Department of Chemistry, Korea University, Jochiwon 339-700, Korea.
ACS Nano. 2010 Apr 27;4(4):2391-401. doi: 10.1021/nn100163k.
Single-crystalline rock-salt PbS nanowires (NWs) were synthesized using three different routes; the solvothermal, chemical vapor transport, and gas-phase substitution reaction of pregrown CdS NWs. They were uniformly grown with the [100] or [110], [112] direction in a controlled manner. In the solvothermal growth, the oriented attachment of the octylamine (OA) ligands enables the NWs to be produced with a controlled morphology and growth direction. As the concentration of OA increases, the growth direction evolves from the [100] to the higher surface-energy [110] and [112] directions under the more thermodynamically controlled growth conditions. In the synthesis involving chemical vapor transport and the substitution reaction, the use of a lower growth temperature causes the higher surface-energy growth direction to change from [100] to [110]. The high-resolution X-ray diffraction pattern and X-ray photoelectron spectroscopy results revealed that a thinner oxide-layer was produced on the surface of the PbS NWs by the substitution reaction. We fabricated field effect transistors using single PbS NW, which showed intrinsic p-type semiconductor characteristics for all three routes. For the PbS NW with a thinner oxide layer, the carrier mobility was measured to be as high as 10 cm(2) V(-1) s(-1).
使用三种不同的方法合成了单晶岩盐 PbS 纳米线 (NWs):溶剂热法、化学气相输运法和预生长 CdS NW 的气相取代反应法。它们以受控的方式均匀地沿 [100] 或 [110]、[112] 方向生长。在溶剂热生长中,辛胺 (OA) 配体的定向附着使 NWs能够以受控的形态和生长方向生长。随着 OA 浓度的增加,在更热力学控制的生长条件下,生长方向从 [100] 演变为更高表面能的 [110] 和 [112] 方向。在涉及化学气相输运和取代反应的合成中,较低的生长温度导致更高表面能的生长方向从 [100] 变为 [110]。高分辨率 X 射线衍射图谱和 X 射线光电子能谱结果表明,取代反应在 PbS NW 表面生成了更薄的氧化层。我们使用单个 PbS NW 制造了场效应晶体管,所有三种方法都显示出本征 p 型半导体特性。对于氧化层较薄的 PbS NW,载流子迁移率高达 10 cm(2) V(-1) s(-1)。