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With the development of future information devices towards smaller size, lower power consumption and higher performance, the size of materials used to build devices will be further reduced. Traditional “top-down” technology has encountered a bottleneck in the development of information devices on a nanoscale, while the vapor deposition technology has attracted great attention due to its ability to construct nanostructures on an atomic scale, and is considered to have the most potential to break through the existing manufacturing limits and build nano-structures directly with atoms as a “bottom-up” method. During molecular beam epitaxy, atoms and molecules of materials are deposited on the surface in an “atomic spray painting” way. By such a method, some graphene-like two-dimensional materials (e.g., silicene, germanene, stanene, borophene) have been fabricated with high quality and show many novel electronic properties, and the ultrathin films (several atomic layers) of other materials have been grown to achieve certain purposes, such as NaCl ultrathin layers for decoupling the interaction of metal substrate with the adsorbate. In an atomic layer deposition process, which can be regarded as a special modification of chemical vapor deposition, the film growth takes place in a cyclic manner. The self- limited chemical reactions are employed to insure that only one monolayer of precursor (A) molecules is adsorbed on the surface, and the subsequent self- limited reaction with the other precursor (B) allows only one monolayer of AB materials to be built. And the self- assembled monolayers composed of usually long- chain molecules can be introduced as the active or inactive layer for area- selective atomic layer deposition growth, which is very useful in fabricating nano- patterned structures. As the reverse process of atomic layer deposition, atomic-layer etching processes can remove certain materials in atomic precision. In this paper we briefly introduce the principles of the related technologies and their applications in the field of nano- electronic device processing and manufacturing, and find how to realize the precise control of the thickness and microstructure of functional materials on an atomic scale.
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Keywords:
- vapor deposition /
- atomic manufacturing /
- molecular beam epitaxy /
- atomic layer deposition
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图 3 (a) Pt(111)表面锗烯的理论计算结构; (b)−(g) 不同位置的Ge原子对以及Ge单原子与最近邻基底Pt原子间电子局域函数的计算模拟; (h)−(j) 锗烯的实验结果(LEED, STM图像及表观高度)[37]
Fig. 3. (a) Theoretical model of germanene on Pt (111) surface, and the electron localization functions of the cross-sections between the germanium pairs (b)−(f) and between one germanium atom and its nearest Pt neighbor (g). (h)−(j) The experimental results of LEED pattern, STM image and the apparent height along the indicated line in the STM image, respectively[37].
图 4 (a) Cu(111)表面制备的锗烯; (b), (c) Cu(111)基底和锗烯的原子分辨图像; (d) 双层锗烯的吸附结构模型; (e) 相应的STM图像模拟, 与实验结果(c)吻合; (f) 单层(红色)和双层(黑色)锗烯的电子结构(STS谱), 插图为Cu(111)基底STS谱用于标定针尖状态[38]
Fig. 4. (a) STM image of germanene on Cu(111); (b), (c) the atomic-resolved STM images of Cu (111) substrate and germanene, respectively; (d) the adsorption model of bilayer germanene; (e) the simulated STM image with the features fitting very well with the experimental observations; (f) the STS of monolayer (red) and bilayer (black) germanene, and inset is STS taken on the bare Cu(111) to verify the condition of the tip[38].
图 5 (a)−(c) 在Cu(111)表面MBE生长的不同取向的硒化铜蜂窝状结构的STM图像; (d) 用于标定针尖状态的Cu(111)表面标准STS谱; (e) CuSe结构的STS谱[52]
Fig. 5. (a)−(c) The STM images of honeycomb structures with equivalent orientations on Cu(111) by means of MBE growth; (d) the standard STS of Cu(111) for checking tip status; (e) electronic structure (STS) of CuSe structures[52].
图 6 (a) 在Cu(100)上外延生长的NaCl薄膜[36], 以及在其上的CoPc分子轨道的实验(b)和理论(c)图像[53]
Fig. 6. (a) MBE growth of NaCl layers on Cu(100)[36], on top of which the quasi-free molecular orbital of adsorbed CoPc can be observed. (b) and (c) are the STM image and theoretical simulation of molecular orbital, respectively[53].
图 13 (a) 左边选区ALD的原理示意图, 右边为自组装钝化层的单体分子结构; (b) 自组装薄膜的缺陷(pinhole)影响ALD沉积过程的选择性; (c) 自组装分子的光聚合官能团(二炔基)在光诱导下聚合有效抑制缺陷产生; (d) 通过选区ALD沉积ZnO掩膜刻蚀后的微结构, 结构最窄宽度约为15 nm[101]
Fig. 13. (a) Schematic diagram of area-selective ALD growth (left), and the monomer molecular structures forming inactive SAMs (right); (b) the pinhole defect affects the selectivity of ALD deposition; (c) photopolymeric functional groups (diacetylenyl) of SAMs can effectively inhibit defect formation in terms of photo-induced polymerization; (d) SEM micrograph of the microstructure obtained by etching with ZnO mask of area-selective ALD, and the width of narrowest structure reaches 15 nm[101].
图 15 双层石墨烯ALE刻蚀前后的光学显微图像(a), (b)以及相应的AFM图像(c), (d)和在各位点的拉曼谱(e)[136]
Fig. 15. Optical microscopic images (a), (b) and AFM images (c), (d) of bilayer graphene before and after one cycle of ALE etching. (e) Raman spectrum of graphene taken at twelve points indicated in (a), (b) before and after etching[136].
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[1] 冯黎, 朱雷 2020 功能材料与器件学报 26 191
Feng L, Zhu L 2020 J. Funct. Mater. Devices 26 191
[2] 庞玉莲, 邹应全 2015 信息记录材料 16 36Google Scholar
Pang Y L, Zou Y Q 2015 Info. Rec. Mater. 16 36Google Scholar
[3] Striccoli M 2017 Science 357 353Google Scholar
[4] Okazaki S 2015 Microelectron. Eng. 133 23Google Scholar
[5] Hong F, Blaikie R 2019 Adv. Opt. Mater. 7 1801653Google Scholar
[6] 王霞, 吕浩, 赵秋玲, 张帅一, 谭永炎 2016 光谱学与光谱分析 36 3461
Wang X, Lü H, Zhao Q L, Zhang S Y, Tan Y Y 2016 Spectrosc. Spect. Anal. 36 3461
[7] Fang F Z 2016 Front. Mech. Eng. Chin. 11 325Google Scholar
[8] Luo C, Li J F, Yang X, Wu X, Zhong S Y, Wang C L, Sun L T 2020 ACS Appl. Nano Mater. 3 4747
[9] Martín-Palma R J, Lakhtakia A 2013 Engineered Biomimicry (Boston: Elsevier) pp383−398
[10] LaPedus M 2018 工艺与制造 35 39
LaPedus M 2018 Prog. Fabri. 35 39
[11] Ashurbekova K, Ashurbekova K, Botta G, Yurkevich O, Knez M 2020 Nanotechnology 31 342001Google Scholar
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[13] Mattox D M 1992 Plat. Surf. Finish. 79 60
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[18] Yang R B, Bachmann J, Pippel E, Berger A, Woltersdorf J, Gösele U, Nielsch K 2009 Adv. Mater. 21 3170Google Scholar
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[24] Howson R P, Spencer A G, Lewin R W 1988 Vacuum 38 947
[25] Kelly P J, Arnell R D 2000 Vacuum 56 159Google Scholar
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