基于力匹配的CsPbI3极化和非极化力场生成方法

IF 3.2 3区 化学 Q2 CHEMISTRY, PHYSICAL
Cecilia Vona, Mathias Dankl, Ariadni Boziki, Martin P. Bircher and Ursula Rothlisberger*, 
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引用次数: 0

摘要

卤化铅钙钛矿已成为一种高效的太阳能电池材料。然而,到目前为止,这一类中最有希望的成员是多晶,其中宽带隙δ相与光活性钙钛矿α形式竞争,并且目前尚未很好地理解稳定一相的内在物理相互作用。基于适当参数化力场(FF)的经典分子动力学模拟可以在广泛的温度(和压力)范围内进行计算研究,并有助于确定在原子水平上控制相对相稳定性的潜在因素。在本文中,我们提出了一种基于力匹配的方法,用于从高级参考数据中自动生成极化(pol)和非极化(npol) FFs,并将其应用于全无机卤化铅材料CsPbI3作为具有δ/α多态性的原型系统。这些力匹配的npol和pol FFs是基于广泛温度范围内第一性原理分子动力学模拟的大量参考数据确定的。虽然这两种ff都能够描述钙钛矿和非钙钛矿δ相,但更精细的结构细节以及相对相稳定性,可以用极化版本更好地再现。对这些从头推导的原子间势进行比较,可以直接了解控制两个竞争相之间相互作用的相互作用的物理起源。结果表明,相对于高对称(立方)钙钛矿α相,显极化是在较低温度下稳定强各向异性δ相的关键因素。α和δ相之间的这种基本差异似乎是普遍存在的,因此可能也适用于其他具有δ/α多态性的钙钛矿化合物,为室温下稳定光活性钙钛矿相的合成工作提供了合理的指导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Force-Matching-Based Approach for the Generation of Polarizable and Nonpolarizable Force Fields Applied to CsPbI3

Lead halide perovskites have emerged as highly efficient solar cell materials. However, to date, the most promising members of this class are polymorphs in which a wide-band-gap δ phase competes with the photoactive perovskite α form and the intrinsic physical interactions that stabilize one phase over the other are currently not well understood. Classical molecular dynamics simulations based on suitably parametrized force fields (FF) enable computational studies over broad temperature (and pressure) ranges and can help to identify the underlying factors that govern relative phase stability at the atomic level. In this article, we present a force-matching-based approach for the automatized generation of polarizable (pol) as well as nonpolarizable (npol) FFs from high-level reference data and apply it to the all-inorganic lead halide material CsPbI3 as a prototype system exhibiting a δ/α polymorphism. These force-matched npol and pol FFs have been determined based on extensive reference data from first-principles molecular dynamics simulations over a wide range of temperatures. While both FFs are able to describe the perovskite as well as the nonperovskite δ phase, finer structural details, as well as the relative phase stability, are better reproduced with the polarizable version. A comparison of these ab initio-derived interatomic potentials allows direct insight into the physical origin of the interactions that govern the interplay between the two competing phases. It turns out that explicit polarization is the essential factor that stabilizes the strongly anisotropic δ phase over the high-symmetry (cubic) perovskite α phase at lower temperatures. This fundamental difference between α and δ phases appears universal and might thus also hold for other perovskite compounds with δ/α polymorphism providing rational guidance for synthetic efforts to stabilize the photoactive perovskite phase at room temperature.

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来源期刊
The Journal of Physical Chemistry C
The Journal of Physical Chemistry C 化学-材料科学:综合
CiteScore
6.50
自引率
8.10%
发文量
2047
审稿时长
1.8 months
期刊介绍: The Journal of Physical Chemistry A/B/C is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, and chemical physicists.
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