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17 protocols using se powder

1

Synthesis of Semiconductor Nanoparticles

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Oleic acid (OA, 90%), 1-octadecene (1-ODE, 90%), trioctylphosphine (TOP, 97%), zinc acetate (99.99%), sulfur (99.998%), zinc diethyldithiocarbamate (Zn DDTC, 97%), ZnO (99.999%), cadmium acetate (99.995%), Se powder (99.99%) zinc acetate dihydrate (≥98%), lithium hydroxide monohydrate (≥98%), and poly[(9,9-dioctylfluorenyl-2,7-diyl)-co-(4,4′-(N-(4-sec-butylphenyl)diphenylamine))] (TFB) were purchased from Sigma Aldrich.
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2

WSe2 Growth via Tube Furnace

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A one-zone tube furnace was used to grow WSe241 (link). Hundred milligram Se powder (Sigma-Aldrich, 99.5%) was loaded at upstream, and kept at 300 °C during growth. A mixture of WO2.9 (30 mg, Alfa Aesar, 99.99%) and NaCl (10 mg, Sigma-Aldrich, 99.5%) was loaded at the center of reaction zone. The temperature of reaction zone gradually increased to 830 °C in 22 min, and cooled down to room temperature after staying at 830 °C for 15 min. Pure Ar and H2 (90/10 sccm) were used as carrying gas.
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3

Synthesis and Characterization of Ti3AlC2 Composite Materials

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Ti3AlC2 (98%) was purchased from the Forsman Scientific Co., Ltd. (Beijing, China). Polyvinylidene fluoride (≥ 99.5%) was purchased from Micxy Chemical Co., Ltd. (Chengdu, China). Nickel form (110 mesh per inch) was purchased from Chuan Dong Chemical Co., Ltd. (Chongqing, China). Carbon black was purchased from Cabot Corporation (Boston, USA). Hydrochloric acid (HCl, ACS grade, 36-38%), lithium fluoride (LiF, ACS grade, ≥ 99%), n-methyl-2-pyrrolidone (ACS grade, ≥ 99.8%), NiCl2 (ACS grade, ≥ 99%), Se powder (ACS grade, ≥ 99%), KOH (ACS grade, ≥ 99%), and EDTA-Na2 (ACS grade, ≥ 99%) were purchased from Sigma-Aldrich. All chemical materials were used as received without further purification.
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4

Synthesis of CdSe Nanoparticles with TiO2

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Cadmium oxide (CdO), Se powder, Octadecane (ODE) (90%), oleic acid (OA), Trioctylphosphine (TOP) were purchased from Sigma-Aldrich for CdSe preparation. Degussa P25-TiO2 nanocrystallite was supplied by Evonik Aeroxide. All of the chemicals were used without any further purification.
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5

Selenization of MoO3 to MoSe2 Films

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The sample was prepared by PLD followed by selenization. A highly pure MoO3 target of approximately 20 mm diameter was placed in a rotating target holder. The target was exposed to a laser beam for several minutes to remove surface contaminants. A sapphire substrate approximately 20 × 20 mm2 was placed in a rotating substrate holder. The distance between the substrate and target was 25 cm. The chamber pressure was 25 mTorr, established by flowing high pure argon (Ar) at 10 sccm. A KrF excimer laser (λ = 248 nm, CompexPro 102 F) with 20 ns pulse width, 200 mJ/cm2 power density, 3 Hz repetition rate deposited thin MoO3 films in 45 s. The substrate temperature during deposition was 700 °C. The as-deposited MoO3 films were then converted to MoSe2 by selenization in a two-zone hot-wall furnace. Se powder (Sigma Aldrich, 99.99%) was placed in the low temperature zone at 450 °C, and the film located in the high temperature zone at 900 °C. A mixture of Ar and H2 were employed as carrier gases to transport Se vapor from the colder to the hotter zone. H2 also assist in reducing MoO3.
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6

Synthesis of AuTe2Se4/3 Single Crystals

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Single crystals of AuTe2Se4/3 were grown using the self-flux method. Total 2–4 g starting materials with high purity Au powder (99.99%, Sigma Aldrich), Te powder (99.999%, Sigma Aldrich), and Se powder (99.99%, Sigma Aldrich) were stoichiometrically weighted and sealed in an evacuated silica tube in high vacuum (10−5 mbar) and subsequently mounted into a muffle furnace. The furnace was heated up to 800 °C in 40 h and dwelled 10 h. Afterward, the furnace was slowly cooled down to 450 °C in 4 days and then shut down. Separated crystals from ingot are generally thin with maximum planar size 4 × 1 mm2. The single crystals of AuTe2Se4/3 were ribbon shape with shining mirror-like surfaces.
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7

Synthesis of PtSe2 Nanosheets

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All the chemicals such as chloroplatinic acid, Se powder, hexamethylenetetramine, and NaBH4 were purchased from Sigma-Aldrich for the synthesis of PtSe2 nanosheets.
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8

Synthesis of Colloidal Semiconductor Nanocrystals

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1-Octadecene (90%), oleic acid (90%), CdO
(≥99.99%), Se powder (100 mesh, 99.99%), trichloroethylene
(anhydrous, ≥99%), 1-hexanethiol (97%), and 1-octadecanethiol
(98%) were purchased from Sigma-Aldrich. 1-Decanethiol (96%) and 1-tetradecanethiol
(94%) were purchased from Alfa Aesar. 1H,1H,2H,2H-Perfluoro-1-hexanethiol
(97%) was purchased from Synquest Laboratories. Hydrochloric acid
(37%) and HPLC grade hexane were purchased from Bio-Lab.
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9

Synthesis of Chalcogenide Nanocrystals

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1-Octadecene
(90%), oleic acid (90%), CdO
(≥99.99%), Se powder (100 mesh, 99.99%), trichloroethylene
(anhydrous, ≥ 99%), 1-butanethiol (99%), 1-pentanethiol (98%),
1-hexanethiol (97%), 1-heptanethiol (98%), 1-octanethiol (≥98.5%),
1-nonanethiol (98%), 1-decanethiol (96%), 2-methyl-1-butanethiol (99%),
3-methyl-1-butanethiol (97%), 2-ethyl-1-hexanethiol (97%), 2-methyl-1-hexanoic
acid (98%), 5-methyl-1-hexanoic acid (98%), 4-methyl-1-octanoic acid
(98%), 4-ethyl-1-octanoic acid (98%), 4-methyl-1-nonanoic acid (99%),
LiAlH4, p-toluenesulfonyl chloride (99%),
thiourea (99%), toluene-d8 (99.6% D),
and chloroform-d1 (99.8% D) were purchased
from Sigma-Aldrich, Alfa Aesar, or Acros Organics.
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10

Synthesis and Characterization of Selenium Nanoparticles

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CuCl2·2H2O (≥99%), Se powder (≥99.5%), sodium borohydride (NaBH4, 99%), mercaptosuccinic acid (MSA, 99%) were purchased from Sigma-Aldrich. Mono-(6-mercapto-6-deoxy)-β-cyclodextrin (CD) was purchased from Shangdong Binzhou Zhiyuan Biotechnology Co. Ltd. JQ1 was purchased from Shanghai Selleck Chemicals Co. Ltd. Indoximod (IND) was purchased from Beijing annoron Co. Ltd. 2,7-dichlorofluorescein diacetate (DCFH-DA) was purchased from AAT Bioquest Inc., Thermo Fisher Scientific. Milli-Q water (>18 MΩ cm) was used in the experiments. All chemicals and reagents were used as received without any further purification.
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