In recent years,significant progress has been achieved in the creation of innovative functional materials for energy storage and conversion.Due to their distinct physicochemical characteristics,ultrathin nanosheets co...In recent years,significant progress has been achieved in the creation of innovative functional materials for energy storage and conversion.Due to their distinct physicochemical characteristics,ultrathin nanosheets composed of common layered transition metal sulfide materials(MoS2)have demonstrated promise as high-capacity anode materials for lithium-ion batteries(LIBs).Nevertheless,their practical application is severely limited by the tendency of monolayer nanosheets to restack due to strong van der Waals forces,dramatic volume changes during successive cycles,and low intrinsic conductivity.Recent research advances have shown that composite structures and nanowire morphologies with specific morphologies effectively overcome these issues.This paper reviews the recent research progress on molybdenum disulfide-based composites as anode materials for LIBs and discusses in detail the struc-tural characteristics of pure molybdenum disulfide and other composite forms of molybdenum disulfide.In addition,the phase engineering,defect engineering,and lithium storage mechanisms of molybdenum disulfide and the synthesis of molybdenum disulfide-based nanocomposites by different preparation methods are focused on.Finally,we review the design(structure),recent developments,and challenges of novel anode materials and consider their electrochemical performance in Li-ion batteries.展开更多
Photocatalytic H_(2) evolution from seawater splitting presents a promising approach to tackle the fossil energy crisis and mitigate carbon emission due to the abundant source of seawater and sunlight on the earth.How...Photocatalytic H_(2) evolution from seawater splitting presents a promising approach to tackle the fossil energy crisis and mitigate carbon emission due to the abundant source of seawater and sunlight on the earth.However,the development of efficient photocatalysts for seawater splitting remains a formidable challenge.Herein,a 2D/2D ZnIn_(2)S_(4)/WO_(3)(ZIS/WO_(3))heterojunction nanostructure is fabricated to efficiently separate the photoinduced carriers by steering electron transfer from the conduction band minimum of WO_(3) to the valence band maximum of ZIS via constructing internal electric field.Subsequently,plasmonic Au nanoparticles(NPs)as a novel photosensitizer and a reduction cocatalyst are anchored on ZIS/WO_(3) surface to further enhance the optical absorption of ZIS/WO_(3) heterojunction and accelerate the catalytic conversion.The obtained Au/ZIS/WO_(3) photocatalyst exhibits an outstanding H_(2) evolution rate of 2610.6 or 3566.3μmol g^(-1)h~(-1)from seawater splitting under visible or full-spectrum light irradiation,respectively.These rates represent an impressive increase of approximately 7.3-and 6,6-fold compared to those of ZIS under the illumination of the same light source.The unique 2D/2D structure,internal electric field,and plasmonic metal modification together boost the photocatalytic H_(2) evolution rate of Au/ZIS/WO_(3),making it even comparable to H_(2) evolution from pure water splitting.The present work sheds light on the development of efficient photocatalysts for seawater splitting.展开更多
Redox p-type organic compounds are promising cathode materials for dual-ion batteries.However,the triphenylamine-based polymers usually with agglomerate and intertwined molecular chain nature limit the maximum reactio...Redox p-type organic compounds are promising cathode materials for dual-ion batteries.However,the triphenylamine-based polymers usually with agglomerate and intertwined molecular chain nature limit the maximum reaction of their active sites with large-sized anions.Herein,we demonstrate the application of a small molecule with rigid spirofluorene structu re,namely 2,2’,7,7’-tetrakis(diphenylamine)-9,9’-spirobifluorene(Spiro-TAD),as a cathode material for lithium dual-ion batteries.The inherent sterical structure endows the Spiro-TAD with good chemical stability and large internal space for fast diffusion kinetics of anions in the organic electrolyte.As a result,the Spiro-TAD electrode shows significant insolubility and less steric hindrance,and gives a high actual capacity of 109 mA h g^(-1)(active groups utilization ratio approximately 100%) at 50 mA g^(-1)with a high discharge voltage of 3.6 V(vs.Li+/Li),excellent rate capability(60 mA h g^(-1)at 2000 mA g^(-1)) and extremely stable cycling life(98.4% capacity retention after 1400 cycles at 500 mA g^(-1)) in half cells.Such good electrochemical performance is attributed to the robust and rapid adsorption/desorption of ClO4-anions,which can be proved by the in-situ FTIR and XPS.Moreover,an all-organic lithium dual-ion battery(a-OLDIBs) is constructed using the Spiro-TAD as cathode and 3,4,9,10-Perylenetetracarboxylic diimide(PTCDI) as anode and displays long-term cycling performance of 87.5 mA h g^(-1)after 800 cycles.This study will stimulate further developments in designing all organic battery systems.展开更多
For patients with osteoporosis,the therapeutic outcomes of osteoimplants are substantially affected by the impaired proliferation,migration,and osteogenic differentiation abilities of bone marrow mesenchymal stem cell...For patients with osteoporosis,the therapeutic outcomes of osteoimplants are substantially affected by the impaired proliferation,migration,and osteogenic differentiation abilities of bone marrow mesenchymal stem cells(BMSCs).展开更多
Usually it is generally believed that the Er element forms the Er_(2)Fe_(14)B phase,which will seriously deteriorate the magnetic properties.Distinctly,here we report the balance of corrosion resistance and coercivity...Usually it is generally believed that the Er element forms the Er_(2)Fe_(14)B phase,which will seriously deteriorate the magnetic properties.Distinctly,here we report the balance of corrosion resistance and coercivity in Nd-Fe-B sintered magnets through using simple Er_(30)Cu_(70) additive whose price is much lower than Dy and Tb.By reasonably controlling Er_(30)Cu_(70) addition,the corrosion resistance is improved at the minimum limit of reducing the magnetic properties.Through studying the influence mechanism of Er element,it is found that the main effect of Er elements is to replace the Nd elements at the edge of the main phase grains to form a(Er,Nd)_(2)Fe_(14)B shell with low H_(A),resulting in the reduction of magnetic properties.The improvement of corrosion resistance mainly comes from the more stable Cu element introduced at the grain boundary.At the same time,the target magnets also show different advantages under different heat treatment methods.Above findings may spur progress towards developing the lowcost permanent magnets that rival the commercial Nd-Fe-B counterpart.展开更多
With the thermal simulated technology, the continuous cooling transforming curve (SH-CCT) of domestic X80 was measured, and the variation rule of the microstructure of coarsened-grain heat-affected zone(CGHAZ) for...With the thermal simulated technology, the continuous cooling transforming curve (SH-CCT) of domestic X80 was measured, and the variation rule of the microstructure of coarsened-grain heat-affected zone(CGHAZ) for X80 pipeline steel was also investigated. The results indicate that the hardenability and the hydrogen cracking susceptibility of domestic X80 are fairly low.展开更多
Lead-free halide perovskite materials possess low toxicity,broadband luminescence and robust stability compared with conventional lead-based perovskites,thus holding great promise for eyes-friendly white light LEDs.Ho...Lead-free halide perovskite materials possess low toxicity,broadband luminescence and robust stability compared with conventional lead-based perovskites,thus holding great promise for eyes-friendly white light LEDs.However,the traditionally used preparation methods with a long period and limited product yield have curtailed the commercialization of these materials.Here we introduce a universal hydrochloric acid-assistant powder-to-powder strategy which can accomplish the goals of thermal-,pressure-free,eco-friendliness,short time,low cost and high product yield,simultaneously.The obtained Cs_(2)Na_(0.9)Ag_(0.1)In_(0.95)Bi_(0.05)Cl_(6)microcrystals exhibit bright self-trapped excitons emission with quantum yield of(98.3±3.8)%,which could retain(90.5±1.3)%and(96.8±0.8)%after continuous heating or ultraviolet-irradiation for 1000 h,respectively.The phosphor converted-LED exhibited near-unity conversion efficiency from ultraviolet chip to self-trapped excitons emission at~200 mA.Various ions doping(such as Cs_(2)Na_(0.9)Ag_(0.1)InCl_(6):Ln^(3+))and other derived lead-free perovskite materials(such as Cs_(2)ZrCl_(6)and Cs_(4)MnBi_(2)Cl_(12))with high luminous performance are all realized by our proposed strategy,which has shown excellent availability towards commercialization.展开更多
Energy transformation is imminent,and hydrogen energy is one of the important new energy sources.One of the keys to increasing the rate of hydrogen evolution during electrolysis is the use of high-performance catalyst...Energy transformation is imminent,and hydrogen energy is one of the important new energy sources.One of the keys to increasing the rate of hydrogen evolution during electrolysis is the use of high-performance catalysts for oxygen evolution reactions(OER).Single-atom alloys(SAAs)have garnered significant attention because they partially reduce costs and combine the advantages of both single-atom catalysts(SACs)and alloy catalysts.Herein,an efficient pyrolysis strategy based on a mixing and drying process is designed to anchor ultra-small Co cluster particles,combined with Ru single atoms dispersed on nitrogen-doped ultra-thin carbon nanosheets(Ru_(1)Co SAA/NC).The prepared electrocatalyst exhibits superior OER activity and superb stability,demonstrating an overpotential of 238 mV for OER with a current density of 10 mA·cm^(-2) in 0.5 mol/L H_(2)SO_(4).And we also utilized in-situ XAS to detect the oxidation state of Ru sites during OER.All in all,this method achieves cost reductions and efficiency improvements through the design of SAAs,offering new prospects for the structural transformation of clean energy.展开更多
The enhancement in the efficiency of triplet-triplet annihilation upconversion(TTA-UC)is mainly determined by the triplet energy transfer(TET)and triplet-triplet annihilation(TTA)between the sensitizers and annihilato...The enhancement in the efficiency of triplet-triplet annihilation upconversion(TTA-UC)is mainly determined by the triplet energy transfer(TET)and triplet-triplet annihilation(TTA)between the sensitizers and annihilators.The TET process works efficiently by adjusting the concentration ratio of the sensitizers and annihilators.The efficiency of TTA is determined by the properties of the annihilator.Because TTA is a Dexter-type energy transfer and is affected by the diffusion rate,the energy levels of the excited states and the molecular size are both crucial in TTA.In this study,four isomerized dimers of 9,10-diphenlanthracene(DPA)and anthracene(An)were designed and prepared as annihilators for TTA-UC.The singlet and triplet energy levels could be adjusted by altering the connection position while maintaining the molecular weight and size.When PtOEP was used as the sensitizer,the maximum upconversion efficiency of 9-[4-(9-anthracenyl)phenyl]-10-phenylanthracene(9DPA-9An)was~11.18%.This is four times higher than that of 9,10-diphenyl-2,9-bianthracene(2DPA-9An,2.63%).The calculation of the energies of T_(1)and the higher triplet state(T_(3),because E(T_(2))is similar to the E(T)of these dimers)for these dimers has provided insights into the underlying reasons.These indicated that the energy gap value of 2×E(T_(1))-E(T_(3))is the determining factor for TTA efficiency.This work may provide a better understanding of the excited-state energy levels,which is crucial for designing novel annihilators to enhance the TTA-UCefficiency.展开更多
Self-healing hydrogels with the shear-thinning property are novel injectable materials and are superior to traditional injectable hydrogels.The self-healing hydrogels based on 2-ureido-4[1 H]-pyrimidinone(UPy)have rec...Self-healing hydrogels with the shear-thinning property are novel injectable materials and are superior to traditional injectable hydrogels.The self-healing hydrogels based on 2-ureido-4[1 H]-pyrimidinone(UPy)have recently received extensive attention due to their dynamic reversibility of UPy dimerization.However,generally,UPy-based self-healing hydrogels exhibit poor stability,cannot degrade in vivo and can hardly be excreted from the body,which considerably limit their bio-application.Here,using poly(l-glutamic acid)(PLGA)as biodegradable matrix,branchingα-hydroxy-ω-amino poly(ethylene oxide)(HAPEO)as bridging molecule to introduce UPy,and ethyl acrylate polyethylene glycol(MAPEG)to introduce double bond,the hydrogel precursors(PMHU)are prepared.A library of the self-healing hydrogels has been achieved with well self-healable and shear-thinning properties.With the increase of MAPEG grafting ratio,the storage modulus of the self-healing hydrogels decreases.The self-healing hydrogels are stable in solution only for 6 h,hard to meet the requirements of tissue regeneration.Consequently,ultraviolet(UV)photo-crosslinking is involved to obtain the dual crosslinking hydrogels with enhanced mechanical properties and stability.When MAPEG grafting ratio is 35.5%,the dual crosslinking hydrogels can maintain the shape in phosphate-buffered saline solution(PBS)for at least 8 days.Loading with adipose-derived stem cell spheroids,the self-healing hydrogels are injected and self-heal to a whole,and then they are crosslinked in situ via UV-irradiation,obtaining the dual crosslinking hydrogels/cell spheroids complex with cell viability of 86.7%±6.0%,which demonstrates excellent injectability,subcutaneous gelatinization,and biocompatibility of hydrogels as cell carriers.The novel PMHU hydrogels crosslinked by quadruple hydrogen bonding and then dual photo-crosslinking of double bond are expected to be applied for minimal invasive surgery or therapies in tissue engineering.展开更多
Magnetic semiconductors with Curie temperatures higher than room temperature show potential for developing spintronic devices with combined data processing and storage functions for next-generation computing systems.I...Magnetic semiconductors with Curie temperatures higher than room temperature show potential for developing spintronic devices with combined data processing and storage functions for next-generation computing systems.In this study,we present an n-type Co_(19.8)Fe_(8.6)Nb_(4.3)B_(6.0)O_(61.3) magnetic semiconductor with a high Curie temperature of~559 K.This magnetic semiconductor has a room-temperature resistivity of~2.10×10^(4)Ωcm and a saturation magnetization of~76 emu/cm^(3).The n-type Co_(19.8)Fe_(8.6)Nb_(4.3)B_(6.0)O_(61.3)magnetic semiconductor was deposited on p-type silicon to form a heterojunction,exhibiting a rectifying characteristic.Our results provide the design principles for discovering high Curie temperature magnetic semiconductors with determined conduction types,which would play an essential role in realizing nonvolatile spin-based transistors that break free from the confines of currently established Si-based information technology.展开更多
What is the most favorite and original chemistry developed in your research group?Ring-opening polymerization-induced self-assembly of N-carboxyanhydrides(NCA-PISA),and fusion-induced particle assembly(FIPA).How do yo...What is the most favorite and original chemistry developed in your research group?Ring-opening polymerization-induced self-assembly of N-carboxyanhydrides(NCA-PISA),and fusion-induced particle assembly(FIPA).How do you get into this specific field?Could you please share some experiences with our readers?NCA-PISA was developed to solve the biodegradability problem of nanoparticles by traditional PISA,while FIPA was inspired by nature.展开更多
The oxygen octahedral rotation(OOR)forms fundamental atomic distortions and symmetries in perovskite oxides and definitely determines their properties and functionalities.Therefore,epitaxial strain and interfacial str...The oxygen octahedral rotation(OOR)forms fundamental atomic distortions and symmetries in perovskite oxides and definitely determines their properties and functionalities.Therefore,epitaxial strain and interfacial structural coupling engineering have been developed to modulate the OOR patterns and explore novel properties,but it is difficult to distinguish the 2 mechanisms.Here,different symmetries are induced in Na_(0.5)Bi_(0.5)TiO_(3)(NBT)epitaxial films by interfacial oxygen octahedral coupling rather than epitaxial strain.The NBT film grown on the Nb:SrTiO_(3)substrate exhibits a paraelectric tetragonal phase,while with La_(0.5)Sr_(0.5)MnO_(3)as a buffer layer,a monoclinic phase and robust ferroelectricity are obtained,with a remanent polarization of 42μC cm^(-2)and a breakdown strength of 7.89 MV cm^(-1),which are the highest record among NBT-based films.Moreover,the interfacial oxygen octahedral coupling effect is demonstrated to propagate to the entire thickness of the film,suggesting an intriguing long-range effect.This work provides a deep insight into understanding the structure modulation in perovskite heterostructures and an important avenue for achieving unique functionalities.展开更多
At present,in order to overcome electromagnetic interference and prevent electromagnetic harm,the research of new and efficient electromagnetic wave absorbing materials has become the research focus in the field of ma...At present,in order to overcome electromagnetic interference and prevent electromagnetic harm,the research of new and efficient electromagnetic wave absorbing materials has become the research focus in the field of materials science.The one-dimensional structure can promote the impedance matching and attenuation characteristics of the absorbing materials.Electrospinning,as an effective method to prepare nanofibers with high length-diameter ratio,has been widely concerned because it is suitable for struc-tural design of various materials.In this paper,the research progress and absorption properties of nano-fiber materials prepared by electrospinning combined with different processes are introduced.展开更多
基金supported by the China Postdoctoral Science Foundation (grant Nos.2019M662405,2019M650612)Natural Science Foundation of Shandong Province (grant Nos.ZR2019BF047,ZR2020KE059)+1 种基金School City Integration in Zibo (grant No.2019ZBXC299)Heilongjiang Touyan Team Program,and the Fundamental Research Funds for the Central Universities (grant No.HIT.0CEF.2021003).
文摘In recent years,significant progress has been achieved in the creation of innovative functional materials for energy storage and conversion.Due to their distinct physicochemical characteristics,ultrathin nanosheets composed of common layered transition metal sulfide materials(MoS2)have demonstrated promise as high-capacity anode materials for lithium-ion batteries(LIBs).Nevertheless,their practical application is severely limited by the tendency of monolayer nanosheets to restack due to strong van der Waals forces,dramatic volume changes during successive cycles,and low intrinsic conductivity.Recent research advances have shown that composite structures and nanowire morphologies with specific morphologies effectively overcome these issues.This paper reviews the recent research progress on molybdenum disulfide-based composites as anode materials for LIBs and discusses in detail the struc-tural characteristics of pure molybdenum disulfide and other composite forms of molybdenum disulfide.In addition,the phase engineering,defect engineering,and lithium storage mechanisms of molybdenum disulfide and the synthesis of molybdenum disulfide-based nanocomposites by different preparation methods are focused on.Finally,we review the design(structure),recent developments,and challenges of novel anode materials and consider their electrochemical performance in Li-ion batteries.
基金supported by the National Natural Science Foundation of China(21872104,21501131,21978216 and 22272082)the Natural Science Foundation of Tianjin for Distinguished Young Scholar(20JCJQJC00150)the Analytical&Testing Center of Tiangong University for PL work。
文摘Photocatalytic H_(2) evolution from seawater splitting presents a promising approach to tackle the fossil energy crisis and mitigate carbon emission due to the abundant source of seawater and sunlight on the earth.However,the development of efficient photocatalysts for seawater splitting remains a formidable challenge.Herein,a 2D/2D ZnIn_(2)S_(4)/WO_(3)(ZIS/WO_(3))heterojunction nanostructure is fabricated to efficiently separate the photoinduced carriers by steering electron transfer from the conduction band minimum of WO_(3) to the valence band maximum of ZIS via constructing internal electric field.Subsequently,plasmonic Au nanoparticles(NPs)as a novel photosensitizer and a reduction cocatalyst are anchored on ZIS/WO_(3) surface to further enhance the optical absorption of ZIS/WO_(3) heterojunction and accelerate the catalytic conversion.The obtained Au/ZIS/WO_(3) photocatalyst exhibits an outstanding H_(2) evolution rate of 2610.6 or 3566.3μmol g^(-1)h~(-1)from seawater splitting under visible or full-spectrum light irradiation,respectively.These rates represent an impressive increase of approximately 7.3-and 6,6-fold compared to those of ZIS under the illumination of the same light source.The unique 2D/2D structure,internal electric field,and plasmonic metal modification together boost the photocatalytic H_(2) evolution rate of Au/ZIS/WO_(3),making it even comparable to H_(2) evolution from pure water splitting.The present work sheds light on the development of efficient photocatalysts for seawater splitting.
基金Project(51778226)supported by the National Natural Science Foundation of ChinaProject(2018JJ3159)supported by the Hunan Provincial Natural Science Foundation for Youths,China。
基金supported by the National Natural Science Foundation of China (21905205 and 22109037)the Natural Science Foundation of Tianjin City (20JCYBJC00380)+1 种基金the Advanced Talents Incubation Program of Hebei University (521000981408)the Haihe Laboratory of Sustainable Chemical Transformations(YYJC202110)。
文摘Redox p-type organic compounds are promising cathode materials for dual-ion batteries.However,the triphenylamine-based polymers usually with agglomerate and intertwined molecular chain nature limit the maximum reaction of their active sites with large-sized anions.Herein,we demonstrate the application of a small molecule with rigid spirofluorene structu re,namely 2,2’,7,7’-tetrakis(diphenylamine)-9,9’-spirobifluorene(Spiro-TAD),as a cathode material for lithium dual-ion batteries.The inherent sterical structure endows the Spiro-TAD with good chemical stability and large internal space for fast diffusion kinetics of anions in the organic electrolyte.As a result,the Spiro-TAD electrode shows significant insolubility and less steric hindrance,and gives a high actual capacity of 109 mA h g^(-1)(active groups utilization ratio approximately 100%) at 50 mA g^(-1)with a high discharge voltage of 3.6 V(vs.Li+/Li),excellent rate capability(60 mA h g^(-1)at 2000 mA g^(-1)) and extremely stable cycling life(98.4% capacity retention after 1400 cycles at 500 mA g^(-1)) in half cells.Such good electrochemical performance is attributed to the robust and rapid adsorption/desorption of ClO4-anions,which can be proved by the in-situ FTIR and XPS.Moreover,an all-organic lithium dual-ion battery(a-OLDIBs) is constructed using the Spiro-TAD as cathode and 3,4,9,10-Perylenetetracarboxylic diimide(PTCDI) as anode and displays long-term cycling performance of 87.5 mA h g^(-1)after 800 cycles.This study will stimulate further developments in designing all organic battery systems.
基金This review work was supported by the National Natural Science Foundation of China(32222041,82072425,82072498,and 21875092)the Natural Science Foundation of Jiangsu Province(BK20220059 and BE2020666)+2 种基金the Priority Academic Program Development of Jiangsu Higher Education Institutions(PAPD)the Special Project of Diagnosis and Treatment Technology for Key Clinical Diseases in Suzhou(LCZX202003)the“jiangsu Specially Appointed Professor”Program and Postgraduate Research&Practice Innovation Program of Jiangsu Province(KYCX22_3217).
文摘For patients with osteoporosis,the therapeutic outcomes of osteoimplants are substantially affected by the impaired proliferation,migration,and osteogenic differentiation abilities of bone marrow mesenchymal stem cells(BMSCs).
基金Project supported by the Natural Science Foundation of Guangxi(2021GXNSFDA075009)the National Natural Science Foundation of China(52261004)。
文摘Usually it is generally believed that the Er element forms the Er_(2)Fe_(14)B phase,which will seriously deteriorate the magnetic properties.Distinctly,here we report the balance of corrosion resistance and coercivity in Nd-Fe-B sintered magnets through using simple Er_(30)Cu_(70) additive whose price is much lower than Dy and Tb.By reasonably controlling Er_(30)Cu_(70) addition,the corrosion resistance is improved at the minimum limit of reducing the magnetic properties.Through studying the influence mechanism of Er element,it is found that the main effect of Er elements is to replace the Nd elements at the edge of the main phase grains to form a(Er,Nd)_(2)Fe_(14)B shell with low H_(A),resulting in the reduction of magnetic properties.The improvement of corrosion resistance mainly comes from the more stable Cu element introduced at the grain boundary.At the same time,the target magnets also show different advantages under different heat treatment methods.Above findings may spur progress towards developing the lowcost permanent magnets that rival the commercial Nd-Fe-B counterpart.
基金Project(51778226)supported by the National Natural Science Foundation of ChinaProject(2018JJ3159)supported by the Hunan Provincial Natural Science Foundation for Youths,China。
文摘With the thermal simulated technology, the continuous cooling transforming curve (SH-CCT) of domestic X80 was measured, and the variation rule of the microstructure of coarsened-grain heat-affected zone(CGHAZ) for X80 pipeline steel was also investigated. The results indicate that the hardenability and the hydrogen cracking susceptibility of domestic X80 are fairly low.
基金supported by the National Natural Science Foundation of China(22005152,22275101).
文摘Lead-free halide perovskite materials possess low toxicity,broadband luminescence and robust stability compared with conventional lead-based perovskites,thus holding great promise for eyes-friendly white light LEDs.However,the traditionally used preparation methods with a long period and limited product yield have curtailed the commercialization of these materials.Here we introduce a universal hydrochloric acid-assistant powder-to-powder strategy which can accomplish the goals of thermal-,pressure-free,eco-friendliness,short time,low cost and high product yield,simultaneously.The obtained Cs_(2)Na_(0.9)Ag_(0.1)In_(0.95)Bi_(0.05)Cl_(6)microcrystals exhibit bright self-trapped excitons emission with quantum yield of(98.3±3.8)%,which could retain(90.5±1.3)%and(96.8±0.8)%after continuous heating or ultraviolet-irradiation for 1000 h,respectively.The phosphor converted-LED exhibited near-unity conversion efficiency from ultraviolet chip to self-trapped excitons emission at~200 mA.Various ions doping(such as Cs_(2)Na_(0.9)Ag_(0.1)InCl_(6):Ln^(3+))and other derived lead-free perovskite materials(such as Cs_(2)ZrCl_(6)and Cs_(4)MnBi_(2)Cl_(12))with high luminous performance are all realized by our proposed strategy,which has shown excellent availability towards commercialization.
基金supported by the National Natural Science Foundation of China(22375019)Beijing Natural Science Foundation(Grant No.2212018)Beijing Institute of Technology Research Fund Program for Young Scholars(2022CX01011).
文摘Energy transformation is imminent,and hydrogen energy is one of the important new energy sources.One of the keys to increasing the rate of hydrogen evolution during electrolysis is the use of high-performance catalysts for oxygen evolution reactions(OER).Single-atom alloys(SAAs)have garnered significant attention because they partially reduce costs and combine the advantages of both single-atom catalysts(SACs)and alloy catalysts.Herein,an efficient pyrolysis strategy based on a mixing and drying process is designed to anchor ultra-small Co cluster particles,combined with Ru single atoms dispersed on nitrogen-doped ultra-thin carbon nanosheets(Ru_(1)Co SAA/NC).The prepared electrocatalyst exhibits superior OER activity and superb stability,demonstrating an overpotential of 238 mV for OER with a current density of 10 mA·cm^(-2) in 0.5 mol/L H_(2)SO_(4).And we also utilized in-situ XAS to detect the oxidation state of Ru sites during OER.All in all,this method achieves cost reductions and efficiency improvements through the design of SAAs,offering new prospects for the structural transformation of clean energy.
基金supported by the National Natural Science Foundation of China(22133006,21703287)the Natural Science Foundation of Shandong Province(ZR2023QB067,ZR2022MB065)+1 种基金the Science and Technology Program of the University of Jinan(XKY2068-140200568)Major Subject of the University of Jinan(1420702).
文摘The enhancement in the efficiency of triplet-triplet annihilation upconversion(TTA-UC)is mainly determined by the triplet energy transfer(TET)and triplet-triplet annihilation(TTA)between the sensitizers and annihilators.The TET process works efficiently by adjusting the concentration ratio of the sensitizers and annihilators.The efficiency of TTA is determined by the properties of the annihilator.Because TTA is a Dexter-type energy transfer and is affected by the diffusion rate,the energy levels of the excited states and the molecular size are both crucial in TTA.In this study,four isomerized dimers of 9,10-diphenlanthracene(DPA)and anthracene(An)were designed and prepared as annihilators for TTA-UC.The singlet and triplet energy levels could be adjusted by altering the connection position while maintaining the molecular weight and size.When PtOEP was used as the sensitizer,the maximum upconversion efficiency of 9-[4-(9-anthracenyl)phenyl]-10-phenylanthracene(9DPA-9An)was~11.18%.This is four times higher than that of 9,10-diphenyl-2,9-bianthracene(2DPA-9An,2.63%).The calculation of the energies of T_(1)and the higher triplet state(T_(3),because E(T_(2))is similar to the E(T)of these dimers)for these dimers has provided insights into the underlying reasons.These indicated that the energy gap value of 2×E(T_(1))-E(T_(3))is the determining factor for TTA efficiency.This work may provide a better understanding of the excited-state energy levels,which is crucial for designing novel annihilators to enhance the TTA-UCefficiency.
基金financially supported by the National Natural Science Foundation of China(No.51773113)。
文摘Self-healing hydrogels with the shear-thinning property are novel injectable materials and are superior to traditional injectable hydrogels.The self-healing hydrogels based on 2-ureido-4[1 H]-pyrimidinone(UPy)have recently received extensive attention due to their dynamic reversibility of UPy dimerization.However,generally,UPy-based self-healing hydrogels exhibit poor stability,cannot degrade in vivo and can hardly be excreted from the body,which considerably limit their bio-application.Here,using poly(l-glutamic acid)(PLGA)as biodegradable matrix,branchingα-hydroxy-ω-amino poly(ethylene oxide)(HAPEO)as bridging molecule to introduce UPy,and ethyl acrylate polyethylene glycol(MAPEG)to introduce double bond,the hydrogel precursors(PMHU)are prepared.A library of the self-healing hydrogels has been achieved with well self-healable and shear-thinning properties.With the increase of MAPEG grafting ratio,the storage modulus of the self-healing hydrogels decreases.The self-healing hydrogels are stable in solution only for 6 h,hard to meet the requirements of tissue regeneration.Consequently,ultraviolet(UV)photo-crosslinking is involved to obtain the dual crosslinking hydrogels with enhanced mechanical properties and stability.When MAPEG grafting ratio is 35.5%,the dual crosslinking hydrogels can maintain the shape in phosphate-buffered saline solution(PBS)for at least 8 days.Loading with adipose-derived stem cell spheroids,the self-healing hydrogels are injected and self-heal to a whole,and then they are crosslinked in situ via UV-irradiation,obtaining the dual crosslinking hydrogels/cell spheroids complex with cell viability of 86.7%±6.0%,which demonstrates excellent injectability,subcutaneous gelatinization,and biocompatibility of hydrogels as cell carriers.The novel PMHU hydrogels crosslinked by quadruple hydrogen bonding and then dual photo-crosslinking of double bond are expected to be applied for minimal invasive surgery or therapies in tissue engineering.
基金supported by the National Natural Science Foundation of China (Grant No. 51922053)。
文摘Magnetic semiconductors with Curie temperatures higher than room temperature show potential for developing spintronic devices with combined data processing and storage functions for next-generation computing systems.In this study,we present an n-type Co_(19.8)Fe_(8.6)Nb_(4.3)B_(6.0)O_(61.3) magnetic semiconductor with a high Curie temperature of~559 K.This magnetic semiconductor has a room-temperature resistivity of~2.10×10^(4)Ωcm and a saturation magnetization of~76 emu/cm^(3).The n-type Co_(19.8)Fe_(8.6)Nb_(4.3)B_(6.0)O_(61.3)magnetic semiconductor was deposited on p-type silicon to form a heterojunction,exhibiting a rectifying characteristic.Our results provide the design principles for discovering high Curie temperature magnetic semiconductors with determined conduction types,which would play an essential role in realizing nonvolatile spin-based transistors that break free from the confines of currently established Si-based information technology.
基金This work was supported by the National Natural Science Foundation of China(Nos.21925505,52003195,and 22101207)Shanghai International Scientific Collaboration Fund(No.21520710100)+1 种基金the China Postdoctoral Science Foundation(Nos.2019M661614 and 2020M671197)J.D.is a recipient of the National Science Fund for Distinguished Young Scholars.
文摘What is the most favorite and original chemistry developed in your research group?Ring-opening polymerization-induced self-assembly of N-carboxyanhydrides(NCA-PISA),and fusion-induced particle assembly(FIPA).How do you get into this specific field?Could you please share some experiences with our readers?NCA-PISA was developed to solve the biodegradability problem of nanoparticles by traditional PISA,while FIPA was inspired by nature.
基金supported by the National Key Research Program of China(Grant No.2022YFB3807604)the National Natural Science Foundation of China(Grant Nos.52027817,52072400,52025025,and 52150092).
文摘The oxygen octahedral rotation(OOR)forms fundamental atomic distortions and symmetries in perovskite oxides and definitely determines their properties and functionalities.Therefore,epitaxial strain and interfacial structural coupling engineering have been developed to modulate the OOR patterns and explore novel properties,but it is difficult to distinguish the 2 mechanisms.Here,different symmetries are induced in Na_(0.5)Bi_(0.5)TiO_(3)(NBT)epitaxial films by interfacial oxygen octahedral coupling rather than epitaxial strain.The NBT film grown on the Nb:SrTiO_(3)substrate exhibits a paraelectric tetragonal phase,while with La_(0.5)Sr_(0.5)MnO_(3)as a buffer layer,a monoclinic phase and robust ferroelectricity are obtained,with a remanent polarization of 42μC cm^(-2)and a breakdown strength of 7.89 MV cm^(-1),which are the highest record among NBT-based films.Moreover,the interfacial oxygen octahedral coupling effect is demonstrated to propagate to the entire thickness of the film,suggesting an intriguing long-range effect.This work provides a deep insight into understanding the structure modulation in perovskite heterostructures and an important avenue for achieving unique functionalities.
基金supported by the National Key R&D Program of China (No.2021YFB3502500)Natural Science Foundation of Shandong Province (Nos.2022HYYQ-014,ZR2016BM16)+5 种基金the New 20 Funded Programs for Universities of Jinan (2021GXRC036)Provincial Key Research and Development Program of Shandong (2021ZLGX01)National Natural Science Foundation of China (No.22205131)Shenzhen municipal special fund for guiding local scientific and Technological Development (China 2021Szvup071)the Joint Laboratory Project of Electromagnetic Structure Technology (637-2022-70-F-037)Qilu Young Scholar Program of Shandong University (No.31370082163127).
文摘At present,in order to overcome electromagnetic interference and prevent electromagnetic harm,the research of new and efficient electromagnetic wave absorbing materials has become the research focus in the field of materials science.The one-dimensional structure can promote the impedance matching and attenuation characteristics of the absorbing materials.Electrospinning,as an effective method to prepare nanofibers with high length-diameter ratio,has been widely concerned because it is suitable for struc-tural design of various materials.In this paper,the research progress and absorption properties of nano-fiber materials prepared by electrospinning combined with different processes are introduced.