4.6 Article

Enhancing the Photoluminescence and Stability of Methylammonium Lead Halide Perovskite Nanocrystals with Phenylalanine

期刊

JOURNAL OF PHYSICAL CHEMISTRY C
卷 125, 期 4, 页码 2793-2801

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.0c11095

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资金

  1. NSF [CHE-1904547]
  2. Office of Science, Office of Basic Energy Sciences, of the U.S. Department of Energy [DE-AC02-05CH11231]
  3. NSF Major Research Instrumentation (MRI) Program [1126845]
  4. Hubei Academy of Agricultural Science Visiting Scholar Program [Q2018034]
  5. Direct For Mathematical & Physical Scien [1126845] Funding Source: National Science Foundation
  6. Division Of Materials Research [1126845] Funding Source: National Science Foundation

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This study demonstrated that phenylalanine (Phe) is an effective capping ligand for synthesizing MAPbBr(3) perovskite nanocrystals (PNCs) when used with (3-aminopropyl) triethoxysilane (APTES) and oleic acid (OA) or methylphosphoric acid (MPA). The combined use of Phe, APTES, and OA or MPA was shown to improve PL and stability of PNCs, attributed to Phe's ability to stabilize surface defects related to Pb2+, CH3NH3+, and Br-. A proposed model explained the passivation mechanism involving Phe in conjunction with other amine and acid ligands for perovskite passivation.
The choice of ligand is an important parameter in the synthesis of metal halide perovskites such as methylammonium lead bromide (MAPbBr(3)) perovskite nanocrystals (PNCs). In this work, phenylalanine (Phe) was demonstrated, for the first time, as a highly effective capping ligand for synthesizing MAPbBr(3) PNCs when used in conjunction with (3-aminopropyl) triethoxysilane (APTES) and oleic acid (OA) or methylphosphoric acid (MPA). Ultraviolet-visible absorption and photoluminescence (PL) emission spectroscopy, powder X-ray diffraction, and Fourier transform infrared spectroscopy were used to investigate the optoelectronic, structural, and surface properties of the PNCs. The combined use of Phe, APTES, and OA or MPA is demonstrated to be highly successful in passivating PNCs for achieving both improved PL and enhanced stability. The enhanced passivation by Phe is attributed to the three functional groups in Phe that can stabilize surface defects related to Pb2+, CH3NH3+, and Br- by mediating pH and hydrophobicity. Based on all the experimental results, a model is proposed to explain the passivation mechanism involving Phe in conjunction with other amine and acid ligands. This study demonstrates the effectiveness of multiligand passivation of perovskites involving amino acid as the capping ligand.

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