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从 CuS 到 CuInS 的纳米棒中阳离子交换的动力学分析:铜蓝矿相变温度对其机制的影响

Kinetic Analysis of the Cation Exchange in Nanorods from CuS to CuInS: Influence of Djurleite's Phase Transition Temperature on the Mechanism.

作者信息

Thiel Felix, Palencia Cristina, Weller Horst

机构信息

Department of Physical Chemistry, University of Hamburg, Grindelallee 117, 20146 Hamburg, Germany.

The Hamburg Centre for Ultrafast Imaging, Luruper Chaussee 149, 22761 Hamburg, Germany.

出版信息

ACS Nano. 2023 Feb 28;17(4):3676-3685. doi: 10.1021/acsnano.2c10693. Epub 2023 Feb 7.

Abstract

In the syntheses of ternary I-III-VI compounds, such as CuInS, it is often difficult to balance three precursor reactivities to achieve the desired size, shape, and atomic composition of nanocrystals. Cation exchange reactions offer an attractive two-step alternative, by producing a binary compound with the desired morphology and incorporating another atomic species postsynthetically. However, the kinetics of such cation exchange reactions, especially for anisotropic nanocrystals, are still not fully understood. Here, we present the cation exchange reaction from Cu-deficient djurleite CuS nanorods to wurtzite CuInS, with size and shape retention. With reaction parameters in a broad temperature range between 40 °C and 160 °C, we were able to obtain various intermediates. Djurleite has a bulk phase transition temperature at 93 °C, which influences the cation exchange considerably. Below the phase transition temperature, indium is only incorporated into the surface of the nanorods, while, at temperatures above the phase transition temperature, we observe a Janus-type exchange mechanism and the formation of CuInS bands in the djurleite nanorods. The findings suggest that the diffusion above the phase transition temperature is strongly favored along the copper planes of the copper sulfide nanorods over the diffusion through the sulfur planes. This results in a difference of 37 kJ mol in the activation energy of the cation exchange below and above the phase transition temperature.

摘要

在三元I-III-VI化合物(如CuInS)的合成过程中,通常很难平衡三种前驱体的反应活性,以实现所需的纳米晶体尺寸、形状和原子组成。阳离子交换反应提供了一种有吸引力的两步替代方法,即先制备具有所需形态的二元化合物,然后在合成后引入另一种原子物种。然而,此类阳离子交换反应的动力学,尤其是对于各向异性纳米晶体的动力学,仍未得到充分理解。在此,我们展示了从缺铜铜蓝CuS纳米棒到纤锌矿CuInS的阳离子交换反应,纳米棒的尺寸和形状得以保留。通过在40℃至160℃的宽温度范围内设置反应参数,我们能够获得各种中间体。铜蓝在93℃有一个体相转变温度,这对阳离子交换有很大影响。在相转变温度以下,铟仅掺入纳米棒的表面,而在相转变温度以上,我们观察到一种双面神型交换机制,并在铜蓝纳米棒中形成CuInS带。研究结果表明,相转变温度以上的扩散在硫化铜纳米棒的铜平面上比通过硫平面的扩散更受青睐。这导致相转变温度以下和以上阳离子交换的活化能相差37kJ/mol。

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