TY - JOUR
T1 - Investigation of crystalline silicon surface passivation by positively charged POx/Al2O3 stacks
AU - Black, L.E.
AU - Kessels, W.M.M.
PY - 2018/10/1
Y1 - 2018/10/1
N2 - We investigate the passivation of crystalline Si (c-Si) surfaces by phosphorus oxide (POx) thin films deposited in an atomic layer deposition (ALD) reactor and capped in-situ by ALD Al2O3. Passivation is demonstrated on both n- and p-type (100) Si surfaces, and for POx/Al2O3 stacks deposited at both 25 °C and 100 °C. In contrast to Al2O3 alone, POx/Al2O3 passivation is activated already by annealing at temperatures as low as 250 °C in N2 in all cases. Best results were obtained after annealing at 350 °C and 450 °C for films deposited at 25 °C and 100 °C respectively, with similar implied open-circuit voltages of 723 and 724 mV on n-type (100) Si. In the latter case an outstandingly low surface recombination velocity of 1.7 cm/s and saturation current density of 3.3 fA/cm2 were obtained on 1.35 Ω cm material. Passivation of p-type Si appeared somewhat poorer, with surface recombination velocity of 13 cm/s on 2.54 Ω cm substrates. Passivation was found to be independent of POx film thickness for films of 4 nm and above, and was observed to be stable during prolonged annealing up to 500 °C. This excellent passivation performance on n-type Si is attributed partly to an unusually large positive fixed charge in the range of 3–5 × 1012 cm−2 (determined from capacitance–voltage measurements) for stacks deposited at both temperatures, which is significantly larger than that exhibited by existing positively charged passivation materials such as SiNx. Indeed, passivation performance on n-type silicon is shown to compare favourably to state-of-the-art results reported for PECVD SiNx. POx/Al2O3 stacks thus represent a highly effective positively charged passivation scheme for c-Si, with potential for n-type surface passivation and selective doping applications.
AB - We investigate the passivation of crystalline Si (c-Si) surfaces by phosphorus oxide (POx) thin films deposited in an atomic layer deposition (ALD) reactor and capped in-situ by ALD Al2O3. Passivation is demonstrated on both n- and p-type (100) Si surfaces, and for POx/Al2O3 stacks deposited at both 25 °C and 100 °C. In contrast to Al2O3 alone, POx/Al2O3 passivation is activated already by annealing at temperatures as low as 250 °C in N2 in all cases. Best results were obtained after annealing at 350 °C and 450 °C for films deposited at 25 °C and 100 °C respectively, with similar implied open-circuit voltages of 723 and 724 mV on n-type (100) Si. In the latter case an outstandingly low surface recombination velocity of 1.7 cm/s and saturation current density of 3.3 fA/cm2 were obtained on 1.35 Ω cm material. Passivation of p-type Si appeared somewhat poorer, with surface recombination velocity of 13 cm/s on 2.54 Ω cm substrates. Passivation was found to be independent of POx film thickness for films of 4 nm and above, and was observed to be stable during prolonged annealing up to 500 °C. This excellent passivation performance on n-type Si is attributed partly to an unusually large positive fixed charge in the range of 3–5 × 1012 cm−2 (determined from capacitance–voltage measurements) for stacks deposited at both temperatures, which is significantly larger than that exhibited by existing positively charged passivation materials such as SiNx. Indeed, passivation performance on n-type silicon is shown to compare favourably to state-of-the-art results reported for PECVD SiNx. POx/Al2O3 stacks thus represent a highly effective positively charged passivation scheme for c-Si, with potential for n-type surface passivation and selective doping applications.
KW - Atomic layer deposition
KW - Crystalline silicon
KW - Solar cells
KW - Surface passivation
UR - http://www.scopus.com/inward/record.url?scp=85047922886&partnerID=8YFLogxK
U2 - 10.1016/j.solmat.2018.05.007
DO - 10.1016/j.solmat.2018.05.007
M3 - Article
AN - SCOPUS:85047922886
SN - 0927-0248
VL - 185
SP - 385
EP - 391
JO - Solar Energy Materials and Solar Cells
JF - Solar Energy Materials and Solar Cells
ER -