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Titanium diisopropoxide bis acetylacetonate solution

Manufactured by Merck Group

Titanium diisopropoxide bis(acetylacetonate) solution is a chemical compound used in various laboratory applications. It serves as a precursor for the deposition of titanium-based thin films through chemical vapor deposition (CVD) or atomic layer deposition (ALD) processes. The solution provides a source of titanium for these thin film deposition techniques.

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6 protocols using titanium diisopropoxide bis acetylacetonate solution

1

Perovskite Solar Cell Fabrication

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FTO (7 Ω) was purchased from UNI-ONWARD Corp. Titanium diisopropoxide bis(acetylacetonate) solution (75% in 2-propanol) and AgNO3 (99.9999% trace metal basis) is obtained from Sigma-Aldrich. Perovskite precursors PbI2 (99.9985%) were obtained from Alfa Aesar. The CH3NH3I (98%) and Spiro-OMeTAD were purchased from Lumtec. Li-TFSI was obtained from ACROS. 4-tert-Butylpyridine (TBP) was acquired from Ak Scientific Inc, and Ag slug (4 mm × 6 mm 99.9999%) was from Gredmann.
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2

Fabrication of Mesoporous TiO2 Thin Films

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Fluorine-doped tin oxide (FTO) glass substrates (TCO glass, NSG 10, Nippon sheet glass, Japan) were cleaned by ultrasonication in Hellmanex (2%, deionized water), rinsed thoroughly with deionized water and ethanol, and then treated in oxygen plasma for 15 min. A 30-nm blocking layer (TiO2) was deposited on the cleaned FTO by spray pyrolysis at 450°C using a commercial titanium diisopropoxide bis(acetylacetonate) solution (75% in 2-propanol; Sigma-Aldrich) diluted in anhydrous ethanol (1:9 volume ratio) as a precursor and oxygen as a carrier gas. A mesoporous TiO2 layer was deposited by spin-coating a diluted paste in ethanol (1:8.5 weight ratio) (Dyesol 30NRD:ethanol) (3000 rpm; acceleration, 2000 rpm for 20 s) onto the substrate containing a TiO2 compact layer and then sintered at 450°C for 30 min in dry air.
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3

Fabrication of Li-Doped Mesoporous TiO2 Layers

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Fluorine-doped tin oxide (FTO)-glass substrates (TCO glass, NSG 10, Nippon sheet glass, Japan) were chemically etched using Zn powder and 4 M HCl and cleaned by ultrasonication in Hellmanex (2%, deionized water), rinsed thoroughly with deionized water and ethanol, and then treated with oxygen plasma for 15 min. A 30 nm blocking layer (TiO2) was deposited on the cleaned FTO by spray pyrolysis at 450°C using a commercial titanium diisopropoxide bis(acetylacetonate) solution (75% in 2-propanol, Sigma-Aldrich) diluted in anhydrous ethanol (1:9, volume ratio) as precursor and oxygen as a carrier gas. A 150 nm mesoporous TiO2 layer was deposited by spin coating a diluted paste (1:6 wt. ratio) (Dyesol 30NRD: ethanol) (4000 rpm, acceleration 2000 rpm for 20 s) onto the substrate containing TiO2 compact layer and then sintered at 450°C for 30 min in dry air. For Li treatment of mesoporous TiO2, 150 μL of LiTFSI solution in acetonitrile (10mg/mL, freshly prepared in an argon atmosphere) was spin coated (3000 rpm, acceleration 2000 rpm for 20 s) after a loading time of 10 s. Thereafter, Li treated substrates were sintered at 450°C for 30 min.
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4

Perovskite Solar Cell Fabrication Process

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The perovskite films in this work were deposited on top of cover glasses or ITO glass. The substrate glasses were cleaned extensively by deionized water, acetone, and isopropanol. For the HTL deposition, the PTAA (Sigma-Aldrich) was dissolved in toluene with a concentration of 5 mg mL−1 and spin-coated on the substrates at 5000 rpm for 30 s. The spun PTAA films were annealed at 100 °C for 10 min. For the ETL deposition, a compact titanium dioxide (TiO2) layer of about 40 nm was deposited by spray pyrolysis of 7 mL 2-propanol solution containing 0.6 mL titanium diisopropoxide bis(acetylacetonate) solution (75% in 2-propanol, Sigma-Aldrich) and 0.4 mL acetylacetone at 450 °C in air. The FA0.95Cs0.05PbI3 precursor solution was prepared by dissolving 0.4 M Pb2+ in dimethyl sulfoxide (DMSO) and dimethylformamide (v/v = 3/7) mixed solvent. Perovskite films were deposited using a three-step spin-coating procedure with the first step of 100 rpm for 3 s, the second step of 3500 rpm for 10 s, and the last step of 5000 rpm for 30 s. Toluene (1 mL) was applied on the spinning substrates at 20 s of the third step. After spin coating, the substrates were annealed at 170 °C for 27 min. The encapsulated perovskite films were capped with PMMA (Mw about 120,000) film by spin-coating 15 mg ml−1 PMMA in chlorobenzene solution at 4000 rpm for 35 s.
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5

Fabrication of Perovskite Solar Cells

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Solar cells were prepared under high-humidity ambient atmosphere. First, FTO-coated glass substrates were cleaned by ultrasonication in detergent, deionized water, acetone and isopropanol for 15 min, respectively. Then, the substrates were dried with a N2 gun and subjected to an ultraviolet/ozone cleaning system for 15 min. Subsequently, the titanium diisopropoxide bis(acetylacetonate) solution (75% in 2-propanol, Sigma-Aldrich) diluted in isopropanol (0.15 M) was spin-coated onto the FTO substrates at 4000 r.p.m. for 30 s and annealed at 150 °C for 10 min.
A commercial TiO2 paste (Dyesol 18NRT, Greatcell) diluted in ethanol (1:2.5, weight ratio) was dropped onto the compact TiO2 and spun at 3000 r.p.m. for 30 s. After drying at 100 °C, the TiO2 thin films were annealed at 500 °C for 30 min and then slowly cooled to room temperature. The mesoporous TiO2 was treated with a TiCl4 aqueous solution (40 mM) at 70 °C for 30 min. After that, the substrate was washed with ethanol and deionized water. The CH3NH3PbI3 film was fabricated using the sequential deposition method. Finally, a counter electrode was prepared by doctor blading the commercial carbon paste onto the perovskite film and annealed at 100 °C for 30 min.
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6

Fabrication of Mesoporous TiO2 Thin Films

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Fluorine-doped tin oxide (FTO)-glass substrates (TCO glass, NSG 10, Nippon sheet glass, Japan) were cleaned by ultrasonication in Hellmanex (2%, deionized water), rinsed thoroughly with de-ionized water and ethanol, and then treated in oxygen plasma for 15 min. A compact layer of TiO 2 of ca 30 nm was subsequently deposited via spray pyrolysis at 450 °C using a commercial titanium diisopropoxide bis(acetylacetonate) solution (75% in 2-propanol, Sigma-Aldrich) diluted in anhydrous ethanol (1:9, volume ratio) as precursor and oxygen as carrier gas.
A mesoporous TiO 2 layer was then deposited by spin coating a diluted paste (1:3.5 wt. ratio)
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