Electronic interface properties of silicon substrates after ozone based wet-chemical oxidation studied by SPV measurements

被引:20
作者
Angermann, Heike [1 ]
Wolke, Klaus [2 ]
Gottschalk, Christiane [3 ]
Moldovan, Ana [4 ]
Roczen, Maurizio [1 ]
Fittkau, Jens [3 ]
Zimmer, Martin [4 ]
Rentsch, Jochen [4 ]
机构
[1] Helmholtz Zentrum Berlin Mat & Energie GmbH, D-12489 Berlin, Germany
[2] Technol Consulting Wolke, D-75382 Althengstett, Germany
[3] MKS ASTex GmbH, D-13355 Berlin, Germany
[4] Fraunhofer ISE, D-79110 Freiburg, Germany
关键词
Silicon solar cell substrates; Ozone; Wet-chemical oxidation; H-termination; Surface photovoltage; Interface states; HYDROGEN TERMINATION; SURFACE-MORPHOLOGY; SI-SURFACES; PASSIVATION; OXIDE; CENTERS; SI(111); STATES; SPECTROSCOPY; DENSITY;
D O I
10.1016/j.apsusc.2012.03.170
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
The preparation of ultra-thin oxide layers on mono-crystalline silicon substrate surfaces with ozone dissolved in ultra pure water at ambient temperature was investigated as a low cost alternative to current wet-chemical cleaning and passivation processes in solar cell manufacturing. Surface photovoltage technique was applied as fast, nondestructive, and surface sensitive method, to provide detailed information about the influence of oxidation rate and substrate surface morphology on electronic properties of the oxidised silicon interfaces and subsequently prepared hydrogen terminated surfaces. Sequences of wet-chemical oxidation in ozone containing ultra pure water and subsequent oxide removal in diluted hydrofluoric acid solution could be utilised to prepare hydrophobic substrates, which are predominantly required as starting point for layer deposition and contact formation. On so prepared hydrogen-terminated substrates values of interface state densities D-it,D-min approximate to 5 x 10(11) eV(-1) cm(-2) could be achieved, comparable to values obtained on the same substrates by the standard RCA process followed by HF dip. (c) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:8387 / 8396
页数:10
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