Publications by authors named "Liangchen Qian"

Achieving rational control over chemical and energetic properties at the perovskite/electron transport layer (ETL) interface is crucial for realizing highly efficient and stable next-generation inverted perovskite solar cells (PSCs). To address this, we developed multifunctional ferrocene (Fc)-based interlayers engineered to exhibit adjustable passivating and electrochemical characteristics. These interlayers are designed to minimize non-radiative recombination and, to modulate the work function (WF) and uniformity of the perovskite surface, thereby enhancing device performance.

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Perovskite/silicon tandem solar cells (TSCs) are promising candidates for commercialization due to their outstanding power conversion efficiencies (PCEs). However, controlling the crystallization process and alleviating the phases/composition inhomogeneity represent a considerable challenge for perovskite layers grown on rough silicon substrates, ultimately limiting the efficiency and stability of TSC. Here, this study reports a "halide locking" strategy that simultaneously modulates the nucleation and crystal growth process of wide bandgap perovskites by introducing a multifunctional ammonium salt, thioacetylacetamide hydrochloride (TAACl), to bind with all types of cations and anions in the mixed halide perovskite precursor.

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Article Synopsis
  • Robust contact schemes are essential for enhancing stability and simplifying the manufacturing of perovskite solar cells (PSCs).
  • The researchers developed a method to deposit SnO/Ag while protecting the perovskite, using atomic layer deposition for SnO to create a strong electron transport layer.
  • By optimizing oxygen vacancy defects in the SnO layer, they achieved power conversion efficiencies over 25% and demonstrated superior stability, maintaining over 95% efficiency after 2000 hours of testing at high temperature.
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The electron transporting layer (ETL) used in high performance inverted perovskite solar cells (PSCs) is typically composed of C, which requires time-consuming and costly thermal evaporation deposition, posing a significant challenge for large-scale production. To address this challenge, herein, we present a novel design of solution-processible electron transporting material (ETM) by grafting a non-fullerene acceptor fragment onto C. The synthesized BTPC exhibits an exceptional solution processability and well-organized molecular stacking pattern, enabling the formation of uniform and structurally ordered film with high electron mobility.

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