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GaAs(111)表面硅烯、锗烯的几何及电子性质研究

张弦 郭志新 曹觉先 肖思国 丁建文

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GaAs(111)表面硅烯、锗烯的几何及电子性质研究

张弦, 郭志新, 曹觉先, 肖思国, 丁建文

Atomic and electronic structures of silicene and germanene on GaAs(111)

Zhang Xian, Guo Zhi-Xin, Cao Jue-Xian, Xiao Si-Guo, Ding Jian-Wen
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  • 基于密度泛函理论的第一性原理计算方法, 系统研究了硅烯、锗烯在GaAs(111) 表面的几何及电子结构. 研究发现, 硅烯、锗烯均可在As-中断和Ga-中断的GaAs(111) 表面稳定存在, 并呈现蜂窝状六角几何构型. 形成能计算结果证明了其实验制备的可行性. 同时发现硅烯、锗烯与GaAs表面存在共价键作用, 这破坏了其Dirac电子性质. 进一步探索了利用氢插层恢复硅烯、锗烯Dirac电子性质的方法. 发现该方法可使As-中断面上硅烯、锗烯的Dirac电子性质得到很好恢复, 而在Ga-中断面上的效果不够理想. 此外, 基于原子轨道成键和杂化理论揭示了GaAs表面硅烯、锗烯能带变化的物理机理. 研究结果为硅烯、锗烯在半导体基底上的制备及应用奠定了理论基础.
    By using first-principles method in the density-functional theory, we clarify the atomic and electronic structures of silicene and germanene on 1×1 GaAs(111). We find stable structures for silicene and germanene on both the As-terminated and Ga-terminated GaAs surfaces. The structures of silicene and germanene are similar to those of the free-standing ones, which present a honeycomb-hexagonal geometry. The cohesive energies of silicene and germanene on both As and Ga sides of GaAs surfaces are comparable to those of their bulk structures and/or those on Ag(111) substrates which have been widely observed in experiment, showing the possibility of synthesizing them on both sides of GaAs surfaces in experiment. The corresponding binding energies are in a range of 0.56-1.37 eV per Si (Ge) atom, 10 times larger than the usual van der Waals interaction, showing the covalent interaction between silicene (germanene) and GaAs surfaces. The band structure calculations show that such a covalent interaction induces the absence of Dirac electrons for silicene and germanene on GaAs surfaces. We then explore the method of recovering the Dirac electrons by using hydrogen (H) intercalation. It is found that the intercalated H atoms are chemically bonded to GaAs surface, and the silicene (germanene) shifts upward distance from GaAs surface increasing from 2.50-2.58 Å to 3.49-3.86 Å, where a covalent van-der-Waals interaction transition happens between silicene (germanene) and GaAs surface. Moreover, the distances between silicene (germanene) and H atoms are 30% and 8% larger than the atomic-radius sum of Si (Ge) and H on As-terminated and Ga-terminated GaAs surfaces, respectively. This shows that the interaction between silicene (germanene) and H on the As-terminated GaAs surface is obviously weaker than the typical covalent interaction, while on the Ga-terminated GaAs surface, it is comparable to the typical covalent interaction. This difference is induced by the difference in electronegativity between As and Ga atoms. We further find that the H intercalation recovers the Dirac electrons well on the As-terminated GaAs(111) due to the weaker Si (Ge)-H interaction, while it does not on the Ga-terminated GaAs(111) due to the stronger Si (Ge)-H interaction. The results are confirmed by performing calculations for silicene (germanene) on larger GaAs(111) surfaces, i.e., the 3×3 GaAs surface. Our study provides the theoretical basis for the preparation and application of silicene and germanene on semiconductor surfaces.
      通信作者: 郭志新, zxguo08@gmail.com
    • 基金项目: 国家自然科学基金(批准号: 11204259, 11374252, 11474245, 51372214)、湖南省自然科学基金(批准号: 2015JJ6106)、新世纪优秀人才计划(批准号: NCET-12-0722)和教育部长江学者和创新团队计划(IRT13093)资助的课题.
      Corresponding author: Guo Zhi-Xin, zxguo08@gmail.com
    • Funds: Project supported by the National Natural Science Foundation of China (Grant Nos. 11204259, 11374252, 11474245, 51372214), the Natural Science Foundation of Hunan Province, China (Grant No. 2015JJ6106), the Program for New Century Excellent Talents in University, China (Grant No. NCET-12-0722) and the Program for Changjiang Scholars and Innovative Research Team in University, China (Grant No. IRT13093).
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    Slonczewski J C, Weiss P R 1958 Phys. Rev. 109 272

    [2]

    Novoselov K S, Geim A K, Morozov S V, Jiang D, Katsnelson M L, Grigorieva I V, Dubonos S V, Firsov A A 2005 Nature 438 197

    [3]

    Zhang Y, Tan Y W, Stormer H L, Kim P 2005 Nature 438 201

    [4]

    Son Y W, Cohen M L, Louie S G 2007 Nature 444 347

    [5]

    Okada S, Oshiyama A 2001 Phys. Rev. Lett. 87 146803

    [6]

    Geim A K, Novoselov K S 2007 Nat. Mat. 6 183

    [7]

    Cahangirov S, Topsakal M, Aktrk E, Sahin H, Ciraci S 2009 Phys. Rev. Lett. 102 236804

    [8]

    Liu C C, Feng W, Yao Y 2011 Phys. Rev. Lett. 107 076802

    [9]

    Vogt P, de Padova P, Quaresima C, Avila J, Frantzeskakis E, Asensio M C, Resta A, Ealet B, Le Lay G 2012 Phys. Rev. Lett. 108 155501

    [10]

    Chen L, Liu C C, Feng B, He X, Cheng P, Ding Z, Meng S, Yao Y, Wu K 2012 Phys. Rev. Lett. 109 056804

    [11]

    Fleurence A, Friedlein R, Ozaki T, Kawai H, Wang Y, Yamada-Takamura Y 2012 Phys. Rev. Lett. 108 245501

    [12]

    Meng L, Wang Y, Zhang L, Du S, Wu R, Li L, Zhang Y, Li G, Zhou H, Hofer W A, Gao H J 2013 Nano Lett. 13 685

    [13]

    Li L, Lu S, Pan J, Qin Z, Wang Y Q, Wang Y, Cao G Y, Du S, Gao H J 2014 Adv. Mater. 26 4820

    [14]

    Dàvila M E, Xian L, Cahangirov S, Rubio A, Le Lay G 2014 New J. Phys. 16 095002

    [15]

    Guo Z X, Furuya S, Iwata J I, Oshiyama A 2013 J. Phys. Soc. Jpn. 82 063714

    [16]

    Guo Z X, Furuya S, Iwata J I, Oshiyama A 2013 Phys. Rev. B 87 235435

    [17]

    Guo Z X, Oshiyama A 2014 Phys. Rev. B 89 155418

    [18]

    Kresse G, Hafner J 1994 Phys. Rev. B 49 14251

    [19]

    Kresse G, Furthmuller J 1996 Phys. Rev. B 54 11169

    [20]

    Blöchl P E 1994 Phys. Rev. B 50 17953

    [21]

    Klimeš J, Bowler D R, Michaelides A 2011 Phys. Rev. B 83 195131

    [22]

    Woolf D A, Westwood D I, Williams R H 1993 Appl. Phys. Lett. 62 1370

    [23]

    Clementi E, Raimondi D L, Reinhardt W P 1963 J. Chem. Phys. 38 2686

    [24]

    Riedl C, Coletti C, Iwasaki T, Zakharov A A, Starke U 2009 Phys. Rev. Lett. 103 246804

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出版历程
  • 收稿日期:  2015-03-03
  • 修回日期:  2015-04-27
  • 刊出日期:  2015-09-05

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