Patent Application
20240043270
The present invention relates to a method for catalytically producing hydrogen by means of energy radiation, specifically relates to a composite catalyst and use thereof in catalytically producing hydrogen by means of energy radiation.
In the field of new energy resources, hydrogen has been considered as the most ideal and pollution-free green energy in the new century since the only product of hydrogen combustion is water. As the most abundant elements in nature, hydrogen widely exists in water, fossil fuel and various carbohydrates. As a major industrial raw material, hydrogen is also the most important industrial gas and special gas, and is used as an important raw material for synthesizing ammonia, methanol, and hydrochloric acid, and also used as a reducing agent for metallurgy, a hydrodesulfurizing agent for petroleum refining and the like.
However, traditional hydrogen producing methods consuming huge amounts of conventional energy lead over high cost for producing hydrogen and limit promotion and application of hydrogen energy. Scientists imaged to use the inexhaustible and low-cost solar energy as the primary energy for producing hydrogen energy, which opens broader prospect in development of hydrogen energy. Scientists found water could be decomposed into oxygen and hydrogen that are essential in a fuel cell by solar energy, by utilizing a photocatalytical material as a “media”, and such a technology of producing hydrogen and oxygen by merely utilizing solar and water was called “one of the ideal technologies for human”.
Plasmonic metal catalysts could immensely enhance local energy on surfaces of a nanosturcture due to plasmon effect. Accordingly, in a case of the overall reaction conditions are mild, the catalytic reaction could be efficiently promoted such that it is possible to conduct a reaction that could not be conducted under normal temperature and normal pressure. In recent years, it has been realized to decompose water into hydrogen and oxygen, but so far, it is still necessary to develop higher effective, more stable and cost effective catalysts.
The concept of single atom catalysis received widespread concern and research since it was proposed in recent years. As development of advanced characteristic technology, single atom catalysts provide the possibility to explain the structure-activity relationship of catalysts from molecular and atomic level, and to connect heterogeneous catalysis with homogeneous catalysis. Single atom catalysts show different activities, selectivities and stabilities from conventional nano catalysts, due to its special structures.
Therefore, it is possible to develop catalysts for producing hydrogen with efficiencies, stabilities and cost that satisfy commercial requirements, by coupling advantages of both plasmon effect and single atom catalysis.
On the basis of the technical problems exist in the technical background, the present invention clarifies a novel plasmonic catalytic technology, the plasmonic catalyst comprises atomic sites such as single atomic sites and/or atomic clusters having 2-25 atoms, the technology provides a unique method of preparing hydrogen by decomposing a hydrogen-containing source, preferably water, by light radiation and/or thermal radiation in the presence of a cost effective catalyst.
One aspect of the present invention is a method for producing hydrogen by means of energy radiation, comprising:
In certain embodiments, the atomic sites further comprise one or two or more chemical elements selected from Ru, Rh, Ag, Au, Pt, Pd, Os and Ir, preferably one or two selected from Ru and Au.
In certain embodiments, the energy radiation is at least one selected from light radiation and heat radiation, preferably light radiation.
In certain embodiments, a distance between the nano-base structure and the atomic sites is 5 nm or less, preferably 1 nm or less, more preferably less than 0.1 nm, most preferably the nano-base structure and the atomic site are in close contact with each other.
In certain embodiments, the atomic sites are bonded with the nano-base structure, for example by physical manner or chemical manner.
In certain embodiments, a mass percentage of the atomic sites and the nano-base structure is 50% or less, preferably 0.01% to 30%, preferably 0.01% to 5%, more preferably to 2%, most preferably 0.1% to 1%.
In certain embodiments, the atomic sites are loaded on surface, internal pores of the nano-base structure or distributed in internal crystal lattices of the nano-base structure, preferably respective atomic sites are dispersed uniformly, and
In certain embodiments, the nano-base structure is selected from a group consisting of Mn, Co, Ce, Fe, Al, Ca, Ce, Cu, Ni, Ti, Zn, Si, Mo, Bi, V, C, N and oxides, nitrides, sulfites, carbides, hydroxides, chlorides thereof and metal-organic frameworks (MOF), preferably metal-organic frameworks, TiO2 or Al2O3.
In certain embodiments, the composite catalyst is a catalyst in which Co and Fe are loaded on or bonded to a metal-organic framework (CoFe-MOF), a catalyst in which Co and Mn are loaded on or bonded to a metal-organic framework (CoMn-MOF), a catalyst in which Fe and Co are loaded on or bonded to TiO2 (FeCo—TiO2), or a catalyst in which Ru and Co are loaded on or bonded to TiO2 (RuCo—TiO2).
In preferable embodiments, the nano-base structure is about 1 nm to about 1000 nm, preferably about 70 nm to about 1000 nm, about 100 nm to about 800 nm, about 200 nm to 500 nm in at least one dimension of length, width and height.
In preferable embodiments, the nano-base structure each independently is about 1 nm to about 3000 nm in length, width or height, preferably about 100 nm to about 3000 nm, about 500 nm to about 2500 nm, or about 1000 nm to about 2000 nm in length, and/or about 1 nm to about 1000 nm, about 70 nm to about 1000 nm, about 100 nm to about 800 nm, or about 200 nm to about 500 nm in width or height, or
In certain embodiments, the nano-base structure each independently has a shape of spherical, spike, flake, needle, blade of grass, columnar, polyhedral, 3D cone, cuboidal, sheet, hemispherical, irregular 3D shape, porous structure or any combinations thereof.
In certain embodiments, a plurality of the atomic sites are arranged in a patterned configuration, preferably in a plurality of layers, on the nano-base structure, or
In certain embodiments, the energy radiation allows the reaction progresses at a temperature between about 20° C. to about 500° C., preferably about 50° C. to about 300° C., about to about 250° C., about 90° C. to about 200° C., about 100° C. to about 200° C., about 100° C. to about 180° C., about 110° C. to about 160° C., about 120° C. to about 150° C., about 130° C. to about 150° C., and
In certain embodiments, the reaction is initiated by utilizing light radiation or heat radiation, and the reaction is continued to progress by utilizing light radiation or heat radiation, wherein
In certain embodiments, temperatures of the composite catalyst, and the hydrogen-containing source are raised by the light radiation, preferably the light radiation is the sole source for raising the temperatures.
In certain embodiments, the hydrogen-containing source is selected from a group consisting of water, saturated alcohols, carboxylic acids, phenols and any combination thereof, preferably water.
In certain embodiments, when the atomic sites include two or more chemical elements and are single atoms, the two or more elements may be arranged at intervals, or may be arranged randomly.
In certain embodiments, when the atomic sites are atomic clusters, compositions of respective atomic clusters may be the same or different, for example, respective atomic clusters may include different elementary composition, and/or include different numbers of atoms.
The invention demonstrated, unexpectedly, that a hydrogen-containing source, preferably water, could be converted to hydrogen molecules, using light radiation and/or heat radiation as energy input, in the presence of composite catalysts having plasmon effect.
Before further description of the present invention, certain terms employed in the specification, examples and appended claims are defined in the following section. The definitions listed herein should be read in light of the remainder of the disclosure and understood as by those skilled in the art. Unless defined otherwise, all technical and scientific terms as used herein have the same meaning as commonly understood by a person of ordinary skill in the art to which this invention belongs.
The term “catalyst” as used herein refers to substances that exhibit effects to increase the rate of a chemical reaction by reducing the activation energy of the reaction. The rate increasing effect is referred as “catalysis”. Catalysts are not consumed in a catalytic reaction, therefore they can continue to catalyze the reaction of further quantities of reactant with a small amount.
The term “plasmon donor” as used herein refers to conductor whose real part of dielectric constant thereof is negative. Plasmon provider provides surface plasmons when excited by electromagnetic radiation.
The term “temperature-dependence” as used herein refers to properties that may vary when temperature changes by a given level. The temperature difference to alter the property may be any degrees, such as 0.1° C., 1° C., 5° C., 10° C., 100° C., or 1000° C.
The term “chemical element” as used herein refers to chemical substance consisting of atoms having the same number of protons in their atomic nuclei. Specifically, chemical elements are those recorded in the periodic table of chemical elements. Chemical elements include natural elements and synthetic elements. Chemical elements also include elements not discovered yet with more than 118 protons in the atomic nuclei.
The term “bond” or “load” as used herein refers to bonded to or loaded on the surface, in the internal holes or internal lattices by physical manner or chemical manner, wherein the physical manner includes Van der Waals force, metallic bond and other conventional physical bonding manner, and the chemical manner includes ionic bond, covalent bond, coordination bond and other conventional chemical bonding manner.
The term “alloy” as used herein refers to a mixture of metals or a mixture of metal and other elements. Alloys are defined by metallic bonding character. An alloy may be a solid solution of metal elements (a single phase) or a mixture of metallic phases (two or more solutions).
The term “catalyst activity per unit” as used herein refers to a molar quantity of a product produced in unit time by active catalyst per unit mass, under certain reaction conditions. Specifically, catalyst activity per unit =a molar quantity of a reaction product/a mass of active catalyst/reaction time.
The term “close contact” as used herein refers to there is substantially no gap between the two components, e.g. a distance between the two components is 1 nm or less, 0.1 nm or less, or substantially 0 nm, preferably metallic bonds or coordinate bonds are formed between the two components.
The term “saturated alcohols” as used herein refers to saturated hydrocarbon compounds substituted by —OH group, for example, C1-C15 saturated alcohols, preferably C1-C8 saturated alcohols, more preferably C1-C4 saturated alcohols, such as methanol, ethanol, propanol, isopropanol, butanol, isobutanol.
The term “carboxylic acids” as used herein refers to saturated hydrocarbon compounds substituted by —COOH group, for example, C1-C15 carboxylic acids, preferably C1-C8 carboxylic acids, more preferably C1-C4 carboxylic acids, such as formic acid, acetic acid, propionic acid, isopropylic acid, butyric acid, isobutyric acid.
The term “phenols” as used herein refers to compounds comprising —OH group directly connecting to an aromatic ring, wherein the aromatic ring is a monocycle, bicycle or tricycle comprising 5-20 carbon atoms, preferably 5-20 carbon atoms, most preferably 5-15 carbon atoms, more preferably 6-12 carbons atoms, for example, the aromatic ring is benzene, naphthalene.
The term “metal-organic frameworks (MOF)” as used herein refers to organic-inorganic hybrid materials having intermolecular pores or metal-organic skeleton structure having periodic network structures formed from organic ligands and metal ions or clusters by means of self-assembly. The MOF may contain transition metals, rare-earth metals, main group metals such as alkali metals and alkaline-earth metals, for example, Cu, Zn, Cd, Fe, Ti, Mn, Al and Co, preferably Ti may be contained, non-metallic elements such as O, N, S, P, halogen (such as F, Cl, Br, I) and the like may be further contained. The MOF may be prepared by known methods in the art such as evaporation solvent method, diffusion method, hydrothermal or solvothermal method, ultrasonic and microwave method and the like.
One aspect of the present invention is composite catalysts used for producing hydrogen molecules by light radiation and/or heat radiation.
Without wishing to be bound by theory, the plasmonic composite catalyst of the present invention interacts with the raw materials of the reaction to reduce the activation energy of the reaction so as to initiate the reaction by utilizing light radiation and/or heat radiation, and to increase the reaction rate.
The plasmonic composite catalyst includes two structures: atomic sites and nano-base structure, wherein the atomic sites and the nano-base structure are contact with each other. In preferred embodiments, in the plasmonic composite catalyst, a mass percentage of the atomic sites and the nano-base structure is 50% or less, preferably 0.01% to 30%, preferably 0.01% to 5%, more preferably 0.01% to 2%, most preferably 0.1% to 1%.
The term “atomic sites” as used herein refers to mutually independent metal single atoms and/or mutually independent atomic clusters including 2-25, preferably 2-20 metal atoms, the metal single atoms and/or the atomic clusters are stably bonded to or loaded on surface and/or in internal pores and/or internal crystal lattices of the nano-base structure, preferably uniformly dispersed on the nano-base structure, more preferably uniformly dispersed on the surface of the nano-base structure. The metal single atoms or atoms in the atomic clusters are present in a valance state between zero valance state and the highest valance state that the metal usually present, an average valance state of the metal is, for example, 0 to +4, or 0 to +3, or 0 to +2, or 0 to +1, preferably 0. The distances between atoms in the atomic clusters are less than 1 nm, preferably 0.1-0.5 nm.
Atoms in the atomic sites are bonded to atoms in the nano-base structure by physical manner or chemical manner, for example coupling by Van der Waals force, metallic bond and other conventional physical bonding manner, or bonding by ionic bond, covalent bond, coordination bond and other conventional chemical bonding manner, or forming complex by coordinate bonds.
When the atomic sites are mutually independent metal single atoms, the interaction between the metal single atoms and the atoms in the nano-base structure may prevent the metal single atoms from being agglomerated, and thus make it more stable. In certain embodiments, in the catalytic metal single atomic sites, all of the catalytic metal are present in form of isolated atoms, that is, a degree of dispersion of the catalytic metal atoms is 100%, and thus the catalytic metal atoms can be utilized to the maximum; preferably, all of the catalytic metal atoms are directly fixed to the surface of the nano-base structure and become 100% interface atoms, and thus the interaction of metal-base interface can be fully utilized to optimize the catalytic performance.
When the atomic sites are mutually independent metal atomic clusters, the metal atomic clusters are bonded with atoms in the nano-base structure by physical manner or chemical manner. The metal atomic clusters are stably dispersed on the nano-base structure and/or in the nano-base structure.
When the atomic sites are single atoms of single metal element, in certain embodiments, the single metal element works as both plasmon providers and catalytic property providers, the nano-base structure provides physical supporting function; in other embodiments, the single metal element works as plasmon provider, and the nano-base structure provides physical supporting function and works as catalytic property provider.
When the atomic sites are metal atomic clusters, in some embodiments, some atomic clusters comprising specific elements work as plasmon provider, other atomic clusters comprising specific elements word as catalytic property provider, the nano-base structure provides physical supporting function; in other embodiments, the atomic clusters work as plasmon provider, and the nano-base structure provides physical supporting function and works as catalytic property provider.
In other embodiments, the atomic sits and the nano-base structure work together as both plasmon provider and catalytic property provider, and the nano-base structure provides physical supporting function.
The term “nano-base structure” as used herein refers to a structure having a range of nanometer-scale dimension, i.e, about 1 nm to about 1000 nm, preferably about 70 nm to about 1000 nm, about 100 nm to about 800 nm, about 200 nm to about 500 nm in at least one dimension of length, width, and height. The nano-base structure can have one dimension which exceeds 1000 nm, for example, have a length in a range of micrometer-scale, such as 1 μm to 5 μm. In certain cases, tubes and fibers with only two dimensions within a range of nanometer-scale are also considered as the nano-base structures. Material having nano-base structure may exhibit size-related properties that differ significantly from those observed in bulk materials.
The nano-base structure of the present invention each independently is about 1 nm to about 3000 nm in length, width or height. The length thereof is preferably about 100 nm to about 3000 nm, more preferably about 500 nm to about 2500 nm, further more preferably about 1000 nm to about 2000 nm. The width or height thereof is preferably about 1 nm to about 1000 nm, preferably about 70 nm to about 1000 nm, more preferably about 100 nm to about 800 nm, further more preferably about 200 nm to about 500 nm.
The nano-base structure of the present invention each independently has an aspect ratio (i.e., a ratio of length to width/height) of about 1 to about 20, preferably an aspect ratio of about 1 to about 10, or about 2 to about 8. The nano-base structure of the present invention can also have a relatively small aspect ratio such as about 1 to about 2.
The nano-base structure of the present invention each independently has a shape of spherical, spike, flake, needle, blade of grass, columnar, polyhedral, 3D cone, cuboidal, sheet, hemispherical, irregular 3D shape, porous structure or any combinations thereof.
The nano-base structure is selected from a group consisting of Mn, Co, Ce, Fe, Al, Ca, Ce, Cu, Ni, Ti, Zn, Si, Mo, Bi, V, C, N and oxides, nitrides, sulfites, carbides, hydroxides, chlorides thereof and metal-organic frameworks.
The term “nano-base structure” as used herein comprises more than 25, preferably more than 30 atoms.
A plurality of the nano-base structures of the present invention can be arranged in a patterned configuration, preferably in a plurality of layers, or a plurality of the nano-base structures may be randomly dispersed in a medium. For example, the nano-base structures may be bound to a substrate. In such case, the nano-base structures are generally not aggregated together, but rather, are arranged or stacked in an orderly pattern. Alternatively, a plurality of the nano-base structures can be dispersed in a liquid medium, in which each nano-base structure is free to move with respect to any other nano-base structures.
For example, the nano-base structure could have a spike or blade of grass-like geometric configuration. Optionally, the nano-base structure has a flaky geometric configuration with a relative thin thickness. Preferably, the nano-base structure has a configuration of nano-jungle, nano-grass, and/or nano-snowflake. The nano-base structure could have a relative large aspect ratio, such nanostructure could have a construction of nano-spike, nano-snowflake or nano-needle. The aspect ratio could be about 1 to about 20, about 1 to about 10, or about 2 to about 8. Preferably, the length of the nano-base structure could be 5 about 100 nm to about 3000 nm, about 500 nm to about 2500 nm, or about 1000 nm to about 2000 nm; the width or height could be about 1 nm to about 1000 nm, about 70 nm to about 1000 nm, about 100 nm to about 800 nm, or about 200 nm to about 500 nm.
The nano-base structures may be bound to a substrate. Accordingly, the nano-base structures are generally not aggregated together, but rather, are arranged in an orderly pattern. The substrate can be formed of metal or polymer material (e.g., polyimide, PTFE, polyester, polyethylene, polypropylene, polystyrene, polyacrylonitrile, etc.)
In other embodiments, the nano-base structure has a shape of spherical, columnar, polyhedral, 3D cone, cuboidal, sheet, hemispherical, irregular 3D shape, porous structure or any combinations thereof. Such nano-base structures each independently is about 1 nm to about 1000 nm, preferably about 70 nm to about 1000 nm, about 100 nm to about 800 nm, or about 200 nm to about 500 nm in length, width or height.
Furthermore, the plasmonic atomic catalyst of the present invention could function in various states, such as dispersed, congregated, or attached/grew on surface of other materials. In preferred embodiments, the plasmonic atomic catalyst are dispersed in a medium, the medium is preferably the reactants of the reaction, such as water.
Another aspect of the present invention is a method for producing hydrogen molecules by light radiation and/or heat radiation, comprising:
Under catalytic effects of the plasmonic composite catalyst, the energy radiation, i.e., light radiation and/or heat radiation, initiates the reaction of the hydrogen-containing source. The reaction decomposing hydrogen-containing source, preferably water to produce hydrogen molecules is an endothermic reaction. Without wishing to be bound by theory, the plasmonic composite catalyst could convert and transmit energy of light radiation and heat radiation, so as to keep the reaction of the present invention progressing. In certain temperature range, raising the temperature leads to a higher energy conversion rate of producing hydrogen molecules.
The light radiation and/or heat radiation step is carried out at a temperature between about 20° C. to about 800° C., about 20° C. to about 500° C., about 50° C. to about 300° C., about to about 250° C., about 90° C. to about 200° C., about 100° C. to about 200° C., about 100° C. to about 180° C., about 110° C. to about 160° C., about 120° C. to about 150° C., about 130° C. to about 150° C. A catalyst activity per unit for producing hydrogen is more than 0.2 οmol g−1 h−1, preferably more than 0.5 μmol g−1 h−1, preferably more than 3 μmol g−1 h−1, preferably more than 5 μmol g−1 h−1, and more than 7 μmol g−1 h−1 in the preferred temperature range.
The term “heat” as used herein refers to thermal energy transferred from one system to another as a result of thermal interactions. Heat may be transferred into the reaction system from an external heat source, alternatively, heat may be carried by one component of the reaction so as to be transferred to other components involved in the reaction. In other words, the one component that carries heat before reaction is an internal heat source. In certain embodiments, temperatures of the plasmonic composite catalyst and the hydrogen-containing source during the reaction of the present invention are raised by heat radiation.
In the reaction of the present invention, the light radiation mimics the wavelength composition and the strength of solar light, thus the temperature of the radiated catalyst and reactants could be raised. When the radiation intensity reaches a certain level, the temperatures of the plasmonic composite catalyst and the hydrogen-containing source are raised by the light radiation. Preferably, light radiation is the sole source for raising the temperature.
In the reaction of the present invention, after the reaction is initiated, the reaction is continued to progress under light radiation. The term “light” as used herein refers to electromagnetic wave having a wavelength from about 250 nm to about 2000 nm. In other words, light refers to the radiance of visible light. Preferably, in the reaction of the present invention, the power of light radiation is less than the power of solar radiation (i.e., the solar constant). For example, the power of light radiation is 200-1500 W/m2, preferably 200-1000 W/m2, and most preferably 500-1000 W/m2. The light radiation could be solar light or light emitted from artificial light sources, wavelength of the light radiation is between about 250 nm to about 2000 nm.
The reaction time varies depending on reaction scale, radiation intensity, temperature and other factors, the reaction is continuously performed utilizing a well-established apparatus with a continuous feed of the hydrogen-containing source. The reaction time could be 0.1 hour or more, preferably 0.1 hour to 1000 hours, preferably 0.1 hour to 500 hours, preferably 0.5 hour to 100 hours, preferably 1 hour to 50 hours, preferably 2 hours to 30 hours, most preferably 4 hours to 20 hours.
The reaction could be carried out at low pressure, normal pressure or high pressure, the reaction pressure could be properly selected based on reaction scale, radiation intensity, temperature and other factors, for example, the reaction pressure could be at least 1 bar, e.g. 1 bar to 30 bar, preferably 1 bar to 20 bar, more preferably 1.5 bar to 5 bar.
In the reaction of the present invention, reaction materials include hydrogen-containing source such as water, saturated alcohols, carboxylic acids, and phenols, preferably water such as pure water or hard water, and water may be gaseous or liquid.
Hydrogen molecules could be produced by the reaction of the present invention. Without wishing to be bound by theory, decompositions and recombinations of various reaction raw materials molecules on the atomic sites and the nano-base structure of the plasmonic composite catalysts could be included in the reaction mechanism of the present invention.
CoFe-MOF composite catalyst (Co and Fe were loaded on or bonded to MOF) and CoMn-MOF composite catalyst (Co and Mn were loaded on or bonded to MOF) were prepared according following method:
4.2 mL of isopropyl titanate and 7.06 g of terephthalic acid were added to a mixed solution containing 108 mL of N,N-dimethylformamide and 12 mL of methanol. The mixture was magnetically stirred for 30 min at a temperature of 25° C., until a transparent and uniform solution was obtained. The solution was transferred into a 200 mL stainless steel high-pressure reactor, then the reactor was put in an oven and heated to 150° C. to conduct a reaction for 16 hours. After cooling down to the room temperature, three methanol washes, centrifugation and separation, and drying at 80° C. for 16 hours in an oven, a MOF base was obtained and reserved. After characterized by SEM, the MOF base showed a morphology of columnar nanoparticles having a diameter of 700 nm and a height of 200 nm.
2 g of the MOF base and 100 mL of methanol were added into a 250 mL beaker and magnetically stirred evenly. 8.8 mg of iron nitrate nonahydrate (Fe(NO3).9H2O) and 12 mg of cobalt nitrate hexahydrate (Co(NO3)2.6H2O) were weighed in a 100 mL beaker, 20 mL of methanol was added and then stirred until dissolved. The mixed liquid was added to the MOF dispersion. The CoFe-MOF composite catalyst was obtained after stirring for 1 h, washing by methanol, filtrating and separating with a Buchner funnel, and drying at 80° C. for 16 hours in an oven. The CoMn-MOF composite catalyst was obtained by replacing iron (III) nitrate nonahydrate in the above procedure by 8.8 mg of MnCl2.
The XPS characterization result showed that, in the obtained composite catalyst, Co, Mn and Fe were chemically bonded (coordination bonded) with atoms in the MOF base.
RuCo—TiO2 (Ru and Co were loaded on or bonded to TiO2) composite catalyst and FeCo—TiO2 (Fe and Co were loaded on or bonded to TiO2) composite catalyst were prepared according following method:
0.2 g of titanium dioxide (TiO2, anatase, 5-10 nm, hydrophilic type) was weighed and put in a 500 mL beaker, then 200 mL of deionized water was added, after magnetically stirred for 15 min, 100 mL of 1 mol/L ammonium carbonate ((NH4)2CO3) solution was add and stirred for 5 min, the obtained solution was labeled as solution A. 0.0014 g of cobalt nitrate hexahydrate (Co(NO3)2.6H2O) and 0.0015 g of iron nitrate nonahydrate (Fe(NO3).9H2O) were dissolved in 100 mL of deionized water and treated with ultrasonication for 10 min, and the solution was added, dropwise, into the solution A. The obtained suspension was aged at room temperature for 2.5 h, the precipitate was centrifugally washed for 3 times at 12500 rpm and then dried at for 12 h in an oven, and the CoFe—TiO2 composite catalyst was obtained. The RuCo—TiO2 composite catalyst was obtained by replacing the mixed solution of cobalt nitrate and iron nitrate with a mixed solution containing 0.0020 g of ruthenium trichloride hydrate (RuCl3.xH2O) and 0.0014 g of cobalt nitrate hexahydrate (Co(NO3)2.6H2O). The high-resolution electron microscopy image of the RuCo—TiO2 composite catalyst was shown in
The CoFe-MOF composite catalyst prepared in Example 1 was used, in which the MOF (metal-organic framework) mainly containing Ti metal element functioned as the nano-base structure. After characterized by SEM, the MOF base was columnar nanoparticles having a diameter of 700 nm and a height of 200 nm; the atomic sites including Co and Fe were atomic clusters having 2-4 metal atoms and dispersed on the surface of the MOF, and intervals between the atomic clusters were 5-20 nm.
1 g of CoFe-MOF composite catalyst and 6 mL of ultrapure water were added into a sealable pressure-bearing glass tube having a volume of 35 mL, 4 bar Ar was filled into the tube after air in the tube was replaced with Ar. The glass tube was laid flat on glass wool, so that the catalyst and water were tiled evenly, and a halogen lamp with controlled voltage was employed to radiate vertically from above. The intensity of the incident light was about 1000 W/m2. Thermocouples were connected to the lower part of the glass tube to monitor the temperature. The temperature of the glass tube was controlled to 50° C.±10° C., the radiation was continued for 18 h to conduct the photocatalytic reaction.
After the photocatalytic reaction, hydrogen content of the gas in the reaction tube was characterized by a gas chromatography with a thermal conductivity detector (TCD).
A gas chromatography of the product obtained from the photocatalytic reaction utilizing the CoFe-MOF composite catalyst was shown in
The CoMn-MOF composite catalyst prepared according to Example 1, having the same MOF with Example 2, was used; atomic sites including Co and Mn were atomic clusters having 2-4 metal atoms and dispersed on the surface of the MOF, and intervals between the atomic clusters were 5-20 nm.
1 g of the CoMn-MOF composite catalyst and 1 mL of ultrapure water were added into a sealable pressure-bearing glass tube having a volume of 35 mL, and photocatalytic reaction was carried out under the same manner as Example 2.
After the photocatalytic reaction, the gas obtained in the reaction was characterized by a gas chromatogram in the same manner as Example 2. A gas chromatography of the product obtained from the photocatalytic reaction utilizing the CoMn-MOF composite catalyst was shown in
The same CoMn-MOF composite catalyst used in Example 3 was used.
0.5 g of CoMn-MOF composite catalyst and 6 mL of ultrapure water were added into a sealable pressure-bearing iron tube having a volume of 35 mL, 4 bar Ar was filled into the tube after air in the tube was replaced with Ar. The iron tube was placed in a temperature-controlled oven, and heated to initiate the reaction. The temperature in the oven was controlled to 130° C.±th° C., and the reaction was continued for 18 h.
The gas was characterized by means of gas chromatogram in the same manner as Example 2. The gas chromatography of the product obtained from the thermal catalytic reaction utilizing the CoMn-MOF composite catalyst was shown in
Except the reaction temperature, the photocatalytic reaction was carried out in the same manner as Example 2 by utilizing the same CoFe-MOF composite catalyst as used in Example 2, and the catalyst activity per unit for producing hydrogen was calculated. The results were shown in following table:
As can be seen from the above experimental results, in a range of 50 to 150° C., the energy conversion rate for producing hydrogen in the photocatalytic reaction increased as the temperature raised. When the temperature exceeded 150° C., with side reactions increasing, the energy conversion rate for producing hydrogen declined.
The catalyst was the RuCo—TiO2 composite catalyst with TiO2 as nano-base structure, and showed a morphology of irregular spherical particles having diameters of 600-1500 nm after characterized by SEM. Isolated Ru, Co metal single atoms or atomic clusters were distributed uniformly on the surface of TiO2, and intervals between the metal single atoms or the atomic clusters are 5-20 nm.
The RuCo—TiO2 composite catalyst was used, 0.2 g of the RuCo—TiO2 composite catalyst was added into a sealable pressure-bearing iron tube having a volume of 35 mL, and thermal catalytic reaction was carried out under the same manner as Example 4. The temperature in the oven was controlled to 130° C.±tu° C., and the reaction was continued for 18 h.
The reacted gas was characterized by means of gas chromatogram in the same manner as Example 2. By calculation, the hydrogen content was 6863 ppm, and the catalyst activity per unit for producing hydrogen was about 10.77 μmol g−1 h−1. After continuously reacted for 10 cycles (180 h), the catalytic activity of the catalyst for producing hydrogen did not decline.
The catalyst was the FeCo—TiO2 composite catalyst with TiO2 as nano-base structure prepared according to claim 1, and showed a morphology of irregular spherical particles having diameters of 600-2000 nm after characterized by SEM. Isolated Fe, Co metal single atoms or atomic clusters were distributed uniformly on the surface of TiO2, and intervals between the metal single atoms or the atomic clusters are 5-20 nm.
The FeCo—TiO2 composite catalyst was used, 1 g of the FeCo—TiO2 composite catalyst was added into a sealable pressure-bearing iron tube having a volume of 35 mL, and thermal catalytic reaction was carried out under the same manner as Example 4. The temperature in the oven was controlled to 150° C.±10° C., and the reaction was continued for 18 h. After continuously reacted for 30 cycles (540 h), the catalytic activity of the catalyst for producing hydrogen did not decline.
The gas was characterized by means of gas chromatogram in the same manner as Example 2. By calculation, the hydrogen content was 16830 ppm, and the catalyst activity per unit for producing hydrogen was about 5.283 μmol g−1 h−4.
As can be seen from the results of Examples 2 to 7, in a case of the overall reaction conditions were mild, e.g., in a case of the power of the light radiation was lower than that of the solar light, the method of the present application could directly convert readily available raw materials into hydrogen with high efficiency, by utilizing cost-effective catalysts.
In this specification and the appended claims, the singular forms “a”, “an”, and “the” include plural reference, unless the context clearly indicates otherwise. Unless defined otherwise, all technical and scientific terms as used herein have the same meaning as commonly understood to a person of ordinary skill in the art. Methods recited herein may be carried out in any order that is logically possible, in addition to a particular order disclosed.
The representative examples are intended to help illustrate the invention, and are not intended to, nor should they be construed to, limit the scope of the invention. Indeed, various modifications of the invention and many further embodiments thereof, in addition to those shown and described herein, will become apparent to those skilled in the art from the full contents of this document, including the examples and the references to the scientific and patent literature included herein. The examples contain important additional information, exemplification and guidance that can be adapted to the practice of this invention in its various embodiments and equivalents thereof.
| Number | Date | Country | Kind |
|---|---|---|---|
| PCT/CN2020/135865 | Dec 2020 | WO | international |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/CN2021/128722 | 11/4/2021 | WO |
