4.7 Article

CsPbBr3@SiO2 Core-Shell Nanoparticle Films for Superhydrophobic Coatings

Journal

ACS APPLIED NANO MATERIALS
Volume 4, Issue 6, Pages 6306-6315

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsanm.1c01199

Keywords

all-inorganic perovskite; superhydrophobicity; nanoparticle film; self-cleaning; photoluminescence

Funding

  1. National Natural Science Foundation of China [51772229]
  2. Overseas Expertise Introduction Project (111 project) for Discipline Innovation of China

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Lead halide perovskite nanocrystals have great potential for photoelectronic applications, but maximizing their stability remains a challenge. A novel surface functionalization method was developed, resulting in superhydrophobic SiO2-coated CsPbBr3 nanoparticle films with excellent water repellency, self-cleaning properties, and high stability. The luminescent films showed a 46% increase in photoluminescence intensity over 180 days, and CsPb2Br5-based luminescent films maintained 75% of their initial intensity after 10 days of water soaking. White-light-emitting diode devices using these nanoparticles achieved over 20% external quantum efficiency and maintained high stability even after 2 weeks.
Lead halide perovskite nanocrystals are extremely promising for photoelectronic application. However, maximizing their stability toward water, UV irradiation, or heat is yet a great challenge for the commercialization process. Herein, we develop a novel and facile surface functionalization approach that combined coating by the SiO2 layer with surface modification by intrinsically hydrophobic methyl groups for the fabrication of superhydro-phobic SiO2 -coated CsPbBr3 (referred as SH-CsPbBr3@SiO2) nanoparticle films. The SiO2 coating is realized by the hydrolysis of tetramethyl orthosilicate in the presence of ammonia. Hexame-thyldisilazane is introduced for nanoparticle surface modification and thus offers the nanoparticle films' superhydrophobic performances. By optimizing the surface coating and modification, the static water contact angle and sliding angle on the representative SH-CsPbBr3@SiO2 core-shell nanoparticle film can reach 160 and 3 degrees, respectively. As a synergetic contribution from SiO2 coating and modification by methyl groups, the as-fabricated green-emissive SH-CsPbBr3@SiO2 films exhibit excellent water repellency, self-cleaning, and ultrahigh stability toward water, heat, and UV illumination. It is of great interest that the photoluminescence (PL) intensity of the SH-CsPbBr3@SiO2 sample increases by 46% after 180 days under ambient conditions due to the phase transformation from CsPbBr3 to CsPb2 Br 5 and Pb(OH)Br. The resulting CsPb2Br5-based luminescent film shows excellent aqueous stability with remaining 75% of its initial PL intensity after soaking in water for 10 days. The white-light-emitting diode device fabricated using the green-emissive nanoparticles reports more than 20% external quantum efficiency (EQE), and no noticeable decrease in EQE is observed even after 2 weeks. This work elucidates a facile surface engineering strategy to prepare luminescent films with ultrahigh stability.

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