Electric Field as A Novel Switch to Enhance Optical Absorption Spectra of Defect Blue Phosphorene Thin-films

Nguyen Vo Anh Duy, Dang Minh Triet, Dinh Van Anh
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Abstract

Improvement of the optical absorption coefficient is essential to enhance the light conversion efficiency of thin-film organic solar cells. Here we report the use of an external electric field as a novel switch to improve the optical absorption capacity of two-dimensional defect blue phosphorene (BlueP) systems. Using the density functional theory with van der Waals functionals, we investigate the structural, electronic, magnetic and optical absorption properties of the pristine, single-vacancy (SV) BlueP thin films, and a BlueP system absorbing a Vanadium adatom. We demonstrate that a SV BlueP layer would exhibit half-metallic and its absorption spectrum under an electric field parallel to the material plane is significantly enhanced in the ultra-violet region. More interestingly, when a Vanadium transition metal is absorbed on a pristine BlueP, the applied electric field perpendicular to the BlueP plane not only doubles the optical absorption coefficient, but also switches ON/OFF the magnetic moments of this system. The prominent red shift of the absorption spectra towards the visible light range under selected polarized directions paves a novel way to engineer solar cell devices with BlueP materials.
电场作为一种增强缺陷蓝磷薄膜光吸收光谱的新开关
提高光吸收系数是提高薄膜有机太阳能电池光转换效率的关键。本文报道了利用外电场作为一种新型开关来提高二维缺陷蓝磷烯(BlueP)系统的光吸收能力。利用范德华泛函的密度泛函理论,研究了原始单空位(SV) BlueP薄膜的结构、电子、磁性和光学吸收特性,以及吸收钒原子的BlueP体系。研究表明,在平行于材料平面的电场作用下,SV蓝光层呈现半金属性质,其吸收光谱在紫外区显著增强。更有趣的是,当钒过渡金属在原始的BlueP上被吸收时,垂直于BlueP平面的外加电场不仅使光学吸收系数加倍,而且还开关了该系统的磁矩。在选择的偏振方向下,吸收光谱向可见光范围的显著红移为用蓝ep材料设计太阳能电池器件铺平了新的道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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