Cooperative Regulation of ns2 Lone-Pair Expression Realizes Distinct Excitonic Emissions in Hybrid Germanium, Tin, and Lead Halides

IF 14.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Journal of the American Chemical Society Pub Date : 2024-12-17 DOI:10.1021/jacs.4c15554
Jiang Han, Yawen Li, Peijie Zhang, Bin Xu, Xiaofan Xu, Zewei Quan
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Abstract

Lone-pair expression is significantly influenced by geometric constraints in hybrid metal halides (HMHs). Two-dimensional (2D) HMHs possess reduced structural dimensionality, allowing for a wide range of off-center displacement of the metal center. However, the effect of lone-pair-induced off-center distortion on the geometric configuration of inorganic units, electronic properties, and exciton emissions in 2D HMHs remains unclear. In this study, 2D DMPMBr4 (DMP = N,N′-dimethylpiperazine) HMHs of group 14 elements (M = Ge, Sn, and Pb) are developed, exhibiting pronounced stereochemical activity of ns2 lone-pair electrons. Such 2D HMHs are chosen as a model system to demonstrate the influence of the stereochemical activity of ns2 lone-pair electrons on the geometric configuration of inorganic units, electronic properties, and exciton emissions. The off-center distortion D is introduced to describe the degree of lone-pair expression in these HMHs, and a quantitative relationship between the D and FE/STE emissions is established. When the D is reduced to less than 0.24, the off-center distortion of the units is sufficiently suppressed to limit the lone-pair expression, facilitating the excitonic transition from the STE state to the FE state upon compression. Substituting metal cations with those having more inactive ns2 lone-pair electrons exerts a similar effect to pressure in promoting the excitonic transitions in the DMPMBr4 series. This study uncovers the relationship between the stereochemical activity of ns2 lone-pair electrons and excitonic emissions, which could accelerate the development of HMHs with the desired optical properties.

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杂化金属卤化物(HMHs)中的孤对表达受几何限制的影响很大。二维(2D)混合金属卤化物的结构维度较低,因此金属中心的偏心位移范围较大。然而,孤对引起的偏心变形对二维 HMHs 中无机单元的几何构型、电子特性和激子发射的影响仍不清楚。本研究开发了 14 族元素(M = Ge、Sn 和 Pb)的二维 DMPMBr4(DMP = N,N′-二甲基哌嗪)HMHs,表现出明显的 ns2 孤对电子立体化学活性。我们选择这种二维 HMHs 作为模型系统,以证明 ns2 孤对电子的立体化学活性对无机单元的几何构型、电子特性和激子发射的影响。我们引入了偏心畸变 D 来描述这些 HMHs 中孤电子对的表达程度,并建立了 D 与 FE/STE 发射之间的定量关系。当 D 减小到小于 0.24 时,单元的偏心畸变被充分抑制,从而限制了孤对表达,促进了压缩时从 STE 状态到 FE 状态的激子转变。用具有更多不活泼 ns2 孤对电子的金属阳离子替代 DMPMBr4 系列中的金属阳离子,在促进激子跃迁方面会产生与压力类似的效果。这项研究揭示了 ns2 孤对电子的立体化学活性与激子发射之间的关系,这将加速具有所需光学特性的 HMHs 的开发。
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来源期刊
CiteScore
24.40
自引率
6.00%
发文量
2398
审稿时长
1.6 months
期刊介绍: The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.
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