Let S = （a1,...,am;b1,...,bn）, where a1,...,am and b1,...,bn are two nonincreasing sequences of nonnegative integers. The pair S= （a1,..., am; b1,..., bn） is said to be a bigraphic pair if there is a simple bipart...Let S = （a1,...,am;b1,...,bn）, where a1,...,am and b1,...,bn are two nonincreasing sequences of nonnegative integers. The pair S= （a1,..., am; b1,..., bn） is said to be a bigraphic pair if there is a simple bipartite graph G = （X ∪ Y, E） such that a1,…, am and b1,..., bn are the degrees of the vertices in X and Y, respectively. Let Z3 be the cyclic group of order 3. Define σ（Z3, m, n） to be the minimum integer k such that every bigraphic pair S = （a1,..., am; b1,..., bn） with am, b ≥ 2 and σ（S） = a1 ＋ ... ＋ am ≥ k has a Z3-connected realization. For n = m, Yin [Discrete Math., 339, 2018-2026 （2016）] recently determined the values of σ（Z3,m,m） for m ≥ 4. In this paper, we completely determine the values of σ（Z3, m, n） for m ≥ n ≥4.展开更多
Two new metal-organic frameworks（MOFs）, namely, [Co_2（L_1）（bix）（μ_3-OH）]·2H_2O（1） and [Co_2（L_2）（bix）（μ_3-OH）]·2.5H_2O（2）（H_3L_1 = 5-oxyacetate isophthalic acid, H_3L_2 = 3,5-bis-oxyacet...Two new metal-organic frameworks（MOFs）, namely, [Co_2（L_1）（bix）（μ_3-OH）]·2H_2O（1） and [Co_2（L_2）（bix）（μ_3-OH）]·2.5H_2O（2）（H_3L_1 = 5-oxyacetate isophthalic acid, H_3L_2 = 3,5-bis-oxyacetate-benzoic acid, bix = 1,4-bis（imidazol-1-ylmethyl）benzene）, have been synthesized under hydrothermal conditions. Their structures were determined by single-crystal X-ray diffraction analysis and further characterized by elemental analysis, IR spectra, and powder X-ray diffraction（PXRD） analysis. Both complexes 1 and 2 demonstrate identical three-dimensional（3D）（3,8）-connected tfz-d nets with（4~3）_2（4~6·6^（18）·8~4） topologies, where the tetranuclear [Co_4（μ_3-OH）_2] clusters act as 8-connected nodes and aromatic multicarboxylic ligands as 3-connected nodes. The results show that the ligands with different geometrical conformations can form products with the same topological structures. Their thermal and magnetic properties were also investigated.展开更多
It is still challenging for exploring high-active photocatalysts to efficiently remove levofloxacin(LFX)by activating peroxymonosulfate(PMS).Herein,we constructed a novel Z scheme ZnFe_(2)O_(4)/g-C_(3)N_(4)/CQDs(ZCC)h...It is still challenging for exploring high-active photocatalysts to efficiently remove levofloxacin(LFX)by activating peroxymonosulfate(PMS).Herein,we constructed a novel Z scheme ZnFe_(2)O_(4)/g-C_(3)N_(4)/CQDs(ZCC)heterojunction by anchoring ZnFe_(2)O_(4)on tubular-like g-C_(3)N_(4)induced by CQDs(denoted as CNC)using microwave-assisted thermal methods.The ZCC exhibits the highest photocatalytic activity in activating PMS for LFX degradation,endowing a removal rate~95.3%,which is 4.8 and 7.3 times that of pure ZnFe_(2)O_(4)(19.8%)and g-C_(3)N_(4)(13.1%),separately.The enhanced photocatalytic activity of ZCC can be attributed to the distinctive morphology of CNC,enhanced light response,increased specific surface area and abundant pore structure.Besides,the formed Z scheme heterojunction and CQDs acting as a transmission bridge of the photogenerated charges(e−and h+)can accelerate transfer and inhibit recombination of e−and h+.Radical capture experiments and electron spin resonance(ESR)measurements revealed that SO4•-and O2•-play a predominant role in degradation process of LFX.Liquid chromatography-mass spectrometry(LC-MS)was applied to identify intermediates and propose feasible degradation pathways of LFX.In conclusion,this study presents a promising strategy for regulating the photocatalytic activity of g-C_(3)N_(4)by simultaneously integrating CQDs induction and Z scheme heterojunction construction.展开更多
Herein,we established a Zn_(3)(OH)_(2)(V_(2)O_(7))(H_(2)O)_(2)/V-Zn(O,S)Z-scheme heterojunction labeled ZnVO/V-Zn(O,S)with a heterovalent V^(4+)/V^(5+)states and oxygen vacancies in both phases via a one-step in-situ ...Herein,we established a Zn_(3)(OH)_(2)(V_(2)O_(7))(H_(2)O)_(2)/V-Zn(O,S)Z-scheme heterojunction labeled ZnVO/V-Zn(O,S)with a heterovalent V^(4+)/V^(5+)states and oxygen vacancies in both phases via a one-step in-situ hydrolysis method.The NaBH_(4) regulated the ZnVO/V-Zn(O,S)-3 with rich Vo and suitable n(V^(4+))/n(V^(5+))ratio achieved an excellent photocatalytic nitrogen fixation activity of 301.7μmol/(g×h)and apparent quantum efficiency of 1.148%at 420 nm without any sacrificial agent,which is 11 times than that of V-Zn(O,S).The Vo acts as the active site to trap and activate N_(2) molecules and to trap and activate H_(2)O to produce the H for N_(2) molecules photocatalytic reduction.The rich Vo defects can also reduce the competitive adsorption of H_(2)O and N_(2) molecules on the surface active site of the catalyst.The heterovalent vanadium states act as the photogenerated electrons,quickly hopping between V^(4+)and V^(5+)to transfer for the photocatalytic N_(2) reduction reaction.Additionally,the Z-scheme heterojunction effectively minimizes photogenerated carrier recombination.These synergistic effects collectively boost the photocatalytic nitrogen fixation activity.This study provides a practical method for designing Z-scheme heterojunctions for efficient photocatalytic N_(2) fixation under mild conditions.展开更多
采用原位水热法,将WO_(3)纳米棒负载在层状的g-C_(3)N_(4)上制备具有高吸附性和光催化活性的Z型g-C_(3)N_(4)/WO_(3)复合光催化剂。通过XRD、XPS和SEM对复合材料的形貌和结构进行了表征,并测试其光致发光光谱、光电流和紫外可见漫反射光...采用原位水热法,将WO_(3)纳米棒负载在层状的g-C_(3)N_(4)上制备具有高吸附性和光催化活性的Z型g-C_(3)N_(4)/WO_(3)复合光催化剂。通过XRD、XPS和SEM对复合材料的形貌和结构进行了表征,并测试其光致发光光谱、光电流和紫外可见漫反射光谱;考察了在可见光下g-C_(3)N_(4)/WO_(3)复合材料对土霉素的降解效果及复合材料的可重复利用性能,并结合自由基淬灭实验初步推测了g-C_(3)N_(4)/WO_(3)的光催化机理。结果表明,WO_(3)纳米棒负载到g-C_(3)N_(4)纳米片上并形成异质结;g-C_(3)N_(4)/WO_(3)异质结增强了可见光响应且降低了光生载流子复合率;添加0.6 g g-C_(3)N_(4)的g-C_(3)N_(4)/WO_(3)复合光催化剂具有最佳的光催化活性,在可见光照射下120 min对土霉素的降解率达到86%,优于单组分的g-C_(3)N_(4)和WO_(3),且稳定性较好;在g-C_(3)N_(4)/WO_(3)降解土霉素过程中,空穴(h+)为主要活性物质。展开更多
基金Supported by National Natural Science Foundation of China(Grant No.11561017)Natural Science Foundation of Hainan Province(Grant No.2016CXTD004)
文摘Let S = （a1,...,am;b1,...,bn）, where a1,...,am and b1,...,bn are two nonincreasing sequences of nonnegative integers. The pair S= （a1,..., am; b1,..., bn） is said to be a bigraphic pair if there is a simple bipartite graph G = （X ∪ Y, E） such that a1,…, am and b1,..., bn are the degrees of the vertices in X and Y, respectively. Let Z3 be the cyclic group of order 3. Define σ（Z3, m, n） to be the minimum integer k such that every bigraphic pair S = （a1,..., am; b1,..., bn） with am, b ≥ 2 and σ（S） = a1 ＋ ... ＋ am ≥ k has a Z3-connected realization. For n = m, Yin [Discrete Math., 339, 2018-2026 （2016）] recently determined the values of σ（Z3,m,m） for m ≥ 4. In this paper, we completely determine the values of σ（Z3, m, n） for m ≥ n ≥4.
基金supported by the application basis research key project of Yunnan Province science and technology department(201401CB00299)the major project of Qujing Normal University(2012ZD002)
文摘Two new metal-organic frameworks（MOFs）, namely, [Co_2（L_1）（bix）（μ_3-OH）]·2H_2O（1） and [Co_2（L_2）（bix）（μ_3-OH）]·2.5H_2O（2）（H_3L_1 = 5-oxyacetate isophthalic acid, H_3L_2 = 3,5-bis-oxyacetate-benzoic acid, bix = 1,4-bis（imidazol-1-ylmethyl）benzene）, have been synthesized under hydrothermal conditions. Their structures were determined by single-crystal X-ray diffraction analysis and further characterized by elemental analysis, IR spectra, and powder X-ray diffraction（PXRD） analysis. Both complexes 1 and 2 demonstrate identical three-dimensional（3D）（3,8）-connected tfz-d nets with（4~3）_2（4~6·6^（18）·8~4） topologies, where the tetranuclear [Co_4（μ_3-OH）_2] clusters act as 8-connected nodes and aromatic multicarboxylic ligands as 3-connected nodes. The results show that the ligands with different geometrical conformations can form products with the same topological structures. Their thermal and magnetic properties were also investigated.
基金Project(32272823) supported by the National Natural Science Foundation of ChinaProject(145309315) supported by the Research Foundation of Education Bureau of Heilongjiang Province of ChinaProject(YSTSXK202309) supported by the Plant Food Processing Technology Advantages Characteristic Discipline “Science and Technology Research” Special Project in Heilongjiang Province,China。
文摘It is still challenging for exploring high-active photocatalysts to efficiently remove levofloxacin(LFX)by activating peroxymonosulfate(PMS).Herein,we constructed a novel Z scheme ZnFe_(2)O_(4)/g-C_(3)N_(4)/CQDs(ZCC)heterojunction by anchoring ZnFe_(2)O_(4)on tubular-like g-C_(3)N_(4)induced by CQDs(denoted as CNC)using microwave-assisted thermal methods.The ZCC exhibits the highest photocatalytic activity in activating PMS for LFX degradation,endowing a removal rate~95.3%,which is 4.8 and 7.3 times that of pure ZnFe_(2)O_(4)(19.8%)and g-C_(3)N_(4)(13.1%),separately.The enhanced photocatalytic activity of ZCC can be attributed to the distinctive morphology of CNC,enhanced light response,increased specific surface area and abundant pore structure.Besides,the formed Z scheme heterojunction and CQDs acting as a transmission bridge of the photogenerated charges(e−and h+)can accelerate transfer and inhibit recombination of e−and h+.Radical capture experiments and electron spin resonance(ESR)measurements revealed that SO4•-and O2•-play a predominant role in degradation process of LFX.Liquid chromatography-mass spectrometry(LC-MS)was applied to identify intermediates and propose feasible degradation pathways of LFX.In conclusion,this study presents a promising strategy for regulating the photocatalytic activity of g-C_(3)N_(4)by simultaneously integrating CQDs induction and Z scheme heterojunction construction.
文摘Herein,we established a Zn_(3)(OH)_(2)(V_(2)O_(7))(H_(2)O)_(2)/V-Zn(O,S)Z-scheme heterojunction labeled ZnVO/V-Zn(O,S)with a heterovalent V^(4+)/V^(5+)states and oxygen vacancies in both phases via a one-step in-situ hydrolysis method.The NaBH_(4) regulated the ZnVO/V-Zn(O,S)-3 with rich Vo and suitable n(V^(4+))/n(V^(5+))ratio achieved an excellent photocatalytic nitrogen fixation activity of 301.7μmol/(g×h)and apparent quantum efficiency of 1.148%at 420 nm without any sacrificial agent,which is 11 times than that of V-Zn(O,S).The Vo acts as the active site to trap and activate N_(2) molecules and to trap and activate H_(2)O to produce the H for N_(2) molecules photocatalytic reduction.The rich Vo defects can also reduce the competitive adsorption of H_(2)O and N_(2) molecules on the surface active site of the catalyst.The heterovalent vanadium states act as the photogenerated electrons,quickly hopping between V^(4+)and V^(5+)to transfer for the photocatalytic N_(2) reduction reaction.Additionally,the Z-scheme heterojunction effectively minimizes photogenerated carrier recombination.These synergistic effects collectively boost the photocatalytic nitrogen fixation activity.This study provides a practical method for designing Z-scheme heterojunctions for efficient photocatalytic N_(2) fixation under mild conditions.
文摘采用原位水热法,将WO_(3)纳米棒负载在层状的g-C_(3)N_(4)上制备具有高吸附性和光催化活性的Z型g-C_(3)N_(4)/WO_(3)复合光催化剂。通过XRD、XPS和SEM对复合材料的形貌和结构进行了表征,并测试其光致发光光谱、光电流和紫外可见漫反射光谱;考察了在可见光下g-C_(3)N_(4)/WO_(3)复合材料对土霉素的降解效果及复合材料的可重复利用性能,并结合自由基淬灭实验初步推测了g-C_(3)N_(4)/WO_(3)的光催化机理。结果表明,WO_(3)纳米棒负载到g-C_(3)N_(4)纳米片上并形成异质结;g-C_(3)N_(4)/WO_(3)异质结增强了可见光响应且降低了光生载流子复合率;添加0.6 g g-C_(3)N_(4)的g-C_(3)N_(4)/WO_(3)复合光催化剂具有最佳的光催化活性,在可见光照射下120 min对土霉素的降解率达到86%,优于单组分的g-C_(3)N_(4)和WO_(3),且稳定性较好;在g-C_(3)N_(4)/WO_(3)降解土霉素过程中,空穴(h+)为主要活性物质。
