TY - JOUR
T1 - Reducing energy loss and stabilising the perovskite/poly (3-hexylthiophene) interface through a polyelectrolyte interlayer
AU - Zhang, Wenxiao
AU - Wan, Li
AU - Fu, Sheng
AU - Li, Xiaodong
AU - Fang, Junfeng
N1 - Publisher Copyright:
© 2020 The Royal Society of Chemistry.
PY - 2020/4/14
Y1 - 2020/4/14
N2 - Efficient hole transport materials in n-i-p structured perovskite solar cells (PSCs) have been confined to 2,2′,7,7′-tetrakis(N,N-di-p-methoxyphenylamine)-9,9′-spirobifluorene (Spiro-OMeTAD) and poly(triarylamine) (PTAA). However, the need for hygroscopic dopants has limited improvements in the stability of the devices. Here, we have successfully fabricated stable PSCs using a dopant-free poly (3-hexylthiophene) (P3HT) HTL. Through introducing a polyelectrolyte buffer layer (P3CT-BN), the P3HT film morphology, perovskite built-in electric field, surficial defects and the hole transfer speed were all optimized, along with significant suppression of interfacial recombination. Hence, the efficiency was improved from 13.13% to 19.23%, with a substantially improved VOC from 0.90 V to 1.10 V and FF from 63.1% to 74.2%. Simultaneously, the un-encapsulated devices also exhibited improved stability, retaining 80% of the peak PCE in the atmosphere (50% relative humidity) for 2300 h or heating at 85 °C in N2 for 400 h and 79% of the original PCE under simultaneous damp heat (60 °C/60-70% humidity) in air.
AB - Efficient hole transport materials in n-i-p structured perovskite solar cells (PSCs) have been confined to 2,2′,7,7′-tetrakis(N,N-di-p-methoxyphenylamine)-9,9′-spirobifluorene (Spiro-OMeTAD) and poly(triarylamine) (PTAA). However, the need for hygroscopic dopants has limited improvements in the stability of the devices. Here, we have successfully fabricated stable PSCs using a dopant-free poly (3-hexylthiophene) (P3HT) HTL. Through introducing a polyelectrolyte buffer layer (P3CT-BN), the P3HT film morphology, perovskite built-in electric field, surficial defects and the hole transfer speed were all optimized, along with significant suppression of interfacial recombination. Hence, the efficiency was improved from 13.13% to 19.23%, with a substantially improved VOC from 0.90 V to 1.10 V and FF from 63.1% to 74.2%. Simultaneously, the un-encapsulated devices also exhibited improved stability, retaining 80% of the peak PCE in the atmosphere (50% relative humidity) for 2300 h or heating at 85 °C in N2 for 400 h and 79% of the original PCE under simultaneous damp heat (60 °C/60-70% humidity) in air.
UR - https://www.scopus.com/pages/publications/85083104596
U2 - 10.1039/d0ta01860k
DO - 10.1039/d0ta01860k
M3 - 文章
AN - SCOPUS:85083104596
SN - 2050-7488
VL - 8
SP - 6546
EP - 6554
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
IS - 14
ER -