Title Advancements in organic small molecule hole-transporting materials for perovskite solar cells: past and future
Authors Murugan, Pachaiyappan
Hu, Ting
Hu, Xiaotian
Chen, Yiwang
Affiliation Nanchang Univ, Coll Chem & Chem Engn, 999 Xuefu Ave, Nanchang 330031, Jiangxi, Peoples R China
Nanchang Univ, Inst Polymers & Energy Chem, 999 Xuefu Ave, Nanchang 330031, Jiangxi, Peoples R China
Nanchang Univ, Sch Phys & Mat Sci, 999 Xuefu Ave, Nanchang 330031, Jiangxi, Peoples R China
Jiangxi Normal Univ, Inst Adv Sci Res iASR, Key Lab Fluorine & Silicon Energy Mat & Chem, Minist Educ, 99 Ziyang Ave, Nanchang 330022, Jiangxi, Peoples R China
Peking Univ, Yangtze Delta Inst Optoelect, Nantong 226010, Peoples R China
Keywords P-TYPE DOPANT
ENERGY-LEVEL SHIFTS
HIGH-PERFORMANCE
LOW-COST
HIGHLY EFFICIENT
SPIRO-OMETAD
COPPER PHTHALOCYANINE
CHARGE-TRANSPORT
RATIONAL DESIGN
PHOTOVOLTAIC PERFORMANCE
Issue Date Feb-2022
Publisher JOURNAL OF MATERIALS CHEMISTRY A
Abstract This review article discusses the current designs and synthetic procedures for organic small molecules as hole-transporting materials (HTMs) with a focus on their structure-property correlation, conductivity, and photovoltaic performance, as well as their high hole mobility and stability. In comparison to non-planar spiro-like compounds, various pi-conjugated aromatic and planar molecules have been studied as being important for the generation of new HTMs. Since heteroatoms, such as oxygen, sulfur, nitrogen and silica, have been shown to have an impact on the search for more stable and cost-effective HTMs and perovskite solar cells (PSCs), developing a new molecular architecture with efficient pi-pi stacking to increase charge mobility or integrating dopant molecular structure into HTM would be a viable approach for generating dopant-free HTMs. A deeper understanding of perovskite/HTM can also provide insight into the design of novel molecular architectures capable of achieving effective and stable systems.
URI http://hdl.handle.net/20.500.11897/638610
ISSN 2050-7488
DOI 10.1039/d1ta11039j
Indexed SCI(E)
Appears in Collections: 待认领

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