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Preparation method of Sb2S3 nanowire

A nanowire and solution technology, applied in chemical instruments and methods, inorganic chemistry, antimony compounds, etc., can solve the problems of high cost, complicated preparation method operation, long reaction cycle, etc., and achieve low cost, simple preparation method, and short reaction cycle short effect

Inactive Publication Date: 2010-12-01
SHAANXI UNIV OF SCI & TECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

[0004] However, the above-mentioned preparation method is complicated to operate, has a long reaction cycle, and is expensive

Method used

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  • Preparation method of Sb2S3 nanowire
  • Preparation method of Sb2S3 nanowire
  • Preparation method of Sb2S3 nanowire

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0019] (1) Weigh 10mmol of Sb 2 Cl 3 , Pour it into 2ml of ethylene glycol, stir with a stirrer until Sb 2 Cl 3 Dissolve completely; then, pour 10ml of deionized water into it while stirring to form a white emulsion A;

[0020] (2) Weigh 15mmol of Na 2 S·9H 2 O is dissolved in 10ml of deionized water to form solution B;

[0021] (3) Drop solution B into solution A at a rate of 2 drops / sec to form an orange-red precursor;

[0022] (4) Add CO(NH 2 ) 2 , Make up 30ml solution C;

[0023] (5) Place solution C in a 50ml reaction kettle, place the reaction kettle in a thermostat to heat, and when the temperature rises to 240°C, keep it for 12 hours. After the reaction, rinse the product with deionized water until the pH is 7. Then dry in a vacuum oven at 80℃ for 4h to obtain Sb 2 S 3 Nanowires.

[0024] The obtained product was analyzed by Rigaku D / max2550VB+ / PC X-ray diffractometer, and figure 1 It can be seen that all the diffraction peaks correspond to the standard card (JCPDS-42-1393, a=...

Embodiment 2

[0027] (1) Weigh 10mmol of Sb 2 Cl 3 , Pour it into 2ml of ethylene glycol, stir with a stirrer until Sb 2 Cl 3 Dissolve completely; then, pour 10ml of deionized water into it while stirring to form a white emulsion A;

[0028] (2) Weigh 15mmol of Na 2 S·9H 2 O is dissolved in 10ml of deionized water to form solution B;

[0029] (3) Drop solution B into solution A at a rate of 2 drops / sec to form an orange-red precursor (;

[0030] (4) Add CO(NH 2 ) 2 , Make up 30ml solution C;

[0031] (5) Place solution C in a 50ml reaction kettle, heat the reaction kettle in a thermostat, and keep it warm for 8 hours when the temperature rises to 240°C. After the reaction is over, rinse the product with deionized water until the pH is 7. Then dry in a vacuum oven at 80℃ for 4h to obtain Sb 2 S 3 Nanowires.

Embodiment 3

[0033] (1) Weigh 10mmol of Sb 2 Cl 3 , Pour it into 2ml of ethylene glycol, stir with a stirrer until Sb 2 Cl 3 Dissolve completely; then, pour 10ml of deionized water into it while stirring to form a white emulsion A;

[0034] (2) Weigh 15mmol of Na 2 S·9H 2 O was dissolved in 10ml of deionized water to form solution B; (3) Solution B was dropped into solution A at a rate of 2 drops / sec to form an orange-red precursor;

[0035] (4) Add CO(NH 2 ) 2 , Make up 30ml solution C;

[0036] (5) Place solution C in a 50ml reaction kettle, place the reaction kettle in a thermostat for heating, and when the temperature rises to 240°C, keep it for 12 hours. After the reaction is over, rinse the product with deionized water until the pH is 7. Then dry it in a vacuum oven at 80℃ for 4h to obtain Sb 2 S 3 Nanowires.

[0037] See Figure 3 to Figure 6 As shown, the Sb obtained by this method 2 S 3 The diameter of the nanowire is about 200nm, the length is 20μm, and it grows along the [001] crystal ...

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Abstract

The invention provides a preparation method of an Sb2S3 nanowire. 10 mmol of Sb2Cl3 is dissolved into 2 ml of glycol; after the Sb2Cl3 is totally dissolved, 10 ml of deionized water is added while stirring to form white emulsion A; 15 mmol of Na2S.9H2O is dissolved into 10 ml of deionized water to form solution B; the solution B is added into the solution A at the rate of 2 drips / second to form a precursor; mineralizer is added into the precursor to prepare 30 ml of solution C, and the solution C is put in an agitated reactor; the agitated reactor is put into an incubator; when temperature rises to 240 DEG C, temperature is kept for 8-16 hours; and after reaction ends, the product is washed by deionized water to be neutral and is dried for 4h in vacuum in the incubator of 80 DEG C. The invention has simple preparation method, short reaction period and low cost.

Description

【Technical Field】 [0001] The present invention relates to a nano Sb 2 S 3 The preparation method of the material, especially a kind of Sb 2 S 3 Preparation method of nanowires. 【Background technique】 [0002] Antimony sulfide (Sb 2 S 3 ) Is an important direct band gap inorganic semiconductor material for V-VI, with an orthorhombic crystal structure and a band gap energy of 1.72 eV at room temperature. Due to its high photosensitivity and thermoelectric properties, antimony sulfide is considered an ideal material for solar energy. In addition, antimony sulfide is also considered to be widely used in infrared field, thermoelectric cooling technology and optoelectronic technology. [0003] In recent years, many researchers have used chemical vapor deposition (CVD), template method, evaporation condensation method, and hydrothermal (solvothermal) method to prepare antimony sulfide crystal phases with various morphologies. For example: Hu H M, Mo M S, YangB J, etc. (Solvothermal synt...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C01G30/00
Inventor 刘运朱刚强薛飞
Owner SHAANXI UNIV OF SCI & TECH
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