4.8 Article

Flexible, All-Inorganic CsPbBr3 Perovskite Solar Cells Tailored by Heat-resistant Muscovite Substrates

期刊

CHEMSUSCHEM
卷 14, 期 6, 页码 1512-1516

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cssc.202002796

关键词

energy storage; flexible substrates; perovskites; photovoltaics; solar cells

资金

  1. Guangdong Basic and Applied Basic Research Foundation [2020A1515110548]
  2. National Natural Science Foundation of China [61774139, 62004083, U1802257]
  3. Natural Science Foundation of Guangdong Province [2019B151502061, 2020A1515011123]
  4. Postdoctoral Research Foundation of China [2020M683185, 2019M663379]
  5. Fundamental Research Funds for the Central Universities [21620348, 21618409, 21619311]

向作者/读者索取更多资源

This study successfully fabricated a flexible CsPbBr3 PSC with an efficiency of 5.71% using a heat-resistant conductive muscovite substrate, achieving high mechanical flexibility and providing a new path for increasing efficiency in the future without lowering the crystallization temperature of state-of-the-art materials.
All-inorganic CsPbBr3 perovskite solar cells (PSCs) have attracted tremendous attention, owing to their excellent stability and rising power conversion efficiency. However, the mechanical flexibility of these solar cells has ground to a standstill because of the high-temperature requirement for ideal CsPbBr3 perovskite films. In this study, a flexible CsPbBr3 PSC with an efficiency of 5.71 % has been made by means of fabricating a heat-resistant conductive muscovite substrate, which demonstrates very high mechanical flexibility with nearly unchanged resistance even after 4000 bending cycles (12000 cycles of concave and convex bending for PSCs), owing to the weak van der Waals force and layered structure. Implementation of the muscovite substrate enables the fabrication of flexible PSCs under high-temperature conditions, providing a new path to increase the efficiency without lowering the crystallization temperature of state-of-the-art electron-transporting materials and perovskite films in the future.

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