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
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
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
With the advantages of similar theoretical basis to lithium batteries,relatively low budget and the abundance of sodium resources,sodium ion batteries(SIBs)are recognized as the most competitive alternative to lithium...With the advantages of similar theoretical basis to lithium batteries,relatively low budget and the abundance of sodium resources,sodium ion batteries(SIBs)are recognized as the most competitive alternative to lithium-ion batteries.Among various types of cathodes for SIBs,advan-tages of high theoretical capacity,nontoxic and facile synthesis are introduced for layered transition metal oxide cathodes and therefore they have attracted huge attention.Nevertheless,layered oxide cathodes suffer from various degradation issues.Among these issues,interface instability including surface residues,phase transitions,loss of active transition metal and oxygen loss takes up the major part of the degra-dation of layered oxides.These degradation mechanisms usually lead to irreversible structure collapse and cracking generation,which signifi-cantly influence the interface stability and electrochemical performance of layered cathodes.This review briefly introduces the background of researches on layered cathodes for SIBs and their basic structure types.Then the origins and effects on layered cathodes of degradation mech-anisms are systematically concluded.Finally,we will summarize various interface modification methods including surface engineering,doping modification and electrolyte composition which are aimed to improve interface stability of layered cathodes,perspectives of future research on layered cathodes are mentioned to provide some theoretical proposals.展开更多
Fabric-based composites with superior mechanical properties and excellent perceptive function are highly desirable.However,it remains a huge challenge to attain structure-function integration,especially for hybrid fab...Fabric-based composites with superior mechanical properties and excellent perceptive function are highly desirable.However,it remains a huge challenge to attain structure-function integration,especially for hybrid fabric composites.Herein,a skin-inspired interface modification strategy is proposed toward this target by constructing a hybrid smart fabric system consisting of two types of smart fabrics:carbon nanotube(CNT)/MXene-modified aramid fabrics and zinc oxide nanorod(ZnO NR)-modified carbon fabrics.Based on that,flexible piezoelectric pressure sensors with skin-like hierarchical perception interfaces are fabricated,which demonstrate superb sensitivity of 2.39 V·kPa^(-1)and are capable of various wearable monitoring tasks.Besides,the interface-modified hybrid fabric reinforced plastics can also be fabricated,which are proven to possess 13.6%higher tensile strength,10.1%elastic modulus.More impressively,their average energy absorption can be improved by 111.9%,accompanied with inherent damage alert capability.This offers a paradigm to fabricate structure-function integrated hybrid smart fabric composites for the smart clothing and intelligent aerial vehicles.展开更多
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
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
A TiO2/P3HT hybrid solar cell was fabricated by infiltrating P3HT into the pores of TiO2 nanorod arrays. To further enhance the photovoltaic performance, anthracene-9-carboxylic acid was employed to modify the interfa...A TiO2/P3HT hybrid solar cell was fabricated by infiltrating P3HT into the pores of TiO2 nanorod arrays. To further enhance the photovoltaic performance, anthracene-9-carboxylic acid was employed to modify the interface of TiO2/P3HT before P3HT was coated. Results revealed that the interface treatment significantly enhances the photovoltaic performance of the cell. The efficiency of the hybrid solar cells reaches 0.28% after interface modification, which is three times higher compared with the un-modified one. We find that except for the increased exciton dissociation efficiency recognized by the previous reports, the suppressing of electron back recombination is another important factor leading to the enhanced photovoltaic performance.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
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
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
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
We use a single-molecule self-assembled layer of an aromatic organophosphonic acid(2PACz) to modify the cathode interface layer in inverted organic solar cells(OSCs). The modified OSCs not only have an obvious improve...We use a single-molecule self-assembled layer of an aromatic organophosphonic acid(2PACz) to modify the cathode interface layer in inverted organic solar cells(OSCs). The modified OSCs not only have an obvious improvement in power conversion efficiency(PCE), but also demonstrate greatly enhanced air stability. Ultraviolet photoelectron spectroscopy shows that the work function of cathode interlayer after modification by 2PACz is more suitable for electron extraction. In addition, the surface energy is reduced without affecting the film deposition, which will be beneficial to reduce the interfacial traps. As a result,the PCE of OSCs based on the PBDB-T:IT-M system is increased, and its stability in air is greatly improved(remaining 88% of its initial PCE after 555 h in air). Therefore, we provide a new strategy for constructing high-performance non-fullerene OSCs with enhanced air stability.展开更多
Due to the long carrier lifetime,high carrier mobility,and high absorption coefficient of perovskite materials,the power conversion efficiency(PCE)of perovskite solar cells(PSCs)has increased from 3.8%in 2009 to 25.7%...Due to the long carrier lifetime,high carrier mobility,and high absorption coefficient of perovskite materials,the power conversion efficiency(PCE)of perovskite solar cells(PSCs)has increased from 3.8%in 2009 to 25.7%in 2021,which have already surpassed the PCE of thin-film solar cells and closes to the efficiency of Si-based photovoltaics(26.7%).Therefore,PSCs have become a promising clean energy technology for commercialization.However,the low defect formation energy of perovskite leads to a higher defect density than other conventional photovoltaic materials.It results in severe non-radiative recombination,limiting its further development and the commercialization.In this review,we summarize the mechanism and strategies for high-quality perovskite absorber fabrications to minimize the bulk and surface/interface defects of halide perovskite,including film quality development and interface modification.Strategies are proposed for further promoting the film quality and the corresponding device performance.Finally,we highlight the challenges that need to be overcome to control over the defect properties of halide perovskite.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
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 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 Key Research and Development Program of China (grant no.2022YFB2502000)the National Natural Science Foundation of China (grant no.U21A2033251771076)+1 种基金Guangdong Basic and Applied Basic Research Foundation (grant nos.2020B1515120049,2021A151-5010332,and 2021A1515010153)R&D Program in Key Areas of Guangdong Province (grant no.2020B0101030005).
文摘With the advantages of similar theoretical basis to lithium batteries,relatively low budget and the abundance of sodium resources,sodium ion batteries(SIBs)are recognized as the most competitive alternative to lithium-ion batteries.Among various types of cathodes for SIBs,advan-tages of high theoretical capacity,nontoxic and facile synthesis are introduced for layered transition metal oxide cathodes and therefore they have attracted huge attention.Nevertheless,layered oxide cathodes suffer from various degradation issues.Among these issues,interface instability including surface residues,phase transitions,loss of active transition metal and oxygen loss takes up the major part of the degra-dation of layered oxides.These degradation mechanisms usually lead to irreversible structure collapse and cracking generation,which signifi-cantly influence the interface stability and electrochemical performance of layered cathodes.This review briefly introduces the background of researches on layered cathodes for SIBs and their basic structure types.Then the origins and effects on layered cathodes of degradation mech-anisms are systematically concluded.Finally,we will summarize various interface modification methods including surface engineering,doping modification and electrolyte composition which are aimed to improve interface stability of layered cathodes,perspectives of future research on layered cathodes are mentioned to provide some theoretical proposals.
基金supported by the National Natural Science Foundation of China(Nos.52205298,52375280 and 51775022)Project funded by China Postdoctoral Science Foundation(Nos.2022M710302 and 2022TQ0023)the Fundamental Research Funds for the Central Universities.
文摘Fabric-based composites with superior mechanical properties and excellent perceptive function are highly desirable.However,it remains a huge challenge to attain structure-function integration,especially for hybrid fabric composites.Herein,a skin-inspired interface modification strategy is proposed toward this target by constructing a hybrid smart fabric system consisting of two types of smart fabrics:carbon nanotube(CNT)/MXene-modified aramid fabrics and zinc oxide nanorod(ZnO NR)-modified carbon fabrics.Based on that,flexible piezoelectric pressure sensors with skin-like hierarchical perception interfaces are fabricated,which demonstrate superb sensitivity of 2.39 V·kPa^(-1)and are capable of various wearable monitoring tasks.Besides,the interface-modified hybrid fabric reinforced plastics can also be fabricated,which are proven to possess 13.6%higher tensile strength,10.1%elastic modulus.More impressively,their average energy absorption can be improved by 111.9%,accompanied with inherent damage alert capability.This offers a paradigm to fabricate structure-function integrated hybrid smart fabric composites for the smart clothing and intelligent aerial vehicles.
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 the China Postdoctoral Science Foundation(Nos.2012M511690,2014T70747)the Research Fund for the Doctoral Program of Higher Education of China(No.20130143130002)+2 种基金the National Natural Science Foundation of China(Nos.11174071,11304088,51372180)the Natural Science Foundation of Hubei Province(Nos.2011CDB056,2013CFA008)the Science and Technology Planning Project of Wuhan City(No.201210711237)
文摘A TiO2/P3HT hybrid solar cell was fabricated by infiltrating P3HT into the pores of TiO2 nanorod arrays. To further enhance the photovoltaic performance, anthracene-9-carboxylic acid was employed to modify the interface of TiO2/P3HT before P3HT was coated. Results revealed that the interface treatment significantly enhances the photovoltaic performance of the cell. The efficiency of the hybrid solar cells reaches 0.28% after interface modification, which is three times higher compared with the un-modified one. We find that except for the increased exciton dissociation efficiency recognized by the previous reports, the suppressing of electron back recombination is another important factor leading to the enhanced photovoltaic performance.
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Financial support from the National Natural Science Foundation of China (No. 51973020)。
文摘We use a single-molecule self-assembled layer of an aromatic organophosphonic acid(2PACz) to modify the cathode interface layer in inverted organic solar cells(OSCs). The modified OSCs not only have an obvious improvement in power conversion efficiency(PCE), but also demonstrate greatly enhanced air stability. Ultraviolet photoelectron spectroscopy shows that the work function of cathode interlayer after modification by 2PACz is more suitable for electron extraction. In addition, the surface energy is reduced without affecting the film deposition, which will be beneficial to reduce the interfacial traps. As a result,the PCE of OSCs based on the PBDB-T:IT-M system is increased, and its stability in air is greatly improved(remaining 88% of its initial PCE after 555 h in air). Therefore, we provide a new strategy for constructing high-performance non-fullerene OSCs with enhanced air stability.
基金support from the National Natural Science Foundation of China(52172182,21975028)。
文摘Due to the long carrier lifetime,high carrier mobility,and high absorption coefficient of perovskite materials,the power conversion efficiency(PCE)of perovskite solar cells(PSCs)has increased from 3.8%in 2009 to 25.7%in 2021,which have already surpassed the PCE of thin-film solar cells and closes to the efficiency of Si-based photovoltaics(26.7%).Therefore,PSCs have become a promising clean energy technology for commercialization.However,the low defect formation energy of perovskite leads to a higher defect density than other conventional photovoltaic materials.It results in severe non-radiative recombination,limiting its further development and the commercialization.In this review,we summarize the mechanism and strategies for high-quality perovskite absorber fabrications to minimize the bulk and surface/interface defects of halide perovskite,including film quality development and interface modification.Strategies are proposed for further promoting the film quality and the corresponding device performance.Finally,we highlight the challenges that need to be overcome to control over the defect properties of halide perovskite.
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.
