Photosynthesis of H_(2)O_(2)via sustainable biomass-derived carbon catalysts facilitate the conversion of renewable resources into valuable chemicals.However,the regulatory function of surface functional groups over r...Photosynthesis of H_(2)O_(2)via sustainable biomass-derived carbon catalysts facilitate the conversion of renewable resources into valuable chemicals.However,the regulatory function of surface functional groups over reaction kinetics has not been sufficiently investigated.Herein,hydrothermal carbon spheres(CS)rich in oxygencontaining functional groups demonstrated a remarkably high H_(2)O_(2)production rate(653μmol/(g·h))in both pure water and actual seawater,even in the absence of any sacrificial agent.Meanwhile,the catalyst demonstrates outstanding activity(92%conversion and>99%selectivity)in the visible-light-driven photocatalytic oxidation of benzylamine to imines.Comprehensive analysis reveals that CS was rich in surface oxygen-containing functional groups,a feature strongly associated with its high photocatalytic efficiency.The observed positive Zeta potential of CS in seawater likely diminished the electrostatic repulsion against the positively charged intermediates,thereby facilitating their accumulation at the liquid-solid interface.This work proposes a strategic framework for developing metal-free photocatalysts from biomass,offering a sustainable pathway for photocatalytic applications.展开更多
Photocatalysis has demonstrated considerable potential as a highly efficient approach to the valorization of biomass under mild conditions,while the selectivity control is a long-standing challenge,notably when the ta...Photocatalysis has demonstrated considerable potential as a highly efficient approach to the valorization of biomass under mild conditions,while the selectivity control is a long-standing challenge,notably when the targets are complex and reactive biopolyols.In this study,we have successfully achieved selectivity control of photocatalytic biopolyols reforming to formic acid(FA)or CO by modulating the surface hydroxyl groups on TiO_(2) semiconductor.Photogenerated holes typically localize at bridging oxygen atoms(O2c)on the TiO_(2) surface,while shifting to terminal hydroxyl groups upon their introduction.The state of holes strongly affects the hole transfer process,which in turn influences the course of the reaction and thus controls the selectivity.By modulating the surface hydroxyl groups,the model substrate glycerol was selectively converted to CO(49%yield)and FA(50%yield).A range of other biopolyols,exemplified by erythritol,have demonstrated the same reaction selectivity.This work provides an effective strategy to manipulate reaction pathways by means of regulating the catalyst surface structure itself.展开更多
There are limitations to using hard carbon(HC)in K^(+)storage due to its insufficient high-current reversible capacity and plateau potential,which result from the lack of effective active sites and low intercalation c...There are limitations to using hard carbon(HC)in K^(+)storage due to its insufficient high-current reversible capacity and plateau potential,which result from the lack of effective active sites and low intercalation capabilities.The construction of HC cathodes with more available functional groups and ordered carbon nanocrystal structures is essential for improving K^(+)storage efficiency.Herein,a new perspective is proposed for synthesizing hard carbon nanosheets(HCNS)with abundant hydroxyl groups(O-H)/carboxylic groups(O-C=O)and rational carbon nanocrystals by interfacial assembly and carbonization.Systematic in ex-situ observations,dynamic analysis and theory calculations elucidate that the superior electrochemical capability of HCNS is ascribed to the synergistic effect of abundant available functional groups and ordered graphitic microcrystalline.Consequently,the HCNS exhibits outstanding K^(+)storage capabilities in terms of superb energy density(146.2 Wh/kg),high power density(1,7800 Wh/kg),and ultralong lifespan(102.9%capacity retention after 10,000 cycles).It was also found that the HC structure correlates with the discharge/charge plateau,confirming the'adsorption-insertion'charge storage mechanism.Furthermore,the proposed work provides a theoretical basis for making high-performance HC anodes by understanding the effect of their microstructure on K^(+)storage.展开更多
The fluorination strategy has been proven effective in significantly enhancing the photovoltaic performance of organic solar cells(OSCs) based on non-fused ring electron acceptors(NFREAs).However,research on the impac...The fluorination strategy has been proven effective in significantly enhancing the photovoltaic performance of organic solar cells(OSCs) based on non-fused ring electron acceptors(NFREAs).However,research on the impact of fluorination positions at side chains on NFREAs device performance remains scant.In this study,we introduce two isomeric NFREAs,designated as GA-2F-E and GA-2F,distinguished by their fluorination positions at the side chains.Both NFREAs share a thiophene[3,2-b]thiophene core,but their side chains differ:GA-2F-E features two(4-butylphenyl)-N-(4-fluorophenyl) amino groups,whereas GA-2F's side chains consist of bis(4-fluorophenyl)amino and bis(4-butylphenyl)amino groups attached to opposite sides of the core.To delve into the influence of fluorination positions on the optoelectronic properties,aggregation behavior,and overall efficiency of the acceptor molecules,a comprehensive investigation was conducted.The findings reveal that,despite similar photophysical properties and comparable absorption bandwidths,GA-2F-E,with fluorine atoms positioned on both sides of the molecular framework,demonstrates more compact π-π stacking,reduced bimolecular recombination,superior exciton transport,and a more balanced,higher mobility.As a result of these advantages,OSCs optimized with D18:GA-2F-E achieve a remarkable power conversion efficiency(PCE) of 16.45 %,surpassing the 15.83 %PCE of devices utilizing D18:GA-2F.This research underscores the potential of NFREAs in future applications and highlights the significance of fluorination positions in enhancing OSC performance,paving the way for the development of more efficient NFREAs.展开更多
Let M be a compact n-manifold of positive sectional curvature.We will review classical results on the fundamental group of M,a motivation on the c(n)-cyclic conjecture that the fundamental group of M contains a cyclic...Let M be a compact n-manifold of positive sectional curvature.We will review classical results on the fundamental group of M,a motivation on the c(n)-cyclic conjecture that the fundamental group of M contains a cyclic subgroup of index bounded above by c(n),a constant depending only on n,and we will survey partial results(up to date)on the c(n)-cyclic conjecture.展开更多
Let T_(n) and S_(n) be the full transformation semigroup and the symmetric group on X_(n)={1,2,...,n},respectively.Let G be a transitiveimprimitive subgroupof S_(n) with nontrivial blocksΔand letαbe a transformation...Let T_(n) and S_(n) be the full transformation semigroup and the symmetric group on X_(n)={1,2,...,n},respectively.Let G be a transitiveimprimitive subgroupof S_(n) with nontrivial blocksΔand letαbe a transformation in T_(n)\S_(n).The kernel ofαis the partition of X_(n) induced by the equivalence relation{(x,y)|xα=yα};the kernel type ofαis the partition of n given by the sizes of the parts of the kernel.A transformation semigroup is called synchronizing if it contains a constant map.Then a group G synchronizes a transformationαif the semigroup(G,α)contains a constant map.In this paper,we study a transitive imprimitive permutation group G together with a non-invertible transformationαthat generate a synchronizing semigroup.We mainly discuss 7 cases where G synchronizes a special transformationαwith each kernel class A_(i)(A_(1)j)satisfying|A_(i)∩Δ|=1(|A_(1)j∩Δ|=1)for all blocksΔofG,that is,the kernel type ofαis(|A_(1)|,1,...,1),(|A_(1)1|,...,|A_(1m)|,|A_(2)|,...,|Ar|),or(|A_(1)|,...,|A_(t)|,1,...,1),or the rank is 2,3,4,or n-2.展开更多
This paper investigates the in uence of local SS-quasinormal maximal subgroups of Sylow subgroups on the structure of nite groups.We present several new criteria on p-nilpotency of nite groups by utilizing a small qua...This paper investigates the in uence of local SS-quasinormal maximal subgroups of Sylow subgroups on the structure of nite groups.We present several new criteria on p-nilpotency of nite groups by utilizing a small quantity of local SS-quasinormal maximal subgroups of Sylow p-subgroups.As applications,we obtain some sucient conditions for a nite group to be in a saturated formation containing the class of supersolvable groups.展开更多
Let G be a finite group and H a subgroup of G.The normal index of H in G is defined as the order of K/H_(G),where K is a normal supplement of H in G such that|K|is minimal and H_(G)≤K■G.Let p be a prime which divide...Let G be a finite group and H a subgroup of G.The normal index of H in G is defined as the order of K/H_(G),where K is a normal supplement of H in G such that|K|is minimal and H_(G)≤K■G.Let p be a prime which divides the order of a group G.In this paper,some characterizations of G being p-solvable or p-supersolvable were obtained by analyzing the normal index of certain subgroups of G.These results can be viewed as local version of recent results in the literature.展开更多
Let G be a group and H;K be subgroups of G.H is called a TI-subgroup of G if H∩H^(g)=1 or H for every g∈G.K is called P-subnormal in G if there is a chain of subgroups K=K_(0)≤K_(1)≤K_(2)≤…≤K_(n-1)≤K_(n)=G suc...Let G be a group and H;K be subgroups of G.H is called a TI-subgroup of G if H∩H^(g)=1 or H for every g∈G.K is called P-subnormal in G if there is a chain of subgroups K=K_(0)≤K_(1)≤K_(2)≤…≤K_(n-1)≤K_(n)=G such that|K_(i):K_(i-1)|∈P for i∈{1;2;…;n}.Furthermore,K is called K-P-subnormal in G if there is a chain of subgroups K=K_(0)≤K_(1)≤K_(2)≤…≤K_(n-1)≤K_(n)=G such that either K_(i-1)is normal in Ki or|K_(i):K_(i-1)|∈P for i∈{1;2;…;n}.In this paper,some properties of a nite group in which some particular subgroups are TI-subgroups or P-subnormal subgroups or K-P-subnormal subgroups are given.展开更多
International trade serves as a crucial pathway for enhancing global food security and equality amid severe food crises worldwide.Under globalization,economic development has profoundly influenced food trade,while dis...International trade serves as a crucial pathway for enhancing global food security and equality amid severe food crises worldwide.Under globalization,economic development has profoundly influenced food trade,while disparities in food purchasing power among different economic development groups have led to uneven food security outcomes.However,the varying contributions of international trade to food security across these groups remain to be quantitatively elucidated.This study categorized countries into four economic development groups—high,high-medium,medium-low,and low—and examined changes in their food security scores from 2010 to 2019.The cross-group contributions of international trade to food security across these groups were compared.The results revealed that the food security score of the high economic development group was 9.22 times higher than that of the low economic development group.From 2010 to 2019,the high economic development group exhibited a significant upward trend in food security scores,whereas the low economic development group showed a significant decline.Moreover,international trade contributed significantly to both cross-group and within-group food security in the high economic development group,while its contribution to the low economic development group remained negligible.These findings demonstrated that international trade has further widened the food security gap between the high and low economic development groups,and its limited contribution to the low economic development group has failed to reverse the declining trend in their food security scores.This study quantified the divergent impacts of international trade on food security across economic development groups,providing valuable insights for optimizing global food trade policies—particularly in addressing the food security challenges faced by low econominc development group.展开更多
With the transformation and upgrading of industries,along with the rapid advancement of artificial intelligence(AI)technologies,higher vocational education in art and design is facing new developmental challenges.As a...With the transformation and upgrading of industries,along with the rapid advancement of artificial intelligence(AI)technologies,higher vocational education in art and design is facing new developmental challenges.As an emerging integrative ecosystem,the municipal industry-education consortium offers a strategic pathway to address these challenges by deepening collaboration between education and industry and fostering the coordinated development of both sectors.Grounded in the framework of the municipal industry-education consortium,this study proposes a top-level organizational model for art and design specialty groups characterized by industry-chain-driven development,interdisciplinary integration,and growth-employment orientation.It further explores multiple development pathways,including innovations in consortium council governance,dynamic talent cultivation models,shared curriculum systems,dual-track teaching teams,and multi-tiered practice bases.Collectively,these pathways establish a comprehensive specialty group system in which core specialties drive development,supporting specialties ensure interdependence,and extended specialties foster mutual advancement.The findings provide theoretical insights and practical guidance for advancing the modernization and high-quality transformation of vocational art and design education,contributing to the cultivation of innovative and application-oriented professionals aligned with industrial restructuring and the development of new productive forces.展开更多
In this paper,we introduce the set of maximal subgroups with non-trivial core and their corresponding second maximal subgroups.A correlation characterization of the group class J_(pr)is presented by establishing the r...In this paper,we introduce the set of maximal subgroups with non-trivial core and their corresponding second maximal subgroups.A correlation characterization of the group class J_(pr)is presented by establishing the relationship between the core and the second maximal subgroups in these classifications.展开更多
Let P be a Sylow p-subgroup of a group G with the smallest generator number d, where p is a prime. Denote by Md（P） = （P1, P2,..., Pd） a set of maximal subgroups of P such that φ（P） = ∩n^d=1Pn. In this paper, w...Let P be a Sylow p-subgroup of a group G with the smallest generator number d, where p is a prime. Denote by Md（P） = （P1, P2,..., Pd） a set of maximal subgroups of P such that φ（P） = ∩n^d=1Pn. In this paper, we investigate the structure of a finite group G under the assumption that the maximal subgroups in Md（P） are weakly s-permutably embedded in G, some interesting results are obtained which generalize some recent results. Finally, we give some further results in terms of weakly s-permutably embedded subgroups.展开更多
A subgroup H of a group G is called F-z-supplemented in G if there exists a subgroup K of G, such that G = HK and H∩K≤ Z∞F（G）, where Z∞F（G） is the F-hypercenter of G. We obtain some results about the F-z-suppl...A subgroup H of a group G is called F-z-supplemented in G if there exists a subgroup K of G, such that G = HK and H∩K≤ Z∞F（G）, where Z∞F（G） is the F-hypercenter of G. We obtain some results about the F-z-supplemented subgroups and use them to determine the structure of some groups.展开更多
During the initial impoundment period of a canyon-shaped reservoir,the water body fluctuated violently regarding water level,hydrological condition,and thermal stratification.These variations may alter the structure o...During the initial impoundment period of a canyon-shaped reservoir,the water body fluctuated violently regarding water level,hydrological condition,and thermal stratification.These variations may alter the structure of phytoplankton community,resulting in algal blooms and seriously threatening the ecological security of the reservoir.It is of great significance to understand the continuous changes of phytoplankton in the initial impoundment period for the protection of reservoir water quality.Therefore,a two-year in-situ monitoring study was conducted on water quality and phytoplankton in a representative canyonshaped reservoir named Sanhekou and the interannual changes of phytoplankton community and its response to environmental changes during the initial impoundment period were discussed at taxonomic versus functional classification levels.The results showed that the total nitrogen and permanganate index levels were relatively high in the first year due to rapid water storage and heavy rainfall input,and the more stable hydrological conditions in the second year promoted the increase of algae density and the transformation of community,and the proportion of cyanobacteria increased significantly.The succession order of phytoplankton in the first year of the initial impoundment periodwas Chlorophyta-Bacillariophyta-Chlorophyta,or J/F/X1-P/MP/W1-A/X1/MP,respectively.And the succession order in the second year was Cyanobacteria/Chlorophyta-Bacillariophyta-Chlorophyta,or L_(M)/G/P-P/A/X1-X1/J/G.Water temperature,relativewater column stability,mixing depth,and pHwere crucial factors affecting phytoplankton community succession.This study revealed the interannual succession law and driving factors of phytoplankton in the initial impoundment period and provided an important reference for the operation management and ecological protection of canyon-shaped reservoirs.展开更多
Lithium-ion capacitors(LICs)combine the high power dens-ity of electrical double-layer capacitors with the high energy density of lithium-ion batteries.However,they face practical limitations due to the narrow operati...Lithium-ion capacitors(LICs)combine the high power dens-ity of electrical double-layer capacitors with the high energy density of lithium-ion batteries.However,they face practical limitations due to the narrow operating voltage window of their activated carbon(AC)cathodes.We report a scalable thermal treatment strategy to develop high-voltage-tolerant AC cathodes.Through controlled thermal treatment of commer-cial activated carbon(Raw-AC)under a H_(2)/Ar atmosphere at 400-800℃,the targeted reduction of degradation-prone functional groups can be achieved while preserving the critical pore structure and increasing graph-itic microcrystalline ordering.The AC treated at 400℃(HAC-400)had a significant increase in specific capacity(96.0 vs.75.1 mAh/g at 0.05 A/g)and better rate capability(61.1 vs.36.1 mAh/g at 5 A/g)in half-cell LICs,along with an 83.5%capacity retention over 7400 cycles within an extended voltage range of 2.0-4.2 V in full-cell LICs.Scalability was demonstrated by a 120 g batch production,enabling fabrication of pouch-type LICs with commercial hard carbon anodes that delivered a higher energy density of 28.3 Wh/kg at 1 C,and a peak power density of 12.1 kW/kg compared to devices using raw AC.This simple,industry-compatible approach may be used for producing ad-vanced cathode materials for practical high-performance LICs.展开更多
Acceptor-donor-acceptor(A-D-A)type molecules,of which the novel non-fused azacyclic end-group pyrazoli-nones were modified with chlorine substitution on the phenyl ring,were synthesized.The non-fused azacyclic end-gro...Acceptor-donor-acceptor(A-D-A)type molecules,of which the novel non-fused azacyclic end-group pyrazoli-nones were modified with chlorine substitution on the phenyl ring,were synthesized.The non-fused azacyclic end-group py-razolinones have the advantages of simple synthesis steps,low cost and environmental friendliness,compared to the classical end-group dicyanomethyleneindianone.The properties of the synthesized A-D-A type molecules with non-fused azacyclic end groups were characterized by theoretical calculation,UV-vis absorption,cyclic voltammetry,X-ray diffraction and space charge limited current.It is shown that the strong UV-vis absorptions of the synthesized A-D-A type molecules are located in the wavelength range of 500~700 nm,with a moderate band gap of nearly 1.7 eV.At the same time,the influence of end-group chlorination on the properties of A-D-A type molecules was compared and explored.It is proven that this kind of A-D-A type molecule with non-fused azacyclic end groups has the potential to be applied as interfacial modified layer of the active layer in perovskite solar cell devices.展开更多
The photocatalytic hydrogen peroxide(H_(2)O_(2))production by graphitic carbon nitride is a sustainable and environment-benign alternative approach of conventional anthraquinone autoxidation technology,but it is great...The photocatalytic hydrogen peroxide(H_(2)O_(2))production by graphitic carbon nitride is a sustainable and environment-benign alternative approach of conventional anthraquinone autoxidation technology,but it is great challenges to promote two-electron O_(2)reduction and water oxidation.Herein,we present the well-dispersed graphitic carbon nitride quantum dots decorated with cyano groups(Na-CNQD and K-CNQD)by thermal polymerization of melamine in the presence of metal fluoride.The quantum confinement and edge effect have endowed the photocatalysts with rich active sites,wide light absorption range and the inhibited charge recombination.The cyano moieties function as O_(2)reduction centers to accept the photogenerated electrons and facilitate their rapid transfer to O_(2)molecules.This process enables the selective two-electron reduction of O_(2),leading to the production of H_(2)O_(2).Concurrently,the valence band holes on the heptazine moiety oxidize water into H_(2)O_(2).These synergistic effects promote photocatalytic H_(2)O_(2)production from O_(2)and H_(2)O without the need for additional photosensitizers,organic scavengers and co-catalysts.In contrast,pristine carbon nitride nanosheets remain inactive under the same conditions.This study offers new strategies for rational design of carbon-based materials for solar-to-chemical energy conversion.展开更多
As a new electrochemical technology,capacitive deionization(CDI)has been increasingly applied in environmental water treatment and seawater desalination.In this study,functional groups modified porous hollow carbon(HC...As a new electrochemical technology,capacitive deionization(CDI)has been increasingly applied in environmental water treatment and seawater desalination.In this study,functional groups modified porous hollow carbon(HC)were synthesized as CDI electrode material for removing Na^(+)and Cl^(−)in salty water.Results showed that the average diameter of HC was approximately 180 nm,and the infrared spectrum showed that its surface was successfully modified with sulfonic and amino groups,respectively.The sulfonic acid functionalized HC(HC-S)showed better electrochemical and desalting performance than the amino-functionalized HC(HC–N),with a maximum Faradic capacity of 287.4 F/g and an adsorptive capacity of 112.97 mg/g for NaCl.Additionally,92.63%capacity retention after 100 adsorption/desorption cycles demonstrates the excellent stability of HC-S.The main findings prove that HC-S is viable as an electrodematerial for desalination by high-performance CDI applications.展开更多
Introducing functional polar groups into polyolefins can significantly improve the material properties,but there are still challenges in achieving this goal,with the core difficulty being that polar groups are prone t...Introducing functional polar groups into polyolefins can significantly improve the material properties,but there are still challenges in achieving this goal,with the core difficulty being that polar groups are prone to interact with metal active species,affecting the efficiency of the copolymerization.With the rapid advancement in catalyst,a variety of copolymerization strategies are developed aimed at producing more versatile polyolefin materials.Although early transition metal catalysts play an indispensable role in the traditional polyolefin industry,their inherent strong oxophilicity becomes a significant constraint in copolymerization involving polar olefins,limiting their application scope.This review summarizes the progress made in recent years in the efficient copolymerization of non-polar olefins with polar comonomers catalyzed by groups 3 and 4 single-site catalysts.We classify the catalysts into four categories,Sc-,Ti-,Zr-,Hf-,based on the type of metal centers,and provide insights into the influence of catalyst structures and the type of comonomers on the copolymerization behavior.The introduction of polar monomers fundamentally improves the comprehensive performance of the products,greatly broadens the application scope of polyolefin materials,and meets the growing market demand for multifunctional and high-performance materials.展开更多
基金Supported by the Natural Science Foundation of Shanxi Province(202203021222233,202203021212398,202203021212403)。
文摘Photosynthesis of H_(2)O_(2)via sustainable biomass-derived carbon catalysts facilitate the conversion of renewable resources into valuable chemicals.However,the regulatory function of surface functional groups over reaction kinetics has not been sufficiently investigated.Herein,hydrothermal carbon spheres(CS)rich in oxygencontaining functional groups demonstrated a remarkably high H_(2)O_(2)production rate(653μmol/(g·h))in both pure water and actual seawater,even in the absence of any sacrificial agent.Meanwhile,the catalyst demonstrates outstanding activity(92%conversion and>99%selectivity)in the visible-light-driven photocatalytic oxidation of benzylamine to imines.Comprehensive analysis reveals that CS was rich in surface oxygen-containing functional groups,a feature strongly associated with its high photocatalytic efficiency.The observed positive Zeta potential of CS in seawater likely diminished the electrostatic repulsion against the positively charged intermediates,thereby facilitating their accumulation at the liquid-solid interface.This work proposes a strategic framework for developing metal-free photocatalysts from biomass,offering a sustainable pathway for photocatalytic applications.
基金supported by the National Natural Science Foundation of China,China(22372023)the Liaoning Revitalization Talents Program,China(XLYC2403019)。
文摘Photocatalysis has demonstrated considerable potential as a highly efficient approach to the valorization of biomass under mild conditions,while the selectivity control is a long-standing challenge,notably when the targets are complex and reactive biopolyols.In this study,we have successfully achieved selectivity control of photocatalytic biopolyols reforming to formic acid(FA)or CO by modulating the surface hydroxyl groups on TiO_(2) semiconductor.Photogenerated holes typically localize at bridging oxygen atoms(O2c)on the TiO_(2) surface,while shifting to terminal hydroxyl groups upon their introduction.The state of holes strongly affects the hole transfer process,which in turn influences the course of the reaction and thus controls the selectivity.By modulating the surface hydroxyl groups,the model substrate glycerol was selectively converted to CO(49%yield)and FA(50%yield).A range of other biopolyols,exemplified by erythritol,have demonstrated the same reaction selectivity.This work provides an effective strategy to manipulate reaction pathways by means of regulating the catalyst surface structure itself.
基金supported by the National Natural Science Foundation of China(Nos.22269020,42167068,U23A20582)Gansu Province Higher Education Industry Support Plan Project(No.2023CYZC-17)2024 Major Cultivation Projectfor University Research and Innovation Platforms(No.2024CXPT-10).
文摘There are limitations to using hard carbon(HC)in K^(+)storage due to its insufficient high-current reversible capacity and plateau potential,which result from the lack of effective active sites and low intercalation capabilities.The construction of HC cathodes with more available functional groups and ordered carbon nanocrystal structures is essential for improving K^(+)storage efficiency.Herein,a new perspective is proposed for synthesizing hard carbon nanosheets(HCNS)with abundant hydroxyl groups(O-H)/carboxylic groups(O-C=O)and rational carbon nanocrystals by interfacial assembly and carbonization.Systematic in ex-situ observations,dynamic analysis and theory calculations elucidate that the superior electrochemical capability of HCNS is ascribed to the synergistic effect of abundant available functional groups and ordered graphitic microcrystalline.Consequently,the HCNS exhibits outstanding K^(+)storage capabilities in terms of superb energy density(146.2 Wh/kg),high power density(1,7800 Wh/kg),and ultralong lifespan(102.9%capacity retention after 10,000 cycles).It was also found that the HC structure correlates with the discharge/charge plateau,confirming the'adsorption-insertion'charge storage mechanism.Furthermore,the proposed work provides a theoretical basis for making high-performance HC anodes by understanding the effect of their microstructure on K^(+)storage.
基金financially supported by the National Natural Science Foundation of China (Nos.22375024,21975031,51933001,and 21734009)。
文摘The fluorination strategy has been proven effective in significantly enhancing the photovoltaic performance of organic solar cells(OSCs) based on non-fused ring electron acceptors(NFREAs).However,research on the impact of fluorination positions at side chains on NFREAs device performance remains scant.In this study,we introduce two isomeric NFREAs,designated as GA-2F-E and GA-2F,distinguished by their fluorination positions at the side chains.Both NFREAs share a thiophene[3,2-b]thiophene core,but their side chains differ:GA-2F-E features two(4-butylphenyl)-N-(4-fluorophenyl) amino groups,whereas GA-2F's side chains consist of bis(4-fluorophenyl)amino and bis(4-butylphenyl)amino groups attached to opposite sides of the core.To delve into the influence of fluorination positions on the optoelectronic properties,aggregation behavior,and overall efficiency of the acceptor molecules,a comprehensive investigation was conducted.The findings reveal that,despite similar photophysical properties and comparable absorption bandwidths,GA-2F-E,with fluorine atoms positioned on both sides of the molecular framework,demonstrates more compact π-π stacking,reduced bimolecular recombination,superior exciton transport,and a more balanced,higher mobility.As a result of these advantages,OSCs optimized with D18:GA-2F-E achieve a remarkable power conversion efficiency(PCE) of 16.45 %,surpassing the 15.83 %PCE of devices utilizing D18:GA-2F.This research underscores the potential of NFREAs in future applications and highlights the significance of fluorination positions in enhancing OSC performance,paving the way for the development of more efficient NFREAs.
文摘Let M be a compact n-manifold of positive sectional curvature.We will review classical results on the fundamental group of M,a motivation on the c(n)-cyclic conjecture that the fundamental group of M contains a cyclic subgroup of index bounded above by c(n),a constant depending only on n,and we will survey partial results(up to date)on the c(n)-cyclic conjecture.
基金Supported by NSFC (No.12401024)the Scientific Research Innovation Project of Lingnan Normal University (Nos.LT2401,LT2410)。
文摘Let T_(n) and S_(n) be the full transformation semigroup and the symmetric group on X_(n)={1,2,...,n},respectively.Let G be a transitiveimprimitive subgroupof S_(n) with nontrivial blocksΔand letαbe a transformation in T_(n)\S_(n).The kernel ofαis the partition of X_(n) induced by the equivalence relation{(x,y)|xα=yα};the kernel type ofαis the partition of n given by the sizes of the parts of the kernel.A transformation semigroup is called synchronizing if it contains a constant map.Then a group G synchronizes a transformationαif the semigroup(G,α)contains a constant map.In this paper,we study a transitive imprimitive permutation group G together with a non-invertible transformationαthat generate a synchronizing semigroup.We mainly discuss 7 cases where G synchronizes a special transformationαwith each kernel class A_(i)(A_(1)j)satisfying|A_(i)∩Δ|=1(|A_(1)j∩Δ|=1)for all blocksΔofG,that is,the kernel type ofαis(|A_(1)|,1,...,1),(|A_(1)1|,...,|A_(1m)|,|A_(2)|,...,|Ar|),or(|A_(1)|,...,|A_(t)|,1,...,1),or the rank is 2,3,4,or n-2.
基金Supported by NSF of China(12061011)NSF of Guangxi(2023GXN-SFAA026333)。
文摘This paper investigates the in uence of local SS-quasinormal maximal subgroups of Sylow subgroups on the structure of nite groups.We present several new criteria on p-nilpotency of nite groups by utilizing a small quantity of local SS-quasinormal maximal subgroups of Sylow p-subgroups.As applications,we obtain some sucient conditions for a nite group to be in a saturated formation containing the class of supersolvable groups.
基金Supported by the National Natural Science Foundation of China(Grant No.12071092)Guangdong Basic and Applied Basic Research Foundation(Grant No.2025A1515012072)+1 种基金the Natural Science Research Project of Anhui Educational Committee(Grant No.2024AH051298)the Scientific Research Foundation of Bozhou University(Grant No.BYKQ202419).
文摘Let G be a finite group and H a subgroup of G.The normal index of H in G is defined as the order of K/H_(G),where K is a normal supplement of H in G such that|K|is minimal and H_(G)≤K■G.Let p be a prime which divides the order of a group G.In this paper,some characterizations of G being p-solvable or p-supersolvable were obtained by analyzing the normal index of certain subgroups of G.These results can be viewed as local version of recent results in the literature.
文摘Let G be a group and H;K be subgroups of G.H is called a TI-subgroup of G if H∩H^(g)=1 or H for every g∈G.K is called P-subnormal in G if there is a chain of subgroups K=K_(0)≤K_(1)≤K_(2)≤…≤K_(n-1)≤K_(n)=G such that|K_(i):K_(i-1)|∈P for i∈{1;2;…;n}.Furthermore,K is called K-P-subnormal in G if there is a chain of subgroups K=K_(0)≤K_(1)≤K_(2)≤…≤K_(n-1)≤K_(n)=G such that either K_(i-1)is normal in Ki or|K_(i):K_(i-1)|∈P for i∈{1;2;…;n}.In this paper,some properties of a nite group in which some particular subgroups are TI-subgroups or P-subnormal subgroups or K-P-subnormal subgroups are given.
基金supported by National Natural Science Foundation of China(Grants No.42361144888 and 42401308)National Key Research and Development Program of China(Grant No.2024YFF1309200).
文摘International trade serves as a crucial pathway for enhancing global food security and equality amid severe food crises worldwide.Under globalization,economic development has profoundly influenced food trade,while disparities in food purchasing power among different economic development groups have led to uneven food security outcomes.However,the varying contributions of international trade to food security across these groups remain to be quantitatively elucidated.This study categorized countries into four economic development groups—high,high-medium,medium-low,and low—and examined changes in their food security scores from 2010 to 2019.The cross-group contributions of international trade to food security across these groups were compared.The results revealed that the food security score of the high economic development group was 9.22 times higher than that of the low economic development group.From 2010 to 2019,the high economic development group exhibited a significant upward trend in food security scores,whereas the low economic development group showed a significant decline.Moreover,international trade contributed significantly to both cross-group and within-group food security in the high economic development group,while its contribution to the low economic development group remained negligible.These findings demonstrated that international trade has further widened the food security gap between the high and low economic development groups,and its limited contribution to the low economic development group has failed to reverse the declining trend in their food security scores.This study quantified the divergent impacts of international trade on food security across economic development groups,providing valuable insights for optimizing global food trade policies—particularly in addressing the food security challenges faced by low econominc development group.
基金General Project of the 2023 Annual Scheme for Shenzhen’s Education Science“14th Five-Year”Plan:Construction of Art and Design Specialty Groups in Higher Vocational Education Based on the Municipal Industry-Education Consortium(yb23018)2024 University-Level Teaching Achievement Award Cultivation Project of Shenzhen Polytechnic University:“Innovation and Implementation of a Sustainable Talent Development Model Based on Municipal Industry-Education Collaboration and Art-Technology Integration”。
文摘With the transformation and upgrading of industries,along with the rapid advancement of artificial intelligence(AI)technologies,higher vocational education in art and design is facing new developmental challenges.As an emerging integrative ecosystem,the municipal industry-education consortium offers a strategic pathway to address these challenges by deepening collaboration between education and industry and fostering the coordinated development of both sectors.Grounded in the framework of the municipal industry-education consortium,this study proposes a top-level organizational model for art and design specialty groups characterized by industry-chain-driven development,interdisciplinary integration,and growth-employment orientation.It further explores multiple development pathways,including innovations in consortium council governance,dynamic talent cultivation models,shared curriculum systems,dual-track teaching teams,and multi-tiered practice bases.Collectively,these pathways establish a comprehensive specialty group system in which core specialties drive development,supporting specialties ensure interdependence,and extended specialties foster mutual advancement.The findings provide theoretical insights and practical guidance for advancing the modernization and high-quality transformation of vocational art and design education,contributing to the cultivation of innovative and application-oriented professionals aligned with industrial restructuring and the development of new productive forces.
基金Supported by the National Natural Science Foundation of China(Grant Nos.1237101812201236)+1 种基金the Fundamental Research Funds for the Central Universities(Grant No.B240201093/2013)the Natural Science Foundation of the Anhui Higher Education Institutions(Grant No.2022AH051907)。
文摘In this paper,we introduce the set of maximal subgroups with non-trivial core and their corresponding second maximal subgroups.A correlation characterization of the group class J_(pr)is presented by establishing the relationship between the core and the second maximal subgroups in these classifications.
基金the National Natural Science Foundation of China(Grant Nos.1120108211171353)+2 种基金China Postdoctoral Science Foundation(Grant No.2013T60866)the Natural Science Foundation of Guangdong Province(Grant No.S201204007267)Outstanding Young Teachers Training Project of Guangdong Province(GrantNo.Yq2013061)
文摘Let P be a Sylow p-subgroup of a group G with the smallest generator number d, where p is a prime. Denote by Md（P） = （P1, P2,..., Pd） a set of maximal subgroups of P such that φ（P） = ∩n^d=1Pn. In this paper, we investigate the structure of a finite group G under the assumption that the maximal subgroups in Md（P） are weakly s-permutably embedded in G, some interesting results are obtained which generalize some recent results. Finally, we give some further results in terms of weakly s-permutably embedded subgroups.
文摘A subgroup H of a group G is called F-z-supplemented in G if there exists a subgroup K of G, such that G = HK and H∩K≤ Z∞F（G）, where Z∞F（G） is the F-hypercenter of G. We obtain some results about the F-z-supplemented subgroups and use them to determine the structure of some groups.
基金supported by the National Key R&D Program of China(No.2022YFC3203602)the Natural Science Foundation of China(No.52370018)+1 种基金Shaanxi Provincial Youth Innovation Team Project(No.22JP040)Shaanxi Provincial Key Scientific and Technological Innovation Team(No.2023-CX-TD-32).
文摘During the initial impoundment period of a canyon-shaped reservoir,the water body fluctuated violently regarding water level,hydrological condition,and thermal stratification.These variations may alter the structure of phytoplankton community,resulting in algal blooms and seriously threatening the ecological security of the reservoir.It is of great significance to understand the continuous changes of phytoplankton in the initial impoundment period for the protection of reservoir water quality.Therefore,a two-year in-situ monitoring study was conducted on water quality and phytoplankton in a representative canyonshaped reservoir named Sanhekou and the interannual changes of phytoplankton community and its response to environmental changes during the initial impoundment period were discussed at taxonomic versus functional classification levels.The results showed that the total nitrogen and permanganate index levels were relatively high in the first year due to rapid water storage and heavy rainfall input,and the more stable hydrological conditions in the second year promoted the increase of algae density and the transformation of community,and the proportion of cyanobacteria increased significantly.The succession order of phytoplankton in the first year of the initial impoundment periodwas Chlorophyta-Bacillariophyta-Chlorophyta,or J/F/X1-P/MP/W1-A/X1/MP,respectively.And the succession order in the second year was Cyanobacteria/Chlorophyta-Bacillariophyta-Chlorophyta,or L_(M)/G/P-P/A/X1-X1/J/G.Water temperature,relativewater column stability,mixing depth,and pHwere crucial factors affecting phytoplankton community succession.This study revealed the interannual succession law and driving factors of phytoplankton in the initial impoundment period and provided an important reference for the operation management and ecological protection of canyon-shaped reservoirs.
文摘Lithium-ion capacitors(LICs)combine the high power dens-ity of electrical double-layer capacitors with the high energy density of lithium-ion batteries.However,they face practical limitations due to the narrow operating voltage window of their activated carbon(AC)cathodes.We report a scalable thermal treatment strategy to develop high-voltage-tolerant AC cathodes.Through controlled thermal treatment of commer-cial activated carbon(Raw-AC)under a H_(2)/Ar atmosphere at 400-800℃,the targeted reduction of degradation-prone functional groups can be achieved while preserving the critical pore structure and increasing graph-itic microcrystalline ordering.The AC treated at 400℃(HAC-400)had a significant increase in specific capacity(96.0 vs.75.1 mAh/g at 0.05 A/g)and better rate capability(61.1 vs.36.1 mAh/g at 5 A/g)in half-cell LICs,along with an 83.5%capacity retention over 7400 cycles within an extended voltage range of 2.0-4.2 V in full-cell LICs.Scalability was demonstrated by a 120 g batch production,enabling fabrication of pouch-type LICs with commercial hard carbon anodes that delivered a higher energy density of 28.3 Wh/kg at 1 C,and a peak power density of 12.1 kW/kg compared to devices using raw AC.This simple,industry-compatible approach may be used for producing ad-vanced cathode materials for practical high-performance LICs.
文摘Acceptor-donor-acceptor(A-D-A)type molecules,of which the novel non-fused azacyclic end-group pyrazoli-nones were modified with chlorine substitution on the phenyl ring,were synthesized.The non-fused azacyclic end-group py-razolinones have the advantages of simple synthesis steps,low cost and environmental friendliness,compared to the classical end-group dicyanomethyleneindianone.The properties of the synthesized A-D-A type molecules with non-fused azacyclic end groups were characterized by theoretical calculation,UV-vis absorption,cyclic voltammetry,X-ray diffraction and space charge limited current.It is shown that the strong UV-vis absorptions of the synthesized A-D-A type molecules are located in the wavelength range of 500~700 nm,with a moderate band gap of nearly 1.7 eV.At the same time,the influence of end-group chlorination on the properties of A-D-A type molecules was compared and explored.It is proven that this kind of A-D-A type molecule with non-fused azacyclic end groups has the potential to be applied as interfacial modified layer of the active layer in perovskite solar cell devices.
基金supported by the National Natural Science Foundation of China(22361024 and 22471055)Natural Science Foundation of Jiangxi Province(20232ACB203001)+1 种基金Natural Science Foundation of Hebei Province(B2024202021,B2022202039)S&T Program of Hebei(236Z4308G)。
文摘The photocatalytic hydrogen peroxide(H_(2)O_(2))production by graphitic carbon nitride is a sustainable and environment-benign alternative approach of conventional anthraquinone autoxidation technology,but it is great challenges to promote two-electron O_(2)reduction and water oxidation.Herein,we present the well-dispersed graphitic carbon nitride quantum dots decorated with cyano groups(Na-CNQD and K-CNQD)by thermal polymerization of melamine in the presence of metal fluoride.The quantum confinement and edge effect have endowed the photocatalysts with rich active sites,wide light absorption range and the inhibited charge recombination.The cyano moieties function as O_(2)reduction centers to accept the photogenerated electrons and facilitate their rapid transfer to O_(2)molecules.This process enables the selective two-electron reduction of O_(2),leading to the production of H_(2)O_(2).Concurrently,the valence band holes on the heptazine moiety oxidize water into H_(2)O_(2).These synergistic effects promote photocatalytic H_(2)O_(2)production from O_(2)and H_(2)O without the need for additional photosensitizers,organic scavengers and co-catalysts.In contrast,pristine carbon nitride nanosheets remain inactive under the same conditions.This study offers new strategies for rational design of carbon-based materials for solar-to-chemical energy conversion.
基金supported by the National Science Foundation of China(No.21606191)the Natural Science Foundation of Shandong Province(No.ZR2020ME024).
文摘As a new electrochemical technology,capacitive deionization(CDI)has been increasingly applied in environmental water treatment and seawater desalination.In this study,functional groups modified porous hollow carbon(HC)were synthesized as CDI electrode material for removing Na^(+)and Cl^(−)in salty water.Results showed that the average diameter of HC was approximately 180 nm,and the infrared spectrum showed that its surface was successfully modified with sulfonic and amino groups,respectively.The sulfonic acid functionalized HC(HC-S)showed better electrochemical and desalting performance than the amino-functionalized HC(HC–N),with a maximum Faradic capacity of 287.4 F/g and an adsorptive capacity of 112.97 mg/g for NaCl.Additionally,92.63%capacity retention after 100 adsorption/desorption cycles demonstrates the excellent stability of HC-S.The main findings prove that HC-S is viable as an electrodematerial for desalination by high-performance CDI applications.
基金supported by the National Natural Science Foundation of China(No.U23B6011)。
文摘Introducing functional polar groups into polyolefins can significantly improve the material properties,but there are still challenges in achieving this goal,with the core difficulty being that polar groups are prone to interact with metal active species,affecting the efficiency of the copolymerization.With the rapid advancement in catalyst,a variety of copolymerization strategies are developed aimed at producing more versatile polyolefin materials.Although early transition metal catalysts play an indispensable role in the traditional polyolefin industry,their inherent strong oxophilicity becomes a significant constraint in copolymerization involving polar olefins,limiting their application scope.This review summarizes the progress made in recent years in the efficient copolymerization of non-polar olefins with polar comonomers catalyzed by groups 3 and 4 single-site catalysts.We classify the catalysts into four categories,Sc-,Ti-,Zr-,Hf-,based on the type of metal centers,and provide insights into the influence of catalyst structures and the type of comonomers on the copolymerization behavior.The introduction of polar monomers fundamentally improves the comprehensive performance of the products,greatly broadens the application scope of polyolefin materials,and meets the growing market demand for multifunctional and high-performance materials.
