Abstract

Compared with traditional inorganic ferroelectric materials, organic molecular ferroelectric materials possess many advantages, such as light weight, flexibility, no heavy metal atoms and low cost, and have received extensive attention for a long time. In recent years, atomic-thick two-dimensional (2D) inorganic ferroelectric materials have achieved breakthrough and attracted much attention. However, there are few reports on the design and research of two-dimensional organic ferroelectric materials. In this paper, we theoretically propose a 2D monolayer organic ferroelectric molecular crystal with the cyclobutene-1,2-dicarboxylic acid (CBDC) molecules as the building block based on density functional theory calculations. The bulk of CBDC molecular crystals clearly shows layered structure due to the chain-like arrangement of hydrogen bonds in crystal. It is found that the internal hydrogen bond chains give rise to the anisotropic cleavage energy values along different crystal planes of the CBDC molecular crystal bulk. Theoretical calculation suggests that the CBDC based 2D monolayer organic ferroelectric molecular crystal can be achieved by the mechanical/chemical peeling along the (102) crystal plane because of the lowest cleavage energy. It is predicted that the in-plane spontaneous polarization of the CBDC (102) molecular crystal monolayer is ~0.39 × 10<sup>–6</sup> μC/cm, which is comparable to those of some inorganic counterparts. Calculations also indicate that the CBDC (102) molecular crystal monolayer shows a high polarization reversal barrier and is sensitive to the external uniaxial stress. The CBDC (102) monolayer organic ferroelectric molecular crystal reveals high in-plane spontaneous polarization with polarization reversal barrier easily modulated by the interface strain engineering, thereby rendering it great potential in lightweight, metal-free and flexible ferroelectric devices.

Highlights

  • 图 14 石墨烯基底上的 CBDC (102) 单层分子晶体经过 5 ps 从头算分子动力学模拟后的结构图 (NPT 系 综, 温 度 300 K, 时间步长 1 fs) (a) 正视图; (b) 侧视图. 图 (a) 中绿 色曲线指示了多条有序排列的氢键链, 为清晰起见, 图 (a) 中的石墨烯衬底已被隐去 Fig. 14. (a) Top and (b) side views of snapshot of the twodimensional CBDC (102) monolayer supported on a graphene sheet, after 5 ps of AIMD simulation

  • 计算表明 CBDC (102) 分子晶 体单层的铁电极化反转势垒达到了 0.76 eV/f.u., 显著高于钙钛矿体系中 BaTiO3, 预示了该分子晶 体单层有望展现出良好的鲁棒性和较高的铁电转

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Summary

Introduction

二维有机拓扑绝缘体的研究进展 Research progress of two-dimensional organic topological insulators 物理学报. 二维铁电In2Se3/InSe垂直异质结能带的应力调控 Strain control of two-dimensional ferroelectric In2Se3/InSe vertical heterojunction energy band 物理学报. 超高真空条件下分子束外延生长的单层二维原子晶体材料的研究进展 Research progress of monolayer two-dimensional atomic crystal materials grown by molecular beam epitaxy in ultra-high vacuum conditions 物理学报. 二维材料/铁电异质结构的研究进展 Research progress and device applications of multifunctional materials based on two-dimensional film/ferroelectrics heterostructures 物理学报. 二维层间滑移铁电研究进展 Research progress of two-dimensional interlayer-sliding ferroelectricity 物理学报. 本文基于密度泛函理论方法设计了一种以环丁烯1,2-二 羧 酸 (cyclobutene-1,2-dicarboxylic acid, CBDC) 分子为结构单元的二维单层有机铁电分子晶体 .

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