Department of Chemistry, Northwestern University , Evanston, Illinois 60208, United States.
ACS Nano. 2014 Sep 23;8(9):9219-23. doi: 10.1021/nn5029967. Epub 2014 Sep 8.
We report the photoluminescence (PL) properties of colloidal Si nanocrystals (NCs) up to 800 K and observe PL retention on par with core/shell structures of other compositions. These alkane-terminated Si NCs even emit at temperatures well above previously reported melting points for oxide-embedded particles. Using selected area electron diffraction (SAED), powder X-ray diffraction (XRD), liquid drop theory, and molecular dynamics (MD) simulations, we show that melting does not play a role at the temperatures explored experimentally in PL, and we observe a phase change to β-SiC in the presence of an electron beam. Loss of diffraction peaks (melting) with recovery of diamond-phase silicon upon cooling is observed under inert atmosphere by XRD. We further show that surface passivation by covalently bound ligands endures the experimental temperatures. These findings point to covalently bound organic ligands as a route to the development of NCs for use in high temperature applications, including concentrated solar cells and electrical lighting.
我们报告了胶体硅纳米晶体(NCs)在 800K 下的光致发光(PL)性质,并观察到其 PL 保持性能与其他组成的核/壳结构相当。这些烷烃封端的 Si NCs 甚至在远高于先前报道的氧化物嵌入颗粒熔点的温度下发射。通过选区电子衍射(SAED)、粉末 X 射线衍射(XRD)、液滴理论和分子动力学(MD)模拟,我们表明在实验 PL 温度范围内,熔化不起作用,并且在电子束存在下观察到β-SiC 的相转变。在惰性气氛下通过 XRD 观察到,随着冷却,衍射峰的损失(熔化)伴随着金刚石相硅的恢复。我们进一步表明,通过共价键合配体进行表面钝化可以承受实验温度。这些发现表明,通过共价键合的有机配体为开发用于高温应用的 NCs 提供了一种途径,包括聚光太阳能电池和电照明。