TY - GEN
T1 - Functional Interface Passivation of Hybrid PEDOT:PSS Silicon Solar Cells via Silicon Hydrosilylation
AU - Lin, Chi Te
AU - Li, You Lan
AU - Chang, Yu Chun
AU - Lin, Bo Hua
AU - Meng, Hsin Fei
AU - Yu, Peichen
N1 - Publisher Copyright:
© 2020 IEEE.
Copyright:
Copyright 2021 Elsevier B.V., All rights reserved.
PY - 2020/6/14
Y1 - 2020/6/14
N2 - Hybrid PEDOT:PSS-silicon heterojunction solar cells have the advantages of low temperature, low cost and solution process. However, as a low-quality native oxide layer can easily form on the surface of silicon substrates, the hybrid solar cells still suffer from charged carrier recombination at the defective interface, hence affecting the device characteristics. In this work, we employ a thermally induced silicon hydrosilylation technique to form a self-assembled monolayer(SAM) on the hydrogen-terminated silicon substrate, in order to prevent the oxidation and passivate the surface of silicon. The quality of this monolayer passivation is characterized by the contact angle, X-ray photoelectron spectroscopy (XPS) analyses. We have found that the SAM passivation can effectively reduce the contact resistance between silicon and the aluminum electrode, leading to an improved open-circuit voltage and fill-factor. However, as the silicon surface with the SAM passivation becomes hydrophobic, it is difficult to apply aqueous PEDOT:PSS solution onto silicon. Therefore, we further apply a low-damage oxygen plasma treatment to modify the terminal functional group of the monolayer to form a hydrophilic surface. The power conversion efficiency of the modified devices is between 10-12%. Although the PCE does not surpass the reference device due to possible chemical reactions between the PEDOT:PSS and SAM, the proposed low- damage oxygen-plasma treatment provide a viable solution for modifying the functional passivation of hybrid PEDOT:PSS silicon solar cells using SAMs.
AB - Hybrid PEDOT:PSS-silicon heterojunction solar cells have the advantages of low temperature, low cost and solution process. However, as a low-quality native oxide layer can easily form on the surface of silicon substrates, the hybrid solar cells still suffer from charged carrier recombination at the defective interface, hence affecting the device characteristics. In this work, we employ a thermally induced silicon hydrosilylation technique to form a self-assembled monolayer(SAM) on the hydrogen-terminated silicon substrate, in order to prevent the oxidation and passivate the surface of silicon. The quality of this monolayer passivation is characterized by the contact angle, X-ray photoelectron spectroscopy (XPS) analyses. We have found that the SAM passivation can effectively reduce the contact resistance between silicon and the aluminum electrode, leading to an improved open-circuit voltage and fill-factor. However, as the silicon surface with the SAM passivation becomes hydrophobic, it is difficult to apply aqueous PEDOT:PSS solution onto silicon. Therefore, we further apply a low-damage oxygen plasma treatment to modify the terminal functional group of the monolayer to form a hydrophilic surface. The power conversion efficiency of the modified devices is between 10-12%. Although the PCE does not surpass the reference device due to possible chemical reactions between the PEDOT:PSS and SAM, the proposed low- damage oxygen-plasma treatment provide a viable solution for modifying the functional passivation of hybrid PEDOT:PSS silicon solar cells using SAMs.
KW - photovoltaic cells
KW - self-assemble monolayer
KW - thermally induce hydrosilation
UR - http://www.scopus.com/inward/record.url?scp=85099579030&partnerID=8YFLogxK
U2 - 10.1109/PVSC45281.2020.9300835
DO - 10.1109/PVSC45281.2020.9300835
M3 - Conference contribution
AN - SCOPUS:85099579030
T3 - Conference Record of the IEEE Photovoltaic Specialists Conference
SP - 618
EP - 620
BT - 2020 47th IEEE Photovoltaic Specialists Conference, PVSC 2020
PB - Institute of Electrical and Electronics Engineers Inc.
T2 - 47th IEEE Photovoltaic Specialists Conference, PVSC 2020
Y2 - 15 June 2020 through 21 August 2020
ER -