TY - JOUR
T1 - Polymer synergy for efficient hole transport in solar cells and photodetectors
AU - Liu, Junwei
AU - Zhou, Zhihua
AU - Gao, Yuping
AU - Wu, Yin
AU - Wang, Jingjing
AU - Li, Haojin
AU - Wang, Qian
AU - Zhou, Kangkang
AU - Xian, Kaihu
AU - Chen, Yu
AU - Zhao, Wenchao
AU - Zhang, Fei
AU - Yin, Hang
AU - Liu, Yongsheng
AU - Zhao, Kui
AU - Yan, Jinyue
AU - Ye, Long
N1 - Publisher Copyright:
© 2023 The Royal Society of Chemistry.
PY - 2023/8/8
Y1 - 2023/8/8
N2 - Hole transport materials (HTMs) have greatly advanced the progress of solution-based electronic devices in the past few years. Nevertheless, most devices employing dopant-free organic HTMs can only deliver inferior performance. In this work, we introduced a novel “polymer synergy” strategy to develop versatile dopant-free polymer HTMs for quantum dot/perovskite solar cells and photodetectors. With this synergy strategy, the optical, electrical and aggregation properties of polymer HTMs can be modulated, resulting in complementary absorption, high hole mobility, favorable energy landscape and moderate aggregation. Moreover, a clear orientational transition was observed for the developed HTMs with a 9-fold increase in the face-on/edge-on ratio, providing a highway-like carrier transport for electronic devices, as revealed by in situ characterization and ultrafast transient absorption. With these benefits, the photovoltaic and photodetection performance of quantum dot devices were boosted from 11.8% to 13.5% and from 2.95 × 1012 to 3.41 × 1013 Jones (over a 10-fold increase), respectively. Furthermore, the developed polymer HTMs can also significantly enhance the photovoltaic and photodetection performance of perovskite devices from 15.1% to 22.7% and from 2.7 × 1012 to 2.17 × 1013Jones with the same device structure, indicating their great application potential in the emerging optoelectronics.
AB - Hole transport materials (HTMs) have greatly advanced the progress of solution-based electronic devices in the past few years. Nevertheless, most devices employing dopant-free organic HTMs can only deliver inferior performance. In this work, we introduced a novel “polymer synergy” strategy to develop versatile dopant-free polymer HTMs for quantum dot/perovskite solar cells and photodetectors. With this synergy strategy, the optical, electrical and aggregation properties of polymer HTMs can be modulated, resulting in complementary absorption, high hole mobility, favorable energy landscape and moderate aggregation. Moreover, a clear orientational transition was observed for the developed HTMs with a 9-fold increase in the face-on/edge-on ratio, providing a highway-like carrier transport for electronic devices, as revealed by in situ characterization and ultrafast transient absorption. With these benefits, the photovoltaic and photodetection performance of quantum dot devices were boosted from 11.8% to 13.5% and from 2.95 × 1012 to 3.41 × 1013 Jones (over a 10-fold increase), respectively. Furthermore, the developed polymer HTMs can also significantly enhance the photovoltaic and photodetection performance of perovskite devices from 15.1% to 22.7% and from 2.7 × 1012 to 2.17 × 1013Jones with the same device structure, indicating their great application potential in the emerging optoelectronics.
UR - http://www.scopus.com/inward/record.url?scp=85169508847&partnerID=8YFLogxK
U2 - 10.1039/d3ee02033a
DO - 10.1039/d3ee02033a
M3 - Article
AN - SCOPUS:85169508847
SN - 1754-5692
VL - 16
SP - 4474
EP - 4485
JO - Energy and Environmental Science
JF - Energy and Environmental Science
IS - 10
ER -