CN113036165A - Nitrogen-sulfur doped defected carbon nanotube and preparation method thereof - Google Patents

Nitrogen-sulfur doped defected carbon nanotube and preparation method thereof Download PDF

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CN113036165A
CN113036165A CN202110157818.4A CN202110157818A CN113036165A CN 113036165 A CN113036165 A CN 113036165A CN 202110157818 A CN202110157818 A CN 202110157818A CN 113036165 A CN113036165 A CN 113036165A
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carbon nanotube
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CN113036165B (en
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范海云
何建平
宋力
王涛
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Nanjing University of Aeronautics and Astronautics
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    • C01B32/00Carbon; Compounds thereof
    • C01B32/15Nano-sized carbon materials
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    • H01M4/86Inert electrodes with catalytic activity, e.g. for fuel cells
    • H01M4/90Selection of catalytic material
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
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    • H01M4/86Inert electrodes with catalytic activity, e.g. for fuel cells
    • H01M4/90Selection of catalytic material
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Abstract

The invention discloses a nitrogen-sulfur doped defected carbon nanotube and a preparation method thereof, and the prepared carbon nanotube material has high-efficiency electrocatalytic activity and durability. The method comprises the following steps: dicyandiamide as carbon/nitrogen source, Co (NO)3)2·6H2O is a metal source, by the sulfur-containing inorganic Salt Co (SCN)2Introducing heteroatom S, and carrying out primary heat treatment on the mixture precursor in an inert atmosphere to form N, S double-doped defected carbon nanotubes, wherein the defect is generated because the heteroatom S is diffused to a cobalt-containing region from a carbon region to form sulfide in the heat treatment process, so that abundant vacancies are left in a carbon skeleton, and the formation of pyridine nitrogen active sites is promoted. Thanks to the structural and compositional advantages, the N, S double-doped defected carbon nanotubes exhibit excellent ORR electrocatalytic activity and can be used as high-efficiency catalysts for fuel cells and zinc-air batteries.

Description

Nitrogen-sulfur doped defected carbon nanotube and preparation method thereof
Technical Field
The invention belongs to the field of functional materials, and particularly relates to a nitrogen-sulfur doped defected carbon nanotube and a preparation method thereof.
Background
Fuel cells have been considered as the most ideal energy storage devices, and zinc-air cells have been one of the most promising energy devices in the next-generation energy devices due to their advantages of low cost, environmental friendliness, high energy density, and convenience in use. Currently, research on zinc-air batteries is mainly focused on an Oxygen Reduction Reaction (ORR) catalyst of a cathode, and a large amount of noble metal catalyst is required due to low efficiency of electrode reaction caused by slow kinetic process, however, the noble metal-based catalyst is expensive and poor in stability, so that the large-scale application of the zinc-air battery is greatly limited. Therefore, more and more research is being conducted to develop a non-noble metal catalyst with high activity and high stability so as to improve the electrode reaction efficiency of the energy device.
Among many non-noble metal-based catalysts, carbon-based materials have the characteristics of good stability, low price, easy structure adjustment and the like, and are widely researched materials in the field of catalysis, however, among many carbon-based materials, carbon nanotubes have more obvious advantages, not only have high electron conductivity, but also can improve the activity of the carbon nanotubes by doping heterogeneous elements, and in addition, the complete one-dimensional structure of the carbon nanotubes also ensures the chemical stability of the carbon nanotubes, so that the carbon-based catalyst is an excellent electrocatalyst. At present, most of carbon nanotubes doped with heterogeneous elements (P, S) are based on modification of commercial carbon nanotubes, sulfur doping is usually performed by using an organic sulfur source, such as thiourea, trithiocyanuric acid, and the like, and related researches show that N, S doped carbon nanotubes can be obtained by introducing thiourea, melamine, and the like to perform modification treatment on the commercial carbon nanotubes. The ex-situ method has long steps, and because the atomic radius (0.102nm) of S is larger than that of C (0.077nm), the S element is difficult to be introduced into the pure carbon nanotube, and the doping effect is poor. Based on the above, in-situ rapid growth of N, S doped carbon nanotubes is a good choice. However, at present, many reports of in-situ nitrogen-doped carbon nanotubes exist, and research on in-situ catalytically grown carbon nanotubes doped with elements such as P and S is very little. In addition, the selection of the sulfur source is also important, and the organic sulfur source is mostly adopted to realize the doping of S in the research, but the inorganic sulfur source is cheaper, safe and environment-friendly.
Disclosure of Invention
The invention provides a nitrogen-sulfur doped defected carbon nanotube and a preparation method thereof, and the prepared carbon nanotube material not only has a stable structure and low price, but also has high-efficiency electrocatalytic activity and excellent durability.
In order to achieve the purpose, the invention adopts the following technical scheme:
a nitrogen-sulfur doped defected carbon nanotube is a N, S double-doped defected carbon nanotube, the carbon nanotube material is bamboo-like, the end part of a carbon nanotube is open and presents a hollow structure, and the end part of the carbon nanotube is closed with particles wrapped by a carbon layer; the pipe diameter of the carbon nano tube is 50-150 nm.
A preparation method of nitrogen-sulfur doped defected carbon nano-tubes comprises the following steps:
(1) a certain amount of Co (NO)3)2·6H2Dissolving O in a mixed solvent of absolute ethyl alcohol and deionized water, dispersing dicyandiamide in the solution, performing ultrasonic treatment to fully dissolve the dicyandiamide, and then violently stirring the mixed solution at room temperature for 1 hour to obtain a uniformly mixed solution;
(2) stirring and evaporating the mixed solution at 70-80 ℃ to dryness to obtain a single precursor;
(3) fully grinding the precursor prepared in the step (2) for later use;
(4) heating the precursor ground in the step (3) to 800-1100 ℃ under the protection of nitrogen atmosphere, wherein the heating rate is 6 ℃ for min-1Setting the heat preservation time to be 2h, and then cooling to room temperature to obtain a carbonized product, namely Co @ N-CNTs;
(5) weighing Co (SCN)2By replacing part of Co (NO)3)2·6H2O, synthesizing to obtain Co @ N, S-CNTs-1 according to the preparation method of Co @ N-CNTs; weighing Co (SCN)2Complete substitution of Co (NO)3)2·6H2And preparing the Co @ N, S-CNTs-2 from O.
In the above steps, the amount of dicyandiamide in step 1 is mixed with Co (NO)3)2·6H2The molar ratio of O is 10:1, absolute ethyl alcohol andthe volume ratio of the deionized water is 2: 1;
when synthesizing Co @ N, S-CNTs-1 in step 5, Co (SCN)2By replacing part of Co (NO)3)2·6H2O,Co(SCN)2With Co (NO)3)2·6H2The mass ratio of O is 1: 1.
The nitrogen-sulfur doped carbon nanotubes can be used as a catalyst for fuel cells or zinc-air cells.
Has the advantages that: the invention provides a nitrogen-sulfur doped defected carbon nano tube and a preparation method thereof, wherein inorganic cobalt thiocyanate is used as a sulfur source, and the defected carbon nano tube containing N, S double doping is grown through the in-situ catalysis of transition metal, so that the effective doping of a heterogeneous element S is realized, and the formation of carbon defects is caused by the introduction of S atoms, so that the electrocatalytic activity of a carbon nano tube material is obviously improved. The formation of the carbon nanotubes is derived from the catalytic action of metal cobalt, the carbon nanotubes with typical bamboo-like characteristics are formed, the pipe diameter of the carbon nanotubes is about 50-150nm, the end parts of some carbon nanotubes are open and present a hollow structure, and the end parts of some carbon nanotubes are closed and have particles wrapped by a carbon layer. Since during heat treatment the hetero atoms S tend to diffuse from the carbon region to the cobalt-containing region to form sulfides, leaving rich vacancies in the carbon skeleton, while also promoting the formation of pyridine nitrogen active sites, the half-wave potential of the synthetic catalyst is 0.86V (relative to RHE) and better than Pt/C (0.83V) thanks to the advantages of this structure and composition. The carbon nano tube catalyst provided by the invention shows higher power density (62.1mW cm) when applied to a zinc-air battery-2) Is superior to Pt/C (58.7mW cm)-2). The catalytic material with a stable structure, high efficiency and durability is prepared by a simple extensible method with low cost, a new thought is provided for the development of energy devices, and the development of clean energy can be assisted.
Drawings
FIG. 1 is an SEM image of Co @ N-CNTs according to an embodiment of the present invention;
FIG. 2 is an SEM image of Co @ N, S-CNTs-1 according to an embodiment of the present invention;
FIG. 3 is an SEM image of Co @ N, S-CNTs-2 according to an embodiment of the present invention;
FIG. 4 is a Raman spectrum of Co @ N-CNTs, Co @ N, S-CNTs-1, Co @ N, S-CNTs-2 according to the present invention.
Detailed Description
The invention is described in detail below with reference to the following figures and specific examples:
embodiments relate to reagent and equipment sources:
Co(NO3)2·6H2o, available from alatin reagent, inc;
Co(SCN)2from Shanghai Michelin Biochemical technology, Inc.;
dicyandiamide, available from carbofuran technologies ltd;
absolute ethanol was analytically pure AR, purchased from south beijing chemicals ltd;
an electrochemical workstation: shanghai chenhua instruments ltd, CHI 760E;
scanning electron microscope: hitachi, Japan S-4800, acceleration voltage 10 kV;
raman spectroscopy: horiba Scientific LabRAM HR Evolution
Example 1
A preparation method of nitrogen-sulfur doped defected carbon nano-tubes comprises the following steps:
(1) accurately weighing 4mmol Co (NO)3)2·6H2O, and dissolved in a mixed solvent of absolute ethanol (50ml) and deionized water (25 ml). 40mmol of dicyandiamide was dispersed in the above solution and sufficiently dissolved by ultrasonic treatment. Then, the mixed solution is stirred vigorously for 1 hour at room temperature;
(2) transferring the mixed solution to a water bath kettle, stirring and evaporating at 80 ℃ to dryness to obtain a single precursor;
(3) fully grinding the precursor prepared in the step (2) for later use;
(4) putting the sample ground in the step (3) into a porcelain boat, heating to 800-1100 ℃ under the protection of nitrogen atmosphere, wherein the heating rate is 6 ℃ for min-1. The heat preservation time is set to be 2 hours, and a carbonized product is obtained after the carbonized product is cooled to the room temperatureNamely Co @ N-CNTs.
Example 2
A preparation method of nitrogen-sulfur doped defected carbon nano-tubes comprises the following steps:
(1) accurately weighing 2mmol Co (NO)3)2·6H2O and 2mmol Co (SCN)2And dissolved in a mixed solvent of absolute ethanol (50ml) and deionized water (25 ml). Then, 40mmol of dicyandiamide was dispersed in the above solution and sufficiently dissolved by ultrasonic treatment. The mixed solution is stirred vigorously for 1h at room temperature;
(2) transferring the mixed solution to a water bath kettle, stirring and evaporating at 80 ℃ to dryness to obtain a single precursor;
(3) fully grinding the precursor prepared in the step (2) for later use;
(4) putting the sample ground in the step (3) into a porcelain boat, heating to 800-1100 ℃ under the protection of nitrogen atmosphere, wherein the heating rate is 6 ℃ for min-1. The heat preservation time is set to be 2h, and a carbonized product, namely Co @ N, S-CNTs-1, is obtained after cooling to the room temperature.
Example 3
A preparation method of nitrogen-sulfur doped defected carbon nano-tubes comprises the following steps:
(1) accurately weigh 4mmol Co (SCN)2And dissolved in a mixed solvent of absolute ethanol (50ml) and deionized water (25 ml). 40mmol of dicyandiamide was dispersed in the above solution and sufficiently dissolved by ultrasonic treatment. Then, the mixed solution is stirred vigorously for 1 hour at room temperature;
(2) transferring the mixed solution to a water bath kettle, stirring and evaporating at 80 ℃ to dryness to obtain a single precursor;
(3) fully grinding the precursor prepared in the step (2) for later use;
(4) putting the sample ground in the step (3) into a porcelain boat, heating to 800-1100 ℃ under the protection of nitrogen atmosphere, wherein the heating rate is 6 ℃ for min-1. The heat preservation time is set to be 2h, and a carbonized product, namely Co @ N, S-CNTs-2, is obtained after the carbonized product is cooled to the room temperature.
In examples 1 to 3, the scanning electron microscope observation results of the carbon nanotubes are shown in fig. 1 to 3, all the carbon nanotubes exhibit a typical bamboo-like structure, part of the ends of the carbon nanotubes are closed and particles coated by the carbon layer are formed, and part of the ends of the carbon nanotubes are open and present a hollow structure. The diameter of the carbon nano tube is about 50-150 nm.
Raman spectra for the samples prepared in examples 1-3 are shown in FIG. 4, with nitrogen-doped Co @ N-CNTs alone having D, G, 2D peaks representing the typical structure of carbon nanotubes, whereas in Co @ N, S-CNTs-1 and Co @ N, S-CNTs-2, the 2D peak disappeared at 675cm-1A peak of sulfide appears, and ID/IGThe ratio of (a) to (b) increases in turn, which indicates that an increase in the sulfur content leads to a significant increase in the degree of defectivity.
The above description is only for the purpose of illustrating preferred embodiments and applications of the present invention, and should not be construed as limiting the present invention, and all modifications, substitutions and alterations based on the technical spirit of the present invention are intended to be included in the scope of the present invention. It will be apparent to those skilled in the art that various changes and modifications can be made without departing from the invention, and these changes and modifications are to be considered as within the scope of the invention.

Claims (6)

1. The nitrogen-sulfur-doped defected carbon nanotube is characterized in that the carbon nanotube is N, S double-doped defected carbon nanotube, the carbon nanotube material is bamboo-like, part of the end part of the carbon nanotube is open and has a hollow structure, and the end part of the carbon nanotube is closed with particles wrapped by a carbon layer.
2. The nitrogen-sulfur doped defected carbon nanotube of claim 1, wherein the tube diameter of the carbon nanotube is 50-150 nm.
3. The nitrogen-sulfur doped defected carbon nanotubes of claim 1 or 2 can be used as a catalyst for fuel cells or zinc-air cells.
4. A preparation method of a nitrogen-sulfur doped defected carbon nanotube is characterized by comprising the following steps:
(1) a certain amount of Co (NO)3)2·6H2Dissolving O in a mixed solvent of absolute ethyl alcohol and deionized water, dispersing dicyandiamide in the solution, performing ultrasonic treatment to fully dissolve the dicyandiamide, and then violently stirring the mixed solution at room temperature for 1 hour to obtain a uniformly mixed solution;
(2) stirring and evaporating the mixed solution at 70-80 ℃ to dryness to obtain a single precursor;
(3) fully grinding the precursor prepared in the step (2) for later use;
(4) heating the precursor ground in the step (3) to 800-1100 ℃ under the protection of nitrogen atmosphere, wherein the heating rate is 6 ℃ for min-1Setting the heat preservation time to be 2h, and then cooling to room temperature to obtain a carbonized product, namely Co @ N-CNTs;
(5) weighing Co (SCN)2By replacing part of Co (NO)3)2·6H2O, synthesizing to obtain Co @ N, S-CNTs-1 according to the preparation method of Co @ N-CNTs; weighing Co (SCN)2Complete substitution of Co (NO)3)2·6H2And preparing the Co @ N, S-CNTs-2 from O.
5. The method of claim 4, wherein the dicyandiamide and Co (NO) are mixed in step 13)2·6H2The molar ratio of O is 10:1, and the volume ratio of absolute ethyl alcohol to deionized water in the mixed solvent is 2: 1.
6. The method of claim 4, wherein the step 5 of synthesizing Co @ N, S-CNTs-1 is performed by Co (SCN)2By replacing part of Co (NO)3)2·6H2O,Co(SCN)2With Co (NO)3)2·6H2The mass ratio of O is 1: 1.
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114620712A (en) * 2022-03-21 2022-06-14 陕西艾诺威邦信息科技有限公司 Preparation method of anode catalyst carrier for direct methanol fuel cell
CN115074092A (en) * 2022-05-09 2022-09-20 清华大学 Nitrogen-containing sulfur-containing carbon nanotube and preparation method and application thereof
CN115491713A (en) * 2022-09-22 2022-12-20 电子科技大学 Preparation method of Ni-N-C monatomic material based on Cl doping

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CN111682224A (en) * 2020-06-19 2020-09-18 郑州大学 Monoatomic cobalt-loaded nitrogen-doped graphite carbon cathode catalyst for rechargeable zinc-air battery and preparation method thereof
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CN115491713A (en) * 2022-09-22 2022-12-20 电子科技大学 Preparation method of Ni-N-C monatomic material based on Cl doping

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