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半导体的光偶极诱导各向异性生长:一种制备手性和复杂纳米结构的简易策略。

Optical dipole-induced anisotropic growth of semiconductors: A facile strategy toward chiral and complex nanostructures.

机构信息

Key Laboratory of Artificial Micro/Nano Structure of Ministry of Education, School of Physics and Technology, Wuhan University, Wuhan 430072, China.

出版信息

Proc Natl Acad Sci U S A. 2023 Mar 21;120(12):e2216627120. doi: 10.1073/pnas.2216627120. Epub 2023 Mar 13.

Abstract

Chiral nanostructures based on semiconductors exhibit pronounced properties of chiral luminescence and optoelectronic responses, which are fundamental for chiroptoelectronic devices. However, the state-of-the-art techniques of generating semiconductors with chiral configurations are poorly developed, most of which are complicated or of low yield, rendering low compatibility to the platform of optoelectronic devices. Here we show polarization-directed oriented growth of platinum oxide/sulfide nanoparticles based on optical dipole interactions and near-field-enhanced photochemical deposition. By rotating the polarization during the irradiation or employing vector beam, both three dimensional and planar chiral nanostructures can be obtained, which is extendable to cadmium sulfide. These chiral superstructures exhibit broadband optical activity with a g-factor of ~0.2 and a luminescence g-factor of ~0.5 in the visible, making them promising candidate for chiroptoelectronic devices.

摘要

基于半导体的手性纳米结构表现出明显的手性发光和光电响应特性,这对手性光电器件至关重要。然而,目前用于产生手性结构半导体的技术发展还不完善,其中大多数技术复杂或产量低,与光电器件平台的兼容性较差。在这里,我们展示了基于光学偶极相互作用和近场增强光化学沉积的铂氧化物/硫化物纳米粒子的偏振定向取向生长。通过在照射过程中旋转偏振或采用矢量光束,可以获得三维和平面手性纳米结构,这一方法还可扩展到硫化镉。这些手性超结构表现出宽带光活性,在可见光范围内的 g 因子约为 0.2,发光 g 因子约为 0.5,这使它们成为手性光电器件的有前途的候选材料。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ac8/10041118/4a7d89e60ead/pnas.2216627120fig01.jpg

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