吩恶嗪
吩噻嗪
钙钛矿(结构)
光电流
材料科学
光致发光
单层
光电子学
化学物理
咔唑
载流子
光化学
价(化学)
串联
超快激光光谱学
轨道能级差
钙钛矿太阳能电池
化学
纳米技术
吸收(声学)
电荷(物理)
太阳能电池
作者
Daniele T. Cuzzupè,Marius Franckevičius,Orestis Karalis,Yekitwork Abebe Temitmie,Mantas Marčinskas,Maria Azhar,Neethinathan Johnee Britto,T. Eberle,Denis Andrienko,Vytautas Getautis,Tadas Malinauskas,Hannes Hempel,Lukas Schmidt‐Mende
出处
期刊:Solar RRL
[Wiley]
日期:2025-12-09
卷期号:10 (6)
被引量:1
标识
DOI:10.1002/solr.202500768
摘要
Hole‐selective self‐assembled monolayers (SAMs) based on carbazole head groups have enabled major performance improvements of perovskite solar cells (PSCs) by eliminating parasitic absorption and nonradiative losses. However, the energy levels of the carbazole‐based, commercially available SAMs poorly match the valence band maximum (VBM) of narrow‐bandgap, lead‐tin (Pb‐Sn) perovskites, relevant for tandem applications. In this work, we expand the library of SAMs compatible with Pb‐Sn PSCs by synthesizing four novel SAMs containing phenoxazine (POz) and phenothiazine (PTz) as their head groups and investigate their interaction with the Pb‐Sn perovskite in detail. We obtain working devices with all SAMs, but despite significant differences between the highest occupied molecular orbital (HOMO) levels of the SAMs, the open‐circuit voltage ( V OC ) and fill factor (FF) across devices remains similar, suggesting that the role of energy level alignment is less relevant at this interface. Through in‐depth analysis including photoluminescence quantum yield (PLQY), transient photocurrent (TPC), and combined time‐resolved surface photovoltage (trSPV) and time‐resolved photoluminescence (trPL) measurements, we unveil the charge extraction dynamics of these systems featuring different head groups and HOMOs. This work highlights that the SAMs’ structure affects the overall charge extraction process and provides insights into the strategies needed to maximize charge extraction for more efficient PSCs.
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