论文标题
有机分子动力学和电荷载体寿命中的碘化物钙钛矿mapbi $ _3 $
Organic Molecular Dynamics and Charge-carrier Lifetime in Lead Iodide Perovskite MAPbI$_3$
论文作者
论文摘要
杂化有机无机钙钛矿(HOIP)的长电荷载体寿命是它们作为太阳能电池材料的显着性能的关键。长寿的微观机制仍在争论中。在这里,通过使用探测局部磁场波动的Muon自旋松弛技术,我们表明,原型hoip甲基铵铅碘化物(MAPBI $ _3 $)的MUON去极化速率($δ$)显示出在两个步骤中,在120 k和190 k的结构中,急剧下降,在160 k和190 k的结构中,我们的结构均高于160 k,我们$δ$的减少与预期行为一致,这是由于MA跳跃旋转绕$ C_3 $和$ C_4 $对称轴的快速发展而吻合的。我们的结果为MA分子的电偶极子旋转与HOIP中的电荷载体寿命之间的旋转之间的密切关系提供了直接的证据。
The long charge carrier lifetime of the hybrid organic-inorganic perovskites (HOIPs) is the key for their remarkable performance as a solar cell material. The microscopic mechanism for the long lifetime is still in debate. Here, by using muon spin relaxation technique that probes the fluctuation of local magnetic fields, we show that the muon depolarization rate ($Δ$) of a prototype HOIP methylammonium lead iodide (MAPbI$_3$) shows a sharp decrease with increasing temperature in two steps above 120 K and 190 K across the structural transition from orthorhombic to tetragonal structure at 162 K. Our analysis shows that the reduction of $Δ$ is quantitatively in agreement with the expected behavior due to the rapid development of MA jumping rotation around the $C_3$ and $C_4$ symmetry axes. Our results provide direct evidence for the intimate relation between the rotation of the electric dipoles of MA molecules and the charge carrier lifetime in HOIPs.