Synergistic Composite Electron Transport Layer and Interfacial Engineering for High-Efficiency and Stable Perovskite Solar Cells
Abstract
The Organic-inorganic perovskite solar cells (PSCs) have achieved remarkable power conversion efficiencies (PCEs), yet their commercialization remains limited by interfacial recombination losses and insufficient operational stability. Here, we present a dual-interface engineering strategy that synergistically combines a Fe<sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">2</sub>O<sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">3</sub>-WO<sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">3</sub> composite electron transport layer (ETL) with an ultrathin piperazine dihydriodide interlayer (IL) to address these challenges. The Fe<sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">2</sub>O<sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">3</sub>-WO<sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">3</sub> composite, prepared via solution processing, integrates the stability and deep conduction band of Fe<sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">2</sub>O<sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">3</sub> with the high electron mobility of WO<sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">3</sub>, forming uniform, transparent, and compact films that facilitate efficient electron extraction and suppressed recombination. Meanwhile, the IL at the perovskite/hole transport interface passivates surface defects, introduces interfacial dipoles for optimized energy-level alignment, and inhibits ion migration. Together, these modifications improve perovskite film morphology, reduce trap density, and enable superior charge transport. Devices incorporating composite ETL and IL achieved a champion PCE of 18.46% with a <italic xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">V<sub>OC</sub></i> of 1.14 V, <italic xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">J<sub>SC</sub></i> of 21.82 mA·cm<sup xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">−2</sup>, and <italic xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">FF</i> of 74.23%, outperforming single-oxide counterparts. Moreover, the dual-engineered devices exhibited enhanced stability, retaining ∼84% of their initial efficiency under prolonged operation. This work demonstrates that composite ETLs combined with molecular interfacial passivation provide a scalable pathway to efficient, stable, and reproducible PSCs.