Ln3+-doped glasses: Advancing molecular logic for integration into photonic and electronic devices

IF 3.3 3区 物理与天体物理 Q2 OPTICS
Rafael F. Salgueiro , Fernando E. Maturi , Victor M.P. da Silva , Danilo Manzani , Carlos D.S. Brites
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Abstract

The rapid miniaturization of electronic devices has pushed the limits of conventional silicon-based technologies, creating a pressing need for novel approaches to sustain the exponential growth of computing power. This study explores the innovative application of Ln3+-doped glasses in developing molecular logic systems as a potential solution. Exploiting Eu3+ and Dy3+, we investigated the luminescence properties under various physical stimuli such as excitation wavelength and temperature. Our findings reveal the capability to construct logic elements of varying complexity, from simple AND and OR gates to advanced FULL-ADDER and FULL-SUBTRACTOR circuits. This work represents the first instance of using Ln3+ exclusively for molecular logic via physical stimuli. The robust and stable optical properties of the doped glasses enable their integration into conventional electronic and photonic devices, potentially revolutionizing the landscape of molecular logic and computing. This research not only enhances the understanding of light-matter interactions in Ln3+-doped systems but also opens new pathways for the development of miniaturized, high-performance innovative computational devices.
掺杂 Ln3+ 的玻璃:推进集成到光子和电子设备中的分子逻辑
电子设备的快速微型化已经突破了传统硅基技术的极限,因此迫切需要新的方法来维持计算能力的指数级增长。本研究探索了掺 Ln3+ 玻璃在开发分子逻辑系统中的创新应用,以此作为一种潜在的解决方案。我们利用 Eu3+ 和 Dy3+ 研究了激发波长和温度等各种物理刺激下的发光特性。我们的研究结果揭示了构建不同复杂程度逻辑元件的能力,从简单的 AND 和 OR 门到先进的全加法器和全减法器电路。这项工作代表了通过物理刺激将 Ln3+ 完全用于分子逻辑的首个实例。掺杂玻璃坚固稳定的光学特性使其能够集成到传统的电子和光子设备中,从而有可能彻底改变分子逻辑和计算的面貌。这项研究不仅加深了人们对掺杂 Ln3+ 系统中光与物质相互作用的理解,还为开发小型化、高性能的创新计算设备开辟了新途径。
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来源期刊
Journal of Luminescence
Journal of Luminescence 物理-光学
CiteScore
6.70
自引率
13.90%
发文量
850
审稿时长
3.8 months
期刊介绍: The purpose of the Journal of Luminescence is to provide a means of communication between scientists in different disciplines who share a common interest in the electronic excited states of molecular, ionic and covalent systems, whether crystalline, amorphous, or liquid. We invite original papers and reviews on such subjects as: exciton and polariton dynamics, dynamics of localized excited states, energy and charge transport in ordered and disordered systems, radiative and non-radiative recombination, relaxation processes, vibronic interactions in electronic excited states, photochemistry in condensed systems, excited state resonance, double resonance, spin dynamics, selective excitation spectroscopy, hole burning, coherent processes in excited states, (e.g. coherent optical transients, photon echoes, transient gratings), multiphoton processes, optical bistability, photochromism, and new techniques for the study of excited states. This list is not intended to be exhaustive. Papers in the traditional areas of optical spectroscopy (absorption, MCD, luminescence, Raman scattering) are welcome. Papers on applications (phosphors, scintillators, electro- and cathodo-luminescence, radiography, bioimaging, solar energy, energy conversion, etc.) are also welcome if they present results of scientific, rather than only technological interest. However, papers containing purely theoretical results, not related to phenomena in the excited states, as well as papers using luminescence spectroscopy to perform routine analytical chemistry or biochemistry procedures, are outside the scope of the journal. Some exceptions will be possible at the discretion of the editors.
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