...
首页> 外文期刊>ACS applied materials & interfaces >In Situ-Doped Silicon Thin Films for Passivating Contacts by Hot-Wire Chemical Vapor Deposition with a High Deposition Rate of 42 nm/min
【24h】

In Situ-Doped Silicon Thin Films for Passivating Contacts by Hot-Wire Chemical Vapor Deposition with a High Deposition Rate of 42 nm/min

机译:在原位掺杂的硅薄膜通过热线化学气相沉积钝化触点,具有42nm / min的高沉积速率

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Hot-wire chemical vapor deposition was used to deposit in situ-doped amorphous silicon layers for poly-Si/ SiOx passivating contacts at a high deposition rate of 42 nm/ min. We investigated the influence of a varied phosphine gas (PH3) concentration during deposition on (i) the silicon film properties and (ii) the passivating contact performances. The microstructural film properties were characterized before and after a high-temperature crystallization step to transform amorphous silicon films into polycrystalline silicon films. Before crystallization, the silicon layers become less dense as the PH3 concentrations increase. After crystallization, an increasing domain size is derived for higher PH3 concentrations. Sheet resistance is found to decrease as domain size increased, and the correlation between mobility and domain size was discussed. The performances of the passivating contact were measured, and a firing stable open circuit voltage of 732 mV, a contact resistivity of 8.1 m Omega.cm(2), and a sheet resistance of 142 Omega/square could be achieved with the optimized PH3 concentration. In addition, phosphorous doping tails into the crystalline silicon were extracted to evaluate the Auger recombination of the passivating contact.
机译:使用热线化学气相沉积以以42nm / min的高沉积速率沉积在原位掺杂的非晶硅层中,用于聚-Si / SiOx钝化触点。我们研究了在沉积期间(i)硅膜特性和(ii)钝化接触性能期间的不同磷气(pH3)浓度的影响。在高温结晶步骤之前和之后的微观结构膜特性以将非晶硅膜转化为多晶硅膜。在结晶之前,随着PH3浓度的增加,硅层变得较少。结晶后,衍生出增加的pH3浓度的域尺寸。发现薄层电阻降低随域尺寸增加,并且讨论了迁移率和域大小之间的相关性。测量钝化触点的性能,并通过优化的pH3浓度来实现8.1MΩcm(2)的接触电阻率的燃烧稳定的开路电压,达到8.1MΩ·厘米(2)的接触电阻率和142ω/平方的薄层电阻。此外,提取磷掺杂尾部进入晶体硅中,以评估钝化接触的螺旋螺旋形。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号