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1

Formamidinium Lead Iodide Perovskite Synthesis

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The formamidinium lead iodide (FAPbI3) perovskite precursors consisted of formamidinium hydroiodide (FAI, Advanced Election Technology), lead iodide (PbI2, Alfa Aesar), 5-aminovaleric acid (5AVA, Aladdin), and passivation molecules [PMs: cadmium iodide (CdI2), or lead acetate (PbAc2), or cadmium acetate (CdAc2), Sigma-Aldrich] with a molar ratio of FAI: PbI2: 5AVA: PMs = 2:1:0.85:x (x = 0~0.2), which were dissolved in N, N-dimethylformamide (DMF). The concentration of Pb2+ should be kept at 0.075 M. The precursors were stirred for 12 h at 55 °C in a nitrogen-filled glovebox before use. The zinc oxide (ZnO) nanocrystals were synthesized according to the literature1 (link),31 (link).
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2

Synthesis of Metal Chalcogenide Nanocrystals

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Copper
chloride (CuCl, anhydrous, 99.99%),
copper(II) acetate monohydrate (C4H6CuO4·H2O, 99.99% trace metals basis), cadmium
iodide (CdI2, 99.990%), mercury bromide (HgBr2, 99.9%), oleylamine (OM, >70%), and octadecene (ODE, 90%) were
purchased
from Sigma-Aldrich. Elemental sulfur (99%) was obtained from Strem
Chemicals, and methanol (anhydrous, 99.9%) and toluene (anhydrous,
99.8%) were from Carlo Erba reagents. All chemicals were used as received
without further purification.
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3

Synthesis of Metal Chalcogenide Nanoparticles

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Copper(II) acetylacetonate (Cu(acac)2, 97%), copper(I)
chloride (CuCl, 99.99%), oleylamine (OLAM,
>70%), octadecene (ODE, 90%), tri-n-octylphosphine
(TOP, 97%), trioctylphosphine oxide (TOPO, 99%), lithium bis(trimethylsilyl)amide
(LiN(SiMe3)2, 97%), N,N-dimethylethylenediamine (NND, ≥98.0%), mercury(II)
chloride (HgCl2, ≥99.5%), cadmium iodide (CdI2, 99%), lead(II) acetylacetonate (Pb(acac)2, ≥95%)
and tin(II) chloride (SnCl2, 98%) were purchased from Sigma-Aldrich,
tellurium powder (99.999%) and selenium powder (99.99%) from Strem
Chemicals, ethanol (anhydrous, ≥99.8%), methanol (anhydrous,
≥99.8%), toluene (anhydrous, ≥99%), and chloroform (anhydrous,
≥99%) from Carlo Erba reagents. All chemicals were used as
received without further purification, and all reactions were carried
out under nitrogen using standard air-free techniques.
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4

Synthesis of Lead and Cadmium Iodides

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All the reagents were from commercial sources and used without further purification.
The hydroidic acid (HI, 57 wt% in water) was from Aldrich; the methylamine (CH 3 NH 2 , 33 wt% in ethanol), diethyl ether (Et 2 O, purity ≥ 99.8%), led iodide (PbI 2 , purity 99%), cadmium iodide (CdI 2 , purity 99.999%), and γ-butyrolactone (purity ≥ 99%) were from Sigma-Aldrich.
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