe...The vertical phase distribution of the activelayer and the effective interface contact between the activelayer and transport layer are crucial for the photovoltaic per-formance of organic solar cells (OSCs). We synthesized an α-diketone-based polymeric donor PBTO, which was applied tobridge the copper(I) thiocyanate CuSCN and the active layer inOSCs. PBTO exhibited perfectly complementary absorptionwith those of PM6 and BTP-eC9, and the poor solubility ofBPTO in toluene renders it a layer. The coordination of con-tact between the PBTO and the CuSCN surface enhanced thebinding strength of both materials. Moreover, due to closersurface energy, PBTO can induce a favorable vertical phasedistribution in the upper active layer to achieve a p-i-n-likeconfiguration, effectively reducing carrier recombination los-ses. Through the multiple roles of the bridging agent PBTO,we achieved a wide range of photon capture, efficient chargetransport, and reduced carrier recombination. Ultimately, thedevice power conversion efficiency reached 19.02%. Our re-search results present a strategy for synergistically improvingcharge transport and optimizing vertical phase distribution inOSCs, offering new insights into the polymer molecular de-sign.展开更多
Currently,conventional organic liquid electrolytes(OLEs)are the main limiting factor for the next generation of high-energy lithium batteries.There is growing interest in inorganic solid-state electrolytes(ISEs).Howev...Currently,conventional organic liquid electrolytes(OLEs)are the main limiting factor for the next generation of high-energy lithium batteries.There is growing interest in inorganic solid-state electrolytes(ISEs).However,ISEs still face various challenges in practical applications,particularly at the interface between ISE and the electrode,which significantly affects the performance of solid-state batteries(SSBs).In recent decades,atomic and molecular layer deposition(ALD and MLD)techniques,widely used to manipulate interface properties and construct novel electrode structures,have emerged as promising strategies to address the interface challenges faced by ISEs.This review focuses on the latest developments and applications of ALD/MLD technology in SSBs,including interface modification of cathodes and lithium metal anodes.From the perspective of interface strategy mechanism,we present experimental progress and computational simulations related to interface chemistry and electrochemical stability in thermodynamic contents.In addition,this article explores the future direction and prospects for ALD/MLD in dynamic stability engineering of interfaces SSBs.展开更多
As an important component to connect the electron transport layer(ETL)and the cathode electrode,the cathode interface layer(CIL)is key to enhancing electron transport and suppressing metal electrode corrosion in inver...As an important component to connect the electron transport layer(ETL)and the cathode electrode,the cathode interface layer(CIL)is key to enhancing electron transport and suppressing metal electrode corrosion in inverted perovskite solar cells(PSCs).In this work,three D-A-D type cathode interface materials(DPP-PhN,DPP-F3N,and ffBT-F3N)are designed and synthesized employing dimethylamino-benzene or bis(dimethylamino)propyl-fluorene as electron donating(D)unit,and pyrrolo[3,4-c]-pyrrole-1,4-dione(DPP)or benzothiadiazole(BT)as electron accepting(A)unit for efficient inverted PSCs.The impact of variations in the A and D units on the energy levels,conductivity,interfacial dipoles,and carrier interfacial dynamics of CILs were systematically studied.On the one hand,DPP-F3N possesses the highest conductivity and the strongest interfacial dipole.On the other hand,the DPP-F3N is most favorable for forming ohmic contacts between the ETL and the cathode electrode to improve electron transport and prevent carrier recombination.As a result,the inverted PSCs using DPP-F3N as the CIL obtained the highest power conversion efficiency(PCE)of 25.19%.However,in terms of stability,the ffBT-F3N-based inverted PSCs show the best stability due to the strong interaction between the ffBT-F3N and the Ag electrode,which could effectively delay the corrosion of the Ag electrode.展开更多
Photocatalysis-self-Fenton system,i.e.,photo-catalytic H_(2)O_(2)generation and utilization in situ for OH radials production to remove organic pollutants with high-fluent degradation and mineralization performance po...Photocatalysis-self-Fenton system,i.e.,photo-catalytic H_(2)O_(2)generation and utilization in situ for OH radials production to remove organic pollutants with high-fluent degradation and mineralization performance pos-sesses such advantages as cleanliness,efficiency and safety.However,its degradation activity always suffers from the Fe(Ⅲ)/Fe(Ⅱ)cycle.For this reason,graphitic carbon interface-modified g-C_(3)N_(4)(CUCN)was fabricated to remarkably improve photocatalysis-self-Fenton degra-dation activity.The experiment results indicated that CUCN-2%photocatalyst,in which the loading percentage of graphitic carbon was 2%,demonstrated the optimum degradation performance among all the counterparts.The mineralization degree for RhB in 3 h over CUCN-2%reached 63.77%,nearly 3.35-fold higher than the pristine g-C_(3)N_(4).The significantly improved mineralization efficiency was ascribed to the promoted Fe(Ⅲ)/Fe(Ⅱ)cycle by photogenerated electrons,which leading to the higher utilization efficiency of H_(2)O_(2)through Fenton reaction,thereby producing more hydroxyl radicals.It is anticipated that our work could provide new insights for the design of photocatalysis-self-Fenton system with exceptional degradation performance for actual photocat-alytic applications.展开更多
Na-based layered transition metal oxides with O_(3)-type structure have been considered to be promising cathodes for Na-ion batteries. However, the intrinsically limited Na-ion conductivity induced by the Otype Na-coo...Na-based layered transition metal oxides with O_(3)-type structure have been considered to be promising cathodes for Na-ion batteries. However, the intrinsically limited Na-ion conductivity induced by the Otype Na-coordinate environment compromises their rate and cycle capability, hindering their practical application. Here, we report an interphase-structure tailoring strategy that improves the electrochemical properties of O_(3)-type layered cathodes achieved through surface coating and doping processes.Specifically, a Zr-doped interphase structure is designed in the model compound NaNi_(1/3)Mn_(1/3)Fe_(1/3)O_(2) using the ionic conductor Na_(3)Zr_(2)Si_(2)PO_(12) as the surface coating material and Zr-dopant provider. We discover that the modified NaNi_(1/3)Mn_(1/3)Fe_(1/3)O_(2)cathode shows a stable Na-storage structure as well as an enhanced rate/cycle capability. Combined with theoretical calculations, it is suggested that the superior electrochemical performances originate from the Zr-doped interphase structure, which has an enlarged Na layer spacing that forms favorable Na-ion diffusion channels. This work highlights a general material interface optimization method which opens a new perspective for fabricating high-performance electrodes for Na-ion batteries and beyond.展开更多
基金supported by the Key Science and Technol-ogy Program of Henan Province(No.232102241020)the Ph.D.Research Startup Foundation of Henan University of Science and Technology(No.400613480015)+1 种基金the Postdoctoral Research Startup Foundation of Henan University of Science and Technology(No.400613554001)the Natural Science Foundation of Henan Province(242300420021).
文摘The poor reversibility and stability of Zn anodes greatly restrict the practical application of aqueous Zn-ion batteries(AZIBs),resulting from the uncontrollable dendrite growth and H_(2)O-induced side reactions during cycling.Electrolyte additive modification is considered one of the most effective and simplest methods for solving the aforementioned problems.Herein,the pyridine derivatives(PD)including 2,4-dihydroxypyridine(2,4-DHP),2,3-dihydroxypyridine(2,3-DHP),and 2-hydroxypyrdine(2-DHP),were em-ployed as novel electrolyte additives in ZnSO_(4)electrolyte.Both density functional theory calculation and experimental findings demonstrated that the incorporation of PD additives into the electrolyte effectively modulates the solvation structure of hydrated Zn ions,thereby suppressing side reactions in AZIBs.Ad-ditionally,the adsorption of PD molecules on the zinc anode surface contributed to uniform Zn deposi-tion and dendrite growth inhibition.Consequently,a 2,4-DHP-modified Zn/Zn symmetrical cell achieved an extremely long cyclic stability up to 5650 h at 1 mA cm^(-2).Furthermore,the Zn/NH_(4)V_(4)O_(10)full cell with 2,4-DHP-containing electrolyte exhibited an outstanding initial capacity of 204 mAh g^(-1),with a no-table capacity retention of 79%after 1000 cycles at 5 A g^(-1).Hence,this study expands the selection of electrolyte additives for AZIBs,and the working mechanism of PD additives provides new insights for electrolyte modification enabling highly reversible zinc anode.
基金The authors are grateful for financial support from the National Natural Science Foundation of China(52202199)Anhui Provincial Natural Science Foundation(2108085QE202)start-up grants from Anhui University(S020318008/007,S020118002/060).
文摘All-solid-state sodium(Na)-metal batteries(ASSSMBs)are considered promising candidates for large-scale energy storage systems due to their abundant sodium resources,unparalleled safety performance,and impressive energy density.Na superionic conductors(NASICONs)are among the best enablers of ASSSMBs in view of their high ionic conductivity,ease of synthesis,and excellent thermal stability and good electrochemical/chemical compatibility with common electrodes.However,challenges surrounding the NASICON/electrode interface,such as high interfacial resistance and dendrite formation,have hindered the development of practical ASSSMBs based on NASICONs.This review starts with an explicit summary of the interface problems between the metallic Na anode and NASICON arising from mechanical,chemical,and electrochemical aspects(i.e.,poor interface contact,insulating side-reaction products,and irregular dendrite growth).Subsequently,we systematically analyze and logically categorize modification strategies for addressing anode interface problems and provide a comprehensive discussion on the underlying enhancement mechanisms.As such,we identify underlying and universal interface enhancement mechanisms by comparatively studying various modification strategies.Furthermore,we briefly summarize the challenges in the cathode/electrolyte interface and early-stage research efforts in constructing stable cathode/electrolyte interface and fabricating high-performance composite cathodes.Finally,key suggestions and future prospectives for the advancement of NASICON-based ASSSMBs are outlined.
基金financial support from National Natural Science Foundation of China(No.21875106,21850410456,21875052,51972172)the Strategic Priority Research Program of Chinese Academy of Sciences(Grant No.XDB36000000)Jiangsu Excellent Postdoctoral Program
文摘The interfacial contacts between the electron transporting layers(ETLs)and the photoactive layers are crucial to device performance and stability for OSCs with inverted architecture.Herein,atomic layer deposition(ALD)fabricated ultrathin Al_(2)O_(3)layers are applied to modify the ETLs/active blends(PM6:BTP-BO-4F)interfaces of OSCs,thus improving device performance.The ALD-Al_(2)O_(3)thin layers on ZnO significantly improved its surface morphology,which led to the decreased work function of ZnO and reduced recombination losses in devices.The simultaneous increase in open-circuit voltage(V_(OC)),short-circuit current density(J_(SC))and fill factor(FF)were achieved for the OSCs incorporated with ALD-Al_(2)O_(3)interlayers of a certain thickness,which produced a maximum PCE of 16.61%.Moreover,the ALD-Al_(2)O_(3)interlayers had significantly enhanced device stability by suppressing degradation of the photoactive layers induced by the photocatalytic activity of ZnO and passivating surface defects of ZnO that may play the role of active sites for the adsorption of oxygen and moisture.
基金National Natural Science Foundation of China (52162028)Natural Science Foundation of Jiangxi Province (20232ACB204011,20224BAB204001)+3 种基金Education Department of Jiangxi Province (GJJ2201001)Jingdezhen Municipal Science and Technology Bureau (2023GY001-16,2023ZDGG001 and 20224SF005-08)Opening Project of National Engineering Research Center for Domestic&Building Ceramics (GCZX2301)State Key Laboratory of New Ceramics and Fine Processing in Tsinghua University (KF202309,KF202414)。
文摘Carbon-based perovskite solar cells have attracted much attention,due to their low cost,simple preparation process and high chemical stability.However,the devices exhibit low photoelectric conversion efficiency,owing to the presence of defects and interface impedance between the perovskite active layer and the contact interface.In order to minimize the interfacial defects and improve the charge transfer performance between the perovskite layer and the contact interface,cetyltrimethylammonium chloride(CTAC)was introduced into the lower interface of HTL-free carbon-based perovskite solar cells,because CTAC can be used as interface modification material to passivate the buried interface of perovskite and promote grain growth.It was found that CTAC can not only passivate the interface defects of perovskite,but also improve the crystalline quality of perovskite.As a result,the photovoltaic conversion efficiency of reaches 17.18%,which is 12.5%higher than that of the control group.After 20 days in air with 60%RH humidity,the cell can still maintain more than 90%of the initial efficiency,which provides a new strategy for interfacial passivation of perovskite solar cells.
基金support from the Instrument Developing Project of the Chinese Academy of Sciences (No.YJKYYQ20210003)Natural Science Foundation of Jilin Province (No. 20210101402JC)support from the National Natural Science Foundation of China (No. 22204159)。
文摘For nano-collision, regulating the interaction between nanoparticles(NPs) and electrode interfaces is crucial for the precise analysis of individual NPs. However, existing ultramicroelectrodes(UMEs) suffer from narrow electrochemical window and poor electrode interface adhesion, severely hindering the application of precise single NP analysis. Here, we propose a simple and effective interface modification strategy. By electrochemically self-assembling poly(diallyldimethylammonium chloride)(PC) on the surface of carbon nanocone electrodes(CNCEs), we successfully prepared PC-modified CNCEs(PC–CNCEs). These electrodes not only possess sufficiently wide electrochemical window but also exhibit strong adhesion to negatively charged Ag NPs on their surfaces. Surface physical analysis and electrochemical molecule detection validated the high-density loading of PC on the modified electrodes. Furthermore, the working principle of PC–CNCEs for single Ag NP collision detection was further verified through the techniques of nanocollision and double-potential steps. Leveraging these significant advantages, PC–CNCEs not only achieved precise measurements of single or mixed-sized Ag NPs but also detected Ag NP solutions at concentrations as low as fmol/L levels. This advancement offers a new strategy for the rapid and precise analysis of NP colloids.
基金the technical support for Nano-X from Suzhou Institute of Nano-Tech and NanoBionics,Chinese Academy of Sciences(SINANO)supported by the National Key R&D Program of China(2021YFB3800300)+2 种基金the National Natural Science Foundation of China(22179059,22239002,92372201)the science and technology innovation fund for emission peak and carbon neutrality of Jiangsu province(BK20231512,BK20220034)the Key R&D project funded by department of science and technology of Jiangsu Province(BE2020003)。
文摘Aluminum(Al)exhibits excellent electrical conductivity,mechanical ductility,and good chemical compatibility with high-ionic-conductivity electrolytes.This makes it more suitable as an anode material for all-solid-state lithium batteries(ASSLBs)compared to the overly reactive metallic lithium anode and the mechanically weak silicon anode.This study finds that the pre-lithiated Al anode demonstrates outstanding interfacial stability with the Li_6PS_5Cl(LPSCl)electrolyte,maintaining stable cycling for over 1200 h under conditions of deep charge-discharge.This paper combines the pre-lithiated Al anode with a high-nickel cathode,LiNi_(0.8)Co_(0.1)Mn_(0.1)O_(2),paired with the highly ionic conductive LPSCl electrolyte,to design an ASSLB with high energy density and stability.Using anode pre-lithiation techniques,along with dual-reinforcement technology between the electrolyte and the cathode active material,the ASSLB achieves stable cycling for 1000 cycles at a 0.2C rate,with a capacity retention rate of up to 82.2%.At a critical negative-to-positive ratio of 1.1,the battery's specific energy reaches up to 375 Wh kg^(-1),and it maintains over 85.9%of its capacity after 100 charge-discharge cycles.This work provides a new approach and an excellent solution for developing low-cost,high-stability all-solid-state batteries.
基金financial supports from the Natural Science Foundation of Shandong Province(ZR2021ME037)the National Natural Science Foundation of China(52472259,22179051 and 61604143)+2 种基金the National Key Research and Development Program of China(2021YFE0111000)the Special Fund of Taishan Scholar Program of Shandong Province(tsqnz20221141)the Foundation of Key Laboratory of Advanced Technique&Preparation for Renewable Energy Materials,Ministry of Education,Yunnan Normal University(OF2022-02)。
文摘A comprehensive understanding of the relevance between molecular structure and passivation ability to screen efficient modifiers is essential for enhancing the performance of perovskite solar cells(PSCs).Here,three similarπ-πstacking molecules namely benzophenone(BPN),diphenyl sulfone(DPS),and diphenyl sulfoxide(DPSO)are used as back-interface modifiers in carbon-based CsPbBr_(3)PSCs.After investigation,the results demonstrate the positive effect of the p-πconjugation characteristic inπ-πstacking molecules on maximizing their passivation ability.The p-πco njugation of DPSO enables a higher coordinative activity of oxygen atom in its S=O group than that in 0=S=O group of DPS and C=O group of BPN,which gives a superior passivation effect of DPSO on defects of perovskite films.The modification of DPSO also significantly improves the p-type behavior of perovskite films and the back-interfacial energetics matching,inducing an increase of hole extraction and a decrease of energy loss.Finally,the unencapsulated carbon-based CsPbBr_(3)PSCs with DPSO achieve a maximum power conversion efficiency of 10.60%and outstanding long-term stability in high-temperature,high-humidity(85℃,85%relative humidity)air environment.This work provides insights into the influence of the structure ofπ-πstacking molecules on their ability to improve the perovskite films quality and therefore the PSCs performance.
基金Project(2023RC3066)supported by the Science and Technology Innovation Program of Hunan Province,ChinaProject(2023JJ50079)supported by the Hunan Provincial Natural Science Foundation,China。
文摘Carbonized melamine foam has been recognized as a promising material for microwave absorption due to its exceptional thermal stability,lightweight,and remarkable dielectric properties.In this study,we investigated the impact of nitric acid oxidation on the surface of carbonized melamine foam and its microwave absorption properties.The treated foam exhibits optimal reflection loss of−21.51 dB at 13.20 GHz,with an effective absorption bandwidth of 7.04 GHz.The enhanced absorption properties are primarily attributed to the strengthened dielectric loss,improved impedance matching,and increased polarization losses resulting from the oxidized surfaces.This research demonstrates a promising new approach for research into surface treatments to improve the performances of microwave absorbers.
基金financially supported by the National Natural Science Foundation of China(Nos.52071117 and 51771063)the Heilongjiang Provincial Science Fund for Distinguished Young Scholars(No.JQ2021E002)。
文摘Diamond/metal composites are widely used in aerospace and electronic packaging fields due to their outstanding high thermal conductivity and low expansion.However,the difference in chemical properties leads to interface incompatibility between diamond and metal,which has a considerable impact on the performance of the composites.To improve the interface compatibility between diamond and metal,it is necessary to modify the interface of composites.This paper reviews the experimental research on interface modification and the application of computational simulation in diamond/metal composites.Combining computational simulation with experimental methods is a promising way to promote diamond/metal composite interface modification research.
基金supported by the National Key R&D Program of China(2022YFB3807700)the National Natural Science Foundation of China(U1964205,51872303,52172253)+3 种基金the Ningbo S&T Innovation 2025 Major Special Programme(2019B10044,2021Z122)the Zhejiang Provincial Key R&D Program of China(2022C01072)the Jiangsu Provincial S&T Innovation Special Programme for carbon peak and carbon neutrality(BE2022007)the Youth Innovation Promotion Association CAS(Y2021080)。
文摘Sulfide solid electrolytes are promising for high energy density and safety in all-solid-state batteries due to their high ionic conductivity and good mechanical properties.However,the application of sulfide solid electrolytes in all-solid-state batteries with lithium anode is restricted by the side reactions at lithium/electrolytes interfaces and the growth of lithium dendrite caused by nonuniform lithium deposition.Herein,a homogeneous LiF-Li_(3)N composite protective layer is in situ formed via a manipulated reaction of pentafluorobenzamide with Li metal.The LiF-Li_(3)N layer with both high interfacial energy and interfacial adhesion energy can synergistically suppress side reactions and inhibit the growth of lithium dendrite,achieving uniform deposition of lithium.The critical current densities of Li_(10)GeP_(2)S_(12)and Li_(6)PS_(5)Cl are increased to 3.25 and 1.25 mA cm^(-2)with Li@LiF-Li_(3)N layer,which are almost triple and twice as those of Li-symmetric cells in the absence of protection layer,respectively.Moreover,the Li@LiF-Li_(3)N/Li10GeP2S12/Li@LiF-Li_(3)N cell can stably cycle for 9000 h at 0.1 mA cm^(-2)under 0.1 mA h cm^(-2),and Li@LiF-Li_(3)N/Li_(6)PS_(5)Cl/Li@LiF-Li_(3)N cell achieves stable Li plating/stripping for 8000 h at 0.1 mA cm^(-2)under10 m A h cm^(-2).The improved dynamic stability of lithium plating/stripping in Li@LiF-Li_(3)N/Li_(10)GeP_(2)S_(12)or Li_(6)PS_(5)Cl interfaces is proved by three-electrode cells.As a result,LiCoO_(2)/electrolytes/Li@LiF-Li_(3)N batteries with Li_(10)GeP_(2)S_(12)and Li_(6)PS_(5)Cl exhibit remarkable cycling stability of 500 cycles with capacity retentions of 93.5%and 89.2%at 1 C,respectively.
基金financial support from the National Natural Science Foundation of China (21571080 and 52202253)the Natural Science Foundation of Jiangsu Province (BK20220914)+2 种基金Project funded by China Postdoctoral Science Foundation (2022M721593)the Jiangsu Funding Program for Excellent Postdoctoral Talent (2022ZB193)the financial support from International Center of Future Science,Jilin University,Changchun,P.R.China (ICFS Seed Funding for Young Researchers)。
文摘Since the electrode/electrolyte interface(EEI)is the main redox center of electrochemical processes,proper manipulation of the EEI microenvironment is crucial to stabilize interfacial behaviors.Here,a finger-paint method is proposed to enable quick physical modification of glass-fiber separator without complicated chemical technology to modulate EEI of bilateral electrodes for aqueous zinc-ion batteries(ZIBs).An elaborate biochar derived from Aspergillus Niger is exploited as the modification agent of EEI,in which the multi-functional groups assist to accelerate Zn^(2+)desolvation and create a hydrophobic environment to homogenize the deposition behavior of Zn anode.Importantly,the finger-paint interface on separator can effectively protect cathodes from abnormal capacity fluctuation and/or rapid attenuation induced by H_(2)O molecular on the interface,which is demonstrated in modified MnO_(2),V_(2)O_(5),and KMn HCF-based cells.The as-proposed finger-paint method opens a new idea of bilateral interface engineering to facilitate the access to the practical application of the stable zinc electrochemistry.
基金Project supported by Beijing Natural Science Foundation,China(Grant No.2202030)the National Natural Science Foundation of China(Grant No.41422050303)+1 种基金the Program of Introducing Talents of Discipline to Universities(Grant No.B14003)the Fundamental Research Funds for Central Universities,China(Grant Nos.FRF-GF-19-001A and FRF-GF-19-002B).
文摘Despite the advanced efficiency of perovskite solar cells(PSCs),electron transportation is still a pending issue.Here the polymer polyvinylpyrrolidone(PVP)is used to enhance the electron injection,which is thanks to the passivation of the defects at the interface between the ZnO electron transporting layer(ETL)and the perovskite.The application of the PVP layer inhibits the device degradation,and 80%of the primary efficiency is kept after 30 d storage in air condition.Additionally,the efficiency of the device is further enhanced by improving the conductivity and crystallinity of the ZnO ETL via Magnesium(Mg)doping in the ZnO nanorods(ZnO NRs).Moreover,the preparation parameters of the ZnO NRs are optimized.By employing the high-crystallinity ZnO ETL and the PVP layer,the power conversion efficiency(PCE)of the champion device is increased from 16.29%to 19.63%.These results demonstrate the advantages of combining mesoscale manipulation with interface modification and doping together.
基金supported by the National Natural Science Foundation of China (Nos. 50990063, 51261130582 and 91233114)
文摘Improved hybrid solar cells consisting of vertical aligned cadmium sulfide （CdS） nanorod arrays and interpenetrating polythiophene （P3HT） have been achieved via modification of CdS nanorod surface by using conjugated N719 dye. The complete infiltration of P3HT between CdS nanorods interspacing was verified by scanning electron microscopy. By employing absorption and photoluminescence spectra, and current-voltage characterization the interaction between N719 molecules and CdS nanorods/P3HT interface was explored, and the role of N719 dye on the improvement of device performance was discussed.
基金supported by the National Natural Science Foundation of China(Grant No.61925405)the National Key Research and Development Program of China(Grant No.2020YFB1506400)。
文摘Perovskite solar cells(PSCs)have witnessed great achievement in the past decade.Most of previous researches focus on the n-i-p structure of PSCs with ultra-high efficiency.While the n-i-p devices usually used the unstable charge transport layers,such as the hygroscopic doped spiro-OMe TAD,which affect the long-term stability.The inverted device with the p-i-n structure owns better stability when using stable undoped organic molecular or metal oxide materials.There are significant progresses in inverted PSCs,most of them related to charge transport or interface engineering.In this review,we will mainly summarize the inverted PSCs progresses related to the interface engineering.After that,we prospect the future direction on inverted PSCs.
基金funded by the UM’s research funds(MYRG2020-00283-IAPME,MYRG2022-00266-IAPME,and MYRG-GRG2023-00224-IAPME-UMDF)the Science and Technology Development Fund,Macao SAR(FDCT 0006/2021/AKP,FDCT 0096/2020/A2,0013/2021/AMJ,and 0082/2022/A2)City University of Hong Kong(Project No.9020002)
文摘Two-dimensional materials have been widely used to tune the growth and energy-level alignment of perovskites.However,their incomplete passivation and chaotic usage amounts are not conducive to the preparation of highquality perovskite films.Herein,we succeeded in obtaining higher-quality CsPbBr_(3)films by introducing large-area monolayer graphene as a stable physical overlay on top of TiO_(2)substrates.Benefiting from the inert and atomic smooth graphene surface,the CsPbBr_(3)film grown on top by the van der Waal epitaxy has higher crystallinity,improved(100)orientation,and an average domain size of up to 1.22μm.Meanwhile,a strong downward band bending is observed at the graphene/perovskite interface,improving the electron extraction to the electron transport layers(ETL).As a result,perovskite film grown on graphene has lower photoluminescence(PL)intensity,shorter carrier lifetime,and fewer defects.Finally,a photovoltaic device based on epitaxy CsPbBr_(3)film is fabricated,exhibiting power conversion efficiency(PCE)of up to 10.64%and stability over 2000 h in the air.
基金supported by the National Natural Science Foundation of China (22379011 and 52373169)。
文摘The vertical phase distribution of the activelayer and the effective interface contact between the activelayer and transport layer are crucial for the photovoltaic per-formance of organic solar cells (OSCs). We synthesized an α-diketone-based polymeric donor PBTO, which was applied tobridge the copper(I) thiocyanate CuSCN and the active layer inOSCs. PBTO exhibited perfectly complementary absorptionwith those of PM6 and BTP-eC9, and the poor solubility ofBPTO in toluene renders it a layer. The coordination of con-tact between the PBTO and the CuSCN surface enhanced thebinding strength of both materials. Moreover, due to closersurface energy, PBTO can induce a favorable vertical phasedistribution in the upper active layer to achieve a p-i-n-likeconfiguration, effectively reducing carrier recombination los-ses. Through the multiple roles of the bridging agent PBTO,we achieved a wide range of photon capture, efficient chargetransport, and reduced carrier recombination. Ultimately, thedevice power conversion efficiency reached 19.02%. Our re-search results present a strategy for synergistically improvingcharge transport and optimizing vertical phase distribution inOSCs, offering new insights into the polymer molecular de-sign.
基金Natural Sciences and Engineering Research Council of Canada(NSERC)Fonds de Recherche du Québec-Nature et Technologies(FRQNT)+3 种基金Centre Québécois sur les Materiaux Fonctionnels(CQMF)Réseau québécois sur l'énergie intelligente(RQEI)École de Technologie Supérieure(ÉTS)Canada Research Chairs Program。
文摘Currently,conventional organic liquid electrolytes(OLEs)are the main limiting factor for the next generation of high-energy lithium batteries.There is growing interest in inorganic solid-state electrolytes(ISEs).However,ISEs still face various challenges in practical applications,particularly at the interface between ISE and the electrode,which significantly affects the performance of solid-state batteries(SSBs).In recent decades,atomic and molecular layer deposition(ALD and MLD)techniques,widely used to manipulate interface properties and construct novel electrode structures,have emerged as promising strategies to address the interface challenges faced by ISEs.This review focuses on the latest developments and applications of ALD/MLD technology in SSBs,including interface modification of cathodes and lithium metal anodes.From the perspective of interface strategy mechanism,we present experimental progress and computational simulations related to interface chemistry and electrochemical stability in thermodynamic contents.In addition,this article explores the future direction and prospects for ALD/MLD in dynamic stability engineering of interfaces SSBs.
基金supported by the National Natural Science Foundation of China(22109142,52102142,52403253)the Natural Science Foundation of Henan Province(232300421360).
文摘As an important component to connect the electron transport layer(ETL)and the cathode electrode,the cathode interface layer(CIL)is key to enhancing electron transport and suppressing metal electrode corrosion in inverted perovskite solar cells(PSCs).In this work,three D-A-D type cathode interface materials(DPP-PhN,DPP-F3N,and ffBT-F3N)are designed and synthesized employing dimethylamino-benzene or bis(dimethylamino)propyl-fluorene as electron donating(D)unit,and pyrrolo[3,4-c]-pyrrole-1,4-dione(DPP)or benzothiadiazole(BT)as electron accepting(A)unit for efficient inverted PSCs.The impact of variations in the A and D units on the energy levels,conductivity,interfacial dipoles,and carrier interfacial dynamics of CILs were systematically studied.On the one hand,DPP-F3N possesses the highest conductivity and the strongest interfacial dipole.On the other hand,the DPP-F3N is most favorable for forming ohmic contacts between the ETL and the cathode electrode to improve electron transport and prevent carrier recombination.As a result,the inverted PSCs using DPP-F3N as the CIL obtained the highest power conversion efficiency(PCE)of 25.19%.However,in terms of stability,the ffBT-F3N-based inverted PSCs show the best stability due to the strong interaction between the ffBT-F3N and the Ag electrode,which could effectively delay the corrosion of the Ag electrode.
基金financially supported by National Natural Science Foundation of China (No. 21906132)Department of Science and Technology of Sichuan Province (Nos. 2020YFG0158 and 2020YFH0162)Sichuan Provincial Engineering Laboratory of Livestock Manure Treatment and Recycling (Sichuan Normal University) (No. 202104)
文摘Photocatalysis-self-Fenton system,i.e.,photo-catalytic H_(2)O_(2)generation and utilization in situ for OH radials production to remove organic pollutants with high-fluent degradation and mineralization performance pos-sesses such advantages as cleanliness,efficiency and safety.However,its degradation activity always suffers from the Fe(Ⅲ)/Fe(Ⅱ)cycle.For this reason,graphitic carbon interface-modified g-C_(3)N_(4)(CUCN)was fabricated to remarkably improve photocatalysis-self-Fenton degra-dation activity.The experiment results indicated that CUCN-2%photocatalyst,in which the loading percentage of graphitic carbon was 2%,demonstrated the optimum degradation performance among all the counterparts.The mineralization degree for RhB in 3 h over CUCN-2%reached 63.77%,nearly 3.35-fold higher than the pristine g-C_(3)N_(4).The significantly improved mineralization efficiency was ascribed to the promoted Fe(Ⅲ)/Fe(Ⅱ)cycle by photogenerated electrons,which leading to the higher utilization efficiency of H_(2)O_(2)through Fenton reaction,thereby producing more hydroxyl radicals.It is anticipated that our work could provide new insights for the design of photocatalysis-self-Fenton system with exceptional degradation performance for actual photocat-alytic applications.
基金The University of Chinese Academy of Sciences,and the Scientific Instrument Developing Project of the Chinese Academy of Sciences (ZDKYYQ20170001):China the Guangdong Basic and Applied Basic Research Foundation (2019A1515111025) China the Japan Synchrotron Radiation Research Institute (2019B1096)Japan。
文摘Na-based layered transition metal oxides with O_(3)-type structure have been considered to be promising cathodes for Na-ion batteries. However, the intrinsically limited Na-ion conductivity induced by the Otype Na-coordinate environment compromises their rate and cycle capability, hindering their practical application. Here, we report an interphase-structure tailoring strategy that improves the electrochemical properties of O_(3)-type layered cathodes achieved through surface coating and doping processes.Specifically, a Zr-doped interphase structure is designed in the model compound NaNi_(1/3)Mn_(1/3)Fe_(1/3)O_(2) using the ionic conductor Na_(3)Zr_(2)Si_(2)PO_(12) as the surface coating material and Zr-dopant provider. We discover that the modified NaNi_(1/3)Mn_(1/3)Fe_(1/3)O_(2)cathode shows a stable Na-storage structure as well as an enhanced rate/cycle capability. Combined with theoretical calculations, it is suggested that the superior electrochemical performances originate from the Zr-doped interphase structure, which has an enlarged Na layer spacing that forms favorable Na-ion diffusion channels. This work highlights a general material interface optimization method which opens a new perspective for fabricating high-performance electrodes for Na-ion batteries and beyond.
