• DocumentCode
    3516781
  • Title

    Comparison between passivation properties of thermal ald Al2O3 deposited with TMA+ O3 and TMA+ H2O

  • Author

    Zhengyue Xia ; Dong, Jingbing ; Li, Xiaoqiang ; Ren, Changrui ; Sidhu, Rubin ; Song, Wentao ; Tao, Longzhong ; Yang, Zhuojian ; Zhang, Bin ; Xing, Guoqiang

  • Author_Institution
    Hareon Solar Technol. Co., Ltd., Jiangyin, China
  • fYear
    2012
  • fDate
    3-8 June 2012
  • Abstract
    ALD Al2O3 can work as excellent passivation dielectric for both p- and n-type c-Si solar cells. In this paper we have demonstrated that ALD Al2O3 passivation properties are dependent on the reactants. Al2O3 synthesized by thermal ALD with TMA+ O3 is a robust candidate to be integrated into both high-temperature (screen printed) with Seff of 1.4 cm/s and low-temperature with Seff of 0.9 cm/s (such as LFC) metallization process flows for c-Si solar cells. Combined with Dit and Qtotal results, we believe a large number of oxygen dangling bonds (O DBs) at c-Si/ Al2O3 interface are the critical factor for restructuring interfacial SiOx during post deposition thermal treatment, and in turn improve passivation properties. However Al2O3 with reactants of TMA+ H2O may be only suitable for low temperature metallization process, as hydrogen which passivates O DBs will escape and make O DBs active during the thermal process, which causes passivation properties to degrade.
  • Keywords
    metallisation; passivation; solar cells; low-temperature; metallization process flows; oxygen dangling bonds; passivation dielectric; passivation properties; post deposition thermal treatment; thermal ALD; thermal atomic layer deposition; Annealing; Electron tubes; Firing; Passivation; Photovoltaic cells; Robustness; Thermal analysis; Crystalline silicon solar cells; passivation;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Photovoltaic Specialists Conference (PVSC), 2012 38th IEEE
  • Conference_Location
    Austin, TX
  • ISSN
    0160-8371
  • Print_ISBN
    978-1-4673-0064-3
  • Type

    conf

  • DOI
    10.1109/PVSC.2012.6317808
  • Filename
    6317808