首页> 外文期刊>Chemistry of Materials: A Publication of the American Chemistry Society >Ligand-Controlled Colloidal Synthesis and Electronic Structure Characterization of Cubic Iron Pyrite (FeS2) Nanocrystals
【24h】

Ligand-Controlled Colloidal Synthesis and Electronic Structure Characterization of Cubic Iron Pyrite (FeS2) Nanocrystals

机译:立方黄铁矿(FeS2)纳米晶的配体控制胶体合成和电子结构表征

获取原文
获取原文并翻译 | 示例
       

摘要

Iron pyrite (FeS2) is a promising photovoltaic absorber because of its Earth abundance, high optical extinction, and infrared band gap (E_g = 0.95 eV), but its use has been hindered because of the difficulty of phase pure synthesis. Pyrite phase purity is a paramount concern, as other phases of iron sulfide have undesirable electronic properties. Here we report the synthesis of phase pure iron pyrite nanocrystals with cubic morphology and a mean dimension of 80 nm. Control over the nanocrystal shape was achieved using an unusual ligand, 1-hexadecanesulfonate. The particles were characterized via synchrotron X-ray spectroscopy, indicating an indirect band gap of 1.00 ± 0.11 eV and a valence bandwidth of nearly 1 eV, Transmission electron microscopy from early reaction stages suggests a nucleation and growth mechanism similar to solution precipitation syntheses typical of metal oxide nanocrystals, rather than the diffusion-limited growth process typical of hot-injection metal chalcogenide nanocrystal syntheses.
机译:黄铁矿(FeS2)由于其地球丰度,高消光性和红外带隙(E_g = 0.95 eV)是一种很有前途的光伏吸收剂,但由于难以进行相纯合成,因此阻碍了它的使用。硫铁矿相纯度是最重要的问题,因为硫化铁的其他相具有不良的电子性能。在这里,我们报告具有立方形态和平均尺寸为80 nm的相纯铁黄铁矿纳米晶体的合成。使用不寻常的配体1-十六烷磺酸盐可以控制纳米晶体的形状。通过同步加速器X射线光谱对颗粒进行了表征,表明间接带隙为1.00±0.11 eV,价带接近1 eV。早期反应阶段的透射电子显微镜表明,成核和生长机理与典型的溶液沉淀合成相似金属氧化物纳米晶体,而不是热注入金属硫族化物纳米晶体合成过程中典型的扩散受限生长过程。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号