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Preparation method for platinum nanowire

A technology of platinum nanowires and chloroplatinic acid, applied in the field of nanomaterials, achieves the effects of high yield, simple synthesis process, high controllability and stability

Active Publication Date: 2015-04-08
YANSHAN UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

Preparation of one-dimensional nanomaterials using chymotrypsin fiber template method has not been reported

Method used

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  • Preparation method for platinum nanowire
  • Preparation method for platinum nanowire
  • Preparation method for platinum nanowire

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0019] Dissolve 1.0 mg of chymotrypsin powder in 1.0 mL of prepared glycine-hydrochloric acid buffer solution with a concentration of 8 mM and pH=2.4 to prepare a chymotrypsin solution, vortex and mix thoroughly, and then add 0.1 ml of trifluoroethanol to the solution, Incubate for 50 h on an air shaker at 20° C. with a rotational speed of 120 r / min to obtain a chymotrypsin fiber suspension. Take 180 μL of chymotrypsin fiber suspension, add 80 μL of chloroplatinic acid with a concentration of 5 mM and pH=1.6 to it, mix thoroughly, and incubate on a shaking table at 10°C and 80 r / min for 20 h, then add 5 mM chloroplatinic acid drop by drop. 90 μL of sodium borohydride was used for reduction, and the reaction was completed by incubating on a shaker at 10°C and 80 r / min for 15 hours to obtain platinum nanowires.

[0020] Such as figure 1 The resulting single platinum nanowire is shown to have a diameter of about 34 nm and a length of about 540 nm.

Embodiment 2

[0022] Dissolve 1.0mg of chymotrypsin powder in 0.67mL of prepared glycine-hydrochloric acid buffer solution with a concentration of 10mM and pH=2.5 to prepare a chymotrypsin solution, vortex and mix thoroughly, and then add 0.09ml of trifluoroethanol to the solution, Incubate for 48 hours on an air shaker at 25° C. with a rotational speed of 135 r / min to obtain a chymotrypsin fiber suspension.

[0023] Take 190 μL of chymotrypsin fiber suspension, add 100 μL of chloroplatinic acid with a concentration of 3 mM and pH=2.0 to it, mix well, place it on a shaker at 16 ° C and 90 r / min for 12 h, and then add the concentration of 10 mM 60 μL of sodium borohydride was used for reduction, and the reaction was completed by incubating on a shaker at 16°C and 90 r / min for 12 hours to obtain platinum nanowires.

[0024] Such as figure 2 As shown, a large number of platinum nanowires can be obtained, and the diameter of the platinum nanowires is about 15 nm, up to a micron.

Embodiment 3

[0026] Take 1.0mg of chymotrypsin powder, dissolve it in 0.5mL of prepared glycine-hydrochloric acid buffer solution with a concentration of 12mM and pH=2.6 to prepare a chymotrypsin solution, vortex and mix well, then add 0.09ml of trifluoroethanol to the solution , and incubated for 45 hours on an air shaker at 30° C. with a rotational speed of 150 r / min to obtain a chymotrypsin fiber suspension.

[0027] Take 180 μL of chymotrypsin fiber suspension, add 200 μL of chloroplatinic acid with a concentration of 2.5 mM and pH=2.5 to it, mix well, place it on a shaking table at 20 °C and 100 r / min for 10 h, and then add the concentration of 80 μL of 8 mM dimethylamine borane was used for reduction, and incubated at 20°C for 10 h on a shaker at 100 r / min to complete the reaction to obtain platinum nanowires.

[0028] Such as image 3 The obtained platinum nanowires have a diameter of about 21 nm and a length of about 900 nm.

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Abstract

The invention discloses a preparation method for a platinum nanowire. The preparation method comprises the following steps of: dissolving each mg of zonolysin into 0.5-1.0ml of glycine-hydrochloric acid buffer solution; fully and uniformly mixing and then adding trifluoroethanol with the volume ratio of 9-15 percent; incubating the mixture in an air shaking table at the temperature of 20-30 DEG C and the rotating speed of 120-150r / min for 45-50h to obtain a zonolysin fiber suspension; adding platinic chloride according to the volume ratio of the zonolysin fiber suspension to the platinic chloride being (0.9-1):(0.4-1); fully and uniformly mixing and then incubating the mixture in the shaking table at the temperature of 10-20 DEG C and the rotating speed of 80-100 / min for 10-20h; adding sodium borohydride or dimethylamine borane for reducing; incubating the reduced product in the shaking table at the temperature of 10-20DEG C and the rotating speed of 80-100r / min for 10-15h for completely reacting; and obtaining the platinum nanowire which is 15-34nm in diameter and as long as micrometer according to the ratio difference of the added raw materials. The preparation method disclosed by the invention has the advantages of mild condition, environment friendliness, low cost, high yield and high controllability and stability of nanowire.

Description

technical field [0001] The invention relates to the field of nanometer materials, in particular to a method for preparing platinum nanowires. Background technique [0002] Platinum nanocrystals have been widely used in many industrial technical fields such as catalytic converters, fuel cells, and petroleum cracking due to their unique electronic structure and catalytic performance. [0003] Due to the high price of platinum and the scarcity of resources, the current research on the control of the size and shape of platinum nanocrystals is mainly to reduce the amount of platinum and improve its cost performance without affecting the performance of platinum. [0004] Compared with the zero-dimensional structure, the one-dimensional structure of platinum nanocrystals has the following advantages: higher aspect ratio, fewer lattice defects, smaller lattice spacing and high surface atomic number. In addition, due to the structural anisotropy, one-dimensional platinum nanowires w...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): B22F9/24C30B7/14C30B29/02C30B29/62
Inventor 高发明鲜义芬李娜侯莉
Owner YANSHAN UNIV