Improved Si/SiOx interface passivation by ultra-thin tunneling oxide layers prepared by rapid thermal oxidation

被引:16
作者
Gad, Kerim M. [1 ]
Voessing, Daniel [1 ]
Balamou, Patrice [2 ,3 ]
Hiller, Daniel [1 ]
Stegemann, Bert [2 ]
Angermann, Heike [3 ]
Kasemann, Martin [1 ]
机构
[1] Univ Freiburg, Dept Microsyst Engn IMTEK, D-79110 Freiburg, Germany
[2] Univ Appl Sci, HTW Berlin, D-12459 Berlin, Germany
[3] Inst Photovolta, Helmholtz Zentrum Berlin Mat & Energie HZB, D-12489 Berlin, Germany
关键词
Silicon oxide-nanolayer; Tunnel oxide; Surface photo voltage measurement; Interface state density; Rapid thermal oxidation; effective minority carrier lifetime; SURFACE-MORPHOLOGY; SILICON INTERFACES; PLASMA OXIDATION; SI-SURFACES; SOLAR-CELL; SIO2/SI(100); RELIABILITY; DEPENDENCE; CONTACTS; STATE;
D O I
10.1016/j.apsusc.2015.07.060
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
We analyze the influence of different oxidation methods on the chemical passivation quality of silicon oxide-nanolayers on crystalline silicon wafers with surface photo voltage and quasi-steady-state photo conductance measurements. We present a simple method by means of rapid thermal oxidation (RTO) and subsequent annealing in forming gas, which requires no complex surface pre-treatment or surface pre-conditioning after cleaning. This technique allows a reproducible preparation of high-quality ultrathin oxide-nanolayers (1.3-1.6 nm) with a nearly intrinsic energetic distribution of interface states and a defect density of states of only 1 x 10(12) cm(-2) eV(-1) at the minimum of the distribution. These results are compared with silicon oxide-nanolayers prepared by wet chemical oxidation and plasma oxidation where only a slight reduction of the interface defect density is achieved by subsequent anneal in forming gas environment. Furthermore, it is shown that applying the RTO oxide-nanolayer as an intermediate layer between Si and an a-SiNx:H layer, leads to a significant improvement of the surface passivation quality. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:1269 / 1276
页数:8
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