Vicente Nuria, Garcia-Belmonte Germà
Institute of Advanced Materials (INAM), Universitat Jaume I , 12006 Castelló, Spain.
J Phys Chem Lett. 2017 Apr 6;8(7):1371-1374. doi: 10.1021/acs.jpclett.7b00189. Epub 2017 Mar 14.
Ions migrate through the hybrid halide perovskite lattice, allowing for a variety of electrochemical applications as perovskite-based electrodes for batteries. It is still unknown how extrinsic defects such as lithium ions interact with the hybrid perovskite structure during the charging process. It is shown here that Li intake/release proceeds by topotactic insertion into the hybrid perovskite host, without drastic structural alterations or rearrangement. Even the perovskite electronic band structure remains basically unaltered upon cycling. The occurrence of conversion or alloying reactions producing metallic lead is discarded. Stable specific capacity ∼200 mA h g is delivered, which entails outstanding Li-ion molar concentration, x in LiCHNHPbBr, approaching 3. Slight distortions of the perovskite lattice upon cycling explain the highly reversible Li intercalation reaction that also exhibits an excellent rate capability.
离子在混合卤化物钙钛矿晶格中迁移,这使得基于钙钛矿的电池电极有多种电化学应用。目前仍不清楚锂离子等外在缺陷在充电过程中如何与混合钙钛矿结构相互作用。本文表明,锂的摄入/释放是通过拓扑插入混合钙钛矿主体进行的,不会发生剧烈的结构改变或重排。即使在循环过程中,钙钛矿的电子能带结构基本保持不变。产生金属铅的转化或合金化反应的发生也被排除。可提供稳定的比容量约200 mA h g,这意味着LiCHNHPbBr中锂离子的摩尔浓度x非常高,接近3。循环过程中钙钛矿晶格的轻微畸变解释了高度可逆的锂嵌入反应,该反应也表现出优异的倍率性能。