Interfacial energetics of silicon in contact with 11 M NH4F(aq), buffered HF(aq), 27 m HF(aq), and 18 M H2SO4

被引:7
|
作者
Michalak, David J.
Gstrein, Florian
Lewis, Nathan S.
机构
[1] CALTECH, Div Chem & Chem Engn, Beckman Inst, Pasadena, CA 91125 USA
[2] CALTECH, Div Chem & Chem Engn, Kavli Nanosci Inst, Pasadena, CA 91125 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2007年 / 111卷 / 44期
关键词
D O I
10.1021/jp074971d
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Open-circuit impedance spectra, channel impedance spectroscopy on solution-gated field-effect devices, and differential capacitance vs potential (Mott - Schottky) measurements were used to determine the energetics of n-Si(111) n-Si(111), and p-Si(111) electrodes in contact with aqueous 11 M (40% by weight) NH4F, buffered HF (BHF), 27 M (48%) HF(aq), and concentrated (18 M) H2SO4. A Mott - Schottky analysis of A(s)(2)C(sc)(-2)-vs-E (where A(s) is the interfacial area, and C-x is the differential capacitance as a function of the electrode potential, E) data yielded reliable barrier heights for some silicon/liquid contacts in this work. Performing a Mott - Schottky analysis, however, requires measurement of the differential capacitance under reverse bias, where oxidation or etching can occur for n-Si and where electroplating of metal contaminants can occur for p-Si. Hence, open-circuit methods would offer desirable, complementary approaches to probing the energetics of such contacts. Accordingly, open-circuit, near-surface channel conductance measurements have been performed using solution-gated n(+)-p-Si(111)-n(+) and p(+)-n-Si(100)-p(+) devices. Additionally, open-circuit impedance spectra were obtained for silicon electrodes in contact with these solutions. The combination of the three techniques indicated that the surfaces of n-Si(111) and n-Si(100) were under accumulation when in contact with either 11 M NH4F(aq) or BHF(aq). The barrier heights for n-Si(111) and n-Si(100) in 11 M NH4F(aq) were -0.065 +/- 0.084 V and -0.20 +/- 0.21 V, respectively, and were -0.03 +/- 0. 19 V and -0.07 +/- 0.24 V, respectively, for these surfaces in contact with buffered HF(aq). Consistently, p-Si(111) surfaces were determined to be in inversion in contact with these electrolytes, exhibiting barrier heights of 0.984 +/- 0.078 V in contact with 11 M NH4F(aq) and 0.97 +/- 0.22 V in contact with buffered HF(aq). In contact with 27 M HF(aq), n-Si(111) and n-Si(111) were in depletion, with barrier heights of 0.577 +/- 0.038 V and 0.400 +/- 0.057 V, respectively, and p-Si(111) was under inversion with a barrier height of 0.856 +/- 0.076 V. Measurements performed in 18 M H2SO4 revealed barrier heights of 0.75 +/- 0.11 V, 0.696 +/- 0.043 V, and 0.889 +/- 0.018 V for n-Si(111), n-Si(100), and p-Si(111), respectively, demonstrating that in 18 M H2SO4, the band edge positions of Si were different for different doping types. The barrier height data demonstrate that the observed low recombination rates of silicon in contact with 11 M NH4F, BHF, or 18 M H2SO4 cannot necessarily be attributed to a reduction in the number of surface trap states. In part, low surface recombination rates are expected for such systems because the very large or very small barrier height for silicon in contact with these liquids provides a potential barrier that prevents one type of photogenerated carrier (either electrons or holes) from reaching the surface, thereby producing a low steady-state surface recombination rate.
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收藏
页码:16516 / 16532
页数:17
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