TY - JOUR
T1 - In Situ Growth of a Robust 1D Capping Layer for Stable and Efficient CsPbI3 Perovskite Solar Cells Without Hole Transporter
AU - Wang, Hailiang
AU - Song, Yongfa
AU - Lin, Zedong
AU - Li, Weiping
AU - Liu, Huicong
AU - Wei, Xiaozhen
AU - Zhang, Qixian
AU - Lv, Chunyu
AU - Zhu, Liqun
AU - Wang, Kexiang
AU - Lan, Yisha
AU - Wang, Lan
AU - Lin, Changqing
AU - Yin, Penggang
AU - Song, Tinglu
AU - Bai, Yang
AU - Chen, Qi
AU - Yang, Shihe
AU - Chen, Haining
N1 - Publisher Copyright:
© 2024 Wiley-VCH GmbH.
PY - 2024/4/26
Y1 - 2024/4/26
N2 - CsPbI3 perovskite is a promising light absorber in perovskite solar cells (PSCs) due to its suitable bandgap (Eg) and high chemical stability, but the perovskite phase is metastable in ambient atmosphere and prone to defect formation. To enhance phase stability and reduce defects, forming a low dimensional (LD) perovskite on CsPbI3 has proved effective. However, the energy levels for most of low-conductivity LD perovskites are not very compatible with those of CsPbI3, which will impair charge separation and device performance. Herein, a new 1D perovskite (5-Azaspiro[4.4]nonan-5-ium lead triiodide, ASNPbI3) with compatible energy levels and a large Eg is reported as a capping layer. The p-type ASNPbI3 forms a p-n heterojunction with n-CsPbI3 with a staggered band alignment, considerably enhancing the carrier separation. Besides, by pre-forming a ASNPbI3 at an intermediate stage, defects are suppressed in perovskite film. Consequently, the CsPbI3 PSCs based on carbon electrode without hole transporter (C-PSCs) achieves a PCE of 18.34%, which is among the highest-reported values for inorganic C-PSCs. Furthermore, the hydrophobic ASNPbI3 capping layer has a high thermal stability that greatly enhances perovskite phase stability. Hence, the CsPbI3 C-PSCs maintains 68% of its initial PCE after 400 h aging at 85°C in a N2 glovebox.
AB - CsPbI3 perovskite is a promising light absorber in perovskite solar cells (PSCs) due to its suitable bandgap (Eg) and high chemical stability, but the perovskite phase is metastable in ambient atmosphere and prone to defect formation. To enhance phase stability and reduce defects, forming a low dimensional (LD) perovskite on CsPbI3 has proved effective. However, the energy levels for most of low-conductivity LD perovskites are not very compatible with those of CsPbI3, which will impair charge separation and device performance. Herein, a new 1D perovskite (5-Azaspiro[4.4]nonan-5-ium lead triiodide, ASNPbI3) with compatible energy levels and a large Eg is reported as a capping layer. The p-type ASNPbI3 forms a p-n heterojunction with n-CsPbI3 with a staggered band alignment, considerably enhancing the carrier separation. Besides, by pre-forming a ASNPbI3 at an intermediate stage, defects are suppressed in perovskite film. Consequently, the CsPbI3 PSCs based on carbon electrode without hole transporter (C-PSCs) achieves a PCE of 18.34%, which is among the highest-reported values for inorganic C-PSCs. Furthermore, the hydrophobic ASNPbI3 capping layer has a high thermal stability that greatly enhances perovskite phase stability. Hence, the CsPbI3 C-PSCs maintains 68% of its initial PCE after 400 h aging at 85°C in a N2 glovebox.
KW - CsPbI perovskite
KW - carbon electrode
KW - low dimensional perovskite
KW - p-n heterojunction
KW - phase stability
UR - http://www.scopus.com/inward/record.url?scp=85183359262&partnerID=8YFLogxK
U2 - 10.1002/aenm.202304038
DO - 10.1002/aenm.202304038
M3 - Article
AN - SCOPUS:85183359262
SN - 1614-6832
VL - 14
JO - Advanced Energy Materials
JF - Advanced Energy Materials
IS - 16
M1 - 2304038
ER -