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1.
采用有利于二维层状结构形成的L-半胱氨酸作为硫源,钼酸钠作为钼源,制备聚乙烯基吡咯烷酮(PVP)辅助水热合成花瓣状微球形貌的MoS2/还原氧化石墨烯复合电极材料(PVP-MoS2/RGO). X射线衍射(XRD)及透射电子显微镜(TEM)证实,经过PVP的适量添加,MoS2有序堆垛结构的片层数目明显减少. 扫描电子显微镜(SEM)显示,添加适量PVP的MoS2/石墨烯材料具有分散性更好的花瓣状微球形貌. 上述的少层有序堆垛结构及复合材料的良好分散性缩短了MoS2中锂离子的嵌入/脱出路径,使其具有更高的容量、循环稳定性和倍率性能.  相似文献   

2.
球磨-溶剂热诱导法合成WS2纳米棒及其摩擦性能   总被引:2,自引:0,他引:2  
采用行星式高能球磨机,将WS2与S粉末混合球磨,得到纳米片状结构的前驱体,然后添加分散剂聚乙二醇(PEG)用溶剂热诱导的方法使纳米片状前驱体发生结构转变,制备了棒状结构的WS2纳米材料。用XRD、SEM、TEM等方法对WS2纳米棒进行了形貌和结构表征,并对其作为润滑油添加剂的摩擦性能进行了初步的研究。  相似文献   

3.
石冈  韩伟  袁珮  范煜  鲍晓军 《催化学报》2013,34(4):659-666
以硫代乙酰胺为硫源,钼酸钠为钼源,乙醇为分散剂,采用化学沉积法制备了MoS3/Al2O3催化剂前驱体,再用H2高温处理得到高分散硫化型MoS2/γ-Al2O3催化剂,运用N2吸附-脱附、X射线光电子能谱以及高分辨透射电子显微镜等技术对MoS2/γ-Al2O3催化剂进行了表征,并以二苯并噻吩作为模型化合物评价了催化剂的加氢脱硫(HDS)活性.结果表明,与浸渍法相比,所制催化剂具有更大的比表面积和孔体积、更高的活性金属分散度、更佳的Mo物种硫化度以及更短的MoS2片层长度和更高的堆积度,因而在二苯并噻吩HDS反应中表现出远优于浸渍法所制催化剂的活性.乙醇可通过S?H-O氢键吸附至MoS3纳米粒子表面,可有效防止其生长和团聚,起到分散剂的作用.  相似文献   

4.
采用水热法成功制备了MoS2/WO3复合半导体光催化剂,分别通过SEM、TEM、EDS、XRD、Raman和DRS对催化剂的形貌,组成及结构进行表征,并用BET模型计算比表面积。对比发现球状MoS2/WO3对罗丹明B(RhB)的光降解效率明显高于纯WO3、片状MoS2/WO3复合半导体。针对球状MoS2/WO3复合半导体,分别研究了MoS2不同负载量(0.5%,1%,2%,5%,10%)对RhB光催化降解性能的影响,结果表明MoS2含量为2%时催化效果最佳。同时,研究了溶液的pH值(pH=1,3,6,7,11)对光催化降解反应活性的影响,结果显示pH=6时降解率最高。当催化剂量增加到1 g·L-1时,30min后RhB降解率达到96.6%。球状MoS2/WO3的瞬态光电流为0.050 6 mA·cm-2,比纯WO3提高了2.4倍。经过5次循环实验,球状MoS2/WO3复合半导体催化剂仍能保持90%的高降解率。  相似文献   

5.
首先在N-甲基吡咯烷酮溶液中超声剥离得到少层的MoS2,将其与石墨相氮化碳(g-C3N4)复合,制得MoS2/g-C3N4复合材料。采用X射线衍射(XRD),扫描电镜(SEM),X射线光电子能谱(XPS),傅里叶变换红外光谱(FTIR),Raman光谱,紫外-可见漫反射吸收光谱(DRS)和光致荧光(PL)技术对复合材料进行表征。可见光下考察MoS2/g-C3N4复合材料光催化降解罗丹明B(RhB)的活性,结果表明:将少量MoS2与g-C3N4复合可明显提高光催化活性,且1%(w/w)MoS2/g-C3N4复合物的光催化活性最高,可能的原因是MoS2和g-C3N4匹配的能带结构,增大了界面间电荷的传输,降低了光生电子-空穴的复合,进而提高了光催化活性。  相似文献   

6.
二硫化钼纳米片(MoS2)受到带电杂质、结构缺陷和易聚集等因素的影响,导致其电子转移性能下降,使其应用受限。将银纳米颗粒(Ag NPs)与少层MoS2纳米片复合,可提升MoS2纳米片的电化学性能。本研究创新性地采用微波还原法,使Ag NPs原位沉积于MoS2,得到Ag NPs/MoS2复合材料。结果表明,将Ag NPs/MoS2复合材料修饰于丝网印刷电极(screen printed elec-trodes,SPE)后,测得的循环伏安(cyclic voltammetry,CV)曲线峰电流值为同浓度单一MoS2修饰电极的1.8倍,方波伏安(square wave voltammetry,SWV)曲线峰电流值为单一MoS2修饰电极的3.4倍,电化学阻抗谱(electrochemical impedance spectroscopy,EIS)的电子转移阻抗值(Ret)仅为167 Ω,相比MoS2/SPE的Ret (320 Ω)显著减小,说明Ag NPs与MoS2复合可显著增强单一MoS2的电化学性能。此外,还推测了高导电性Ag NPs/MoS2复合材料的导电机理。最后,基于Ag NPs/MoS2复合材料构建了电化学传感器并对前列腺特异性抗原(PSA)进行检测。结果表明,该传感器针对PSA的检测限为0.009 ng·mL-1,线性检测范围为0.1~1 000 ng·mL-1,灵敏度为0.011 μA·mL·ng-1。  相似文献   

7.
以碳纳米纤维(CNFs)作为负载基体和反应器采用静电纺丝技术和碳化工艺生长和调控二硫化钼(MoS2)纳米片。通过改变前驱体溶液浓度来调控纳米片的形貌和结构,利用MoS2纳米片的高催化活性和CNFs高比表面积、良好的稳定性以及高电导率的协同作用,研究不同形貌和结构的杂化纳米材料在电催化析氢方面的应用,探索杂化材料形貌与性能之间的潜在规律。运用多种分析测试技术对制备得到的纳米杂化材料进行表征,并对所制备的MoS2/CNFs杂化材料的电催化析氢性能(HER)进行研究,研究表明近似皮芯结构的MoS2/CNFs-10杂化材料的电催化析氢性能最好,初始析氢过电位在220 mV,Tafel斜率为110 mV·dec-1。  相似文献   

8.
采用射频磁控溅射法,在Ar气-H2S混合气氛中,以MoS2靶材为原料,在泡沫铜基底上制备了MoS2薄膜。利用X射线衍射(XRD)、Raman光谱、扫描电子显微镜(SEM)、能量弥散X射线谱(EDS)等手段对样品的结构、形貌和成分进行了表征,并探讨了靶功率和基底温度对MoS2薄膜的结构及形貌的影响。结果表明,靶功率的增加可以提高薄膜结晶度,但功率过高会造成薄膜的龟裂;基底温度升高会使MoS2薄膜结晶度明显提高,且形成蠕虫状形貌。靶功率为80W,基底温度为300℃时,可以制备得到具有较高结晶度的蠕虫状MoS2薄膜。对其进行充放电测试表明,在100mA·g-1的电流密度下,其首次放电比容量为980mAh·g-1,经过40周循环,容量可保持为约920mAh·g-1,容量保持率达到93.9%。  相似文献   

9.
采用机械球磨法成功制备Ag3PO4/MoS2纳米片复合催化剂。运用X射线衍射仪(XRD)、透射电子显微镜(TEM)、扫描电子显微镜(SEM)、紫外可见漫反射光谱(UV-Vis)和荧光发射光谱(PL)对复合催化剂的结构和形貌进行了表征。结果表明,Ag3PO4纳米粒子均匀地附着在MoS2纳米片层结构上,两者形成紧密结合。以亚甲基蓝为模拟污染物,研究复合催化剂在可见光照射下的光催化特性;通过循环实验考察复合催化剂的稳定性。结果显示,含有1%的MoS2纳米片与Ag3PO4形成的复合催化剂在30 min内对亚甲基蓝的降解率为95%,其降解动力学常数是纯相Ag3PO4的2倍。经过5次循环实验后复合催化剂对于亚甲基蓝的降解率为84%,而纯Ag3PO4对于亚甲基蓝的降解率仅为35%。Ag3PO4/MoS2纳米片复合催化剂具有优良的光催化活性和高稳定性,主要归因于二硫化钼纳米片与磷酸银形成异质结,磷酸银激发的电子和二硫化钼纳米片产生的空穴直接复合,从而促使光生电子从磷酸银晶体表面快速分离,减轻了磷酸银的光电子腐蚀,同时也提高了复合物的光催化活性。  相似文献   

10.
采用水热-煅烧法制备Cd2SnO4,之后通过超声混合法得到一系列MoS2/Cd2SnO4复合材料。采用X射线衍射、扫描电子显微镜、X射线光电子能谱对Cd2SnO4和一系列MoS2/Cd2SnO4复合材料进行结构和形貌的表征。研究了MoS2掺杂量对于MoS2/Cd2SnO4复合材料的气敏性能影响。实验结果表明,当MoS2与Cd2SnO4的质量比为2.5%,MoS2/Cd2SnO4复合材料制备的气敏元件在170 ℃时对浓度为100 μL·L-1的甲醛气体的灵敏度为40.0,最低检测限为0.1 μL·L-1。  相似文献   

11.
Microstructures of three Bi-W-Nb-O phases have been examined by using high-resolution transmission electron microscopy. Bi17W2Nb3O39 and Bi17WNb3O36 have incommensurate superstructures derived from the defect fluorite-type δ-Bi2O3 and can be regarded as intermediate phases between the type II solid solutions in the Bi-Nb-O and Bi-W-O systems. Bi8W2Nb2O23 has a Bi2WO6-like subunit cell with a stepped superstructure. Formation mechanisms of various superstructures are discussed.  相似文献   

12.
The near infrared spectra of aqueous solutions of the ethylsulfates of La, Nd, Gd, Tb, Er, Yb, Lu, Y, and Na have been determined from about 0.2 mol-dm–3 to nearly saturation. The extinction coefficients of water have been calculated taking into account the absorption of ethylslfate anions determined in separate experiments. Their values appeared to be nearly the same as that of pure water. The relative contents of free OH groups in 0.5 and 0.7M solutions have been estimated from the absorbances at 1160 nm. They were lower in solutions of the heavy rare-earth ethylsulfates (Tb, Er, Yb, Lu) than in equimolar solutions of the lighter ones (La, Nd), confirming our previous view that secondary hydration of the heavy trivalent rare-earth cations is distinctly stronger than that of the lighter ones. A comparison of the spectra of these aqueous ethylsulfates with those of perchlorates shows that the structure-breaking ability of the C2H5SO 4 ion is much smaller than that of perchlorate anion.  相似文献   

13.
Reactivity of mixtures of La(III) oxide and Cu(II) oxalate/nitrate in hydrated as well as anhydrous state was studied using TG, DTA and XRD. Cu(II) oxide formed in the endothermic decomposition of mixture containing hydrated Cu(II) nitrate and La(III) oxide could not form La2CuO4 while Cu(II) oxide formed in the exothermic decomposition of mixture containing hydrated/anhydrous Cu(II) oxalate and La(III) oxide reacts with La(III) oxide and develops the phases CuLaO3 and La2CuO4. The maximum reactivity with respect to the formation of La2CuO4phase was observed in mixture containing anhydrous Cu(II) oxalate. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   

14.
Tao Lin  Wei Li  Maochu Gong  Yao Yu  Bo Du  Yaoqiang Chen   《Acta Physico》2007,23(12):1851-1856
TiO2,ZrO2-TiO2,andZrO2-TiO2-CeO2 were prepared by co-precipitation method and characterized by X-ray diffraction (XRD), specific surface area measurements (BET), temperature programmed desorption (NH3-TPD), oxygen storage capacity (OSC), and temperature programmed reduction (H2-TPR). The results showed that ZrO2-TiO2-CeO2 exhibited large number of surface strong acid, possessed some oxygen storage capacity, and strong redox property. The three materials were used as supports and the monolith catalysts were prepared with 1% (w) V2O5 and 9% (w)WO3 for selective catalytic reduction (SCR) of NO with ammonia in the presence of excessive O2, and the results of catalytic activity showed that the catalyst used ZrO2-TiO2-CeO2 as support yielded nearly 100% NO conversion at 275 °C at a gas hourly space velocity (GHSV) of 10000 h−1, and it had the best catalytic activity and showed great potential for practical application.  相似文献   

15.
本实验介绍了电感耦合等离子体光谱法测定铜冶炼烟尘中锌含量的分析方法。针对样品碳,硅含量高的特点,有针对性的研究了样品的消解方法,确定采用盐酸、硝酸、氢氟酸、高氯酸对铜冶炼烟尘样品进行消解。同时进行了干扰试验,确定样品中高含量的铜,铅,砷等对样品测定结果没有影响。并对仪器的工作参数进行了优化。方法检出限为为0.011 mg/L,测定下限为0.019 mg/L,3个样品的相对标准偏差在0.54%~0.92%之间,加标回收率在96%~101.14%之间。该方法样品消解完全,流程短,操作简单,快速,测定准确度高,可以满足铜冶炼烟尘中锌含量的测定。  相似文献   

16.
α-Fe2O3掺杂对In2O3电导和气敏性能的影响   总被引:10,自引:1,他引:9  
用化学共沉淀法制备了α Fe2O3掺杂的In2O3纳米晶微粉,研究了α Fe2O3掺杂对In2O3电导和气敏性能的影响. 结果表明, α Fe2O3和In2O3间可形成有限固溶体In2-xFexO3(0≤x≤0.40); Fe3+对In2O3晶格中In3+格位的部分取代,大大增强了阴阳离子间的结合力,导致材料中氧空位VO×数骤降、 自由电子的浓度变稀和电导下降. n(Fe3+):n(In3+)=5 :5的共沉淀粉于800 ℃下灼烧4 h所得的α Fe2O3掺杂In2O3传感器元件,对45 μmol•L-1 C2H5OH的灵敏度达54.0,为相同浓度干扰气体汽油的8倍多.  相似文献   

17.
针对银精矿样品复杂,难消解的特点,研究了不同酸溶法和碱熔法对样品的消解情况,建立了硝酸,盐酸,氢氟酸,高氯酸消解银精矿的方法。根据元素灵敏度和抗干扰性,选定各元素的测定波长。通过酸溶样和碱熔样测定结果比对,验证了方法准确性。建立了四酸消解-电感耦合等离子体光谱法测定银精矿中铜、铅、锌、砷、镉、钙、镁、锰含量的方法,元素的线性相关系数均在0.9999以上。通过共存元素干扰实验,确定了银精矿中高含量元素(铜、铅、锌、铁、锑、铋等)对测定元素结果没有影响。方法检出限:Cu 0.0063 mg/L, Pb 0.0159 mg/L ,Zn 0.0090 mg/L,As 0.0192 mg/L, Cd 0.0093 mg/L ,Ca 0.0084 mg/L, Mg 0.0075 mg/L, Mn 0.0081 mg/L。测定下限:Cu 0.0105mg/L,Pb 0.0265 mg/L, Zn 0.0150 mg/L, As 0.0320 mg/L, Cd 0.0155 mg/L, Ca 0.0140 mg/L, Mg 0.0125 mg/L,Mn 0.0135 mg/L。3个样品的相对标准偏差在0.87%~3.56%之间,加标回收率在95.00%~103.56%之间。方法流程短,操作简单,快速,灵敏度和再现性高,结果准确可靠,可以满足银精矿中铜、铅、锌、砷、镉、钙、镁、锰含量的测定。  相似文献   

18.
The reactivity of Zn3 V2 O8 towards ZnMoO4 was investigated by using DTA and XRD methods. A new compound of the formula Zn2.5 VMoO8 was found. It crystallises in an orthorhombic system. The melting temperature was determinated to be 845±5°C. This revised version was published online in August 2006 with corrections to the Cover Date.  相似文献   

19.
The near infrared spectra of water in aqueous solutions of La(ClO4)3, Pr(ClO4)3, Nd(ClO4)3, Gd(ClO4)3, Er(ClO4)3, Yb(ClO4)3, Lu(ClO4)3, and NaClO4 have been measured in the concentration range from 0.3 to 2.5 mol-dm–3, at 25°C. The relative contents of free OH groups in the 1.0, 1.6, and 2.2M solutions have been calculated from extinction coefficients for water at 1160 nm. They increase with increasing salt concentration and are greater in solutions of the lighter lanthanide perchlorates at any fixed molarity. The results are discussed in terms of the stoichiometry and structure of hydrated cations of trivalent lanthanides.  相似文献   

20.
娄太平  张乐  郭军兴 《化学学报》2010,68(6):466-470
研究了在不同温度下的NaNO3和AgNO3水溶液中Li1.3Ti1.7Al0.3(PO4)3和Na1.3Ti1.7Al0.3(PO4)3离子交换行为.实验表明Li1.3Ti1.7Al0.3(PO4)3和Na1.3Ti1.7Al0.3(PO4)3均显示出了高选择性与Na+和Ag+进行离子交换的特征,且对Ag+的选择性高于Na+.升高温度可显著提高Ag/Li和Ag/Na的交换反应速度.  相似文献   

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