Zinc sulfide: from supertetrahedral atomically precise clusters to quantum dots

IF 2.6 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
CrystEngComm Pub Date : 2024-10-22 DOI:10.1039/D4CE00731J
Ju-Suo Zhong, Yan-Xiang Ling, Xin-Yu Tong, Zhan-Guo Jiang and Cai-Hong Zhan
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Abstract

In this comprehensive review, we have introduced two distinct types of multinuclear zinc sulfide superpolyhedral molecular clusters and zinc sulfide quantum dots. Two distinct categories of hyper polyhedral zinc sulfide clusters are identified: Zn10, categorized under T3 symmetry, and Zn8, classified under P1 symmetry. Both Zn10 and Zn8 clusters feature not only μ1-S and μ2-S species, which are attached to ligands, but also μ3-S and μ4-S species that remain unattached to ligands. Furthermore, the zinc and sulfur atoms within these cluster molecules possess the versatility to be substituted by alternative cations or anions, leading to the formation of corresponding derivatives. By comparing synthetic methodologies, structural attributes, and potential applications of the multinuclear zinc sulfide superpolyhedral molecular clusters and zinc sulfide quantum dots, we have delved into the intricate relationship between zinc sulfide quantum dots and these two classes of zinc sulfide clusters, offering a fresh perspective. From a synthetic standpoint, the preparation of zinc sulfide quantum dots often shares similarities with the synthesis of Zn10 clusters, while some methods also mirror the synthesis of Zn8 clusters utilizing reactors. Quantum dots typically exhibit larger sizes compared to cluster molecules, and their growth is characterized by rapid and continuous expansion, accompanied by a continuous red-shift of the edge band peaks in their UV-vis absorption spectra. In contrast, cluster molecules display discrete and heterogeneous growth patterns, with abrupt transitions from one discrete size to another larger discrete size, mirrored by individual sharp peaks in their UV-vis absorption spectra. Regarding applications, both entities share similar domains of utilization, albeit with distinct underlying mechanisms. By elucidating these differences and similarities, we aim to foster further advancements in the field of zinc sulfide-based materials.

Abstract Image

硫化锌:从超四面体原子精确团簇到量子点
在这篇综述中,我们介绍了两种不同类型的多核硫化锌超多面体分子团簇和硫化锌量子点。我们发现了两类不同的超多面体硫化锌团簇:Zn10 属于 T3 对称型,Zn8 属于 P1 对称型。Zn10 和 Zn8 团簇不仅具有与配体相连的 μ1-S 和 μ2-S 物种,还具有未与配体相连的 μ3-S 和 μ4-S 物种。此外,这些簇分子中的锌原子和硫原子还可以被其他阳离子或阴离子取代,从而形成相应的衍生物。通过比较多核硫化锌超多面体分子团簇和硫化锌量子点的合成方法、结构属性和潜在应用,我们深入探讨了硫化锌量子点与这两类硫化锌团簇之间错综复杂的关系,为我们提供了一个全新的视角。从合成的角度来看,硫化锌量子点的制备通常与 Zn10 团簇的合成有相似之处,而有些方法也与利用反应器合成 Zn8 团簇的方法相似。与团簇分子相比,量子点的尺寸通常较大,其生长特点是快速而持续的扩展,并伴随着其紫外-可见吸收光谱中边缘带峰的持续红移。相比之下,团簇分子则表现出离散和异质的生长模式,从一种离散尺寸突然过渡到另一种更大的离散尺寸,其紫外-可见吸收光谱中的单个尖锐峰也反映了这一点。在应用方面,这两种实体具有相似的利用领域,尽管其基本机制各不相同。通过阐明这些异同,我们希望促进硫化锌基材料领域的进一步发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CrystEngComm
CrystEngComm 化学-化学综合
CiteScore
5.50
自引率
9.70%
发文量
747
审稿时长
1.7 months
期刊介绍: Design and understanding of solid-state and crystalline materials
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