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Abstract All‐inorganic α ‐phase CsPbI 3 perovskite with a suitable bandgap and superb optoelectronic properties is transforming the landscape of perovskite photovoltaics, but its long‐term lability associated with “soft” ionic lattice still imposes a great challenge for practical applications. Herein, a unique solid‐solution fluorination strategy is proposed to deliver an “ideal” perovskite matrix of α ‐phase CsPbI 3 abundant with F ions through interlocking the soft lattice of CsPbI 3 with cubic‐phase CsF·3/2HF. Such a sublattice interlocking can not only stabilize the soft lattice of α ‐phase CsPbI 3 perovskite nanocrystals but also passivate their notorious surface defects, thereby producing a “rigid” solid‐solution‐type perovskite/fluoride CsPbI 3 /CsF (termed as CsPbI 3 :F) nanocomposite with excellent long‐term stability and a near‐unity photoluminescence efficiency. Of particular note is that these CsPbI 3 :F nanocomposites can work well as effective grain boundary anchors to significantly improve the photovoltaic performance of perovskite solar cells because of their F‐rich perovskite lattice, achieving a T 80 stability of 1500 h under continuous maximum power point tracking and AM 1.5G illumination without the need for encapsulation. This work paves a new way to deliver perovskite materials with desirable properties for photovoltaics.
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Youchao Wei
Tan Kah Kee Innovation Laboratory
Xianjin Wang
Shanghai Jiao Tong University
Zhaoyu Wang
Qilu University of Technology
Advanced Functional Materials
Chinese Academy of Sciences
Peking University
Fujian Institute of Research on the Structure of Matter
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Wei et al. (Tue,) studied this question.
synapsesocial.com/papers/68e75a00b6db6435876d0dd2 — DOI: https://doi.org/10.1002/adfm.202316058