Mark Justin, Hanrahan Michael P, Woo Katherine E, Lee Shannon, Rossini Aaron J, Kovnir Kirill
Department of Chemistry, Iowa State University, Ames, Iowa, 50011, USA.
Ames Laboratory, U.S. Department of Energy, Ames, Iowa, 50011, USA.
Chemistry. 2019 May 2;25(25):6392-6401. doi: 10.1002/chem.201900339. Epub 2019 Apr 11.
Lithiation of van der Waals tetrel-arsenides, GeAs and SiAs, has been investigated. Electrochemical lithiation demonstrated large initial capacities of over 950 mAh g accompanied by rapid fading over successive cycling in the voltage range 0.01-2 V. Limiting the voltage range to 0.5-2 V achieved more stable cycling, which was attributed to the intercalation process with lower capacities. Ex situ powder X-ray diffraction confirmed complete amorphization of the samples after lithiation, as well as recrystallization of the binary tetrel-arsenide phases after full delithiation in the voltage range 0.5-2 V. Solid-state synthetic methods produce layered phases, in which Si-As or Ge-As layers are separated by Li cations. The first layered compounds in the corresponding ternary systems were discovered, Li Ge As and Li Si As , which crystallize in the Pbam (No. 55) and P2/m (No. 10) space groups, respectively. Semiconducting layered GeAs and SiAs accommodate the extra charge from Li cations through structural rearrangement in the Si-As or Ge-As layers and eventually by replacement of the tetrel dumbbells with sets of Li atoms. Ge and Si monoarsenides demonstrated high structural flexibility and a mild ability for reversible lithiation.
已对范德华四价元素砷化物GeAs和SiAs的锂化过程展开研究。电化学锂化显示,在0.01 - 2V的电压范围内,初始容量超过950 mAh g,但在连续循环过程中会迅速衰减。将电压范围限制在0.5 - 2V可实现更稳定的循环,这归因于容量较低的嵌入过程。非原位粉末X射线衍射证实,锂化后样品完全非晶化,并且在0.5 - 2V的电压范围内完全脱锂后,二元四价元素砷化物相发生重结晶。固态合成方法可制备层状相,其中Si - As或Ge - As层被Li阳离子分隔。在相应的三元体系中发现了首批层状化合物Li₂GeAs和Li₂SiAs,它们分别结晶于Pbam(编号55)和P2/m(编号10)空间群。半导体层状GeAs和SiAs通过Si - As或Ge - As层中的结构重排,最终通过用Li原子组取代四价元素哑铃状结构来容纳来自Li阳离子的额外电荷。锗和硅的单砷化物表现出高结构灵活性和适度的可逆锂化能力。