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Structural, Optical, Photocatalytic and Electrochemical Studies of PbS Nanoparticles

机译:PBS纳米粒子的结构,光学,光催化和电化学研究

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Oleic acid (OA) and octadecylamine (ODA) capped lead sulphide (PbS) nanoparticles were prepared at 150, 190 and 230 degrees C. X-ray diffraction patterns indicates that the synthesized PbS nanoparticles were in the rock cubic salt crystalline phase. The particle sizes of the as-prepared PbS nanoparticles are in the range 2.91-10.05 nm for OA-Pb S(150), 24.92-39.98 nm for ODA-Pb S(150), 9.26 - 29.08 nm for OA-PbS(190), 34.54 - 48.04 nm for ODA-PbS(190), 17.96-88.07 nm for OA-PbS(230) and 53.60 - 94.42 nm for ODA-PbS(230). SEM images revealed flaky and agglomerated spherical like morphology for the nanoparticles. The energy bandgap of the PbS nanoparticles are in the range 4.14 - 4.25 eV, OA-PbS(230) have the lowest bandgap of 4.14 eV while ODA-PbS(150) have the highest bandgap of 4.25 eV. The PbS nanoparticles were used as photocatalyst for the degradation of Rhodamine B and OA-PbS(150) showed efficiency of 44.11% after 360 mins. Cyclic voltammetry of the PbS nanoparticles showed a reversible redox reaction and linear Randles-Sevcik plots indicates electron transfer process is diffusion controlled.
机译:在150,190和230℃下制备油酸(OA)和十八烷基胺(ODA)封端的硫化物(PBS)纳米颗粒。X射线衍射图案表明合成的PBS纳米颗粒在岩石立方盐结晶相中。用于OA-Pb S(150)的AA-Pb S(150)的粒径为2.91-10.05nm,OA-Pb S(150)的24.92-39.98nm,9.26-29.08nm用于OA-PBS(190 ),用于OA-PBS(230)的OA-PBS(230)和53.60-94.42nm的34.54-48.04nm,ODA-PBS(230)。 SEM图像揭示了纳米颗粒的形态形态的片状和凝聚的球形。 PBS纳米粒子的能量带隙在4.14-4.25eV的范围内,OA-PBS(230)具有4.14eV的最低带隙,而ODA-PBS(150)具有4.25eV的最高带隙。使用PBS纳米颗粒作为光催化剂,用于罗丹明B和OA-PBS(150)的降解,显示360分钟后的效率为44.11%。 PBS纳米粒子的循环伏安法显示可逆氧化还原反应,线性Randles-Sevcik图表示电子转移过程是扩散控制的。

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