4.6 Article

Skillfully deflecting the question: a small amount of piperazine-1,4-diium iodide radically enhances the thermal stability of CsPbI3 perovskite

Journal

JOURNAL OF MATERIALS CHEMISTRY C
Volume 7, Issue 38, Pages 11757-11763

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c9tc03576a

Keywords

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Funding

  1. National Natural Science Foundation of China [21603010, 21875013]
  2. Beijing Natural Science Foundation [2182031]
  3. Fundamental Research Funds for Central Universities
  4. Shenzhen Peacock Plan [KQTD2016053015544057]
  5. HK-RGC General Research Funds (GRF) [16312216]
  6. HK Innovation and Technology Fund [GHP/079/17SZ]

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Inorganic CsPbI3 perovskite holds great promise to prepare high-performance and long-term operational perovskite solar cells (PSCs) because of its ideal band gap and intrinsic superb stability. However, due to the low tolerance factor, the photoactive CsPbI3 perovskite is a high-temperature (330 degrees C) phase that would spontaneously transit to a non-perovskite phase at ambient temperature. Herein, we incorporate piperazine-1,4-diium iodide (PZDI(2)) into CsPbI3 perovskite to stabilize the photoactive phase. PZD cations are proved to be inserted between layered perovskites to form a Ruddlesden-Popper 2D structure. Excitingly, a small amount of PZDI(2) (3%) radically enhances the thermal stability of the CsPbI3 perovskite. Specifically, the CsPbI3 center dot 3%PZDI(2) film exhibits no phase transition after heating at 100 degrees C for 24 h, whereas the pristine CsPbI3 and MAPbI(3) films are seriously degraded after 16 h and 12 h, respectively. The carbon-based PSCs without the hole transport material (C-PSCs) using the CsPbI3 center dot 3%PZDI(2) film show almost no performance decay after storage in air atmosphere at room temperature for 1200 h and at 85 degrees C for 200 h, whereas at 85 degrees C, the pristine CsPbI3 and MAPbI(3) devices inflict over 20% decay after 40 h and 6 h, respectively.

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