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1.
TiO2纳米粒子制备方法对其光催化活性的影响 总被引:20,自引:0,他引:20
分别用胶溶法、金属醇盐水解法和低温水解法制备了TiO2纳米粒子;采用XRD和BET技术,测试了TiO2粒子的粒径、晶型及表面积。以庚烷的气相光催化氧化为探针反应,考察了不同方法、不同温度处理的TiO2粒子的光催化活性。结果表明,以胶溶法和金属醇盐水解法制备的TiO2粒子,随焙烧温度的增加TiO2粒子长大,晶型由锐钛矿向金红石型转变,光催化活性降低。用低温水解法,可在低温下制得金红石型TiO2粒子,但其催化活性很低。说明由原料和制备方法所决定的TiO2粒子的物理化学性质,影响其光催化行为。锐钛矿型TiO2粒子催化活性较金红石型TiO2好。这是由于前者的表面羟基含量较高且带隙能较大的缘故。 相似文献
2.
TiO2 thin films with different crystalline structures were prepared by the CVD method. The relationship between photocatalytic activity of a TiO2 thin film and its crystalline type was investigated. These films were characterized by XRD and AFM. Their photocatalytic properties were tested by the degradation of NO2-. The results showed that the crystalline structures of TiO2 thin films are primary anatase and/or rutile when the preparation temperatures were less than 573 K and higher than 773 K respectively. When the preparation temperature was around 623 K, the structures of TiO2 thin films were mixed crystalline structure, which showed the highest catalytic activity. When the ratio of rutile to anatase in TiO2 thin films fell between 0.5 and 0.7, the highest catalytic activity for the degradation of NO2- was found. 相似文献
3.
以Ti(SO4)2酸溶液为前驱体.氢氧化钠作沉淀剂,采用沉淀法低温焙烧制备了SO4^2-掺杂的金红石型TiO2微粒.用光催化降解正庚烷为反应模型.结合BET、TG-DTA、IR、XRD等表征手段,探讨了制备条件对金红石型SO4^2-/TiO2微粒气相光催化活性的影响,并优化实验条件获得了光催化性能优良的金红石型SO4^2-/TiO2微粒. 相似文献
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A visible light-activated TiO2 photocatalyst was successfully synthesized by the surface organic modification to sol-gel-hydrothermal synthesized TiO2. The surface hydroxyls of TiO2 nanoparticles reacted with the active -NCO groups of tolylene diisocyanate (TDI) to form a surface complex that was confirmed by the FT-IR and XPS spectra. Due to the existence of surface complex, the absorption edge of as-prepared TDI-modified TiO2 nanomaterial extended well into visible region. Compared with unmodified TiO2 and Degussa P25, the TDI-modified TiO2 photocatalysts showed higher activity for the photocatalytic degradation of methylene blue under visible light irradiation. 相似文献
6.
利用静电纺丝技术结合高温煅烧过程制备碳纤维(CNFs)载体材料, 进一步通过溶剂热和化学反应过程获得AgX/TiO2 /CNFs(X=Br, I)复合光催化剂. 利用X射线衍射(XRD)、 扫描电子显微镜(SEM)、 红外光谱(FTIR)等测试手段表征了材料的结构及形貌. 通过在可见光下降解甲基橙考察了催化材料的光催化性能. 结果表明, 该复合材料具有高吸附性、 良好的传导性以及较好的光敏性, 从而使其具有较好的可见光催化活性; 同时以一维碳纤维作为载体, 使其更容易分离、 回收, 更具有实际应用价值. 相似文献
7.
铕掺杂对纳米TiO2的光催化活性的影响 总被引:21,自引:0,他引:21
用溶胶-凝胶法制备了掺杂Eu3+的纳米TiO2,用XRD和TG-DTA对其进行了表征,并以正庚烷为气相有机污染物的实例研究了样品的光催化活性,发现Eu3+进入TiO2晶格中引起了TiO2晶格膨胀,导致晶格畸变增大,抑制了TiO2晶相的转变和粒径的增长.结果表明,Eu3+掺杂可提高TiO2的光催化活性,并且当掺杂摩尔分数为0.3%时,光催化活性最好.随着焙烧温度的升高,光催化活性下降,而利用较高的水解酸度则有利于得到光催化活性较高的样品. 相似文献
8.
碘掺杂对纳米TiO2催化剂光催化活性的影响 总被引:11,自引:0,他引:11
用溶胶-凝胶法制得了碘掺杂纳米TiO2催化剂, 考察了诸因素对相结构的影响, 这对深入揭示I-TiO2光催化降解有机物的本质具有重要意义. 相似文献
9.
Photocatalytic Activity of TiO2 Nanofibers with Doped La Prepared by Electrospinning Method
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La‐TiO2 nanofibers are prepared by a sol‐gel assisted electrospinning method. The structure and morphology of La‐TiO2 nanofibers are characterized by X‐ray diffraction (XRD) and scanning electron microscopy (SEM). XRD analysis shows that the weight percentage of anatase and rutile in the 1.5 mol% La‐TiO2 nanofibers calcined at 600 °C is about 8:2, which is similar to P‐25. The XRD data of La‐TiO2 nanofibers with different La content shows that La3+ dopant has a great inhibition on TiO2 phase transformation. The photocatalytic activity of the as‐prepared La‐TiO2 nanofibers is evaluated by photocatalytic decolorization of Methylene Blue (MB) aqueous solution. The results show that the 1.5 mol% La‐TiO2 nanofibers calcined at 600 °C exhibit high photocatalytic activity, indicating that 600 °C and 1.5 mol% are the appropriate calcination temperature and optimal molar ratio of La to Ti, respectively. 相似文献
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研究了SrCo0.7Fe0.2Mo0.103-δ(SCFM)材料的相组成、微观结构、热膨胀系数、氧渗透性能和化学稳定性,其结果和文献中的SrCo0.8Fe0.2O3-δ(SCF)做了对比.通过EDTA-citric混合方法成功获得了纯相SCFM材料.SCFM材料在500-1050℃显示出比SCF材料更低的热膨胀系数(24×10^-6-29×10^-6/K),表明其具有一种更稳定的结构,尽管由于Mo掺杂造成其透氧率比SCF材料低,但是SCFM的透氧率仍然维持在一个较高水平.证实SCF中的Mo掺杂能够阻止晶格中的有序-无序转变,提高了其在CO2下的化学稳定性. 相似文献
11.
Au改性纳米TiO2材料对NPE-10光催化降解的活性 总被引:7,自引:0,他引:7
以钛酸四丁酯和氯金酸为原料,通过溶胶凝胶法制备了Au掺杂的纳米TiO2光催化剂粉体,并用 XRD, BET,XPS和固体紫外可见吸收光谱等技术对其晶相结构,比表面积,表面组成及紫外可见光响应范围进行了表征,对其光催化降解非离子表面活性剂壬基酚聚氧乙烯醚(NPE-10)的活性进行了考察. 结果表明,掺杂的Au在纳米TiO2粉体材料中可能以两种形态存在,即以Au3+离子形式替代Ti4+进入TiO2晶格和以Au原子态形式暴露于粉体表面.前者使TiO2在480~650 nm出现了更强的光吸收,并大大地增强了粉体表面对氧物种的吸附;后者中处于表面原子态的Au又会成为光生电子的受体,有效地避免了光生电子空穴对的复合. 通过对掺杂量及处理温度的优化,在nAu3+/nTi4+=0.005, 500 ℃煅烧的条件下可以制得具有较高的光催化活性的Au/TiO2粉体. 对NPE-10的光催化氧化试验显示,日光照射4小时后降解效率可以达到91.8%;而用未改性的纳米TiO2,在同样条件下,NPE-10的光催化降解效率仅能达到50.2%,商品Degussa P-25也只能达到66%. 相似文献
12.
Nanostructured TiO2 coating films on silica glass substrates were prepared by the assembly technique. TiO2 colloids were synthesized employing the sol‐gel method using TiCl4 as a precursor. The effect on the surface structures which was caused by the polyethylene glycol (PEG) added to the precursor solution and the photocatalytic activity were studied. The experimental results showed that the cobble‐like TiO2 coating films were synthesized at 500 °C. On the surface of the samples, TiO2 films exhibited uniform shape and a narrow size distribution. The result of proper PEG added to the precursor solution led to the decreasing of the size of TiO2 particles and the increasing of the surface area of the samples. The photocatalytic activity of TiO2 films with PEG was higher than that of samples without PEG. 相似文献
13.
利用银盐与单氰胺水溶液的沉淀反应,通过共混不同质量分数的纳米TiO2粒子制备了TiO2/Ag2NCN复合光催化剂.使用X射线衍射仪(XRD)、扫描电子显微镜(SEM)、傅里叶变换红外(FTIR)光谱仪和紫外-可见(UV-Vis)吸收光谱仪对复合光催化剂的结构进行了表征.结果表明,锐钛矿相TiO2纳米颗粒沉积在Ag2NCN表面形成异质结构,二者间以弱的物理作用力相结合.TiO2的掺杂使得复合颗粒的UV-Vis吸收光谱发生红移,带隙变窄.以亚甲基蓝(MB)为光催化降解对象,研究了TiO2/Ag2NCN复合颗粒的可见光催化活性.结果表明,与单一Ag2NCN相比,复合颗粒表现出增强的光催化性能.对TiO2/Ag2NCN复合颗粒的光催化反应动力学过程及光催化机理进行了探讨. 相似文献
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The development of the photocatalytic production of hydrogen from water splitting has attracted immense attention in recent years. CdS is a potential photocatalyst with a visible light response, though it still suffers from a limited activity for hydrogen production due to the fast recombination of photo-induced electron/hole pairs and the low reaction rate of hydrogen evolution on the surface. Studies on the effect of CdS surface structure and properties on hydrogen production are still very limited. In this work, we prepared three CdS nanocrystals with different morphologies: long rod, short rod, and triangular plate. The prepared samples were well characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET) specific surface area analysis, X-ray photoelectron spectroscopy (XPS), photoluminescence (PL) spectroscopy, and UV-Vis diffuse reflectance spectroscopy (UV-Vis DRS). From the results of TEM, XRD and XPS, we find that the three CdS nanocrystals with different morphologies were successfully synthesized. From the PL spectra, we conclude that the area of exposed nonpolar surface and degree of surface defects increase with an increase in aspect ratio. We also performed the photocatalytic hydrogen production reaction using the three CdS crystals. Long rod-like CdS (lr-CdS) exhibits the highest photocatalytic activity, with a hydrogen production rate of 482 μmol·h-1·g-1, which is 2.6 times that of short rod-like CdS (sr-CdS) (183 μmol·h-1·g-1) and 8.8 times that of triangular plate-like CdS (tp-CdS, 55 μmol h-1·g-1). It is found that lr-CdS shows a higher hydrogen production rate than sr-CdS and tp-CdS. We find that the hydrogen production rate is related to the degree of surface defects. Surface defects can trap the photo-induced electrons/holes, thus decreasing their probability of recombination. In addition, these defects can be used to anchor Pd particles to form a heterojunction structure that facilitates the separation of photo-induced charges. Therefore, we also compared three CdS/Pd nanocrystals synthesized with the three abovementioned morphologies with respect to hydrogen production. With 1% (w, mass fraction) Pd, the hydrogen production rate was greatly enhanced compared to all the CdS catalysts. Compared to the unpromoted CdS, the reaction rate is enhanced 43.1, 10.7 and 6.0 times over those of sr-CdS, lr-CdS and tp-CdS, respectively. Notably, the hydrogen production rate with short rod-like CdS/Pd reaches 7884 μmol·h-1·g-1, which can be favorably compared with the ever-increasing values reported in the literature. Hopefully, this work provides knowledge on the effect of crystal surface structure and properties on photocatalysis. 相似文献
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碳纳米管(CNTs)混酸(H2SO4/HNO3, 体积比为3:1)超声辅助纯化及氧化植入活性基团-COOH, 进一步借助其转化为酰氯基团, 分别于CNTs 表面共价嫁接亲水性赖氨酸及亲脂性正十八胺基团, 赋予赖氨酸表面改性CNTs 显著水溶(6.85 mg·mL-1)和十八胺表面改性CNTs 显著醇溶(10.15 mg·mL-1)性能. 运用低温水热法以亲水性CNTs 复合TiO2, 溶胶-凝胶法以亲脂性CNTs 复合TiO2, 观察到复合催化剂光催化性能随CNTs 溶剂分散性能增加而明显提升. 运用傅里叶变换红外(FTIR)、激光拉曼、X射线衍射(XRD)、Brunauer-Emmett-Teller 低温氮气吸附、透射电镜(TEM)及X光电子能谱(XPS)等手段表征, 系统探讨CNTs 的表面改性机制及CNTs 溶解分散性能与复合催化剂的光活性的关联. 认为表面改性CNTs 借助Ti-O-C键合促进其与纳米TiO2的异质结合, 从而充分利用CNTs的大比表面积及电荷传输性能促进催化剂的污染物光催化降解. 相似文献
16.
多孔TiO2薄膜自洁净玻璃的亲水性和光催化活性 总被引:37,自引:0,他引:37
亲水性多孔TiO2薄膜自洁净玻璃以含聚乙二醇的钛醇盐溶胶前驱体中通过浸渍提拉法制备;随着前驱物中聚乙二醇加入量的增加,多孔TiO2薄膜表面的羟基含量也增加,薄膜表面的亲水性增强,水与薄膜表面的接触角下降为0°.该亲水性多孔TiO2薄膜自洁净玻璃具有明显的自洁净和易清洗功能.紫外-可见光透过光谱分析表明,随着TiO2薄膜中孔径的增大,光的散射增强,透光率减小.该TiO2镀膜玻璃对于紫外线具有吸收作用.甲基橙水溶液的光催化降解实验表明,在TiO2薄膜中引入适当大小的微孔可显著增强薄膜的光催化活性,但当孔径接近400nm时,薄膜的光催化活性减弱. 相似文献
17.
采用溶胶-凝胶法和四丁基氢氧化铵(TBAH)表面改性的方法制备出改性TiO2光催化剂(TBAH-TiO2).利用X射线衍射谱(XRD)、X射线光电子能谱(XPS)、透射电子显微镜(TEM)、傅里叶变换红外光谱(FTIR)和表面光电压谱(SPS)等表征了催化剂的晶体结构、晶粒粒径和能带结构,并研究了其光催化活性.研究结果表明,TBAH-TiO2催化剂的表面主要存在NOx(x=1,2,3)物种,该物种能级(价带上0.20eV)产生了可见光响应,有效地促进了光生电子和光生空穴的分离,使催化剂的可见和紫外光催化活性显著提高,TBAH-TiO2催化剂降解对氯苯酚的可见光和紫外光催化活性分别是TiO2的2.6倍和1.7倍. 相似文献
18.
N掺杂TiO_2纳米粒子表面光生电荷特性与光催化活性 总被引:2,自引:0,他引:2
以尿素为氮源,采用水热法制备了不同N掺杂量的TiO2(N-TiO2)光催化剂.利用X射线衍射(XRD),紫外-可见漫反射光谱(UV-Vis DRS),X射线光电子能谱(XPS)及荧光(PL)光谱等技术对其进行了系统的表征.以罗丹明B(RhB)和甲基橙(MO)溶液的脱色降解为模型反应,分别考察了N-TiO2光催化剂在紫外和可见光区的光催化活性.利用表面光伏(SPV)和瞬态光伏(TPV)技术研究了N-TiO2纳米粒子表面光生电荷的产生和传输机制,并探讨了光生电荷与光催化活性之间的关系.结果显示,随着N含量的增大,TiO2表面光伏响应阈值红移,可见光部分光电压响应强度逐渐增强,瞬态光伏响应达到最大值的时间亦有着不同程度的延迟.这表明适量的N掺杂能够提高TiO2纳米粒子中光生载流子的分离效率,相应地延长载流子的传输时间,增加光生电荷的寿命,从而促进其光催化活性;而过量的N掺杂则增加了TiO2纳米粒子中光生载流子的复合中心,抑制其光催化活性. 相似文献
19.
采用混合溶剂热法在尿素的辅助下成功地制备了新型可见光复合催化剂NiO/Bi7.47Ni0.53O11.73(BiNiO).利用X射线多晶粉末衍射(XRD)仪、X射线光电子能谱(XPS)、扫描电镜(SEM)、透射电镜(TEM)、紫外-可见漫反射谱(UV-Vis DRS)对样品进行了表征,并以甲基橙为目标降解物对其光催化性能进行研究.结果表明:样品是由自组装三维(3D)-Bi7.47Ni0.53O11.73微球和其表面薄层NiO纳米片组成,前驱物在300°C条件下煅烧2 h后所得样品BiNiO-300光催化效果最好,在可见光(波长大于420 nm)照射下,3 h内对甲基橙溶液的脱色率高达98%. 相似文献
20.
结合超临界乙醇干燥技术, 采用沉积-沉淀(DP)和共沉淀(CP)法分别制备了具有单一锐钛矿晶相的Au/TiO2和Au(0.2%, 原子分数)-TiO2光催化剂, 通过XRD、BET、TEM、XPS和Raman手段表征样品中Au的掺杂形态, 以光催化降解甲基橙为模型反应考察了样品的光催化活性. 结果表明, DP法制备的Au/TiO2在110 ℃干燥处理后, 表面存在的Au3+能有效地促进锐钛矿TiO2光催化性能, 其一级反应速率常数比纯锐钛矿TiO2提高了3.2倍, 比商用光催化剂Degussa-P25提高了4.1倍, 而当Au3+被还原为Au0后光催化活性下降. 用CP法制备的Au-TiO2并没有较大地提高锐钛矿TiO2光催化性能, 在焙烧温度达到800 ℃时, Au向表面迁移聚集, 造成锐钛矿TiO2晶格氧空位和缺陷位增加, 使光催化活性下降. 相似文献