Silicon-containing aryl acetylene resin(PSA)is a new type of high-temperature resistant resin with excellent oxidation resistance,whereas antioxidant reaction mechanism of PSA resin under ultra-high temperatures still...Silicon-containing aryl acetylene resin(PSA)is a new type of high-temperature resistant resin with excellent oxidation resistance,whereas antioxidant reaction mechanism of PSA resin under ultra-high temperatures still remains unclear.Herein,the oxidation behavior and mechanisms of PSA resin are systematically investigated combining kinetic analysis and Reax FF molecular dynamics(MD)simulations.Thermogravimetric analysis indicates that the oxidation process of PSA resin undergoes two main steps:oxidative mass gain and oxidative degradation.The distributed activation energy model(DAEM)is employed for describing oxidation processes and the best-fit one is obtained using genetic algorithms and differential evolution.DAEM model demonstrates that the oxidative weight gain stage is dominated by two virtual reactants and the oxidative degradation stage consists of three virtual reactants.Correspondingly,the observation of MD reaction pathways indicates that oxygen oxidation of unsaturated structures occurs in the initial stage,which results in the formation of PSA resin oxides.Furthermore,cracked pieces react with O_(2)to generate CO and other chemicals in the second step.The resin matrix's great antioxidation resilience is illustrated by the formation of SiO_(2).The analysis based on MD simulations exhibits an efficient computational proof with the experiments and DAEM methods.Based on the results,a two-stage reaction mechanism is proposed,which provides important theoretical support for the subsequent study of the oxidation behavior of silica-based resins.展开更多
The integration of nano-semiconductors into electromagnetic wave absorption materials is a highly desirable strategy for intensifying dielectric polarization loss;achieving high-attenuation microwave absorption and re...The integration of nano-semiconductors into electromagnetic wave absorption materials is a highly desirable strategy for intensifying dielectric polarization loss;achieving high-attenuation microwave absorption and realizing in-depth comprehension of dielectric loss mechanisms remain challenges.Herein,ultrafine oxygen vacancy-rich Nb_(2)O_(5)semiconductors are confined in carbon nanosheets(ov-Nb_(2)O_(5)/CNS)to boost dielectric polarization and achieve high attenuation.The polarization relaxation,electromagnetic response,and impedance matching of the ov-Nb_(2)O_(5)/CNS are significantly facilitated by the Nb_(2)O_(5)semiconductors with rich oxygen vacancies,which consequently realizes an extremely high attenuation performance of-80.8 dB(>99.999999%wave absorption)at 2.76 mm.As a dielectric polarization center,abundant Nb_(2)O_(5)–carbon heterointerfaces can intensify interfacial polarization loss to strengthen dielectric polarization,and the presence of oxygen vacancies endows Nb_(2)O_(5)semiconductors with abundant charge separation sites to reinforce electric dipole polarization.Moreover,the three-dimensional reconstruction of the absorber using microcomputer tomography technology provides insight into the intensification of the unique lamellar morphology regarding multiple reflection and scattering dissipation characteristics.Additionally,ov-Nb_(2)O_(5)/CNS demonstrates excellent application potential by curing into a microwave-absorbing,machinable,and heat-dissipating plate.This work provides insight into the dielectric polarization loss mechanisms of nano-semiconductor/carbon composites and inspires the design of high-performance microwave absorption materials.展开更多
Lithium metal batteries are among the strong contenders to satisfy the ever-increasing needs of energy storage systems,which however suffer from poor composition of the solid electrolyte interphase(SEI)layer and uncon...Lithium metal batteries are among the strong contenders to satisfy the ever-increasing needs of energy storage systems,which however suffer from poor composition of the solid electrolyte interphase(SEI)layer and uncontrolled Li dendrites formation.In this regard,we report on the design of an ionreleased MgI_(2)-doped polyacrylonitrile(PAN)based nanofiber(MPANF)separator,which can lead to conducive SEI layer and dendrite-free Li anode.The combination of the lithophilic MgI_(2)nanoparticles with polarized PAN matrix comprehensively functions as a high-compatible interpenetrating network to homogenize ionic transportation and confront dendrite growth.The released I ions introduce the highion-conductivity LiI into SEI layer,which could induce the formation of favorable and protective interface layer in the early stage,as embodied in the enrichment of advantageous components such as LiN_(x)O_(y),Li_(2)O,LiF,and Li_(3)N.Profited from the high-affinity MPANF separator,the Li||Li symmetric cell achieves an ultralow voltage hysteresis of 46 mV with an extended lifespan of 580 h.And a prolonged lifetime of 590cycles with an enhanced specific capacity of 140.1 m Ah g^(-1)and the Coulombic efficiency of 96.2%at 1C can be obtained in full cells.This work may offer a facile and high-affinity alternative to traditional polymeric separators for high-performance and dendrite-free Li metal batteries.展开更多
Selective cleavage of robust C−C bonds to harvest value-added aromatic oxygenates is an intriguing but challenging task in lignin depolymerization.Photocatalysis is a promising technology with the advantages of mild r...Selective cleavage of robust C−C bonds to harvest value-added aromatic oxygenates is an intriguing but challenging task in lignin depolymerization.Photocatalysis is a promising technology with the advantages of mild reaction conditions and strong sustainability.Herein,we show a novel urchin-like Nb_(2)O_(5)hollow microsphere(U-Nb_(2)O_(5)HM),prepared by one-pot hydrothermal method,are highly active and selective for C_(α)−C_(β)bond cleavage of ligninβ-O-4 model compounds under mild conditions,achieving 94%substrate conversion and 96%C−C bond cleavage selectivity.Systematic experimental studies and density functional theory(DFT)calculations revealed that the superior performance of U-Nb_(2)O_(5)HMs arises from more exposed active sites,more efficient free charge separation and the active(001)facet,which facilitates the activation of Cβ−H bond of lignin models and generate key Cβradical intermediates by photogenerated holes,further inducing the C_(α)−C_(β)bond cleavage to produce aromatic oxygenates.This work could provide some suggestions for the fabrication of hierarchical photocatalysts in the lignin depolymerization system.展开更多
基金financially supported by National Natural Science Foundation of China(22008073,22078100,21878091)Shanghai Sailing Program(20YF1410600)。
文摘Silicon-containing aryl acetylene resin(PSA)is a new type of high-temperature resistant resin with excellent oxidation resistance,whereas antioxidant reaction mechanism of PSA resin under ultra-high temperatures still remains unclear.Herein,the oxidation behavior and mechanisms of PSA resin are systematically investigated combining kinetic analysis and Reax FF molecular dynamics(MD)simulations.Thermogravimetric analysis indicates that the oxidation process of PSA resin undergoes two main steps:oxidative mass gain and oxidative degradation.The distributed activation energy model(DAEM)is employed for describing oxidation processes and the best-fit one is obtained using genetic algorithms and differential evolution.DAEM model demonstrates that the oxidative weight gain stage is dominated by two virtual reactants and the oxidative degradation stage consists of three virtual reactants.Correspondingly,the observation of MD reaction pathways indicates that oxygen oxidation of unsaturated structures occurs in the initial stage,which results in the formation of PSA resin oxides.Furthermore,cracked pieces react with O_(2)to generate CO and other chemicals in the second step.The resin matrix's great antioxidation resilience is illustrated by the formation of SiO_(2).The analysis based on MD simulations exhibits an efficient computational proof with the experiments and DAEM methods.Based on the results,a two-stage reaction mechanism is proposed,which provides important theoretical support for the subsequent study of the oxidation behavior of silica-based resins.
基金supported by National Natural Science Foundation of China(No.22078100,No.52102098,and No.22008073)Fundamental Research Funds for the Central Universities(No.222201718002)。
文摘The integration of nano-semiconductors into electromagnetic wave absorption materials is a highly desirable strategy for intensifying dielectric polarization loss;achieving high-attenuation microwave absorption and realizing in-depth comprehension of dielectric loss mechanisms remain challenges.Herein,ultrafine oxygen vacancy-rich Nb_(2)O_(5)semiconductors are confined in carbon nanosheets(ov-Nb_(2)O_(5)/CNS)to boost dielectric polarization and achieve high attenuation.The polarization relaxation,electromagnetic response,and impedance matching of the ov-Nb_(2)O_(5)/CNS are significantly facilitated by the Nb_(2)O_(5)semiconductors with rich oxygen vacancies,which consequently realizes an extremely high attenuation performance of-80.8 dB(>99.999999%wave absorption)at 2.76 mm.As a dielectric polarization center,abundant Nb_(2)O_(5)–carbon heterointerfaces can intensify interfacial polarization loss to strengthen dielectric polarization,and the presence of oxygen vacancies endows Nb_(2)O_(5)semiconductors with abundant charge separation sites to reinforce electric dipole polarization.Moreover,the three-dimensional reconstruction of the absorber using microcomputer tomography technology provides insight into the intensification of the unique lamellar morphology regarding multiple reflection and scattering dissipation characteristics.Additionally,ov-Nb_(2)O_(5)/CNS demonstrates excellent application potential by curing into a microwave-absorbing,machinable,and heat-dissipating plate.This work provides insight into the dielectric polarization loss mechanisms of nano-semiconductor/carbon composites and inspires the design of high-performance microwave absorption materials.
基金supported by the National Natural Science Foundation of China(22078100,22008073,and 52102098)。
文摘Lithium metal batteries are among the strong contenders to satisfy the ever-increasing needs of energy storage systems,which however suffer from poor composition of the solid electrolyte interphase(SEI)layer and uncontrolled Li dendrites formation.In this regard,we report on the design of an ionreleased MgI_(2)-doped polyacrylonitrile(PAN)based nanofiber(MPANF)separator,which can lead to conducive SEI layer and dendrite-free Li anode.The combination of the lithophilic MgI_(2)nanoparticles with polarized PAN matrix comprehensively functions as a high-compatible interpenetrating network to homogenize ionic transportation and confront dendrite growth.The released I ions introduce the highion-conductivity LiI into SEI layer,which could induce the formation of favorable and protective interface layer in the early stage,as embodied in the enrichment of advantageous components such as LiN_(x)O_(y),Li_(2)O,LiF,and Li_(3)N.Profited from the high-affinity MPANF separator,the Li||Li symmetric cell achieves an ultralow voltage hysteresis of 46 mV with an extended lifespan of 580 h.And a prolonged lifetime of 590cycles with an enhanced specific capacity of 140.1 m Ah g^(-1)and the Coulombic efficiency of 96.2%at 1C can be obtained in full cells.This work may offer a facile and high-affinity alternative to traditional polymeric separators for high-performance and dendrite-free Li metal batteries.
基金financially supported by the National Natural Science Foundation of China (No. 22008073)Shanghai Sailing Program (No. 20YF1410600)
文摘Selective cleavage of robust C−C bonds to harvest value-added aromatic oxygenates is an intriguing but challenging task in lignin depolymerization.Photocatalysis is a promising technology with the advantages of mild reaction conditions and strong sustainability.Herein,we show a novel urchin-like Nb_(2)O_(5)hollow microsphere(U-Nb_(2)O_(5)HM),prepared by one-pot hydrothermal method,are highly active and selective for C_(α)−C_(β)bond cleavage of ligninβ-O-4 model compounds under mild conditions,achieving 94%substrate conversion and 96%C−C bond cleavage selectivity.Systematic experimental studies and density functional theory(DFT)calculations revealed that the superior performance of U-Nb_(2)O_(5)HMs arises from more exposed active sites,more efficient free charge separation and the active(001)facet,which facilitates the activation of Cβ−H bond of lignin models and generate key Cβradical intermediates by photogenerated holes,further inducing the C_(α)−C_(β)bond cleavage to produce aromatic oxygenates.This work could provide some suggestions for the fabrication of hierarchical photocatalysts in the lignin depolymerization system.