Zhang Zhilu, Wang Qi, Song Yamin, Bu Yuxiang, Song Xinyu
School of Chemistry and Chemical Engineering, Shandong University, Jinan, 250100, People's Republic of China.
J Phys Chem A. 2022 May 26;126(20):3174-3184. doi: 10.1021/acs.jpca.2c01709. Epub 2022 May 13.
The electronic properties and their modulations for the nitrogen-vacancy (NV) centers in various nanoscale diamonds are of profound current interest because of their potential applications. However, although the NV centers as chromophores in diamond are the most widely studied, surprisingly, little is known about their magnetic spin coupling properties up to now. Here, we for the first time show, using the spin-polarized DFT calculations, that the NV centers can act as unique endohedral σ-diradical magnets in diamond nanoclusters and exhibit quite strong ferromagnetic (FM) or antiferromagnetic (AFM) spin coupling characteristics due to their unique endotetrahedral structures with favorable radical-radical contacts. Although the neutral NV center (NV) in its doublet ground state exhibits quite strong AFM spin coupling among three radical C-sites (i.e., an AFM triradical center), interestingly, excess electron injection can convert it to a FM diradical magnet (i.e., the triplet ground state NV) with almost unchanged -coupling magnitude, and the -coupling of the nanocluster can be noticeably enhanced by F-termination of the surface due to triradical spin delocalization mediated by excess electron. However, interior modification (one C in the endotetrahedron core is substituted by N or B or is hydrogenated) can assign the nanocluster perfect AFM diradical character. The spin coupling strength presents a quasilinear correlation with the distance between the two C radicals in the NV core for the same size of the clusters and a high linear correlation with the energy difference between two singly occupied molecular orbitals. Clearly, the FM and AFM couplings as well as their switching behavior in such NV defect diamond nanoclusters featuring the endohedral σ-diradicals are a novel type of promising magnetic material motifs. These findings open up promising spintronic application prospects of the NV diamonds and provide helpful information for the design of inorganic magnetic materials and logic devices.
由于其潜在应用,各种纳米级金刚石中氮空位(NV)中心的电子特性及其调制目前引起了广泛关注。然而,尽管金刚石中作为发色团的NV中心是研究最广泛的,但令人惊讶的是,到目前为止,人们对它们的磁自旋耦合特性知之甚少。在这里,我们首次使用自旋极化密度泛函理论(DFT)计算表明,NV中心在金刚石纳米团簇中可以作为独特的内包σ-双自由基磁体,并且由于其具有有利的自由基-自由基接触的独特内四面体结构,表现出相当强的铁磁(FM)或反铁磁(AFM)自旋耦合特性。尽管处于双重态基态的中性NV中心(NV)在三个自由基C位点之间表现出相当强的AFM自旋耦合(即一个AFM三自由基中心),但有趣的是,过量电子注入可以将其转变为具有几乎不变耦合强度的FM双自由基磁体(即三重态基态NV),并且由于过量电子介导的三自由基自旋离域,表面的F端基可以显著增强纳米团簇的耦合。然而,内部修饰(内四面体核心中的一个C被N或B取代或氢化)可以赋予纳米团簇完美的AFM双自由基特性。对于相同尺寸的团簇,自旋耦合强度与NV核心中两个C自由基之间的距离呈现准线性相关性,与两个单占据分子轨道之间的能量差呈现高度线性相关性。显然,在这种具有内包σ-双自由基的NV缺陷金刚石纳米团簇中,FM和AFM耦合及其开关行为是一种新型的有前途的磁性材料基序。这些发现为NV金刚石开辟了有前途的自旋电子应用前景,并为无机磁性材料和逻辑器件的设计提供了有用信息。