USPatent applicationPatented

Preparation method of fluorine-doped lamellar black titanium dioxide nano material

Granted 16 Jan 2018 · 2 office actions

Current assignee: SAFRAN ELECTRICAL & POWER · originally Safran

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Inventors: Ruike Li, Wenjian Liu, Meicheng Li, Jiewei Chen +2 · Examiner: Melvin C Mayes · AU 1732 · TC 1700

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Abstract

The method for preparing fluorine-doped lamellar black TiO 2 nanomaterials includes mixing a solution of tetra-n-butyl titanate, n-propanol and hydrofluoric acid together, and then stir the solutions for a period of time. The solution is transferred into an autoclave and reacts at a certain temperature for a period of time. The sample obtained by the reaction is washed and dried. Then, the sample is heated in a protective atmosphere for a period of time so as to produce the fluorine-doped lamellar black TiO 2 nanomaterials. This fluorine-doped lamellar black TiO 2 owns superior optical absorption and electron transport performances.

Description

10 parts
›CROSS-REFERENCE TO RELATED APPLICATIONS

See Application Data Sheet.

›STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT

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›THE NAMES OF PARTIES TO A JOINT RESEARCH AGREEMENT

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INCORPORATION-BY-REFERENCE OF MATERIAL SUBMITTED ON A COMPACT DISC OR AS A TEXT FILE VIA THE OFFICE ELECTRONIC FILING SYSTEM (EFS-WEB)

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›STATEMENT REGARDING PRIOR DISCLOSURES BY THE INVENTOR OR A JOINT INVENTOR

Not applicable.

›BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to the technical field of nano materials and, more specifically, to a method for preparing a fluorine-doped lamellar black titanium dioxide nano material. This nano material owns the advantages of both superior optical absorption and electrochemical performance, so it can be used as a catalyst for photocatalysis application, as well as a photoanode material in dye-sensitized solar cells.

2. Description of Related Art Including Information Disclosed Under 37 CFR 1.97 and 37 CFR 1.98.

Titanium dioxide (TiO 2 ) is an environmentally friendly, chemically stable and low-cost semiconductor material widely used in many fields including photoelectrochemical catalysis, dye-sensitized solar cells, perovskite solar cells, and lithium-ion batteries owing to its excellent charge transport performance, high catalytic activity under light irradiation and other feature. However, common TiO 2 material possesses a distinct disadvantage of wide band gap (˜3 eV), which may restricts its absorption in visible light region and carrier transport/separating ability. Therefore, modifying the electron energy level of TiO 2 to narrow the bandgap, and consequently enhance the light absorption and carrier transport/separation ability of TiO 2 is of great importance to its performance improvement. Herein, we have prepared a new-type fluorine-doped lamellar black TiO 2 nanomaterial by adopting a low-temperature hydrothermal synthesis method, which uses tetra-n-butyl titanate as the titanium source, n-propanol as the solvent and hydrofluoric acid as the surface agent. Specifically, trivalent titanium defects are generated in the black TiO 2 as a result of the fluorine doping, making the electron energy level structure improved to some extent. The black feature of the TiO 2 enables the absorption of more sunlight, and the lamellar-nanosheet structure benefits in increasing the specific surface area, thereby improving the photocatalytic performance of the material.

›BRIEF SUMMARY OF THE INVENTION

The objective of this invention is to prepare a kind of fluorine-doped lamellar black TiO 2 nanomaterial by a simple one-step hydrothermal synthesis method with precusors of tetra-n-butyl titanate as the titanium source, n-propanol as the solvent and hydrofluoric acid as the surface agent. The specific preparation method includes the following steps:

(1) add 20˜30 mL n-propanol into a beaker, then add 1˜3 mL tetrabutyl titanate, and stir it well stir it well;

(2) add 0.2˜0.8 mL hydrofluoric acid into the solution, and then stir the mixed solution for 1 to 3 hours;

(3) transfer the solution prepared to an autoclave, and leave it to have hydrothermal reaction at 160˜200° C. for 12˜24 hours;

(4) keep washing the precipitate obtained after reaction with deionized water and ethanol until the filtrate is neutral, and then dry it;

(5) calcine the dried precipitate at 400˜450° C. in a protective atmosphere, thus the fluorine-doped lamellar black TiO 2 sample is obtained.

The n-propanol added in Step (1) is 20˜30 mL, with tetra-n-butyl titanate of 1˜3 mL.

The hydrofluoric acid added in Step (2) is 0.2˜0.8 mL, with the stirring time of 1˜3 hours.

The reaction temperature of the solution in the autoclave in Step (3) is 160˜200° C., with the reaction time of 12˜24 hours.

The drying temperature for the sample obtained in Step (4) is 50° C.˜60° C., with the drying time of 12˜20 hours.

The protective atmosphere used in Step (5) is a gas mixture of argon and hydrogen, with the calcination time of 2˜4 hours.

The beneficial effects of the present invention: it uses tetra-n-butyl titanate as the titanium source, n-propanol as a solvent and hydrofluoric acid as a surface agent, adopting a simple one-step hydrothermal synthesis method, to prepare a fluorine-doped lamellar black TiO 2 nanomaterial. The advantages of the hydrothermal synthesis method: it can effectively conduct liquid phase control, and features lower energy consumption, good controllability and lower cost. The TiO 2 nanomaterial prepared via the method provided by the present invention possesses modified energy band structure by fluorine-doping, which greatly enhances its performance. Compared with the commercial-purpose P25, which only can absorb ultraviolet light, the synthesized TiO 2 nanomaterial has a relatively strong capacity of absorbing ultraviolet—visible—infrared light in full spectrum, which benefits the improvement in its photocatalytic performance. The material can be widely used in many fields including photoelectrochemistry, perovskite solar cells and dye-sensitized solar cells.

›BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWINGS

FIG. 1 is a contrast diagram of the absorption spectra between a fluorine-doped lamellar black TiO 2 nanomaterials prepared in Embodiment 1 of the present invention and the commercial P25 nanoparticles.

FIG. 2 is a scanning electron microscope (SEM) image of the fluorine-doped lamellar black TiO 2 nanomaterials prepared in Embodiment 1 of the present invention.

FIG. 3 is a contrast diagram of F1s signal in x-ray photo electron spectroscopy (XPS) between the fluorine-doped lamellar black TiO 2 nanomaterials prepared in Embodiment 1 of the present invention and the commercial P25 nanoparticles.

›DETAILED DESCRIPTION OF THE INVENTION

A method for preparing a pinecone-shaped TiO 2 nanomaterial provided by the present invention can be implemented as below, and the specific preparing method includes the following steps:

›Embodiment 1

(1) add 25 mL of n-propanol into a beaker, then add 2 mL of tetrabutyl titanate, and stir it well;

(2) add 0.4 mL of hydrofluoric acid into the solution, and then stir it for 2 hours;

(3) transfer the solution prepared to an autoclave, and leave it to have hydrothermal reaction at 180° C. for 18 hours;

(4) wash the precipitate obtained after reaction with deionized water and ethanol, until the filtrate is neutral, and then dry it;

(5) calcine the sample obtained at 430° C. in a protective atmosphere to obtain the fluorine-doped lamellar black TiO 2 nanomaterials.

›Embodiment 2

(1) add 20 mL of n-propanol into a beaker, then add 1 mL of tetrabutyl titanate, and stir it well;

(2) add 0.15 mL of hydrofluoric acid into the solution, and then stir it for 1 hour;

(3) transfer the solution prepared to an autoclave, and leave it to have hydrothermal reaction at 180° C. for 15 hours;

(4) wash the precipitate obtained after reaction with deionized water and ethanol, until the filtrate is neutral, and then dry it;

(5) calcine the sample obtained at 450° C. in a protective atmosphere to obtain the fluorine-doped lamellar black TiO 2 nanomaterials.

Claims as granted

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Classifications

9 codes
IPC · International Patent Classification
Section B — Performing operations; transporting
  • B01J37/06
  • B01J35/00
  • B01J37/08
  • B01J37/03
  • B01J27/00
  • B01J27/135
Section C — Chemistry; metallurgy
  • C09C1/36
  • C01G23/053
Section H — Electricity
  • H01G9/20

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⤢ drag to zoomJul 2016Oct 2016Jan 2017Apr 2017Jul 2017Oct 2017Jan 2018USPTOApplicantNon-final rejectionResponse after non-finalFinal rejectionRequest for continued examinationNotice of allowance
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Pendency
1.5 y
553 days filing → grant
Office actions
2
non-final + final
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2
1 RCE
Examiner
Melvin C Mayes
art unit 1732 · TC 1700
Citations: 4 back · 0 forward

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