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5 protocols using ybcl3

1

Multistep Solution-Processed Perovskite Films

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The perovskite film was fabricated by a multistep solution‐process. 1 m PbCl2 (Sigma‐Aldrich) in DMSO containing YbCl3 (Sigma‐Aldrich) at a stoichiometric range of 0–9.1 mol% was spin coated onto glass substrates (quartz for optical measurements and TCO for LED device) at 3000 rpm for 30 s. After being dried at 90 °C for 15 min, 0.07 m CsCl methanol solution was spin coated onto PbCl2 film at 3000 rpm for 30 s and continuingly heated at 250 °C for 5 min. This process was repeated for five times to obtain the ideal perovskite films. The obtained perovskite films were rinsed with isopropanol and dried 250 °C again for 5 min. The Cs4PbCl6 phase was obtained when PbCl2 film slowly reacted with CsCl solution by spin coating at 2000 rpm for 30 s.
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2

Synthesis of Rare-Earth Chloride Compounds

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GdCl3, TiCl4, TeCl4, EuCl3, ErCl3, YCl3, YbCl3, CeCl4, MoCl6, and TaCl5 were obtained from Sigma-Aldrich. NaOH was obtained from Sinopharm Chemical Reagent Co. Deionized water used in all experiments was obtained from a Milli-Q water system.
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3

Synthesis and Characterization of Rare-Earth Chlorides

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The following materials were used in this
study: CsCl (Sigma, 99.999%), PbCl2 (Sigma, 99.999%, anhydrous),
LaCl3 (Sigma, >99.99%, anhydrous), CeCl3 (Sigma,
99.99%, anhydrous), PrCl3 (Sigma, 99.99%, anhydrous), NdCl3 (AlfaAesar, 99.9%, anhydrous), SmCl3 (Sigma, 99.9%,
anhydrous), SmI2 (Sigma, 99.9%, anhydrous), EuCl3 (Sigma, 99.99%, anhydrous), EuI2 (Sigma, 99.999%, anhydrous),
GdCl3 (Sigma, 99.99%, anhydrous), TbCl3 (Sigma,
99.99%, anhydrous), DyCl3 (Sigma, 99.99%, anhydrous), HoCl3 (Sigma, 99.9%, anhydrous), ErCl3 (Sigma, 99.9%,
ultra dry), ErI3 (abcr, 99.9%, anhydrous), TmCl3 (Sigma, 99.9%, anhydrous), YbCl3 (Sigma, 99.99%, anhydrous),
LuCl3 (Sigma, 99.99%, anhydrous).
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4

Synthesis of Halide-Based Solid Electrolytes

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The halide SEs were prepared by ball milling and subsequent solid-state reaction. Raw materials of LiCl (99.9%), InCl3 (99.99%), ScCl3 (99.99%,), YCl3 (99.99%), YbCl3 (99.99%), LuCl3 (99.99%) and ZrCl4 (99.9%) were used as starting materials from Sigma-Aldrich. The stoichiometric starting materials were weighed and ball milled at 350 rpm for 12 h sealed in a ZrO2 jar using 18 ZrO2 balls in an Ar-filled glovebox with p(H2O)/p < 0.1 ppm, p(O2)/p < 0.1 ppm. During ball milling, the jar was opened to make the samples homogenous at each 5 h in a glovebox. Then, the resulting mixture was sealed in quartz tubes and annealed at 260 °C for 12 h with a heating rate of 2 °C min−1 and cooled naturally to room temperature. After that, the obtained material was directly stored in an Ar-filled glovebox to prevent any moisture exposition.
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5

Synthesis of Rare-Earth Nanoparticles

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YCl 3 $6H 2 O (99.9%), YbCl 3 $6H 2 O (99.9%), ErCl 3 $6H 2 O (99.9%), NaOH (98%), NH 4 F (98%), 1-octadecene (90%) and Oleylamine (OM) were purchased from Sigma-Aldrich. Fluoresceinyl cypridina luciferin analogue (FCLA) was purchased from Tokyo Kasel Kogyo Co. Tokyo, Japan. ABT737 was purchased from Selleck Chemicals (Houston, TX). All chemicals were used as received without further purification. 2, 9, 16, 23-tetracarboxylic Zinc phthalocyanine and poly (ethylene glycol)-poly (L-histidine) (PEG-PHis) diblock copolymer were synthesized according to the references. [24] .
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