With different pyridine-analogs as auxiliary ligands,three novel Zn（Ⅱ） complexes（1-3） based on 5-（1Htetrazol-1-yl） isophthalic acid（H_2L） have been synthesized and structurally characterized.Single crystal X-...With different pyridine-analogs as auxiliary ligands,three novel Zn（Ⅱ） complexes（1-3） based on 5-（1Htetrazol-1-yl） isophthalic acid（H_2L） have been synthesized and structurally characterized.Single crystal X-ray diffraction analyses of complexes 1-3 show the presence of tetrazolyl group,as well as the coordination behavior of the auxiliary ligands as critical factors determining the structures of such Zn（Ⅱ）-carboxyIate coordination architectures.In addition,the resulting complexes all exhibit luminescence properties in the solid state at room temperature.展开更多
Hexagonal boron nitride(h-BN),with unique structural and properties,has shown enormous potentitoward variety of possible applications.By virtue of partially-ionic character of BN chemical bonds anusually large specifi...Hexagonal boron nitride(h-BN),with unique structural and properties,has shown enormous potentitoward variety of possible applications.By virtue of partially-ionic character of BN chemical bonds anusually large specific surface area,h-BN-related nanostructures exhibit appealing adsorption propertiewhich can be widely applied for separation and purification towards energy and environment treatmenIn this review,recent progress in designing h-BN micro,nano-structure,controlled synthesis,performancoptimizing as well as energy and environment-related adsorption applications are summarized.Strategieto tailor the h-BN can be classified as morphology control,element doping,defect control and surfacmodification,focusing on how to optimize the adsorption performance.In order to insight the intrinsimechanism of tuning strategies for property optimization,the significant adsorption applications of h-Btowards hydrogen storage,CO2 capture,pollutants removal from water and adsorption desulfurization arpresented.展开更多
Three types of β-NaYF_4nanoparticles, uncoated core（NaYF_4：Yb/Ho/Ce）, single-layer coated core@shell（NaYF_4：Yb/Ho/Ce@NaYF_4：Yb） and double-layer coated core@shell@shell（NaYF_4：Yb/Ho@NaYF_4：Yb@NaYF_4：Yb） w...Three types of β-NaYF_4nanoparticles, uncoated core（NaYF_4：Yb/Ho/Ce）, single-layer coated core@shell（NaYF_4：Yb/Ho/Ce@NaYF_4：Yb） and double-layer coated core@shell@shell（NaYF_4：Yb/Ho@NaYF_4：Yb@NaYF_4：Yb） with Ce^（3＋） doped in core, first and second shell, respectively, were synthesized through solvothermal method to investigate the cross-relaxation between Ho^（3＋） and Ce^（3＋） for the tunable upconversion luminescence. By doping Ce^（3＋） into different layers with different doping concentrations, a systematical investigation on the tunable upconversion luminescence from green to red was conducted. The results showed that a remarkable color tuning could be achieved from green to red when increasing the doping concentration of Ce^（3＋） in the same layer of Ho^（3＋）. And if Ce^（3＋） and Ho^（3＋） were separated in different layers, the color tuning would be depressed significantly due to the reduced cross-relaxation between Ho^（3＋） and Ce^（3＋）. Moreover, the UC emission intensity of core@shell and core@shell@shell was enhanced significantly compared with that of unmodified core nanoparticles.展开更多
基金supported by the Natural Science Foundation of Hebei Province(No.B2012202019)the National Natural Science Foundation of China(No.21206027)
文摘With different pyridine-analogs as auxiliary ligands,three novel Zn（Ⅱ） complexes（1-3） based on 5-（1Htetrazol-1-yl） isophthalic acid（H_2L） have been synthesized and structurally characterized.Single crystal X-ray diffraction analyses of complexes 1-3 show the presence of tetrazolyl group,as well as the coordination behavior of the auxiliary ligands as critical factors determining the structures of such Zn（Ⅱ）-carboxyIate coordination architectures.In addition,the resulting complexes all exhibit luminescence properties in the solid state at room temperature.
基金financially supported by the National Natural Science Foundation of China (Nos. 21606113, 21676128, and 21722604)the International Postdoctoral Exchange Fellowship by China Postdoctoral Science Foundation (No. 20170055)
文摘Hexagonal boron nitride(h-BN),with unique structural and properties,has shown enormous potentitoward variety of possible applications.By virtue of partially-ionic character of BN chemical bonds anusually large specific surface area,h-BN-related nanostructures exhibit appealing adsorption propertiewhich can be widely applied for separation and purification towards energy and environment treatmenIn this review,recent progress in designing h-BN micro,nano-structure,controlled synthesis,performancoptimizing as well as energy and environment-related adsorption applications are summarized.Strategieto tailor the h-BN can be classified as morphology control,element doping,defect control and surfacmodification,focusing on how to optimize the adsorption performance.In order to insight the intrinsimechanism of tuning strategies for property optimization,the significant adsorption applications of h-Btowards hydrogen storage,CO2 capture,pollutants removal from water and adsorption desulfurization arpresented.
基金Project supported by the National Key Basic Research Program of China(2013CB921800)the National Natural Science Foundation of China(11374291,11204292,11274299,11311120047)the Fundamental Research Funds for the Central Universities(WK2030020021)
文摘Three types of β-NaYF_4nanoparticles, uncoated core（NaYF_4：Yb/Ho/Ce）, single-layer coated core@shell（NaYF_4：Yb/Ho/Ce@NaYF_4：Yb） and double-layer coated core@shell@shell（NaYF_4：Yb/Ho@NaYF_4：Yb@NaYF_4：Yb） with Ce^（3＋） doped in core, first and second shell, respectively, were synthesized through solvothermal method to investigate the cross-relaxation between Ho^（3＋） and Ce^（3＋） for the tunable upconversion luminescence. By doping Ce^（3＋） into different layers with different doping concentrations, a systematical investigation on the tunable upconversion luminescence from green to red was conducted. The results showed that a remarkable color tuning could be achieved from green to red when increasing the doping concentration of Ce^（3＋） in the same layer of Ho^（3＋）. And if Ce^（3＋） and Ho^（3＋） were separated in different layers, the color tuning would be depressed significantly due to the reduced cross-relaxation between Ho^（3＋） and Ce^（3＋）. Moreover, the UC emission intensity of core@shell and core@shell@shell was enhanced significantly compared with that of unmodified core nanoparticles.
