Improvement Of Effective Lifetime Research Articles

Investigating the degradation behaviours of n+-doped Poly-Si passivation layers: An outlook on long-term stability and accelerated recovery

In this article, we study the kinetics of firing-activated degradation and recovery of industrially processed n + -doped poly-Si on thin oxide passivation layers subjected to illuminated annealing at elevated temperatures. The impact of a comprehensive range of fast-firing conditions on the subsequent degradation and recovery were assessed. The results indicate that the recovery process is dependent on the peak firing temperature, where higher temperatures led to an improvement in effective lifetime of up to 20% compared to the pre-fired state, and a very low surface dark saturation current density of 2.9 fA/cm 2 . By cycling through light soaking and dark anneal conditions, we show that unlike the commonly studied boron-oxygen light-induced degradation (BO-LID) and light- and elevated temperature-induced degradation (LeTID), this newly observed instability in n + -doped poly-Si passivation layers is not reversible, that is, once a degradation/recovery cycle is completed, the lifetime remains very stable under subsequent light soaking. This indicates that the surface related instability may be able to be completely resolved following the completion of the first degradation/recovery cycle. With this in mind, we investigate the potential for high intensity laser illumination (up to 150 kW/m 2 ) to rapidly increase the recovery rates, however, this does not seem sufficient to cycle through degradation and recovery on a timescale that is amenable with mass production. The mitigation of any potential instabilities at the poly-Si interface has significant implications for the reliability of n-type tunneling oxide passivated contact (TOPCon) solar cells. • Firing conditions have a significant impact in stability of polysilicon passivation. • The firing-induced surface instability is different to previous degradation modes. • Cycling between degraded and recovered states does not occur.

Improved Passivation of a-Si:H / c-Si Interfaces Through Film Restructuring

ABSTRACTThe as-deposited passivation quality of amorphous silicon films on crystalline silicon surfaces is dependent on deposition conditions and resulting hydrogen bonding structure. However the initial surface passivation can be significantly improved by low temperature post-deposition anneal. For example an improvement in effective lifetime from 780 μsec as-deposited to 2080 μsec post-anneal is reported in the present work. This work probes the hydrogen bonding environment using monolayer resolution Brewster angle transmission Fourier transform infrared spectroscopy of 100 Å thick films. It is found that there is significant restructuring at the a-Si:H / c-Si interface upon annealing and a gain of mono-hydride bonding at the c-Si surface is detected. Calculations show an additional 3.56 − 4.50 × 1014 cm−2 mono-hydride bonding at c-Si surface due to annealing. The estimation of the surface hydride oscillator strength in transmission mode is reported for the first time to be 7.2 × 10−18 cm on Si (100) surface and 7.5 × 10−18 cm on Si (111).