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NH₄F缓冲HF溶液中硅纳米线的三维蚀刻轮廓和表面形态(通过衰减全反射傅里叶变换红外光谱法):双钝化模型

Three-dimensional etching profiles and surface speciations (via attenuated total reflection-fourier transform infrared spectroscopy) of silicon nanowires in NH4F-buffered HF solutions: a double passivation model.

作者信息

Teo Boon K, Chen W W, Sun X H, Wang S D, Lee S T

机构信息

Department of Chemistry, University of Illinois at Chicago, 845 West Taylor Street, Chicago, Illinois 60607, USA.

出版信息

J Phys Chem B. 2005 Nov 24;109(46):21716-24. doi: 10.1021/jp052984q.

Abstract

A systematic study of the etching behavior, in terms of three-dimensional profiles, of one-dimensional (1-D) silicon nanowires (SiNWs) in NH(4)F-buffered hydrofluoric acid (BHF) solutions of varying concentrations and pH values and the surface speciations of the resulting etched SiNW surfaces, as characterized by attenuated total reflection-Fourier transform infrared (ATR-FTIR) spectroscopy, is reported. It was found that SiNWs are stable only in relatively narrow pH ranges of the BHF solutions. The results are rationalized in terms of a "double passivation" model. When SiNWs are etched in BHF solutions with pH values of 1-3, the surfaces are passivated with hydrogen (inner layer) giving rise to surface moieties such as Si-H(x) species (x = 1-3); at high HF concentrations, the H-terminated Si surfaces are covered with a hydrogen bonding network of HF and related molecules (oligomers, etc.), providing an outer-layer passivation. When SiNWs are etched in BHF solutions with pH values of 11-14 (by adding a strong base such as NaOH), the surfaces are oxygen-terminated with surface moieties such as Si-(O(-))(x)() species (x = 1-3); at high NH(4)F concentrations, the negatively charged Si surfaces are stabilized by NH(4)(+) ions via ionic bonding, again providing outer-layer passivation. In BHF solutions with pH values of 3-11, the surface speciation, consisting of Si-(OH)(x)(O(-))(y) (x + y = 1-3) species, is unstable and etched away rapidly. The surface speciations of SiNWs etched in various BHF solutions were explored via ATR-FTIR spectroscopy. It was found that, while etching SiNWs with HF-rich BHF solutions with pH < 4 gave rise to Si-H(x)() surface species, no surface Si-H(x) species were observed with SiNWs etched in BHF solutions with pH >/= 4 (HF/NH(4)F </= 1:1). In sharp contrast, etching of two-dimensional (2-D) Si wafers with either HF, NH(4)F, or BHF etchants produces Si-H(x) species on the surface. Finally, while HF is a much more efficient etchant than NH(4)F for 2-D Si surfaces, NH(4)F is found to be as efficient an etchant as HF for SiNWs (this work). We believe that these differences can be attributed to the nanometer size (corresponding to the roughness scale in 2-D wafers) of SiNWs on one hand and the lack of "passivation" by the hydrogen bonding network of HF and related molecules at pH >/= 4 on the other. These two factors, among others, contribute to the rapid hydrolysis of the surface Si-H(x)() species (and the etching of the SiNWs), particularly in BHF solutions with low HF/NH(4)F ratios and high pH values (pH >/= 4).

摘要

本文报道了一项系统研究,该研究通过三维轮廓来考察一维(1-D)硅纳米线(SiNWs)在不同浓度和pH值的NH₄F缓冲氢氟酸(BHF)溶液中的蚀刻行为,以及通过衰减全反射-傅里叶变换红外(ATR-FTIR)光谱表征的蚀刻后SiNW表面的表面形态。研究发现,SiNWs仅在BHF溶液相对较窄的pH范围内稳定。研究结果依据“双重钝化”模型进行了合理解释。当SiNWs在pH值为1 - 3的BHF溶液中蚀刻时,表面被氢(内层)钝化,产生诸如Si-Hₓ(x = 1 - 3)物种的表面部分;在高HF浓度下,H端终止的Si表面被HF和相关分子(低聚物等)的氢键网络覆盖,提供外层钝化。当SiNWs在pH值为11 - 14的BHF溶液中蚀刻(通过添加强碱如NaOH)时,表面被氧端终止,产生诸如Si-(O⁻)ₓ(x = 1 - 3)物种的表面部分;在高NH₄F浓度下,带负电荷的Si表面通过NH₄⁺离子通过离子键稳定,再次提供外层钝化。在pH值为3 - 11的BHF溶液中,由Si-(OH)ₓ(O⁻)ᵧ(x + y = 1 - 3)物种组成的表面形态不稳定且迅速被蚀刻掉。通过ATR-FTIR光谱探索了在各种BHF溶液中蚀刻的SiNWs的表面形态。研究发现,虽然用pH < 4的富含HF的BHF溶液蚀刻SiNWs会产生Si-Hₓ表面物种,但在pH≥4(HF/NH₄F≤1:1)的BHF溶液中蚀刻的SiNWs未观察到表面Si-Hₓ物种。形成鲜明对比的是,用HF、NH₄F或BHF蚀刻剂蚀刻二维(2-D)硅片会在表面产生Si-Hₓ物种。最后,虽然对于二维Si表面,HF比NH₄F是更有效的蚀刻剂,但发现NH₄F对于SiNWs是与HF一样有效的蚀刻剂(本研究)。我们认为,这些差异一方面可归因于SiNWs的纳米尺寸(对应于二维硅片中的粗糙度尺度),另一方面可归因于在pH≥4时缺乏HF和相关分子的氢键网络的“钝化”。这两个因素以及其他因素导致表面Si-Hₓ物种的快速水解(以及SiNWs的蚀刻),特别是在低HF/NH₄F比和高pH值(pH≥4)的BHF溶液中。

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