4.7 Article

Hydrophobic Organic Ammonium Halide Modification toward Highly Efficient and Stable CsPbI2.25Br0.75 Solar Cell

期刊

SOLAR RRL
卷 5, 期 7, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/solr.202100178

关键词

hydrophobic organic ammonium halides; inorganic perovskite solar cells; interfacial modifications

资金

  1. National Key Research and Development Program of China [2018YFB1502003, 2019YFE0123400]
  2. Tianjin Distinguished Young Scholars Fund [20JCJQJC00260]
  3. Chinese Thousand Talents Program for Young Professionals
  4. 111 Project [B16027]
  5. National Natural Science Foundation of China [21872080]
  6. Nankai University

向作者/读者索取更多资源

In this study, hydrophobic organic ammonium halides were used to modify inorganic cesium lead halide perovskite solar cells, resulting in enhanced efficiency and stability, with the hexadecyltrimethylammonium chloride (CTAC)-modified device showing the best performance. The CTAC modification also led to the formation of a gradient triple anion inorganic perovskite layer, demonstrating better phase stability and excellent efficiency retention after 35 days in N-2 atmosphere.
Inorganic cesium lead halide perovskite solar cells are promising candidates for next-generation photovoltaic applications. However, their phase instability and relatively low efficiency hinder their commercialization. Herein, hydrophobic organic ammonium halides (CI, Br, and I) are rationally used for the modification of inorganic CsPb(I0.75Br0.25)(3) perovskite solar cells. Benefiting from their passivation effects and hydrophobic long alkyl chain, the modified devices exhibit enhanced efficiency and stability. Among them, the hexadecyltrimethylammonium chloride (CTAC)-modified device shows the best performance with a power conversion efficiency (PCE) of 18.05%. Furthermore, a gradient triple anion inorganic perovskite CsPb(I0.75Br0.25)(3-x)Cl-x layer is formed in situ during the CTAC modification, which demonstrates better phase stability than CsPb(I0.75Br0.25)(3). As a result, the modified device also shows excellent stability, maintaining 94% of the initial efficiency after 35 days in N-2 atmosphere.

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