The interfacial interaction existing in the Ni ZrO 2 composite plating has been investigated. The experimental results show that no new phases were formed in the interfacial regions between matrix Ni and ZrO 2 part...The interfacial interaction existing in the Ni ZrO 2 composite plating has been investigated. The experimental results show that no new phases were formed in the interfacial regions between matrix Ni and ZrO 2 particles, but an orbital interaction through the mutual overlap of the d orbits does exist in the interfacial regions between Ni atoms and Zr 3+ ions.展开更多
Developing classes of Ag@C composites stand out for their one of a kind structure and novel physicochemical properties in later a long time.This review explores the current state-of-the-art progress in the preparation...Developing classes of Ag@C composites stand out for their one of a kind structure and novel physicochemical properties in later a long time.This review explores the current state-of-the-art progress in the preparation methods and the novel properties of Ag@C composites.We provide a definition of the stability of Ag@C composites,and propose strategies to improve the stability.Based on the later inquire,a summary and outlook toward the synthesis and applications of Ag@C composites are presented,aiming to accelerate the exploration of Ag@C composites and further stimulate the applications in various fields.展开更多
Herein,a bottom-down design is presented to successfully fabricate ZIF-derived Co3O4,grown in situ on a one-dimensional(1D)α-MnO2 material,denoted as α-MnO2@Co3O4.The synergistic effect derived from the coupled inte...Herein,a bottom-down design is presented to successfully fabricate ZIF-derived Co3O4,grown in situ on a one-dimensional(1D)α-MnO2 material,denoted as α-MnO2@Co3O4.The synergistic effect derived from the coupled interface constructed betweenα-MnO2 and Co3O4 is responsible for the enhanced catalytic activity.The resultantα-MnO2@Co3O4 catalyst exhibits excellent catalytic activity at a T90%(temperature required to achieve a toluene conversion of 90%)of approximately 229℃,which is 47 and 28℃ lower than those of the pureα-MnO2 nanowire and Co3O4-b obtained via pyrolysis of ZIF-67,respectively.This activity is attributed to the increase in the number of surface-adsorbed oxygen species,which accelerate the oxygen mobility and enhance the redox pairs of Mn^4+/Mn^3+ and Co^2+/Co^3+.Moreover,the result of in situ diffuse reflectance infrared Fourier transform spectroscopy suggests that the gaseous oxygen could be more easily activated to adsorbed oxygen species on the surface of α-MnO2@Co3O4 than on that of α-MnO2.The catalytic reaction route of toluene oxidation over theα-MnO2@Co3O4 catalyst is as follows:toluene→benzoate species→alkanes containing oxygen functional group→CO2 and H2O.In addition,the α-MnO2@Co3O4 catalyst shows excellent stability and good water resistance for toluene oxidation.Furthermore,the preparation method can be extended to other 1D MnO2 materials.A new strategy for the development of high-performance catalysts of practical significance is provided.展开更多
A comprehensive understanding of the role of the electrocatalyst in photoelectrochemical(PEC)water splitting is central to improving its performance.Herein,taking the Si-based photoanodes(n^(+)p-Si/SiO_(x)/Fe/FeOx/MOO...A comprehensive understanding of the role of the electrocatalyst in photoelectrochemical(PEC)water splitting is central to improving its performance.Herein,taking the Si-based photoanodes(n^(+)p-Si/SiO_(x)/Fe/FeOx/MOOH,M=Fe,Co,Ni)as a model system,we investigate the effect of the transition-metal electrocatalysts on the oxygen evolution reaction(OER).Among the photoanodes with the three different electrocatalysts,the best OER activity,with a low-onset potential of∼1.01 VRHE,a high photocurrent density of 24.10 mA cm^(-2)at 1.23 VRHE,and a remarkable saturation photocurrent density of 38.82 mA cm^(-2),was obtained with the NiOOH overlayer under AM 1.5G simulated sunlight(100 mW cm^(-2))in 1 M KOH electrolyte.The optimal interfacial engineering for electrocatalysts plays a key role for achieving high performance because it promotes interfacial charge transport,provides a larger number of surface active sites,and results in higher OER activity,compared to other electrocatalysts.This study provides insights into how electrocatalysts function in water-splitting devices to guide future studies of solar energy conversion.展开更多
Typical cationic and anionic surfactants were chosen and their interactions were calculated by quantum chemical method. Interaction energies are -0.2378 kJ·mol-1, -3.3394kJ·mol-1 and 0.1204kJ·mol-1 for ...Typical cationic and anionic surfactants were chosen and their interactions were calculated by quantum chemical method. Interaction energies are -0.2378 kJ·mol-1, -3.3394kJ·mol-1 and 0.1204kJ·mol-1 for the molecular pairs with fluocarbon and hydrocarbon chain: C4H10/C5H12, C4F10/C5H12, and C4F10 /C5F12, respectively. When hydrophilic group with cationic and anionicions is introduced, interaction energies are -287.40kJ·mol-1, -311.18kJ·mol-1 and -345.83kJ·mol-1. The results show that there is strong static interaction between cationic and anionic surfactants. It has been predicted that mixed monolayer may be formed and surface activity is enhanced favorably, especially for mixtures of cationic and anionic surfactants with fluocarbon and hydrocarbon chains. The anionic surfactants, sodium octadecylbenzenesulfonate perfluopolyetherbenzenesulonate(ANF-I) was synthesized, mixture effects of ANF-I with sodium octadecylbenzenesulfonate or dodecyldimethyl benzylammonium bromide were studied. The results indicate that the efficiency of mixing increased and the theoretical prediction was testified. These results can provide useful information for the design of new surfactants.展开更多
Abstract： In this work, the authors present a study of growth and characterization of composite based on AI and CNT （carbon nanotubes. The composites were prepared by a chemical mixing method and characterized by SE...Abstract： In this work, the authors present a study of growth and characterization of composite based on AI and CNT （carbon nanotubes. The composites were prepared by a chemical mixing method and characterized by SEM analysis, energy dispersed X-ray measurements, X-ray photoelectron spectroscopy and cathodoluminescence spectroscopy. The analysis showed that the composites are formed by macro-cluster of aluminum oxide on a network of CNT without formation of chemical bonds at interface between particles. The results are compared with those obtained for a sample of CNT with AI traces （〈 0.5%）. They show that only the presence of metal traces changes the nanotubes optical properties, with a luminescence signal centered at about 380 nm. These luminescence signals are caused by the adhesion between CNT and AI micro-clusters that promote the formation of band gap with some local energy levels.展开更多
The hierarchical micro/nanoscale layered formation of organic and inorganic components of natural nacre, results in abundant interracial interactions, providing an inspiration for fabricating bioinspired nanocomposite...The hierarchical micro/nanoscale layered formation of organic and inorganic components of natural nacre, results in abundant interracial interactions, providing an inspiration for fabricating bioinspired nanocomposites through constructing the interfacial interactions. Herein, we demonstrated the synergistic interfacial interactions of hydrogen bonding from hydroxypropyl cellu- lose and ionic bonding from copper ions upon the reduced graphene oxide based bioinspired nanocomposites, which show the integrated tensile strength, toughness and excellent fatigue-resistant property, as well as high electrical conductivity. These ex- traordinary properties allow this kind of bioinspired nanocomposites to potentially utilize in the fields of aerospace, flexible electronics devices, etc. This study also opens a door for fabricating excellent mechanical performance graphene-based bioin- spired nanocomposites via synergistic interfacial interactions in the future.展开更多
Graphene dispersions in low-boiling-point green solvents have wide applications in coatings,conducting inks,batteries,electronics and solar cells.Two three-dimensional(3D)cathode interfacial materials(CIMs)(1,3,5,7,9,...Graphene dispersions in low-boiling-point green solvents have wide applications in coatings,conducting inks,batteries,electronics and solar cells.Two three-dimensional(3D)cathode interfacial materials(CIMs)(1,3,5,7,9,11,13,15-octa-(9-bis(30-(N,N-dimethylamino)propyl)-2,7-fluorene)-vinylpentacyclo-octasiloxane)(POSSFN)and(1,3,5,7-tetra-(9-bis(30-(N,N-dimethylamino)propyl)-2,7-fluorene)-adamantane)(ADMAFN)are excellent surfactants for dispersing graphene in ethanol at the concentration of 0.97–1.18 mg mL−1,in agreement with their calculated large adsorption energies on graphene.The results of electron spin resonance,Raman,scanning Kelvin probe microscopy and X-ray photoelectron spectroscopy measurements indicate that the amino groups could n-dope graphene or form dipole interaction with graphene.The two 3D-surfactant-based graphene composites(POSSFN-G and ADMAFN-G)can work as high-performance CIMs in organic solar cells(OSCs),which improve the power conversion efficiency(PCE)of the OSCs based on PM6:Y6 to 15.9%–16.1%.ADMAFN forms dipole interaction with graphene in ADMAFN-G and the composite CIM delivers high PCE of 16.11%in the OSCs,while POSSFN forms n-doped composition with graphene in POSSFN-G which works well as thicker CIM film in the OSCs.展开更多
Mg O has not been explored as a counter electrode materials for dye-sensitized solar cells(DSSCs)due to its lack of electrical conductivity.However,herein,it is reported that Mg O insulator with conductive poly(3,4-et...Mg O has not been explored as a counter electrode materials for dye-sensitized solar cells(DSSCs)due to its lack of electrical conductivity.However,herein,it is reported that Mg O insulator with conductive poly(3,4-ethylenedioxythiophene):polysty-renesulfonate(PEDOT:PSS)exhibited excellent performance as a counter electrode for DSSCs,leading to a high power conversion efficiency of 7.45%.Furthermore,it was revealed that the interface between Mg O and PEDOT:PSS plays an important electro-catalytic role in the Mg O/PEDOT composite counter electrodes.展开更多
文摘The interfacial interaction existing in the Ni ZrO 2 composite plating has been investigated. The experimental results show that no new phases were formed in the interfacial regions between matrix Ni and ZrO 2 particles, but an orbital interaction through the mutual overlap of the d orbits does exist in the interfacial regions between Ni atoms and Zr 3+ ions.
基金Projects(2018YFC1802204,2020YFC1909200)supported by the National Key R&D Program of China。
文摘Developing classes of Ag@C composites stand out for their one of a kind structure and novel physicochemical properties in later a long time.This review explores the current state-of-the-art progress in the preparation methods and the novel properties of Ag@C composites.We provide a definition of the stability of Ag@C composites,and propose strategies to improve the stability.Based on the later inquire,a summary and outlook toward the synthesis and applications of Ag@C composites are presented,aiming to accelerate the exploration of Ag@C composites and further stimulate the applications in various fields.
文摘Herein,a bottom-down design is presented to successfully fabricate ZIF-derived Co3O4,grown in situ on a one-dimensional(1D)α-MnO2 material,denoted as α-MnO2@Co3O4.The synergistic effect derived from the coupled interface constructed betweenα-MnO2 and Co3O4 is responsible for the enhanced catalytic activity.The resultantα-MnO2@Co3O4 catalyst exhibits excellent catalytic activity at a T90%(temperature required to achieve a toluene conversion of 90%)of approximately 229℃,which is 47 and 28℃ lower than those of the pureα-MnO2 nanowire and Co3O4-b obtained via pyrolysis of ZIF-67,respectively.This activity is attributed to the increase in the number of surface-adsorbed oxygen species,which accelerate the oxygen mobility and enhance the redox pairs of Mn^4+/Mn^3+ and Co^2+/Co^3+.Moreover,the result of in situ diffuse reflectance infrared Fourier transform spectroscopy suggests that the gaseous oxygen could be more easily activated to adsorbed oxygen species on the surface of α-MnO2@Co3O4 than on that of α-MnO2.The catalytic reaction route of toluene oxidation over theα-MnO2@Co3O4 catalyst is as follows:toluene→benzoate species→alkanes containing oxygen functional group→CO2 and H2O.In addition,the α-MnO2@Co3O4 catalyst shows excellent stability and good water resistance for toluene oxidation.Furthermore,the preparation method can be extended to other 1D MnO2 materials.A new strategy for the development of high-performance catalysts of practical significance is provided.
文摘A comprehensive understanding of the role of the electrocatalyst in photoelectrochemical(PEC)water splitting is central to improving its performance.Herein,taking the Si-based photoanodes(n^(+)p-Si/SiO_(x)/Fe/FeOx/MOOH,M=Fe,Co,Ni)as a model system,we investigate the effect of the transition-metal electrocatalysts on the oxygen evolution reaction(OER).Among the photoanodes with the three different electrocatalysts,the best OER activity,with a low-onset potential of∼1.01 VRHE,a high photocurrent density of 24.10 mA cm^(-2)at 1.23 VRHE,and a remarkable saturation photocurrent density of 38.82 mA cm^(-2),was obtained with the NiOOH overlayer under AM 1.5G simulated sunlight(100 mW cm^(-2))in 1 M KOH electrolyte.The optimal interfacial engineering for electrocatalysts plays a key role for achieving high performance because it promotes interfacial charge transport,provides a larger number of surface active sites,and results in higher OER activity,compared to other electrocatalysts.This study provides insights into how electrocatalysts function in water-splitting devices to guide future studies of solar energy conversion.
文摘Typical cationic and anionic surfactants were chosen and their interactions were calculated by quantum chemical method. Interaction energies are -0.2378 kJ·mol-1, -3.3394kJ·mol-1 and 0.1204kJ·mol-1 for the molecular pairs with fluocarbon and hydrocarbon chain: C4H10/C5H12, C4F10/C5H12, and C4F10 /C5F12, respectively. When hydrophilic group with cationic and anionicions is introduced, interaction energies are -287.40kJ·mol-1, -311.18kJ·mol-1 and -345.83kJ·mol-1. The results show that there is strong static interaction between cationic and anionic surfactants. It has been predicted that mixed monolayer may be formed and surface activity is enhanced favorably, especially for mixtures of cationic and anionic surfactants with fluocarbon and hydrocarbon chains. The anionic surfactants, sodium octadecylbenzenesulfonate perfluopolyetherbenzenesulonate(ANF-I) was synthesized, mixture effects of ANF-I with sodium octadecylbenzenesulfonate or dodecyldimethyl benzylammonium bromide were studied. The results indicate that the efficiency of mixing increased and the theoretical prediction was testified. These results can provide useful information for the design of new surfactants.
文摘Abstract： In this work, the authors present a study of growth and characterization of composite based on AI and CNT （carbon nanotubes. The composites were prepared by a chemical mixing method and characterized by SEM analysis, energy dispersed X-ray measurements, X-ray photoelectron spectroscopy and cathodoluminescence spectroscopy. The analysis showed that the composites are formed by macro-cluster of aluminum oxide on a network of CNT without formation of chemical bonds at interface between particles. The results are compared with those obtained for a sample of CNT with AI traces （〈 0.5%）. They show that only the presence of metal traces changes the nanotubes optical properties, with a luminescence signal centered at about 380 nm. These luminescence signals are caused by the adhesion between CNT and AI micro-clusters that promote the formation of band gap with some local energy levels.
基金supported by the Excellent Young Scientist Foundation of NSFC(Grant No.51522301)the National Natural Science Foundation of China(Grant Nos.21273017&51103004)+7 种基金Program for New Century Excellent Talents in University(Grant No.NCET-12-0034)Beijing Nova Program(Grant No.Z121103002512020)Fok Ying-Tong Education Foundation(Grant No.141045)Open Project of Beijing National Laboratory for Molecular Sciences,the 111 Project(Grant No.B14009)Aeronautical Science Foundation of China(Grant Nos.20145251035&2015ZF21009)State Key Laboratory for Modification of Chemical Fibers and Polymer Materials,Donghua University(Grant No.LK1508)the Key Research Program of the Chinese Academy of Sciences(Grant No.KJZD-EW-M03)the Fundamental Research Funds for the Central Universities(Grant Nos.YWF-15-HHXY-001&YWF-16-BJ-J-09)
文摘The hierarchical micro/nanoscale layered formation of organic and inorganic components of natural nacre, results in abundant interracial interactions, providing an inspiration for fabricating bioinspired nanocomposites through constructing the interfacial interactions. Herein, we demonstrated the synergistic interfacial interactions of hydrogen bonding from hydroxypropyl cellu- lose and ionic bonding from copper ions upon the reduced graphene oxide based bioinspired nanocomposites, which show the integrated tensile strength, toughness and excellent fatigue-resistant property, as well as high electrical conductivity. These ex- traordinary properties allow this kind of bioinspired nanocomposites to potentially utilize in the fields of aerospace, flexible electronics devices, etc. This study also opens a door for fabricating excellent mechanical performance graphene-based bioin- spired nanocomposites via synergistic interfacial interactions in the future.
基金the National Natural Science Foundation of China(51820105003,51863002 and 51973042)the Excellent Young Scientific and Technological Talents of Guizhou,China(QKHPTRC[2019]5652)。
文摘Graphene dispersions in low-boiling-point green solvents have wide applications in coatings,conducting inks,batteries,electronics and solar cells.Two three-dimensional(3D)cathode interfacial materials(CIMs)(1,3,5,7,9,11,13,15-octa-(9-bis(30-(N,N-dimethylamino)propyl)-2,7-fluorene)-vinylpentacyclo-octasiloxane)(POSSFN)and(1,3,5,7-tetra-(9-bis(30-(N,N-dimethylamino)propyl)-2,7-fluorene)-adamantane)(ADMAFN)are excellent surfactants for dispersing graphene in ethanol at the concentration of 0.97–1.18 mg mL−1,in agreement with their calculated large adsorption energies on graphene.The results of electron spin resonance,Raman,scanning Kelvin probe microscopy and X-ray photoelectron spectroscopy measurements indicate that the amino groups could n-dope graphene or form dipole interaction with graphene.The two 3D-surfactant-based graphene composites(POSSFN-G and ADMAFN-G)can work as high-performance CIMs in organic solar cells(OSCs),which improve the power conversion efficiency(PCE)of the OSCs based on PM6:Y6 to 15.9%–16.1%.ADMAFN forms dipole interaction with graphene in ADMAFN-G and the composite CIM delivers high PCE of 16.11%in the OSCs,while POSSFN forms n-doped composition with graphene in POSSFN-G which works well as thicker CIM film in the OSCs.
基金supported by the U.S.National Science Foundation(NSF-CBET-0931587)the ACS Petroleum Research Fund(PRF-51799-ND10)
文摘Mg O has not been explored as a counter electrode materials for dye-sensitized solar cells(DSSCs)due to its lack of electrical conductivity.However,herein,it is reported that Mg O insulator with conductive poly(3,4-ethylenedioxythiophene):polysty-renesulfonate(PEDOT:PSS)exhibited excellent performance as a counter electrode for DSSCs,leading to a high power conversion efficiency of 7.45%.Furthermore,it was revealed that the interface between Mg O and PEDOT:PSS plays an important electro-catalytic role in the Mg O/PEDOT composite counter electrodes.
