Rational Design of Electric Field-Responsive Building Blocks for All-Organic 2D Magnetoelectric Materials

IF 15.6 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Kílian Jutglar-Lozano, Mercè Deumal, Jordi Ribas-Arino* and Stefan T. Bromley*, 
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Abstract

Development of technologically promising magnetoelectric materials, where magnetic properties can be controlled by electric fields (E-fields), has focused on inorganic systems. Here, we propose a strategy for modulating magnetic exchange coupling (J) in purely organic systems through experimentally realizable E-fields. Our approach leverages two established concepts: (i) E-field-induced twisting of dipolar organic linkers and (ii) control of J via conformational changes in organic diradicals. Using density functional theory calculations, we investigated the effects of applied E-fields on diradicals with two coplanar spin-carrying trioxotriangulene (TOT) radicals connected by dipolar aryl linkers. We find that E-fields induce significant conformational changes in the linkers (twisting) that alters π-conjugation and, in turn, the magnetic J coupling between TOT radicals. In-plane E-fields twist the linkers toward the plane of the radicals, enhancing π-conjugation and increasing AFM coupling. Out-of-plane E-fields induce more orthogonal linker conformations and decrease the coupling strength. The magnetoelectric response depends on a combination of steric hindrance, π-conjugation, and polarization. Significant and measurable cumulative changes in J of up to 3.9 meV could be achieved by using in-plane and out-of-plane E-fields of up to 0.5 V/Å. In some cases, applied E-fields can also induce switching between paramagnetism and antiferromagnetism. Calculations on a 2D covalent organic framework (COF) based on a network of TOT radicals and dipolar linkers confirm that this approach is also viable for extended systems. Such COFS could also display E-field induced ferroelectric responses. Overall, our proof-of-principle study highlights the interplay between molecular structure, E-fields, and magnetism and establishes an innovative and chemically rational framework for developing all-organic magnetoelectric materials.

Abstract Image

全有机二维磁电材料电场响应构件的合理设计
技术上有前途的磁电材料的发展,其中的磁性可以由电场(e场)控制,已经集中在无机系统。在这里,我们提出了一种通过实验可实现的电场来调制纯有机系统中的磁交换耦合(J)的策略。我们的方法利用了两个既定的概念:(i)电场诱导的偶极有机连接体的扭曲和(ii)通过有机双自由基的构象变化来控制J。利用密度泛函理论计算,研究了应用电场对由双极性芳基连接的共面携带自旋的三氧三角烯(TOT)自由基的影响。我们发现,电场在连接体中引起明显的构象变化(扭转),从而改变π共轭,进而改变TOT自由基之间的磁J耦合。平面内电场使连接子向自由基平面扭曲,增强π共轭作用,增加原子力显微镜耦合。面外电场诱导了更多的正交连接构象,降低了耦合强度。磁电响应取决于位阻、π共轭和极化的综合作用。通过使用高达0.5 V/Å的面内和面外电场,可以实现高达3.9 meV的显著且可测量的累积J变化。在某些情况下,外加电磁场还可以诱导顺磁性和反铁磁性之间的切换。基于TOT自由基和偶极连接体网络的二维共价有机骨架(COF)的计算证实了该方法对扩展体系也是可行的。这种COFS还可以显示电场诱导的铁电响应。总的来说,我们的原理验证研究强调了分子结构,电场和磁性之间的相互作用,并为开发全有机磁电材料建立了创新和化学合理的框架。
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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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