Abstract
Hydrogenated nanocrystalline silicon (nc‐Si:H) or hydrogenated nanocrystalline silicon oxide (nc‐SiOx:H) as window layers have ample potential to improve the short‐circuit current density (JSC) of silicon heterojunction (SHJ) solar cells due to their wide optical bandgap. However, the growth of their nanocrystals within a 20 nm‐thickness on intrinsic hydrogenated amorphous silicon (i‐a‐Si:H) poses a challenge. Plasma treatment (PT) after i‐a‐Si:H deposition is usually used to improve passivation performance. Herein, the i/p interface is subjected to CO2 PT: a 20 s post CO2 PT is proven to be beneficial in obtaining improved passivation performance. This can be achieved by activated hydrogen which can be diffused to the wafer surface and can saturate the dangling bonds on it. Extending the CO2 PT time from 20 to 40 s, the oxygen (O) insertion into i‐a‐Si:H starts to increase slowly, which leads to marginal change of microstructure in the p layer. Strained SiSi bonds by oxygen incorporation into the a‐Si:H network generate nucleation sites and consequently accelerate the nucleation of p‐nc‐Si:H on i‐a‐Si:H. Finally, it is demonstrated that the power conversion efficiency (PCE) of planar SHJ solar cells is enhanced from 12.65% to 19.06% by a 20 s CO2 PT at the i/p interface.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
More From: physica status solidi (RRL) – Rapid Research Letters
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.