LPICM, CNRS, Ecole Polytechnique , Université Paris-Saclay , 91128 Palaiseau , France.
DEN - Service de Recherches de Métallurgie Physique, CEA , Université Paris-Saclay , 91191 Gif sur Yvette , France.
ACS Nano. 2018 Apr 24;12(4):3477-3486. doi: 10.1021/acsnano.8b00267. Epub 2018 Mar 26.
Hybrid organic-inorganic perovskites emerged as a new generation of absorber materials for high-efficiency low-cost solar cells in 2009. Very recently, fully inorganic perovskite quantum dots also led to promising efficiencies, making them a potentially stable and efficient alternative to their hybrid cousins. Currently, the record efficiency is obtained with CsPbI, whose crystallographical characterization is still limited. Here, we show through high-resolution in situ synchrotron XRD measurements that CsPbI can be undercooled below its transition temperature and temporarily maintained in its perovskite structure down to room temperature, stabilizing a metastable perovskite polytype (black γ-phase) crucial for photovoltaic applications. Our analysis of the structural phase transitions reveals a highly anisotropic evolution of the individual lattice parameters versus temperature. Structural, vibrational, and electronic properties of all the experimentally observed black phases are further inspected based on several theoretical approaches. Whereas the black γ-phase is shown to behave harmonically around equilibrium, for the tetragonal phase, density functional theory reveals the same anharmonic behavior, with a Brillouin zone-centered double-well instability, as for the cubic phase. Using total energy and vibrational entropy calculations, we highlight the competition between all the low-temperature phases of CsPbI (γ, δ, β) and show that avoiding the order-disorder entropy term arising from double-well instabilities is key to preventing the formation of the yellow perovskitoid phase. A symmetry-based tight-binding model, validated by self-consistent GW calculations including spin-orbit coupling, affords further insight into their electronic properties, with evidence of Rashba effect for both cubic and tetragonal phases when using the symmetry-breaking structures obtained through frozen phonon calculations.
2009 年,混合有机-无机钙钛矿作为新一代高效、低成本太阳能电池的吸收材料而出现。最近,全无机钙钛矿量子点也带来了有前景的效率,使它们成为其混合同类物的潜在稳定和高效替代品。目前,使用 CsPbI 获得的记录效率,但其晶体学特性仍然有限。在这里,我们通过高分辨率原位同步辐射 X 射线衍射测量表明,CsPbI 可以过冷到低于其转变温度,并在室温下暂时保持其钙钛矿结构,稳定对于光伏应用至关重要的亚稳钙钛矿多型体(黑色 γ 相)。我们对结构相变的分析表明,各晶格参数随温度的变化具有高度各向异性。基于几种理论方法进一步检查了所有实验观察到的黑色相的结构、振动和电子性质。尽管黑色 γ 相在平衡时表现出谐和行为,但对于四方相,密度泛函理论揭示了相同的非谐行为,具有布里渊区中心的双势阱不稳定性,与立方相相同。使用总能量和振动熵计算,我们强调了 CsPbI(γ、δ、β)所有低温相之间的竞争,并表明避免由双势阱不稳定性引起的有序-无序熵项是防止形成黄色钙钛矿相的关键。基于对称的紧束缚模型,通过包括自旋轨道耦合的自洽 GW 计算进行验证,进一步深入了解它们的电子性质,对于立方相和四方相,当使用通过冻结声子计算获得的对称破缺结构时,都有证据表明 Rashba 效应。