极地的
纳米尺度
化学物理
偶极子
扫描隧道显微镜
离子键合
材料科学
氧化物
航程(航空)
化学极性
密度泛函理论
量子隧道
纳米技术
静电学
化学
计算化学
离子
物理化学
物理
光电子学
复合材料
有机化学
冶金
天文
作者
Mikołaj Lewandowski,Irene M. N. Groot,Zhihui Qin,Tomasz Ossowski,Tomasz Pabisiak,A. Kiejna,Anastassia Pavlovska,Shamil Shaikhutdinov,Hans‐Joachim Freund,E. Bauer
标识
DOI:10.1021/acs.chemmater.6b03040
摘要
Polar ionic surfaces with bulk termination are inherently unstable because of their diverging electrostatic surface energy. Nevertheless, they are frequently observed in nature, mainly because of charge neutralization by adsorbates, but occur also under atomically clean conditions. Several mechanisms have been invoked to explain the stability of atomically clean polar surfaces, but the frequently observed periodic nanoscale pattern formation has not yet been explained. Here we propose that long-range interactions between alternating electropositive and electronegative regions of different surface terminations minimize the electrostatic energy of the surface and thus stabilize the nanoscale pattern. This is illustrated using the example of polar Fe oxide surfaces by combining scanning tunneling microscopy and spectroscopy results with results from density functional theory-based calculations and dipole–dipole interaction models.
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