Preparation and Photocatalytic Activity of Ce, H3PW12O40 co-doped TiO2 Hollow Fibers

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.

可见光下ZrO_2(Er^(3+))/TiO_2光催化剂的性能研究

本文以氧氯化锆、氧化铒、二氧化钛等为基本原料,利用沉淀超声法合成了一种由上转换材料ZrO2(Er3+)复合TiO2的光催化剂。用荧光光谱仪测量了上转换材料在420nm激发下的上转换发光光谱,并用紫外-可见分光光度计分析了ZrO2(Er3+)/TiO2催化剂的光催化能力。以甲基橙为降解对象,研究了在可见光下不同复合量样品的光催化活性,并与紫外光下的结果进行了对比。结果表明:上转换材料ZrO2(Er3+)复合后的光催化剂其催化性能优于二氧化钛,且很好的提高了TiO2催化剂的光谱响应范围,大大提高了可见光利用率。

纳米(Er^(3+)-Gd^(3+))/TiO_2光催化性能的研究

文章采用超声波共振法合成了不同掺杂量、不同煅烧温度的Er3+、Gd3+共掺杂的纳米TiO2光催化剂,并对所制样品进行XRD、FT-IR、SEM表征;通过降解孔雀石绿溶液来测试样品的光催化性能。结果表明:稀土Er3+、Gd3+共掺杂能抑制TiO2晶粒长大,细化晶粒;稀土掺杂后样品能吸附更多的羟基,羟基自由基具有很强的氧化性,从而提高催化活性;在500℃下煅烧,Er3+-Gd3+的摩尔分数为5%的催化剂,加入0.5mL30%的双氧水后,降低基元反应活化能,有很强的氧化性,能抑制电子-空穴的复合,无灯源照射、常温常压不需通氧条件下的催化时间为80min,降解率达到100%。

Li^+共掺杂对Er^(3+)-Yb^(3+):TiO_2紫外、可见和红外发光同步增强研究(英文)

采用溶胶-凝胶(Sol-gel)法制备了Li+共掺杂的Er3+-Yb3+∶TiO2粉末。976 nm激光激发下在波长350~1700 nm范围内观察到了紫外、蓝色、绿色和红色上转换发光和红外下转换发光。随着Li+共掺杂浓度由0增大到20mol%,Er3+-Yb3+∶TiO2的紫外、可见和红外发光强度同步增强。低Li+共掺杂浓度引起的Li+固溶以及高Li+共掺杂浓度引起的相变过程相继破坏了Er3+的晶体场对称性,导致紫外、可见和红外发光显著增强。结果表明共掺杂Li+是一种提高Er3+掺杂材料发光性能的有效方法。

Sulfur-doped g-C3N4/TiO2 S-scheme heterojunction photocatalyst for Congo Red photodegradation

Constructing step-scheme(S-scheme)heterojunctions has been confirmed as a promising strategy for enhancing the photocatalytic activity of composite materials.In this work,a series of sulfur-doped g-C3N4(SCN)/TiO2 S-scheme photocatalysts were synthesized using electrospinning and calcination methods.The as-prepared SCN/TiO2 composites showed superior photocatalytic performance than pure TiO2 and SCN in the photocatalytic degradation of Congo Red(CR)aqueous solution.The significant enhancement in photocatalytic activity benefited not only from the 1D well-distributed nanostructure,but also from the S-scheme heterojunction.Furthermore,the XPS analyses and DFT calculations demonstrated that electrons were transferred from SCN to TiO2 across the interface of the SCN/TiO2 composites.The built-in electric field,band edge bending,and Coulomb interaction synergistically facilitated the recombination of relatively useless electrons and holes in hybrid when the interface was irradiated by simulated solar light.Therefore,the remaining electrons and holes with higher reducibility and oxidizability endowed the composite with supreme redox ability.These results were adequately verified by radical trapping experiments,ESR tests,and in situ XPS analyses,suggesting that the electron immigration in the photocatalyst followed the S-scheme heterojunction mechanism.This work can enrich our knowledge of the design and fabrication of novel S-scheme heterojunction photocatalysts and provide a promising strategy for solving environmental pollution in the future.

可见光下利用ZrO_2(Er^(3+))/TiO_2光催化降解海水中柴油污染

通过共沉淀法自制上转换材料与TiO_2复合的纳米光催化剂;利用SEM、XRD等方法对光催化剂进行表征;通过改变催化剂掺杂比、pH值、催化剂投入量、光照时间和柴油初始浓度研究了可见光下光催化降解海水中柴油污染的影响因素以及复合光催化剂ZrO_2(Er3+)/TiO_2的利用效率,通过正交试验优化海水中柴油污染的降解;进行动力学分析,计算总反应速率表达式。结果表明,当柴油初始浓度为0.20g/L,催化剂投加量为0.8g/L,催化剂掺杂比为40%,pH为7,光照时间为2.5h时,复合光催化剂的利用效率最高,柴油的去除率达到87.74%。ZrO_2(Er3+)/TiO_2在可见光下能够有效地降解海水中的柴油污染。

Preparation of NaYF_4:Er^(3+)/TiO_2 composite and up-conversion luminescence properties under visible light excitation

The up-conversion luminescence composite NaYF4：Er3＋/TiO2 is prepared using the sol-gel method. The specimen has good crystallinity and two shapes, i.e., viereck and round, while the sizes of viereck and round particles are both micron-sized. The TiO2 has an anatase structure, while the NaYF4 has a hexagonal phase, which can be hardly obtained through the common sol-gel method. Due to the big particle size and the high crystallinity of pure NaYF4： Er3＋, the composite has a small specific surface area that is less than Degussa P25 TiO2. The NaYF4：Er3＋/TiO2 composite shows several emission peaks at 211, 237, and 251 nm under the excitation of 388 nm, at 395 nm and 411 nm under the excitation of 500 nm, and at 467, 481,492, and 508 nm under the excitation of 570 nm.

Aligning Fe_(2)O_(3)photo-sheets on TiO_(2)nanofibers with hydrophilic and aerophobic surface for boosting photoelectrochemical performance

Photoelectrochemical(PEC)nanomaterials are critical to producing clean oxygenation or value-added chemical production by utilizing sustainable solar energy,but are always limited by simultaneous integration of architectural engineering and electronic regulation in one structure.Directed by density functional theory(DFT)calculations and finite element analysis(FEA),the bioinspired ivy-like Fe_(2)O_(3)heterostructures with enriched oxygen defects on TiO_(2)nanofibers are designed for boosting PEC performances.Ivy-like Fe_(2)O_(3)photo-sheets remarkably enhanced the light harvesting by multiple light-mater interactions.The oxygen vacancies on Fe_(2)O_(3)photo-sheets could aid the photons catching and promote the reactivity at active sites.More importantly,demonstrated by a well-designed dynamic observation,the abundant tip-edges within ivy-like Fe_(2)O_(3)photo-sheets enabled the surface of heterostructure with hydrophilic and aerophobic properties.The functionalized surface allowed the rapid desorption of produced bubbles and thus ensured a high density of unoccupied active sites for electrolyte accessing.Featured by these attributes,the Fe_(2)O_(3)@TiO_(2)nanofibers delivered an excellent photocurrent of 40.8 mA/mg,high donor density(1.2×10^(18)cm^(−3)),and rapid oxygen production rate(1 mmol/(L∙h)).This work demonstrates a new strategy on nano-structural design for enhancing light-harvesting and making a hydrophilic/aerophobic surface on low-dimensional oxide nanomaterial,holding great potential on designing high-performance PEC devices for producing survival source gas,carbon-neutral fuel,and valuedchemicals.

稀土掺杂TiO_2在1064nm激光激发下的上转换发光

为研究TiO2材料的上转换发光特性,采用溶胶-凝胶与共沉淀法制备了La3+、Yb3+和Er3+稀土离子掺杂的TiO2粉末。利用SEM和XRD表征发光材料的结构,探讨了试样在1064nm激发光源常温激发作用下,稀土氧化物的掺杂比例、煅烧温度对上转换发光特性的影响。实验表明,1064nm激光常温激发TiO2基掺杂稀土La2O3、Yb2O3、Er2O3的最佳比例为39∶10∶1,经1300℃煅烧可制备出明亮绿色发光的上转换材料。

上转换材料复合介孔TiO_2晶须的可见光催化性能

用溶胶凝胶法制备上转换发光材料Y3Al5O12:Er。反射光谱、发射光谱表明:Y3Al5O12:Er在480 nm光的激发下,产生2个<387 nm的紫外光发射峰。将上转换材料介孔TiO2晶须复合成可见光催化剂,采用X线衍射仪(XRD)、场发射扫描电子显微镜(FESEM)以及低温N2吸附-脱附(BET)等对催化剂进行表征,通过光催化降解亚甲基蓝(MB),对催化剂的活性进行测试。结果表明:复合上转换材料的介孔TiO2晶须在可见光下能够有效降解MB,10%Y3Al5O12:Er的介孔TiO2晶须的MB降解率为73%。

Preparation, characterization and antibacterial properties of cobalt doped titania nanomaterials

Cobalt-doped titania(Co-TiO2)nanomaterials were synthesized by the sol–gel method at different calcination temperatures.Using Escherichia coli(a),Staphylococcus aureus(b)and Candida albicans(c)as target strains,the antibacterial activity in visible light of the nanomaterials were studied.Co-TiO2 nanomaterials were characterized by X-ray diffraction(XRD),scanning electron microscopy(SEM),transmission electron microscopy(TEM),UV–Vis diffuse reflectance spectroscopy(DRS),Fourier transform infrared spectrum(FT-IR)and X-ray photoelectron spectroscopy(XPS).The Co ions in the Co-TiO2 nanomaterial exist in the form of CoTiO3 phase.The antibacterial properties of Co-TiO2 nanomaterials on E.coli(a),S.aureus(b)and C.albicans(c)were investigated with the oscillating flask method and the inhibition zone method.The nanomaterials calcined at 600°C exhibit excellent antibacterial activity.The bacteriostatic rates for E.coli,S.aureus and C.albicans reached 99.5%,91.3%and 93.4%respectively.The diameters of the antibacterial rings were up to 36 mm,37 mm,30 mm respectively,and the clarity of the ring was clear.The antibacterial properties of Co-TiO2 nanomaterials were compared with those of traditional silver sol,zinc oxide sol and Zn-doped TiO2 nanomaterials The mechanism of the influences of Co ions doping on the antibacterial activity of TiO2 nanomaterials was also discussed.The doping of Co ions inhibits the particle size of the antibacterial agent and extends the photocatalytic response range,thereby improving the photocatalytic performance of the antibacterial agent.

高比表面积Y_2O_3:Er^(3+)+TiO_2的制备及上转换发光特性研究

采用共沉淀法和sol-gel法制备了Y2O3:Er3+,Y2O3:Er3+/Yb3+和Y2O3:Er3++TiO2三种样品.通过扫描电子显微镜(SEM)、透射电子显微镜(TEM)、比表面积仪、紫外可见分光光度计及荧光光谱仪分析和测试了样品的表面形貌、比表面积、孔隙度、紫外可见吸收光谱和室温下的荧光光谱.SEM和TEM测试表明共沉淀法制备的样品发光离子分散性很好;sol-gel法制备的Y2O3:Er3++TiO2表面分布着许多的介孔,颗粒直径在10nm左右.对3种样品的孔径分布和表面积测试表明,Y2O3:Er3+和TiO2复合后的性质不是两种物质性质的简单叠加,其比表面积高达135.991m2/g,是纯Y2O3:Er3+的4.8倍,是纯Degussa P25 TiO2的2.5倍,如此高的比表面积有利于提高TiO2的光催化性能.样品的荧光光谱显示其在388,500和570nm的可见光激发下分别对应在237,395和467nm处各有一个上转换发光峰.

Li^+共掺杂对掺Er^(3+):TiO_2粉末上转换发光特性的影响

采用溶胶-凝胶法制备摩尔分数为x(Er3+)=0.1%Er3+,x(Li+)=0~2%Li+共掺杂TiO2粉末。800℃烧结Li+共掺杂促进掺Er3+:TiO2由锐钛矿向金红石相转变,900℃和1000℃烧结Er3+-Li+:TiO2均为单一金红石相。976 nm激光激发下Er3+-Li+:TiO2均获得中心波长为526 nm和550 nm的绿色和663 nm的红色上转换发光,绿色和红色上转换发光均为双光子吸收过程。随着Li+共掺杂浓度逐渐增大,800℃烧结Er3+-Li+:TiO2上转换发光强度逐渐减小,900℃烧结发光强度先增加后减小,1000℃烧结发光强度显著增强。不同烧结温度下Li+共掺杂对Er3+所处晶体场对称性的改变导致上转换发光强度随Li+共掺杂浓度增加出现不同的变化规律。结果表明,Li+共掺杂可有效提高Er3+:TiO2上转换发光强度。

异质结型Er_2O_3/TiO_2复合纳米纤维制备及光催化性能

采用静电纺丝技术与溶剂热法相结合,制备了异质结型Er2O3/TiO2复合纳米纤维光催化材料。利用X射线衍射(XRD)、扫描电镜(SEM)、透射电镜(TEM)、高分辨透射电镜(HRTEM)和紫外-可见吸收光谱(UV-Vis)等分析测试手段对材料进行表征,并以罗丹明B(RB)的脱色降解为模式反应,考察了材料的光催化性能。实验结果表明:Er2O3纳米粒子均匀地负载在TiO2纤维上,形成了异质型Er2O3/TiO2复合纳米纤维光催化材料,拓宽了光谱响应范围,有利于TiO2光生电子和空穴的分离,增强了体系的量子效率。与纯TiO2纳米纤维相比光催化活性明显提高,对RB的紫外光降解率达93.93%。

Er^(3+)∶YAlO_3/Fe掺杂TiO_2复合物的制备及光催化活性研究

对TiO2半导体材料进行改性,分别通过溶胶凝胶、超声波分散和溶液沸腾的方法合成了Er3+∶YAlO3/Fe掺杂TiO2复合物光催化剂,并且采用XRD和SEM进行表征,研究了各种因素在太阳光照射下降解酸性红B的催化活性,也考察了Er3+∶YAlO3的包覆量、Er3+∶YAlO3/Fe掺杂TiO2的量、太阳光照射时间、酸性红B的初始浓度和氯化钠浓度等其降解过程用UV-Vis光谱进行检测。实验结果表明,加入上转光剂之后降解率大幅度增加,改性后的光催化剂可以有效地降解染料废水。

Sol-Gel法制备TiO2纳米晶中Yb3+-Mn2+聚合体到Er3+的有效能量传递(英文)

采用溶胶-凝胶法在烧结温度700℃下制备了5mol%Yb^(3+)和2 m01%Mn^(2+)共掺杂的1 m01%E^(3+)掺杂TiO2纳米发光粉。Yb^(3+)和Mn^(2+)共掺杂不改变TiO_2的相结构。在976 nm半导体激光器激发下,通过在Er^(3+)掺杂TiO_2中共掺杂Yb^(3+)和Mn^(2+)获得了明显的绿色上转换发光的选择性增强。Er^(3+)-Yb^(3+)-Mn^(2+)共掺杂TiO_2的绿色上转换发光为双光子吸收过程。研究表明Er^(3+)-Yb^(3+)-Mn^(2+)共掺杂TiO_2的绿色上转换增强来源于Yb^(3+)-Mn^(2+)聚合体的|~2F_(7/2),~4T_(1g)>能级到Er^(3+)的~4F_(7/2)有效能量能级的有效能量传递。.

Preparation and characterization of upconversion nanocomposite for β-NaYF_4:Yb^(3+),Er^(3+)-supported TiO_2 nanobelts

Hexagonal NaYF4:Yb3+,Er3+ (β-NaYF4:Yb3+,Er3+) nanoparticles supported on TiO2 nanobelts were prepared using two-step pro- cedures of ion-exchangeable process and hydrothermal treatment: layered titanate nanobelts were first ion-exchanged with Y3+, Yb3+ and Er3+ cations to produce titanate nanobelts with these cations, and then, the product nanobelts in NaY solution were treated under hydrothermal con- dition to transform into anatase TiO2 nanobelts supported with β-NaYF4:Yb3+,Er3+ nanoparticles. The final p...