首页 | 本学科首页   官方微博 | 高级检索  
     


DFT+U Analysis on Stability of Low-Index Facets in Hexagonal LaCoO3 Perovskite:Effect of Co3+ Spin States
Authors:Dan Wu  Gong-dong Chen  Chao-yi Ge  Zhen-peng Hu  Xue-hao He  Xin-gang Li
Affiliation:1.Tianjin Key Laboratory of Applied Catalysis Science & Technology(Tianjin), Tianjin 300072, China;Collaborative Innovation Center for Chemical Science & Engineering(Tianjin), Tianjin 300072, China2.Collaborative Innovation Center for Chemical Science & Engineering(Tianjin), Tianjin 300072, China;School of Physics, Nankai University, Tianjin 300071, China3.Department of Chemistry, School of Science, Tianjin University, Tianjin 300072, China
Abstract:By the first-principles calculations,most studies indicated that the (11102)-CoO2 termination of LaCoO3 cannot be stabilized,which disagrees with the experimental observation.Besides the crystal structure,we found that the spin states of Co3+ ions could affect surface stability,which previously were not well considered.By examining the different states of Co3+ ions in hexagonal-phase LaCoO3,including low spin,intermediate spin,and high spin states,the surface grand potentials of these facets are calculated and compared.The results show that the spin states of Co3+ ions have an important influence on stability of the LaCoO3 facets.Different from the previous results,the stability diagrams demonstrate that the (11102)-CoO2 termination can stably exist under O-rich condition,which can get an agreement with the experimental ones.Furthermore,the surface oxygen vacancy formation energies (EOv) of stable facets are computed in different spin states.The EOv of these possible exposed terminations strongly depend on the spin state of Co3+ ions:in particular,the EOv of the HS states is lower than that of other spin states.This indicates that one can tune the properties of LaCoO3 by directly tuning the spin states of Co3+ ions.
Keywords:DFT+U   Spin state   Surface   Perovskite
点击此处可从《化学物理学报(中文版)》浏览原始摘要信息
点击此处可从《化学物理学报(中文版)》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号