Theoretical Study of the Magnetic Mechanism of a Pca21 C4N3 Monolayer and the Regulation of Its Magnetism by Gas Adsorption.

IF 4.2 2区 化学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecules Pub Date : 2024-11-02 DOI:10.3390/molecules29215194
Dongqiu Zhao, Xiao Tang, Xueying Gao, Wanyan Xing, Shuli Liu, Huabing Yin, Lin Ju
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Abstract

For metal-free low-dimensional ferromagnetic materials, a hopeful candidate for next-generation spintronic devices, investigating their magnetic mechanisms and exploring effective ways to regulate their magnetic properties are crucial for advancing their applications. Our work systematically investigated the origin of magnetism of a graphitic carbon nitride (Pca21 C4N3) monolayer based on the analysis on the partial electronic density of states. The magnetic moment of the Pca21 C4N3 originates from the spin-split of the 2pz orbit from special carbon (C) atoms and 2p orbit from N atoms around the Fermi energy, which was caused by the lone pair electrons in nitrogen (N) atoms. Notably, the magnetic moment of the Pca21 C4N3 monolayer could be effectively adjusted by adsorbing nitric oxide (NO) or oxygen (O2) gas molecules. The single magnetic electron from the adsorbed NO pairs with the unpaired electron in the N atom from the substrate, forming a Nsub-Nad bond, which reduces the system's magnetic moment from 4.00 μB to 2.99 μB. Moreover, the NO adsorption decreases the both spin-down and spin-up bandgaps, causing an increase in photoelectrical response efficiency. As for the case of O2 physisorption, it greatly enhances the magnetic moment of the Pca21 C4N3 monolayer from 4.00 μB to 6.00 μB through ferromagnetic coupling. This method of gas adsorption for tuning magnetic moments is reversible, simple, and cost-effective. Our findings reveal the magnetic mechanism of Pca21 C4N3 and its tunable magnetic performance realized by chemisorbing or physisorbing magnetic gas molecules, providing crucial theoretical foundations for the development and utilization of low-dimensional magnetic materials.

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Pca21 C4N3 单层的磁性机理及气体吸附对其磁性调节的理论研究》(Theoretical Study of the Magnetic Mechanism of a Pca21 C4N3 Monolayer and the Regulation of Its Magnetism by Gas Adsorption)。
无金属低维铁磁材料是下一代自旋电子器件的希望候选材料,研究其磁性机理并探索调节其磁性能的有效方法对推动其应用至关重要。我们的研究基于对部分电子态密度的分析,系统地研究了石墨氮化碳(Pca21 C4N3)单层材料的磁性起源。Pca21 C4N3 的磁矩来源于特殊碳原子(C)的 2pz 轨道和氮原子(N)的 2p 轨道在费米能附近的自旋分裂,这种分裂是由氮(N)原子中的孤对电子引起的。值得注意的是,Pca21 C4N3 单层的磁矩可以通过吸附一氧化氮(NO)或氧气(O2)气体分子进行有效调节。吸附的一氧化氮中的单个磁性电子与来自基底的 N 原子中的未成对电子配对,形成 Nsub-Nad 键,从而将系统的磁矩从 4.00 μB 降低到 2.99 μB。此外,NO 的吸附还降低了自旋向下带隙和自旋向上带隙,从而提高了光电响应效率。至于 O2 物理吸附的情况,它通过铁磁耦合使 Pca21 C4N3 单层的磁矩从 4.00 μB 大大提高到 6.00 μB。这种调整磁矩的气体吸附方法是可逆的、简单的和经济的。我们的发现揭示了 Pca21 C4N3 的磁性机理及其通过化学吸附或物理吸附磁性气体分子实现的可调磁性能,为低维磁性材料的开发和利用提供了重要的理论基础。
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来源期刊
Molecules
Molecules 化学-有机化学
CiteScore
7.40
自引率
8.70%
发文量
7524
审稿时长
1.4 months
期刊介绍: Molecules (ISSN 1420-3049, CODEN: MOLEFW) is an open access journal of synthetic organic chemistry and natural product chemistry. All articles are peer-reviewed and published continously upon acceptance. Molecules is published by MDPI, Basel, Switzerland. Our aim is to encourage chemists to publish as much as possible their experimental detail, particularly synthetic procedures and characterization information. There is no restriction on the length of the experimental section. In addition, availability of compound samples is published and considered as important information. Authors are encouraged to register or deposit their chemical samples through the non-profit international organization Molecular Diversity Preservation International (MDPI). Molecules has been launched in 1996 to preserve and exploit molecular diversity of both, chemical information and chemical substances.
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