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A new environmental friendly silver front contact paste for crystalline silicon solar cells

机译:一种用于晶体硅太阳能电池的新型环保银正面接触膏

摘要

This paper reports a new environmental friendly silver front contact paste for crystalline silicon solar cells. Quasi-spherical and high-dispersive silver particles were prepared from silver nitrate in hot ethylene glycol. Polyvinylpirrolidone (PVP) as a protective agent was added into the reduction system. Moreover, Bi-based glass frit powders with glass transition temperature (Tg) of 385 °C were prepared by traditional melting route. The silver front contact paste for crystalline silicon solar cells was prepared using the as-prepared superfine silver particles and Bi-based glass frit powders. The microstructures of the conductive silver thick films were investigated, which indicated that the wetting behavior and etching effect of the glass frit on silicon nitride and silicon were efficient. Besides, silver particles were sintered well with the help of the glass frit during firing processing. The fabricated solar cell containing the Bi-based glass frit as an inorganic binder showed higher Fill Factor (FF) and electrical conversion efficiency (Eff) when compared with those of the solar cell fabricated with commercial Pb-based glass frit. In short, synthesis of silver particles in hot liquid polyols is a useful method for preparing superfine and high-dispersive particles. Moreover, the Bi-based glass frit could be a suitable substitute for Pb-based glass frit for preparing environmental friendly front-side silver paste for crystalline silicon solar cells.
机译:本文报道了一种用于晶体硅太阳能电池的新型环保银前接触膏。由硝酸银在热乙二醇中制得准球形和高分散性的银粒子。将聚乙烯吡咯烷酮(PVP)作为保护剂添加到还原系统中。此外,通过传统的熔融路线制备了玻璃化转变温度(Tg)为385℃的Bi-基玻璃粉粉末。使用所制备的超细银颗粒和Bi基玻璃粉粉末制备用于晶体硅太阳能电池的银前接触浆料。研究了导电银厚膜的微观结构,表明该玻璃料对氮化硅和硅的润湿行为和蚀刻效果是有效的。此外,在烧制过程中,借助于玻璃粉将银颗粒很好地烧结。与使用市售的Pb基玻璃粉制造的太阳能电池相比,所制造的包含Bi基玻璃粉作为无机粘合剂的太阳能电池显示出更高的填充因子(FF)和电转换效率(Eff)。简而言之,在热的液体多元醇中合成银颗粒是制备超细和高分散性颗粒的有用方法。此外,Bi基玻璃料可以替代Pb基玻璃料,以制备用于晶体硅太阳能电池的环保正面银浆。

著录项

  • 作者

    Che Q; Yang H; Lu L; Wang Y;

  • 作者单位
  • 年度 2013
  • 总页数
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类

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