材料科学
硅
光电子学
非晶硅
钝化
异质结
无定形固体
掺杂剂
图层(电子)
兴奋剂
晶体硅
纳米技术
有机化学
化学
作者
Julie Dréon,Quentin Jeangros,Jean Cattin,Jan Haschke,Luca Antognini,Christophe Ballif,Mathieu Boccard
出处
期刊:Nano Energy
[Elsevier]
日期:2020-04-01
卷期号:70: 104495-104495
被引量:211
标识
DOI:10.1016/j.nanoen.2020.104495
摘要
Interest in silicon heterojunction solar cells is growing due to their manufacturing simplicity and record efficiencies. However, a significant limitation of these devices still stems from parasitic light absorption in the amorphous silicon layers. This can be mitigated by replacing the traditional (p) and (n) doped amorphous silicon selective layers by other materials. While promising results have been achieved using molybdenum oxide (MoOx) as a front-side hole-selective layer, charge transport mechanisms in that contact stack have remained elusive and device efficiencies below predictions. We carefully analyze the influence of the MoOx and intrinsic a-Si:H thicknesses on current-voltage properties and discuss transport and performance-loss mechanisms. In particular, we find that thinning down the MoOx and (i)a-Si:H layers (down to 4 nm and 6 nm respectively) mitigates parasitic sub-bandgap MoOx optical absorption and drastically enhances charge transport, while still providing excellent passivation and selectivity. High-resolution transmission microscopy reveals that such thin MoOx layer remains continuous and, while slightly sub-stoechiometric, exhibits a chemistry close to MoO3. A screen-printed device reaching a certified efficiency of 23.5% and a fill factor of 81.8% is demonstrated, bridging the gap with traditional Si-based contacts and demonstrating that dopant-free selective contacts can rival traditional approaches.
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