Graphite‐like carbon nitride(g‐C3N4)‐based compounds have attracted considerable attention because of their excellent photocatalytic performance.In this work,a novel direct Z‐scheme system constructed from two‐di...Graphite‐like carbon nitride(g‐C3N4)‐based compounds have attracted considerable attention because of their excellent photocatalytic performance.In this work,a novel direct Z‐scheme system constructed from two‐dimensional(2D)g‐C3N4nanoplates and zero‐dimensional(0D)MoS2quantum dots(QDs)was prepared through the combination of a hydrothermal process and microemulsion preparation.The morphologies,structures,and optical properties of the as‐prepared photocatalysts were characterized by X‐ray diffraction,X‐ray photoelectron spectroscopy,atomic force microscopy,transmission electron microscopy,and UV‐vis diffuse reflectance spectroscopy.In addition,the photocatalytic performances of the prepared2D/0D hybrid composites were evaluated based on the photodegradation of rhodamine B under visible‐light irradiation.The results demonstrated that the introduction of MoS2QDs to g‐C3N4greatly enhanced the photocatalytic efficiency.For the optimum7%MoS2QD/g‐C3N4photocatalyst,the degradation rate constant was8.8times greater than that of pure g‐C3N4under visible‐light irradiation.Photocurrent and electrochemical impedance spectroscopy results further demonstrated that the MoS2QD/g‐C3N4composites exhibited higher photocurrent density and lower chargetransfer resistance than those of the pure g‐C3N4or MoS2QDs.Active species trapping,terephthalic acid photoluminescence,and nitro blue tetrazolium transformation experiments were performed to investigate the evolution of reactive oxygen species,including hydroxyl radicals and superoxide radicals.The possible enhanced photocatalytic mechanism was attributed to a direct Z‐scheme system,which not only can increase the separation efficiency of photogenerated electron‐hole pairs but also possesses excellent oxidation and reduction ability for high photocatalytic performances.This work provides an effective synthesis approach and insight to help develop other C3N4‐based direct Z‐scheme photocatalytic systems for environmental purification and energy conversion.展开更多
文献[1]给出了从n元布尔函数f的代数正规型得到f(X+Y mod 2n)和f(X*Y mod 2n)的公式,其中Y是常数。基于mod 2n加法进位比特的性质,给出了求X+Y mod 2n或X-Y mod2n的n个分量函数的代数正规型的方法。其总的计算复杂度分别为O(2n)(或O(3n)...文献[1]给出了从n元布尔函数f的代数正规型得到f(X+Y mod 2n)和f(X*Y mod 2n)的公式,其中Y是常数。基于mod 2n加法进位比特的性质,给出了求X+Y mod 2n或X-Y mod2n的n个分量函数的代数正规型的方法。其总的计算复杂度分别为O(2n)(或O(3n))。远远低于经典的用真值表计算布尔函数代数正规型的算法[2]。使用文献[2]的算法仅得到X+Ymod 2n(或X-Y mod 2n)最高位的计算复杂度就达O(2n*22 n)。展开更多
Density functional theory was used at the B3LYP/6-311＋＋G（d,p） level of theory to study the hydrates of 2NH3：H2SO4：nH2O for n = 0～4. Neutrals of the most stable clusters, when n = 0 and 1, spontaneously formed a...Density functional theory was used at the B3LYP/6-311＋＋G（d,p） level of theory to study the hydrates of 2NH3：H2SO4：nH2O for n = 0～4. Neutrals of the most stable clusters, when n = 0 and 1, spontaneously formed and were determined to be hydrogen-bonded molecular complexes of monomeric species. Double ions （clusters containing a NH4＋ cation and a HSO4- anion） or even ternary ions （clusters with two NH4＋ cations and one SO42- anion） spontaneously formed in the most stable clusters of 2NH3：H2SO4：nH2O （n = 2, 3, 4）. The energetics of binding and incremental association was also calculated. Double ions are not energetically favorable until 2NH3：H2SO4：2H2O because of the about equal free energies for forming the neutral （the most stable） and double ion （the second stable） isomers. The free energy of incremental association from free H2O and 2NH3：H2SO4：nH2O has a maximum at n = 2 at room temperature with ΔG ≈ –2 kcal/mol. The comparison of incremental association energies between 2NH3：H2SO4：nH2O, NH3：H2SO4：nH2O and H2SO4：nH2O clusters revealed that NH3 plays an important role in the atmospheric particle nucleation.展开更多
基金supported by National Natural Science Foundation of China(51672113)Six Talent Peaks Project in Jiangsu Province(2015-XCL-026)+3 种基金Natural Science Foundation of Jiangsu Province(BK20171299)State Key Laboratory of Photocatalysis on Energy and Environment(SKLPEE-KF201705),Fuzhou UniversityState Key Laboratory of Advanced Technology for Materials Synthesis and Processing(2016-KF-10),Wuhan University of Technologythe Qing Lan Project Foundation of Jiangsu Province~~
文摘Graphite‐like carbon nitride(g‐C3N4)‐based compounds have attracted considerable attention because of their excellent photocatalytic performance.In this work,a novel direct Z‐scheme system constructed from two‐dimensional(2D)g‐C3N4nanoplates and zero‐dimensional(0D)MoS2quantum dots(QDs)was prepared through the combination of a hydrothermal process and microemulsion preparation.The morphologies,structures,and optical properties of the as‐prepared photocatalysts were characterized by X‐ray diffraction,X‐ray photoelectron spectroscopy,atomic force microscopy,transmission electron microscopy,and UV‐vis diffuse reflectance spectroscopy.In addition,the photocatalytic performances of the prepared2D/0D hybrid composites were evaluated based on the photodegradation of rhodamine B under visible‐light irradiation.The results demonstrated that the introduction of MoS2QDs to g‐C3N4greatly enhanced the photocatalytic efficiency.For the optimum7%MoS2QD/g‐C3N4photocatalyst,the degradation rate constant was8.8times greater than that of pure g‐C3N4under visible‐light irradiation.Photocurrent and electrochemical impedance spectroscopy results further demonstrated that the MoS2QD/g‐C3N4composites exhibited higher photocurrent density and lower chargetransfer resistance than those of the pure g‐C3N4or MoS2QDs.Active species trapping,terephthalic acid photoluminescence,and nitro blue tetrazolium transformation experiments were performed to investigate the evolution of reactive oxygen species,including hydroxyl radicals and superoxide radicals.The possible enhanced photocatalytic mechanism was attributed to a direct Z‐scheme system,which not only can increase the separation efficiency of photogenerated electron‐hole pairs but also possesses excellent oxidation and reduction ability for high photocatalytic performances.This work provides an effective synthesis approach and insight to help develop other C3N4‐based direct Z‐scheme photocatalytic systems for environmental purification and energy conversion.
文摘文献[1]给出了从n元布尔函数f的代数正规型得到f(X+Y mod 2n)和f(X*Y mod 2n)的公式,其中Y是常数。基于mod 2n加法进位比特的性质,给出了求X+Y mod 2n或X-Y mod2n的n个分量函数的代数正规型的方法。其总的计算复杂度分别为O(2n)(或O(3n))。远远低于经典的用真值表计算布尔函数代数正规型的算法[2]。使用文献[2]的算法仅得到X+Ymod 2n(或X-Y mod 2n)最高位的计算复杂度就达O(2n*22 n)。
基金supported by the National Natural Science Foundation of China (20528706)the China Postdoctoral Science Foundation (20090450385)
文摘Density functional theory was used at the B3LYP/6-311＋＋G（d,p） level of theory to study the hydrates of 2NH3：H2SO4：nH2O for n = 0～4. Neutrals of the most stable clusters, when n = 0 and 1, spontaneously formed and were determined to be hydrogen-bonded molecular complexes of monomeric species. Double ions （clusters containing a NH4＋ cation and a HSO4- anion） or even ternary ions （clusters with two NH4＋ cations and one SO42- anion） spontaneously formed in the most stable clusters of 2NH3：H2SO4：nH2O （n = 2, 3, 4）. The energetics of binding and incremental association was also calculated. Double ions are not energetically favorable until 2NH3：H2SO4：2H2O because of the about equal free energies for forming the neutral （the most stable） and double ion （the second stable） isomers. The free energy of incremental association from free H2O and 2NH3：H2SO4：nH2O has a maximum at n = 2 at room temperature with ΔG ≈ –2 kcal/mol. The comparison of incremental association energies between 2NH3：H2SO4：nH2O, NH3：H2SO4：nH2O and H2SO4：nH2O clusters revealed that NH3 plays an important role in the atmospheric particle nucleation.
基金This work was supported in part by the National Natural Science Foundation of China （Grant Nos. 10825101, 10861004, 11101266）, SMSTC grant no. 12XD1405000, Fundamental Research Funds for the Central Universities, and Science ＆ Technology Program of Shanghai Maritime University.
文摘We determine the derivation algebra and the automorphism group of the generalized topological N = 2 superconformal algebra.
