Cheng Pengfei, Sun Lei, Feng Lu, Yang Songqiu, Yang Yang, Zheng Daoyuan, Zhao Yang, Sang Youbao, Zhang Ruiling, Wei Donghui, Deng Weiqiao, Han Keli
State Key Laboratory of Molecular Reaction Dynamics, Dalian Institute of Chemical Physics, Chinese Academy of Science, Dalian, 116023, P. R. China.
Institute of Molecular Sciences and Engineering, Shandong University, Qingdao, P. R. China.
Angew Chem Int Ed Engl. 2019 Nov 4;58(45):16087-16091. doi: 10.1002/anie.201909129. Epub 2019 Sep 24.
Low-dimensional metal halides have recently attracted extensive attention owing to their unique structure and photoelectric properties. Herein, we report the colloidal synthesis of all-inorganic low-dimensional cesium copper halide nanocrystals (NCs) by adopting a hot-injection approach. Using the same reactants and ligands, but different reaction temperatures, both 1D CsCu I nanorods and 0D Cs Cu I NCs can be prepared. Density functional theory indicates that the reduced dimensionality in 1D CsCu I compared to 0D Cs Cu I makes the excitons more localized, which accounts for the strong emission of 0D Cs Cu I NCs. Subsequent optical characterization reveals that the highly luminescent, strongly Stokes-shifted broadband emission of 0D Cs Cu I NCs arises from the self-trapped excitons. Our findings not only present a method to control the synthesis of low-dimensional cesium copper halide nanocrystals but also highlight the potential of 0D Cs Cu I NCs in optoelectronics.
低维金属卤化物因其独特的结构和光电性能,近年来受到了广泛关注。在此,我们报道了采用热注入法胶体合成全无机低维铯铜卤化物纳米晶体(NCs)。使用相同的反应物和配体,但不同的反应温度,可以制备出一维CsCuI纳米棒和零维CsCuI NCs。密度泛函理论表明,与零维CsCuI相比,一维CsCuI维度的降低使激子更加局域化,这解释了零维CsCuI NCs的强发射。随后的光学表征表明,零维CsCuI NCs的高发光、强斯托克斯位移宽带发射源于自陷激子。我们的发现不仅提供了一种控制低维铯铜卤化物纳米晶体合成的方法,还突出了零维CsCuI NCs在光电子学中的潜力。