A series of Ce, H3PW12O40 co-doped TiO2 hollow fibers photocatalysts have been prepared by sol-gel method using ammonium ceric nitrate, H3PW12O40 and tetrabutyltitanate as precursors and cotton fibers as template, fol...A series of Ce, H3PW12O40 co-doped TiO2 hollow fibers photocatalysts have been prepared by sol-gel method using ammonium ceric nitrate, H3PW12O40 and tetrabutyltitanate as precursors and cotton fibers as template, followed by calcination at 500 ℃ in N2 atmosphere for 2 h. Scanning electron microscopy, X-ray diffraction, nitrogen adsorption-desorption mea- surements, and UV-Vis spectroscopy are employed to characterize the morphology, crystal structure, surface structure, and optical absorption properties of the samples. The photo- catalytic performance of the samples has been studied by photodegradation phenol in water under UV and visible light irradiation. The results show that the TiO2 fiber materials have hollow structures, and the co-doped TiO2 hollow fibers exhibit higher photocatalytic activities for the degradation of phenol than un-doped, single-doped TiO2 hollow fibers under UV and visible light. In addition, the recyclability of co-doped TiO2 fibers is also confirmed that the TiO2 fiber retains ca. 90% of its activity after being used four times. It is shown that the co-doped TiO2 fibers can be activated by visible light and may be potentially applied to the treatment of water contaminated by organic pollutants. The synergistic effect of Ce and H3PW12O40 co-doping plays an important role in improving the photocatalytic activity.展开更多
Soil acid phosphomonoesterase activity (APA) plays a vital role in controlling phosphorus (P) cycling and reflecting the current degree of P limitation. Responses of soil APA to elevating nitrogen (N) deposition are i...Soil acid phosphomonoesterase activity (APA) plays a vital role in controlling phosphorus (P) cycling and reflecting the current degree of P limitation. Responses of soil APA to elevating nitrogen (N) deposition are important because of their potential applications in addressing the relationship between N and P in forest ecosystems. A study of responses of soil APA to simulated N deposition was conducted in three succession forests of subtropical China. The three forests include a Masson pine (Pinus massoniana) forest (MPF)-pioneer community, a coniferous and broad-leaved mixed forest (MF)-transition community and a monsoon evergreen broad-leaved forest (MEBF)-climax community. Four N treatments were designed for MEBF: control (without N added), low-N (50 kg N ha-1 year-1), and medium-N (100 kg N ha-1 year-1) and high-N (150 kg N ha-1 year-1), and only three N treatments (i.e., control, low-N, medium-N) were established for MPF and MF. Results showed that soil APA was highest in MEBF, followed by MPF and MF. Soil APAs in both MPF and MF were not influenced by low-N treatments but depressed in medium-N treatments. However, soil APA in MEBF exhibited negative responses to high N additions, indicating that the environment of enhanced N depositions would reduce P supply for the mature forest ecosystem. Soil APA and its responses to N additions in subtropical forests were closely related to the succession stages in the forests.展开更多
LiFePO4 materials have become increasingly popular as a cathode material due to the many benefits they possess including thermal stability, durability, low cost, and long life span. Nevertheless, to broaden the genera...LiFePO4 materials have become increasingly popular as a cathode material due to the many benefits they possess including thermal stability, durability, low cost, and long life span. Nevertheless, to broaden the general appeal of this material for practical electrochemical applications, it would be useful to develop a relatively mild, reasonably simple synthesis method of this cathode material. Herein, we describe a generalizable, 2-step methodology of sustainably synthesizing LiFePO4 by incorporating a template-based, ambient, surfactantless, seedless, U-tube protocol in order to generate size and morphologically tailored, crystalline, phase-pure nanowires. The purity, composition, crystallinity, and intrinsic quality of these wires were systematically assessed using transmission electron microscopy （TEM）, high-resolution TEM （HRTEM）, scanning electron microscopy （SEM）, X-ray diffraction （XRD）, selected area electron diffraction （SAED）, energy dispersive analysis of X-rays （EDAX）, and high-resolution synchrotron XRD. From these techniques, we were able to determine that there is an absence of any obvious defects present in our wires, supporting the viability of our synthetic approach. Electrochemical analysis was also employed to assess their electrochemical activity. Although our nanowires do not contain any noticeable impurities, we attribute their less than optimal electrochemical rigor to differences in the chemical bonding between our LiFePO4 nanowires and their bulk-like counterparts. Specifically, we demonstrate for the first time experimentally that the Fe-O3 chemical bond plays an important role in determining the overall conductivity of the material, an assertion which is further supported by recent ＂first-principles＂ calculations. Nonetheless, our ambient, solution-based synthesis technique is capable of generating highly crystalline and phase-pure energy-storage-relevant nanowires that can be tailored so as to fabricate different sized materials of reproducible, reliable morphology.展开更多
基金ACKNOWLEDGMENTS This work was supported by the National Natural Science Foundation of China （No.41373127） and Liaon- ing Provincial Natural Science Foundation of China （No.2013020121）.
文摘A series of Ce, H3PW12O40 co-doped TiO2 hollow fibers photocatalysts have been prepared by sol-gel method using ammonium ceric nitrate, H3PW12O40 and tetrabutyltitanate as precursors and cotton fibers as template, followed by calcination at 500 ℃ in N2 atmosphere for 2 h. Scanning electron microscopy, X-ray diffraction, nitrogen adsorption-desorption mea- surements, and UV-Vis spectroscopy are employed to characterize the morphology, crystal structure, surface structure, and optical absorption properties of the samples. The photo- catalytic performance of the samples has been studied by photodegradation phenol in water under UV and visible light irradiation. The results show that the TiO2 fiber materials have hollow structures, and the co-doped TiO2 hollow fibers exhibit higher photocatalytic activities for the degradation of phenol than un-doped, single-doped TiO2 hollow fibers under UV and visible light. In addition, the recyclability of co-doped TiO2 fibers is also confirmed that the TiO2 fiber retains ca. 90% of its activity after being used four times. It is shown that the co-doped TiO2 fibers can be activated by visible light and may be potentially applied to the treatment of water contaminated by organic pollutants. The synergistic effect of Ce and H3PW12O40 co-doping plays an important role in improving the photocatalytic activity.
基金the "Strategic Priority Research Program" of the Chinese Academy of Sciences (No.XDA05050208)the National Natural Science Foundation of China (Nos.31070439 and 40730102)the Knowledge Innovation Program of the Chinese Academy of Sciences (Nos.KSCX2-EW-Q-8 and KSCX2-EW-J-28)
文摘Soil acid phosphomonoesterase activity (APA) plays a vital role in controlling phosphorus (P) cycling and reflecting the current degree of P limitation. Responses of soil APA to elevating nitrogen (N) deposition are important because of their potential applications in addressing the relationship between N and P in forest ecosystems. A study of responses of soil APA to simulated N deposition was conducted in three succession forests of subtropical China. The three forests include a Masson pine (Pinus massoniana) forest (MPF)-pioneer community, a coniferous and broad-leaved mixed forest (MF)-transition community and a monsoon evergreen broad-leaved forest (MEBF)-climax community. Four N treatments were designed for MEBF: control (without N added), low-N (50 kg N ha-1 year-1), and medium-N (100 kg N ha-1 year-1) and high-N (150 kg N ha-1 year-1), and only three N treatments (i.e., control, low-N, medium-N) were established for MPF and MF. Results showed that soil APA was highest in MEBF, followed by MPF and MF. Soil APAs in both MPF and MF were not influenced by low-N treatments but depressed in medium-N treatments. However, soil APA in MEBF exhibited negative responses to high N additions, indicating that the environment of enhanced N depositions would reduce P supply for the mature forest ecosystem. Soil APA and its responses to N additions in subtropical forests were closely related to the succession stages in the forests.
文摘LiFePO4 materials have become increasingly popular as a cathode material due to the many benefits they possess including thermal stability, durability, low cost, and long life span. Nevertheless, to broaden the general appeal of this material for practical electrochemical applications, it would be useful to develop a relatively mild, reasonably simple synthesis method of this cathode material. Herein, we describe a generalizable, 2-step methodology of sustainably synthesizing LiFePO4 by incorporating a template-based, ambient, surfactantless, seedless, U-tube protocol in order to generate size and morphologically tailored, crystalline, phase-pure nanowires. The purity, composition, crystallinity, and intrinsic quality of these wires were systematically assessed using transmission electron microscopy （TEM）, high-resolution TEM （HRTEM）, scanning electron microscopy （SEM）, X-ray diffraction （XRD）, selected area electron diffraction （SAED）, energy dispersive analysis of X-rays （EDAX）, and high-resolution synchrotron XRD. From these techniques, we were able to determine that there is an absence of any obvious defects present in our wires, supporting the viability of our synthetic approach. Electrochemical analysis was also employed to assess their electrochemical activity. Although our nanowires do not contain any noticeable impurities, we attribute their less than optimal electrochemical rigor to differences in the chemical bonding between our LiFePO4 nanowires and their bulk-like counterparts. Specifically, we demonstrate for the first time experimentally that the Fe-O3 chemical bond plays an important role in determining the overall conductivity of the material, an assertion which is further supported by recent ＂first-principles＂ calculations. Nonetheless, our ambient, solution-based synthesis technique is capable of generating highly crystalline and phase-pure energy-storage-relevant nanowires that can be tailored so as to fabricate different sized materials of reproducible, reliable morphology.
