CN104034072B - Coating for selective absorption of sunlight spectrum and preparation method thereof and application - Google Patents

Coating for selective absorption of sunlight spectrum and preparation method thereof and application Download PDF

Info

Publication number
CN104034072B
CN104034072B CN201310074921.8A CN201310074921A CN104034072B CN 104034072 B CN104034072 B CN 104034072B CN 201310074921 A CN201310074921 A CN 201310074921A CN 104034072 B CN104034072 B CN 104034072B
Authority
CN
China
Prior art keywords
layer
absorbed layer
coating
target
mentioned
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
CN201310074921.8A
Other languages
Chinese (zh)
Other versions
CN104034072A (en
Inventor
宋斌斌
刘静
汪洪
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BEIJING HANGBO NEW MATERIAL TECHNOLOGY Co Ltd
China Building Materials Academy CBMA
Original Assignee
BEIJING HANGBO NEW MATERIAL TECHNOLOGY Co Ltd
China Building Materials Academy CBMA
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by BEIJING HANGBO NEW MATERIAL TECHNOLOGY Co Ltd, China Building Materials Academy CBMA filed Critical BEIJING HANGBO NEW MATERIAL TECHNOLOGY Co Ltd
Priority to CN201310074921.8A priority Critical patent/CN104034072B/en
Publication of CN104034072A publication Critical patent/CN104034072A/en
Application granted granted Critical
Publication of CN104034072B publication Critical patent/CN104034072B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E10/00Energy generation through renewable energy sources
    • Y02E10/40Solar thermal energy, e.g. solar towers

Landscapes

  • Surface Treatment Of Glass (AREA)

Abstract

The present invention proposes a kind of coating for selective absorption of sunlight spectrum and preparation method thereof and application, and this coating for selective absorption of sunlight spectrum comprises successively: basalis, infrared reflecting layer, absorbed layer and anti-reflection layer; Described absorbed layer is made up of three layers of gradual change solar spectrum absorbed layer, is followed successively by outer absorbed layer, middle absorbed layer and interior absorbed layer, and the material of described interior absorbed layer is TiN x1o y1, the material of described middle absorbed layer is TiN x2o y2, the material of described outer absorbed layer is TiN x3o y3.The optical parametric gradient of described absorbed layer, achieves the efficient absorption of coating to solar spectrum, higher heat endurance and low radiative thermal emissivity.

Description

太阳光谱选择性吸收涂层及其制备方法以及应用Solar Spectrum Selective Absorbing Coating and Its Preparation Method and Application

技术领域technical field

本发明涉及一种中低温下使用的太阳能光热转化材料及其制备方法,特别是涉及一种可用于真空管式和平板式太阳能热水器的太阳光谱选择性吸收涂层及其制备方法。The invention relates to a solar light-to-heat conversion material used at medium and low temperatures and a preparation method thereof, in particular to a solar spectrum selective absorption coating and a preparation method thereof which can be used in vacuum tube and flat solar water heaters.

背景技术Background technique

太阳能光热利用是开发新能源和可再生能源最直接有效的途径之一,其中中低温(80-400℃)下使用的太阳能集热器具有易推广,普及率高的优势,已成为节能减排的重要手段。吸热体是太阳能集热装置的核心组件,早期的吸热体采用黑漆、电镀黑铬或黑镍作为吸收材料,尽管这些材料在太阳光波段具有高吸收率,可将太阳能有效地转化为热,与此同时,由于吸热体温度的升高,材料表面通过热辐射向外辐射电磁波,因此一般实际光热转化效率并不高。Solar thermal utilization is one of the most direct and effective ways to develop new energy and renewable energy. Among them, solar collectors used at medium and low temperatures (80-400°C) have the advantages of easy promotion and high penetration rate, and have become an energy-saving important means of platooning. The heat absorber is the core component of the solar heat collector. The early heat absorbers used black paint, electroplated black chrome or black nickel as the absorbing material, although these materials have a high absorption rate in the sunlight band, which can effectively convert solar energy into At the same time, due to the increase of the temperature of the heat absorber, the surface of the material radiates electromagnetic waves through thermal radiation, so the actual light-to-heat conversion efficiency is generally not high.

太阳光谱选择性吸收涂层在近二三十年内被广泛关注,它可在300nm-2500nm(太阳光98%的能量集中在此波段)的光谱范围内具有高吸收率,与黑体材料不同的是在2500nm以外的红外波段具有低吸收率(即低热辐射率),大大降低了辐射散热,提高了光热转化效率。按应用范围太阳光谱选择性吸收涂层可分为两类:1)真空管式太阳能集热器中使用的太阳光谱选择性吸收涂层,这类涂层应用于真空环境中,对在大气下的热稳定性要求相对较低;2)平板式太阳能集热器中使用的选择性吸收涂层,这类材料直接面对大气,长时间使用结构与成分不应发生变化,应具备较高的热稳定性。The solar spectrum selective absorption coating has been widely concerned in the past 20 to 30 years. It can have a high absorption rate in the spectral range of 300nm-2500nm (98% of the energy of sunlight is concentrated in this band). The difference from black body materials is In the infrared band other than 2500nm, it has low absorption rate (that is, low thermal radiation rate), which greatly reduces radiation heat dissipation and improves light-to-heat conversion efficiency. According to the scope of application, the solar spectrum selective absorption coating can be divided into two categories: 1) the solar spectrum selective absorption coating used in the vacuum tube solar collector. The requirements for thermal stability are relatively low; 2) The selective absorption coating used in flat-plate solar collectors, this kind of material directly faces the atmosphere, and the structure and composition should not change after long-term use, and should have high thermal stability. stability.

现阶段中低温下使用的太阳能集热器多采用真空管式,其吸收材料多为AlN或氧化铝中掺杂不锈钢或Al的陶瓷材料。这类材料的光热转化效率可高达90%以上,然而在大气下易被氧化,限制了这类材料不适用于平板式太阳能集热器中。采用物理气相沉积的方法在氧化物或氮化物中掺杂Ag、Au、W、Mo或Pt等金属已被发现在大气中具有较强的热稳定性,这些材料也已被应用于特殊的高温光热转化装置中,然而制备成本相对较高却限制了此类材料在中低温太阳能集热领域的应用。为了更好的推广平板式集热器,开发一种兼具光热转化效率高、热稳定性强及成本低廉的光热转化材料缺一不可。At present, the solar collectors used at medium and low temperatures mostly adopt the vacuum tube type, and the absorbing materials are mostly ceramic materials doped with stainless steel or Al in AlN or alumina. The light-to-heat conversion efficiency of this type of material can be as high as 90%, but it is easily oxidized in the atmosphere, which limits the application of this type of material in flat-plate solar collectors. Doping metals such as Ag, Au, W, Mo or Pt in oxides or nitrides by physical vapor deposition has been found to have strong thermal stability in the atmosphere, and these materials have also been applied to special high temperatures In photothermal conversion devices, however, the relatively high preparation cost limits the application of such materials in the field of medium and low temperature solar heat collection. In order to better promote flat-plate collectors, it is indispensable to develop a light-to-heat conversion material with high light-to-heat conversion efficiency, strong thermal stability and low cost.

发明内容Contents of the invention

本发明目的在于提供一种中低温下使用的太阳光谱选择性吸收涂层及其制备方法,使其可以实现对太阳光谱的高效吸收,在使用温度范围内具有较高的热稳定性,还可以实现较低的热辐射率。The object of the present invention is to provide a solar spectrum selective absorption coating used at medium and low temperatures and a preparation method thereof, so that it can realize high-efficiency absorption of the solar spectrum, has high thermal stability in the use temperature range, and can also A low thermal radiation rate is achieved.

本发明的目的及解决其技术问题是采用以下技术方案来实现的。依据本发明提出的一种太阳光谱选择性吸收涂层,所述吸收涂层由以下步骤制备得到:The purpose of the present invention and the solution to its technical problems are achieved by adopting the following technical solutions. According to a solar spectrum selective absorption coating proposed by the present invention, the absorption coating is prepared by the following steps:

步骤1,采用Al、Cu或玻璃作为基底层材料,将基底层材料置于真空清洗室中,通入一定量的氩气,进行射频氩离子清洗;Step 1, using Al, Cu or glass as the base layer material, placing the base layer material in a vacuum cleaning chamber, passing a certain amount of argon gas, and performing radio frequency argon ion cleaning;

步骤2,采用磁控溅射铝靶、铜靶或银靶在上述的基底层上制备红外反射层;Step 2, using magnetron sputtering aluminum target, copper target or silver target to prepare an infrared reflective layer on the above-mentioned base layer;

步骤3,在通入氩气和氮气的条件下,将上述的红外反射层置于钛靶下,采用磁控溅射法在上述的红外反射层上制备内吸收层;最后通入一定量的氧气,继续以金属钛为靶材通过反应磁控溅射法在上述内吸收层上制备中吸收层;然后增加氧气流量,继续以金属钛为靶材通过反应磁控溅射法在上述中吸收层上制备外吸收层;Step 3, under the condition of feeding argon and nitrogen, the above-mentioned infrared reflective layer is placed under the titanium target, and the internal absorption layer is prepared on the above-mentioned infrared reflective layer by magnetron sputtering; finally, a certain amount of Oxygen, continue to use metal titanium as the target material to prepare the middle absorption layer on the above-mentioned internal absorption layer by reactive magnetron sputtering method; then increase the flow rate of oxygen, continue to use metal titanium as the target material to absorb in the above-mentioned internal absorption layer Prepare the outer absorbent layer on the layer;

步骤4,将步骤3得到的产品置于硅靶前,通入氩气和氧气,用反应磁控溅射法在上述外吸收层上制备氧化硅层作为减反层;Step 4, placing the product obtained in step 3 in front of the silicon target, introducing argon and oxygen, and preparing a silicon oxide layer on the above-mentioned outer absorbing layer by reactive magnetron sputtering as an antireflection layer;

其中,所述内吸收层的材质为TiNx1Oy1,1.10>x1>0.90,0.70>y1>0.50,所述中吸收层的材质为TiNx2Oy2,0.80>x2>0.70,1.15>y2>1.05,所述外吸收层的材质为TiNx3Oy3,0.55>x3>0.45,1.30>y3>1.10;所述外吸收层的厚度为10nm-50nm,中吸收层的厚度为10nm-50nm,内吸收层的厚度为20nm-50nm;Wherein, the material of the internal absorption layer is TiN x1 O y1 , 1.10>x1>0.90, 0.70>y1>0.50, the material of the middle absorption layer is TiN x2 O y2 , 0.80>x2>0.70, 1.15>y2> 1.05, the material of the outer absorption layer is TiN x3 O y3 , 0.55>x3>0.45, 1.30>y3>1.10; the thickness of the outer absorption layer is 10nm-50nm, the thickness of the middle absorption layer is 10nm-50nm, the inner The thickness of the absorbing layer is 20nm-50nm;

由上述步骤得到的太阳光谱选择性吸收涂层在300nm-2500nm的太阳光波段的吸收率为94.6%-94.7%,在100摄氏度下的热辐射率为3%。The solar spectrum selective absorption coating obtained by the above steps has an absorption rate of 94.6%-94.7% in the solar light band of 300nm-2500nm, and a thermal radiation rate of 3% at 100 degrees Celsius.

另一方面,本发明提供了一种太阳光谱选择性吸收涂层的制备方法,其包括以下步骤:On the other hand, the present invention provides a kind of preparation method of solar spectrum selective absorption coating, it comprises the following steps:

步骤1,采用Al、Cu或玻璃作为基底层材料,将基底层材料置于真空清洗室中,通入一定量的氩气,进行射频氩离子清洗;Step 1, using Al, Cu or glass as the base layer material, placing the base layer material in a vacuum cleaning chamber, passing a certain amount of argon gas, and performing radio frequency argon ion cleaning;

步骤2,采用磁控溅射铝靶、铜靶或银靶在上述的基底层上制备红外反射层;Step 2, using magnetron sputtering aluminum target, copper target or silver target to prepare an infrared reflective layer on the above-mentioned base layer;

步骤3,在通入氩气和氮气的条件下,将上述的红外反射层置于钛靶下,采用磁控溅射法在上述的红外反射层上制备内吸收层;然后通入一定量的氧气,继续以金属钛为靶材通过反应磁控溅射法在上述内吸收层上制备中吸收层;然后增加氧气流量,继续以金属钛为靶材通过反应磁控溅射法在上述中吸收层上制备外吸收层;Step 3, under the condition of feeding argon and nitrogen, the above-mentioned infrared reflective layer is placed under the titanium target, and the internal absorption layer is prepared on the above-mentioned infrared reflective layer by magnetron sputtering; then a certain amount of Oxygen, continue to use metal titanium as the target material to prepare the middle absorption layer on the above-mentioned internal absorption layer by reactive magnetron sputtering method; then increase the flow rate of oxygen, continue to use metal titanium as the target material to absorb in the above-mentioned internal absorption layer Prepare the outer absorbent layer on the layer;

步骤4,将步骤3得到的产品置于硅靶前,通入氩气和氧气,采用反应磁控溅射法在上述外吸收层上制备氧化硅层作为减反层。In step 4, the product obtained in step 3 is placed in front of the silicon target, argon and oxygen are introduced into it, and a silicon oxide layer is prepared on the above-mentioned outer absorbing layer by reactive magnetron sputtering as an antireflection layer.

优选的,前述的太阳光谱选择性吸收涂层的制备方法,其中所述的基底层的厚度为0.2-10mm;所述的红外反射层的厚度为90-500nm;所述的内吸收层、中吸收层和外吸收层的总厚度为40-150nm,所述的减反层的厚度为80-100nm。Preferably, the aforementioned preparation method of the solar spectrum selective absorption coating, wherein the thickness of the base layer is 0.2-10mm; the thickness of the infrared reflection layer is 90-500nm; the internal absorption layer, middle The total thickness of the absorption layer and the outer absorption layer is 40-150nm, and the thickness of the anti-reflection layer is 80-100nm.

优选的,前述的太阳光谱选择性吸收涂层的制备方法,其中所述内吸收层的材质为TiNx1Oy1,其中本层材料中所含的氧一部分来自真空腔室中的残余水气和氧气,另一部则由于在空气中被氧化所致。在波长为400nm-600nm范围内,折射率处于1.9-2.5之间,消光系数处于0.6-1.2之间;在波长为900nm-1100nm范围内,折射率处于2.2-2.8,消光系数处于2.1-2.5;在波长为2000nm-2300nm范围内,折射率处于3.8-4.1,消光系数处于2.8-3.0。Preferably, the aforementioned method for preparing a solar spectrum selective absorption coating, wherein the material of the internal absorption layer is TiN x1 O y1 , wherein part of the oxygen contained in the material of this layer comes from the residual water vapor and Oxygen, and the other part is caused by oxidation in the air. In the wavelength range of 400nm-600nm, the refractive index is between 1.9-2.5, and the extinction coefficient is between 0.6-1.2; in the wavelength range of 900nm-1100nm, the refractive index is 2.2-2.8, and the extinction coefficient is 2.1-2.5; In the wavelength range of 2000nm-2300nm, the refractive index is 3.8-4.1, and the extinction coefficient is 2.8-3.0.

优选的,前述的太阳光谱选择性吸收涂层的制备方法,其中所述中吸收层的材质为TiNx2Oy2,在波长为400nm-600nm范围内,折射率处于2.0-2.4之间,消光系数处于0.5-0.9之间;在波长处于900nm-1100nm范围内,折射率处于2.7-3.1,消光系数处于至1.3-1.5;在波长为2000nm-2300nm范围内,折射率处于3.6-3.8,消光系数处于1.0-1.2。Preferably, the aforementioned method for preparing a solar spectrum selective absorbing coating, wherein the material of the middle absorbing layer is TiN x2 O y2 , within the wavelength range of 400nm-600nm, the refractive index is between 2.0-2.4, and the extinction coefficient Between 0.5-0.9; in the wavelength range of 900nm-1100nm, the refractive index is in the range of 2.7-3.1, and the extinction coefficient is in the range of 1.3-1.5; in the wavelength range of 2000nm-2300nm, the refractive index is in the range of 3.6-3.8, and the extinction coefficient is in the 1.0-1.2.

优选的,前述的太阳光谱选择性吸收涂层的制备方法,其中所述外吸收层的材质为TiNx3Oy3,在波长为400nm-600nm范围内,折射率处于2.2-2.5之间,消光系数处于0.3-0.5之间;此类材料在波长为900nm-1100nm范围内,折射率处于2.6-2.9,消光系数为0.4-0.6;在波长为2000nm-2300nm范围内,折射率处于2.8-3.0,消光系数处于0.2-0.3。Preferably, the aforementioned method for preparing a solar spectrum selective absorbing coating, wherein the material of the outer absorbing layer is TiN x3 O y3 , within the wavelength range of 400nm-600nm, the refractive index is between 2.2-2.5, and the extinction coefficient between 0.3-0.5; such materials have a refractive index of 2.6-2.9 and an extinction coefficient of 0.4-0.6 in the wavelength range of 900nm-1100nm; and a refractive index of 2.8-3.0 in the wavelength range of 2000nm-2300nm The coefficients are in the range of 0.2-0.3.

本发明还提出一种太阳能集热器,其特征在于,在该太阳能集热器中包括上述的太阳光谱选择性吸收涂层。The present invention also proposes a solar heat collector, which is characterized in that the above-mentioned solar spectrum selective absorption coating is included in the solar heat collector.

借由上述技术方案,本发明至少具有下列优点:By virtue of the above technical solutions, the present invention has at least the following advantages:

本发明所公开的太阳光谱选择性吸收涂层通过吸收层光学参数的梯度渐变,可实现涂层对太阳光谱的高效吸收和较高的热稳定性。氮氧化钛吸收材料对红外波段(2.5微米以外)的光波具有高透的性能,当红外波段的光穿透吸收层后会经红外反射层反射,从而实现较低的热辐射率。最外层选取可与吸收层材料光学参数匹配的氧化硅作为减反层,使吸收层能更大限度的吸收太阳光谱。此类涂层具有以下主要优点:a、在太阳光波段可具有94%以上的吸收率(300nm-2500nm),在100摄氏度下的热辐射率可低于4%,总体光热转化效率高达90%以上;b、通过制备梯度渐变吸收层,涂层的力学性能可得到提升,高温下不易脱膜,可增加涂层在高温下的使用寿命;c、涂层不仅可用于真空管式太阳能集热器,也可直接面对大气,应用于平板式太阳能集热器。The solar spectrum selective absorption coating disclosed by the invention can realize efficient absorption of the solar spectrum and high thermal stability of the coating through the gradual change of the optical parameters of the absorption layer. The titanium oxynitride absorbing material has high transmittance to light waves in the infrared band (beyond 2.5 microns). When the light in the infrared band penetrates the absorbing layer, it will be reflected by the infrared reflective layer, thereby achieving a lower thermal radiation rate. The outermost layer selects silicon oxide that can match the optical parameters of the material of the absorbing layer as the anti-reflection layer, so that the absorbing layer can absorb the solar spectrum to a greater extent. This type of coating has the following main advantages: a. It can have an absorption rate of more than 94% in the solar light band (300nm-2500nm), and the thermal radiation rate at 100 degrees Celsius can be lower than 4%, and the overall photothermal conversion efficiency is as high as 90% % or more; b. By preparing a gradient absorbing layer, the mechanical properties of the coating can be improved, and it is not easy to release the film at high temperature, which can increase the service life of the coating at high temperature; c. The coating can not only be used for vacuum tube solar heat collection The device can also directly face the atmosphere and is applied to a flat-plate solar collector.

此外本发明还具有以下特点:In addition, the present invention also has the following characteristics:

a、通过直流溅射的方法制备的红外反射层,选用在整个光波波段具有高消光系数的Al、Cu或Ag等金属,这些高消光系数的金属层对整个波段的光谱具有强反射的作用,特别利于反射透过吸收层的红外光谱(2500nm以外);b、红外反射层之上是三层渐变太阳光谱吸收层,考虑反应气体的渐变会引起吸收层的光学参数的连续变化,采用了连续改变反应气体氧气的方法制备氮氧化钛梯度渐变吸收层;c、内吸收层的主要光学特征为消光系数在整个太阳光谱波段(0.3μm-2.5μm)均大于0.6,且随着波长增长有明显增加的趋势,此材料对整个波段的太阳光谱具有相对较强的吸收效果;d、中吸收层的消光系数在380nm-420nm之间具有一个极小值,低至0.5,而在900nm-1000nm之间会产生一个消光系数的极大值,可达1.5,因此这种材料在900nm-1000nm波段具有较高的吸收率;e、外吸收层在380nm-420nm之间有一个消光系数的低谷,并且在700nm-800nm之间有一个消光系数的峰值,随后消光系数随着波长的增加降低,此材料在700nm-800nm波段对太阳光谱有相对较高的吸收率;f、采用反应磁控溅射的方法制备氧化硅层作为减反层,制备过程中需将氧化硅层在300nm-2500nm微米波段的折射率控制在1.45-1.52之间。a. The infrared reflective layer prepared by DC sputtering is selected from metals such as Al, Cu or Ag with high extinction coefficients in the entire light wave band. These metal layers with high extinction coefficients have a strong reflection effect on the spectrum of the entire band. It is especially beneficial to reflect the infrared spectrum (beyond 2500nm) that passes through the absorbing layer; b, above the infrared reflecting layer is a three-layer gradient solar spectrum absorbing layer. Considering that the gradual change of the reaction gas will cause the continuous change of the optical parameters of the absorbing layer, a continuous The method of changing the reaction gas oxygen to prepare a gradient gradient absorption layer of titanium oxynitride; c. The main optical feature of the internal absorption layer is that the extinction coefficient is greater than 0.6 in the entire solar spectrum band (0.3 μm-2.5 μm), and there is a significant increase with the wavelength This material has a relatively strong absorption effect on the entire solar spectrum; d, the extinction coefficient of the middle absorbing layer has a minimum value between 380nm-420nm, as low as 0.5, and between 900nm-1000nm There will be a maximum extinction coefficient between 1.5, so this material has a high absorption rate in the 900nm-1000nm band; e, the outer absorption layer has a trough in the extinction coefficient between 380nm-420nm, and There is a peak of the extinction coefficient between 700nm-800nm, and then the extinction coefficient decreases with the increase of the wavelength. This material has a relatively high absorption rate for the solar spectrum in the 700nm-800nm band; f, using reactive magnetron sputtering Methods A silicon oxide layer was prepared as an anti-reflection layer. During the preparation process, the refractive index of the silicon oxide layer in the 300nm-2500nm micron band should be controlled between 1.45-1.52.

上述说明仅是本发明技术方案的概述,为了能够更清楚了解本发明的技术手段,并可依照说明书的内容予以实施,以下以本发明的较佳实施例并配合附图详细说明如后。The above description is only an overview of the technical solutions of the present invention. In order to understand the technical means of the present invention more clearly and implement them according to the contents of the description, the preferred embodiments of the present invention and accompanying drawings are described in detail below.

附图说明Description of drawings

图1是本发明提出的太阳光谱选择性吸收涂层的结构示意图。Fig. 1 is a schematic structural view of the solar spectrum selective absorption coating proposed by the present invention.

图2是实例1和实例2的反射光谱图。Fig. 2 is the reflectance spectrogram of example 1 and example 2.

图3是实例2样品在大气中退火后的吸收率和热辐射率示意图。Fig. 3 is a schematic diagram of the absorptivity and thermal emissivity of the samples of Example 2 after annealing in the atmosphere.

具体实施方式detailed description

为更进一步阐述本发明为达成预定发明目的所采取的技术手段及功效,以下结合附图及较佳实施例,对依据本发明提出的太阳光谱选择性吸收涂层及其制备方法其具体实施方式、结构、特征及其功效,详细说明如后。In order to further elaborate the technical means and effects that the present invention adopts to achieve the intended purpose of the invention, the specific implementation of the solar spectrum selective absorption coating and its preparation method according to the present invention will be described below in conjunction with the accompanying drawings and preferred embodiments. , structure, feature and effect thereof, detailed description is as follows.

请参阅图1所示,是本发明提出的太阳光谱选择性吸收涂层的结构示意图。该太阳光谱选择性吸收涂层依次包括基底层4、红外反射层3、吸收层2,和减反层1。所述的基底层4可采用厚度范围为0.5-10mm的玻璃板;也可采用厚度范围为0.2-2mm的金属材料,例如铜或者铝,当采用金属基底层时红外反射层3可不制备。为增加基底层4的表面活性,需要经机械清洗后进行射频离子清洗,从而去除基底层表面的污染层和氧化层。所述的红外反射层3设置于基底层之上,该红外反射层3的作用在于对入射的整个波段的光谱进行反射,特别是对红外光谱,尤其是波长2.5微米以上的红外光进行反射。该红外反射层的材质为铝、铜或者银。该红外反射层的厚度为90-500nm。所述的吸收层2由三层渐变太阳光谱吸收层组成,依次为外吸收层21、中吸收层22和内吸收层23,内吸收层23制备于红外反射层3上。外吸收层21的材质为TiNx3Oy3,厚度为10nm-50nm,该层材料在380nm-420nm之间有一个消光系数的低谷,并且在700nm-800nm之间有一个消光系数的峰值,随后消光系数随着波长的增加降低,该层材料在700nm-800nm波段对太阳光谱有相对较高的吸收率。中吸收层22的材质为TiNx2Oy2,厚度为10nm-50nm,该层材料的消光系数在380nm-420nm之间具有一个极小值,低至0.5,而在900nm-1000nm之间会产生一个消光系数的极大值,可达1.5,因此这种材料在900nm-1000nm波段具有较高的吸收率。内吸收层23的材质为TiNx1Oy1,厚度为20nm-50nm,该层材料的主要光学特征为消光系数在整个太阳光谱波段(300nm-2500nm)均大于0.6,且随着波长增长有明显增加的趋势,此材料对整个波段的太阳光谱具有相对较强的吸收效果。在外收层21之上为减反层1,材质为氧化硅,其对于300nm-2500nm波段的光的折射率在1.45-1.52之间。Please refer to FIG. 1 , which is a schematic structural view of the solar spectrum selective absorption coating proposed by the present invention. The solar spectrum selective absorption coating includes a base layer 4 , an infrared reflection layer 3 , an absorption layer 2 , and an antireflection layer 1 in sequence. The base layer 4 can be a glass plate with a thickness in the range of 0.5-10 mm; it can also be a metal material with a thickness in the range of 0.2-2 mm, such as copper or aluminum, and the infrared reflection layer 3 can be omitted when the metal base layer is used. In order to increase the surface activity of the base layer 4, it is necessary to carry out radio frequency ion cleaning after mechanical cleaning, so as to remove the contamination layer and the oxide layer on the surface of the base layer. The infrared reflective layer 3 is disposed on the base layer, and the function of the infrared reflective layer 3 is to reflect the entire incident spectrum, especially the infrared spectrum, especially the infrared light with a wavelength of 2.5 microns or more. The material of the infrared reflection layer is aluminum, copper or silver. The thickness of the infrared reflection layer is 90-500nm. The absorbing layer 2 is composed of three gradient solar spectrum absorbing layers, which are an outer absorbing layer 21 , a middle absorbing layer 22 and an inner absorbing layer 23 , and the inner absorbing layer 23 is prepared on the infrared reflective layer 3 . The outer absorption layer 21 is made of TiN x3 O y3 with a thickness of 10nm-50nm. The material of this layer has a trough of extinction coefficient between 380nm-420nm and a peak of extinction coefficient between 700nm-800nm, and then the extinction The coefficient decreases with the increase of the wavelength, and the material of this layer has a relatively high absorption rate for the solar spectrum in the 700nm-800nm band. The middle absorbing layer 22 is made of TiN x2 O y2 with a thickness of 10nm-50nm. The extinction coefficient of this layer material has a minimum value between 380nm-420nm, as low as 0.5, and a The maximum value of the extinction coefficient can reach 1.5, so this material has a high absorption rate in the 900nm-1000nm band. The material of the internal absorption layer 23 is TiN x1 O y1 with a thickness of 20nm-50nm. The main optical feature of this layer material is that the extinction coefficient is greater than 0.6 in the entire solar spectrum band (300nm-2500nm), and it increases significantly with the increase of wavelength. The trend of this material has a relatively strong absorption effect on the entire solar spectrum. On the outer receiving layer 21 is the anti-reflection layer 1, which is made of silicon oxide, and its refractive index for light in the 300nm-2500nm band is between 1.45-1.52.

制备方法Preparation

本发明还提出一种制备上述太阳光谱选择性吸收涂层的方法,该方法包括以下步骤:The present invention also proposes a method for preparing the above-mentioned solar spectrum selective absorption coating, the method comprising the following steps:

基底层制备,选择抛光的金属板或者玻璃板,经过机械清洗后进行射频氩离子清洗去除表面污染层和氧化层,增进基底表面活性。For the preparation of the base layer, a polished metal plate or glass plate is selected, and after mechanical cleaning, radio frequency argon ion cleaning is performed to remove the surface contamination layer and oxide layer, and to improve the surface activity of the base layer.

红外反射层制备,通过直流磁控溅射法在上述的基底层表面制备一层金属红外反射层,所选用的靶材可为金属为铝、铜或者银。Infrared reflective layer preparation, a layer of metal infrared reflective layer is prepared on the surface of the above-mentioned base layer by DC magnetron sputtering method, and the selected target material can be aluminum, copper or silver.

吸收层的制备,通过反应磁控溅射法在上述的红外反射层上制备内吸收层,以金属钛作为靶材,通入50sccm氩气和8sccm氮气,制成厚度为20nm-50nm的TiNx1Oy1材质的内吸收层;然后通入2-2.5sccm的氧气,继续以金属钛为靶材通过反应磁控溅射法在上述内吸收层上制备中吸收层,该中吸收层的厚度控制在10-50nm,中吸收层的材质为TiNx2Oy2;然后增加氧气的流量至2.5-3.5sccm,继续以金属钛为靶材通过反应磁控溅射法在上述中吸收层上制备外吸收层,该外吸收层的厚度控制在10-50nm,外吸收层的材质为TiNx3Oy3The preparation of the absorbing layer is to prepare the internal absorbing layer on the above-mentioned infrared reflective layer by reactive magnetron sputtering method, using metal titanium as the target material, and feeding 50sccm argon and 8sccm nitrogen to make TiN x1 with a thickness of 20nm-50nm The internal absorption layer of O y1 material; Pass into the oxygen of 2-2.5sccm then, continue to use metal titanium as the target material to prepare the medium absorption layer on the above-mentioned internal absorption layer by reactive magnetron sputtering method, the thickness control of this medium absorption layer At 10-50nm, the material of the medium absorbing layer is TiN x2 O y2 ; then increase the flow rate of oxygen to 2.5-3.5sccm, and continue to use metal titanium as the target material to prepare external absorption on the above medium absorbing layer by reactive magnetron sputtering layer, the thickness of the outer absorption layer is controlled at 10-50nm, and the material of the outer absorption layer is TiN x3 O y3 .

减反层的制备,采用反应磁控溅射法在上述外吸收层上制备氧化硅层作为减反层,该方法为成熟技术,制备过程中控制氧化硅层在300nm-2500nm波段的折射率控制在1.45-1.52之间。The anti-reflection layer is prepared by using the reactive magnetron sputtering method to prepare a silicon oxide layer on the above-mentioned outer absorption layer as an anti-reflection layer. This method is a mature technology, and the refractive index of the silicon oxide layer is controlled in the 300nm-2500nm band during the preparation process. Between 1.45-1.52.

上述的吸收层为渐变吸收层,其在不同波段的折射率和消光系数如表1所示。The above-mentioned absorbing layer is a graded absorbing layer, and its refractive index and extinction coefficient in different wavelength bands are shown in Table 1.

表1Table 1

实例1Example 1

按照上述的制备方法进行如下操作步骤:Carry out following operation steps according to above-mentioned preparation method:

1)对玻璃基底层进行射频离子清洗,去除表面污染层和氧化层,增进基底表面活性;1) Carry out radio frequency ion cleaning to the glass base layer, remove the surface contamination layer and oxide layer, and increase the surface activity of the base;

2)将基底层传输至铝靶前方,待本底真空优于6×10-6Torr后,通入50sccm氩气,控制压力为5mTorr,开启溅射电源,保持功率1200W,设置传输速率为0.4m/min,使基底层通过铝靶12次,用以制备红外反射铝层;2) Transfer the base layer to the front of the aluminum target. After the background vacuum is better than 6×10 -6 Torr, inject 50 sccm argon gas, control the pressure to 5 mTorr, turn on the sputtering power supply, keep the power at 1200W, and set the transfer rate to 0.4 m/min, make the base layer pass through the aluminum target 12 times to prepare the infrared reflective aluminum layer;

3)将镀有金属铝层的基底层传输至钛靶前方,通入50sccm氩气,8sccm氮气,控制气压5mTorr,开启溅射电源,保持功率1000W,传输速率为0.4m/min,使基底层通过钛靶3次,用以制备材质为TiN0.94O0.60的内吸收层;3) Transfer the base layer coated with a metal aluminum layer to the front of the titanium target, inject 50 sccm argon gas, 8 sccm nitrogen gas, control the air pressure 5mTorr, turn on the sputtering power supply, keep the power at 1000W, and the transfer rate is 0.4m/min, so that the base layer Pass through the titanium target 3 times to prepare an internal absorption layer made of TiN 0.94 O 0.60 ;

4)在其它参数不变的情况下,通入2sccm的氧气,使基底层在钛靶下按0.4m/min的速率运行3次,用以制备材质为TiN0.72O1.11的中吸收层;4) Under the condition that other parameters remain unchanged, 2 sccm of oxygen is introduced to make the base layer run 3 times under the titanium target at a rate of 0.4 m/min, so as to prepare a medium absorbing layer whose material is TiN 0.72 O 1.11 ;

5)随后将氧气流量增加至2.5sccm,传输速度增至0.6m/min,其它参数保持不变,使基底层在钛靶下方运行5次,用以制备材质为TiN0.51O1.12的外吸收层;5) Then increase the oxygen flow rate to 2.5 sccm, increase the transmission speed to 0.6m/min, keep other parameters unchanged, and run the base layer under the titanium target 5 times to prepare the outer absorbing layer made of TiN 0.51 O 1.12 ;

6)完成以上步骤后,将基底层传输至硅靶前方,通入50sccm氩气,26sccm氧气,控制气压5mTorr,开启溅射电源,保持功率2000W,设置传输速度为1m/min,使基底层通过硅靶9次;6) After completing the above steps, transfer the base layer to the front of the silicon target, inject 50sccm argon gas, 26sccm oxygen gas, control the air pressure to 5mTorr, turn on the sputtering power supply, keep the power at 2000W, set the transmission speed to 1m/min, and let the base layer pass through Silicon target 9 times;

7)待完成以上制备步骤后,使样品冷却20min,出片,停机。7) After the above preparation steps are completed, the sample is cooled for 20 minutes, the tablet is released, and the machine is stopped.

采用带积分球的分光光度计测量实例1的涂层样品的反射光谱(300nm-2500nm),如图2所示,该涂层在此波段的吸收率为94.6%;采用热辐射计测量涂层在100摄氏度下的热辐射率为3.7%。Adopt the reflectance spectrum (300nm-2500nm) of the coating sample of example 1 to be measured by the spectrophotometer with integrating sphere, as shown in Figure 2, the absorptivity of this coating is 94.6% in this waveband; Adopt thermal radiometer to measure coating The thermal radiation rate at 100 degrees Celsius is 3.7%.

对实例1制得的涂层样品在真空气氛下的退火处理,来验证制得涂层在真空中的高温稳定性和耐用性。将涂层样品置于真空状态下(小于1×10-5Torr),将样品加热至380摄氏度退火14h,退火后样品的吸收率和热辐射率分别为93.5%和3%,较退火前涂层的吸收率(94.6%)和热辐射率(3.7%)略有变化,但不明显,证明实例1制得的涂层可应用于真空管式太阳能集热器中使用。The annealing treatment of the coating sample prepared in Example 1 in a vacuum atmosphere is performed to verify the high temperature stability and durability of the coating in vacuum. Put the coated sample in a vacuum state (less than 1×10 -5 Torr), heat the sample to 380 degrees Celsius and anneal for 14 hours. The absorptivity (94.6%) and heat radiation rate (3.7%) of the layer change slightly, but not obviously, it proves that the coating prepared in Example 1 can be applied to the evacuated tube solar collector.

实施例2Example 2

按照上述的制备方法进行如下操作步骤:Carry out following operation steps according to above-mentioned preparation method:

1)对Al基底层进行射频离子清洗,去除表面污染层和氧化层,并增进基底表面活性,溅射清洗后的Al板热辐射率低于1.7%,此时Al基底层同时具有红外反射层的作用;1) Carry out radio frequency ion cleaning on the Al base layer to remove the surface contamination layer and oxide layer, and increase the surface activity of the base. The thermal emissivity of the Al plate after sputtering cleaning is lower than 1.7%. At this time, the Al base layer has an infrared reflective layer at the same time role;

2)将基底层传输至磁控溅射钛靶前方,本底真空优于6×10-6Torr后,通入50sccm氩气,8sccm氮气,控制气压5mTorr,开启溅射电源,保持功率1000W,传输速率为0.4m/min,使基底层通过钛靶3次,用以制备材质为TiN0.94O0.60的内吸收层;2) Transfer the base layer to the front of the magnetron sputtering titanium target. After the background vacuum is better than 6×10 -6 Torr, introduce 50 sccm argon gas, 8 sccm nitrogen gas, control the air pressure at 5 mTorr, turn on the sputtering power supply, and keep the power at 1000W. The transmission rate is 0.4m/min, so that the base layer passes through the titanium target 3 times to prepare an internal absorption layer made of TiN 0.94 O 0.60 ;

3)在其它参数不变的情况下,通入2sccm的氧气,使基底层在钛靶下按0.4m/min的速率运行3次,用以制备材质为TiN0.72O1.11的中吸收层;3) Under the condition that other parameters remain unchanged, 2 sccm of oxygen is introduced to make the base layer run 3 times under the titanium target at a speed of 0.4 m/min, so as to prepare a medium absorbing layer whose material is TiN 0.72 O 1.11 ;

4)随后将氧气流量增加至2.5sccm,传输速度增至0.6m/min,其它参数保持不变,使基底层在钛靶下方运行5次,用以制备材质为TiN0.51O1.12的外吸收层;4) Then increase the oxygen flow rate to 2.5sccm, increase the transmission speed to 0.6m/min, and keep other parameters unchanged, so that the base layer runs 5 times under the titanium target to prepare the outer absorption layer made of TiN 0.51 O 1.12 ;

5)将基底层传输至硅靶前方,通入50sccm氩气,26sccm氧气,控制气压5mTorr,开启溅射电源,保持功率2000W,设置传输速度为1m/min,使基底层通过硅靶9次;5) Transfer the base layer to the front of the silicon target, inject 50 sccm argon gas, 26 sccm oxygen gas, control the air pressure to 5mTorr, turn on the sputtering power supply, keep the power at 2000W, set the transmission speed to 1m/min, and make the base layer pass through the silicon target 9 times;

6)待完成以上制备步骤后,使样品冷却20min,出片,停机。6) After the above preparation steps are completed, the sample is cooled for 20 minutes, the tablet is released, and the machine is stopped.

采用带积分球的分光光度计测量实例2涂层样品的反射光谱(300nm-2500nm),如图2所示,涂层在此波段的吸收率为94.7%;采用热辐射计测量涂层在100摄氏度下的热辐射率为5.0%。Adopt the reflectance spectrum (300nm-2500nm) of the spectrophotometer measurement example 2 coating sample of band integrating sphere, as shown in Figure 2, the absorptivity of coating in this band is 94.7%; Adopt thermal radiometer to measure coating at 100 The thermal radiation rate in Celsius is 5.0%.

实例2制得的涂层样品进行大气气氛下的退火处理,来验证制得涂层在大气下的高温稳定性和耐用性。将涂层样品置于马弗炉中依次在100摄氏度、250摄氏度、300摄氏度和350摄氏度下连续退火36h、10h、5h和5h,如图3所示,100℃退火36小时后该涂层的吸收率为94.6%,热辐射率为5.0%;250℃退火10小时后该涂层的吸收率和热辐射率仍未发生明显变化;300℃退火5小时后该涂层的吸收率为93.3%,热辐射率为4%;350℃退火5小时后该涂层的吸收率为91.1%,热辐射率为2.4%。退火后该涂层的吸收率和热辐射率仅出现小幅度的变化,涂层的光热转化效率没有明显的降低,证明实例2制得的涂层可以用于平板式太阳能热水器中使用。The coating sample prepared in Example 2 was annealed in the atmosphere to verify the high-temperature stability and durability of the coating in the atmosphere. The coated sample was placed in a muffle furnace and annealed successively at 100°C, 250°C, 300°C and 350°C for 36h, 10h, 5h and 5h, as shown in Figure 3, the coating was annealed at 100°C for 36 hours The absorption rate is 94.6%, and the thermal radiation rate is 5.0%; the absorption rate and thermal radiation rate of the coating have not changed significantly after annealing at 250 °C for 10 hours; the absorption rate of the coating is 93.3% after annealing at 300 °C for 5 hours , the thermal emissivity is 4%; the absorptivity of the coating is 91.1% and the thermal emissivity is 2.4% after annealing at 350°C for 5 hours. After annealing, the absorptivity and thermal emissivity of the coating only change slightly, and the photothermal conversion efficiency of the coating does not significantly decrease, which proves that the coating prepared in Example 2 can be used in flat-plate solar water heaters.

以上所述,仅是本发明的较佳实施例而已,并非对本发明作任何形式上的限制,虽然本发明已以较佳实施例揭露如上,然而并非用以限定本发明,任何熟悉本专业的技术人员,在不脱离本发明技术方案范围内,当可利用上述揭示的技术内容作出些许更动或修饰为等同变化的等效实施例,但凡是未脱离本发明技术方案的内容,依据本发明的技术实质对以上实施例所作的任何简单修改、等同变化与修饰,均仍属于本发明技术方案的范围内。The above description is only a preferred embodiment of the present invention, and does not limit the present invention in any form. Although the present invention has been disclosed as above with preferred embodiments, it is not intended to limit the present invention. Anyone familiar with this field Those skilled in the art, without departing from the scope of the technical solution of the present invention, can use the technical content disclosed above to make some changes or modify them into equivalent embodiments with equivalent changes, but any content that does not depart from the technical solution of the present invention, according to the present invention Any simple modifications, equivalent changes and modifications made to the above embodiments by the technical essence still belong to the scope of the technical solutions of the present invention.

Claims (8)

1. a coating for selective absorption of sunlight spectrum, is characterized in that, described absorber coatings is prepared by following steps:
Step 1, adopts Al, Cu or glass as base layer material, base layer material is placed in vacuum cleaned room, passes into a certain amount of argon gas, carry out the cleaning of radio frequency argon ion;
Step 2, adopts Magnetron Sputtered Al target, copper target or silver-colored target to prepare infrared reflecting layer on above-mentioned basalis;
Step 3, under the condition passing into argon gas and nitrogen, under above-mentioned infrared external reflection is placed on titanium target, adopt magnetron sputtering method prepare on above-mentioned infrared reflecting layer in absorbed layer; Finally pass into a certain amount of oxygen, continuing take Titanium as absorbed layer during target is prepared on above-mentioned interior absorbed layer by reactive magnetron sputtering method; Then increase oxygen flow, continue to be that target prepares outer absorbed layer by reactive magnetron sputtering method on above-mentioned middle absorbed layer with Titanium;
Step 4, before product step 3 obtained is placed in silicon target, passes into argon gas and oxygen, prepares silicon oxide layer as anti-reflection layer with reactive magnetron sputtering method on above-mentioned outer absorbed layer;
Wherein, the material of described interior absorbed layer is TiN x1o y1, 1.10 > x1 > 0.90,0.70 > y1 > 0.50, the material of described middle absorbed layer is TiN x2o y2, 0.80 > x2 > 0.70,1.15 > y2 > 1.05, the material of described outer absorbed layer is TiN x3o y3, 0.55 > x3 > 0.45,1.30 > y3 > 1.10; The thickness of described outer absorbed layer is 10nm-50nm, and the thickness of middle absorbed layer is 10nm-50nm, and the thickness of interior absorbed layer is 20nm-50nm.
2. a preparation method for coating for selective absorption of sunlight spectrum, is characterized in that comprising the following steps:
Step 1, adopts Al, Cu or glass as base layer material, base layer material is placed in vacuum cleaned room, passes into a certain amount of argon gas, carry out the cleaning of radio frequency argon ion;
Step 2, adopts Magnetron Sputtered Al target, copper target or silver-colored target to prepare infrared reflecting layer on above-mentioned basalis;
Step 3, under the condition passing into argon gas and nitrogen, under above-mentioned infrared external reflection is placed on titanium target, adopt magnetron sputtering method prepare on above-mentioned infrared reflecting layer in absorbed layer; Finally pass into a certain amount of oxygen, continuing take Titanium as absorbed layer during target is prepared on above-mentioned interior absorbed layer by reactive magnetron sputtering method; Then increase oxygen flow, continue to be that target prepares outer absorbed layer by reactive magnetron sputtering method on above-mentioned middle absorbed layer with Titanium;
Step 4, before product step 3 obtained is placed in silicon target, passes into argon gas and oxygen, adopts reactive magnetron sputtering method to prepare silicon oxide layer as anti-reflection layer on above-mentioned outer absorbed layer.
3. the coating for selective absorption of sunlight spectrum prepared of method according to claim 2, it is characterized in that, the thickness of described basalis is 0.2-10mm; The thickness of described infrared reflecting layer is 90-500nm; The gross thickness of described interior absorbed layer, middle absorbed layer and outer absorbed layer is 40-150nm, and the thickness of described anti-reflection layer is 80-100nm.
4. the coating for selective absorption of sunlight spectrum prepared of method according to claim 2, it is characterized in that, the material of described interior absorbed layer is TiN x1o y1, be within the scope of 400nm-600nm at wavelength, refractive index is between 1.9-2.5, and extinction coefficient is between 0.6-1.2; Be that within the scope of 900nm-1100nm, refractive index is in 2.2-2.8 at wavelength, extinction coefficient is in 2.1-2.5; Be that within the scope of 2000nm-2300nm, refractive index is in 3.8-4.1 at wavelength, extinction coefficient is in 2.8-3.0.
5. the coating for selective absorption of sunlight spectrum prepared of method according to claim 2, it is characterized in that, the material of described middle absorbed layer is TiN x2o y2, be within the scope of 400nm-600nm at wavelength, refractive index is between 2.0-2.4, and extinction coefficient is between 0.5-0.9; Be within the scope of 900nm-1100nm at wavelength, refractive index is in 2.7-3.1, and extinction coefficient is in 1.3-1.5; Be that within the scope of 2000nm-2300nm, refractive index is in 3.6-3.8 at wavelength, extinction coefficient is in 1.0-1.2.
6. the coating for selective absorption of sunlight spectrum prepared of method according to claim 2, it is characterized in that, the material of described outer absorbed layer is TiN x3o y3, be within the scope of 400nm-600nm at wavelength, refractive index is between 2.2-2.5, and extinction coefficient is between 0.3-0.5; This type of material is that within the scope of 900nm-1100nm, refractive index is in 2.6-2.9 at wavelength, and extinction coefficient is 0.4-0.6; Be that within the scope of 2000nm-2300nm, refractive index is in 2.8-3.0 at wavelength, extinction coefficient is in 0.2-0.3.
7. a solar thermal collector, is characterized in that, comprises coating for selective absorption of sunlight spectrum according to claim 1.
8. the application of coating for selective absorption of sunlight spectrum according to claim 1 in solar thermal collector.
CN201310074921.8A 2013-03-08 2013-03-08 Coating for selective absorption of sunlight spectrum and preparation method thereof and application Active CN104034072B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201310074921.8A CN104034072B (en) 2013-03-08 2013-03-08 Coating for selective absorption of sunlight spectrum and preparation method thereof and application

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201310074921.8A CN104034072B (en) 2013-03-08 2013-03-08 Coating for selective absorption of sunlight spectrum and preparation method thereof and application

Publications (2)

Publication Number Publication Date
CN104034072A CN104034072A (en) 2014-09-10
CN104034072B true CN104034072B (en) 2016-04-27

Family

ID=51464956

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201310074921.8A Active CN104034072B (en) 2013-03-08 2013-03-08 Coating for selective absorption of sunlight spectrum and preparation method thereof and application

Country Status (1)

Country Link
CN (1) CN104034072B (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105276846B (en) * 2014-11-14 2018-07-06 中国建筑材料科学研究总院 Coating for selective absorption of sunlight spectrum that ABSORPTION EDGE is continuously adjusted and preparation method thereof
CN106091442A (en) * 2016-06-06 2016-11-09 南宁可煜能源科技有限公司 A kind of slective solar energy absorbing coating with double ceramic structure
CN109742187B (en) * 2018-12-29 2020-09-15 苏州焜原光电有限公司 Method for manufacturing multi-section solar cell

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2006070795A1 (en) * 2004-12-28 2006-07-06 Ishihara Sangyo Kaisha, Ltd. Black titanium oxynitride
CN101737983A (en) * 2009-11-25 2010-06-16 北京航空航天大学 Solar spectrum selective absorbing coating and preparation method thereof
CN101818328A (en) * 2010-04-22 2010-09-01 常州博士新能源科技有限公司 Preparation method of multilayer compound solar energy selective absorption plating layer
CN102278833A (en) * 2011-05-16 2011-12-14 山东桑乐光热设备有限公司 High-temperature resistant selective absorption coating and manufacturing method thereof
CN102353165A (en) * 2011-08-26 2012-02-15 郝立冬 Solar flat plate collector board core and manufacturing method thereof

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007119303A (en) * 2005-10-28 2007-05-17 Nippon Sheet Glass Co Ltd Low radiation laminate
JP5185406B2 (en) * 2011-03-14 2013-04-17 株式会社東芝 Sputtering target, interface layer film for phase change optical recording medium using the same, method for producing the same, and phase change optical recording medium

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2006070795A1 (en) * 2004-12-28 2006-07-06 Ishihara Sangyo Kaisha, Ltd. Black titanium oxynitride
CN101737983A (en) * 2009-11-25 2010-06-16 北京航空航天大学 Solar spectrum selective absorbing coating and preparation method thereof
CN101818328A (en) * 2010-04-22 2010-09-01 常州博士新能源科技有限公司 Preparation method of multilayer compound solar energy selective absorption plating layer
CN102278833A (en) * 2011-05-16 2011-12-14 山东桑乐光热设备有限公司 High-temperature resistant selective absorption coating and manufacturing method thereof
CN102353165A (en) * 2011-08-26 2012-02-15 郝立冬 Solar flat plate collector board core and manufacturing method thereof

Also Published As

Publication number Publication date
CN104034072A (en) 2014-09-10

Similar Documents

Publication Publication Date Title
CN103388917B (en) A kind of solar selectively absorbing coating and its preparation method
CN204345956U (en) The continuously adjustable coating for selective absorption of sunlight spectrum of a kind of ABSORPTION EDGE
CN102602071B (en) Solar selective absorbing coating as well as preparation method and application thereof
CN101886847B (en) Medium-high temperature solar thermal collector tube
CN105299935B (en) A kind of coating for selective absorption of sunlight spectrum and preparation method thereof and heat collector
CN101344334B (en) A kind of solar spectrum selective absorption film and preparation method thereof
CN105222381B (en) A kind of double absorption layer coating for selective absorption of sunlight spectrum and preparation method thereof
CN106884145B (en) A kind of coating for selective absorption of sunlight spectrum and preparation method thereof
CN103383155A (en) Ti-alloy nitride selective-absorption film system and preparation method thereof
CN104724951B (en) Dimming glass thin-film material and preparation method thereof
CN104034072B (en) Coating for selective absorption of sunlight spectrum and preparation method thereof and application
CN107588569A (en) Double absorption layer spectral selective absorbing coating and preparation method thereof
CN204535163U (en) A kind of coating for selective absorption of sunlight spectrum and heat collector
CN103105011B (en) Solar selective absorbing film series suitable for medium-high temperature heat usage and preparation method thereof
CN109457219B (en) A medium and low temperature solar spectrum selective absorption coating and preparation method thereof
CN201715767U (en) Multilayer composite solar selection absorption coating
CN115451594B (en) A wide spectrum solar energy absorption enhancement device and preparation method thereof
CN102092960A (en) Low emissivity glass
CN104034071A (en) Dark green solar spectral selection absorbing coating and preparation method and application thereof
CN105970175A (en) Titanium carbide-zirconium carbide high-temperature solar selective absorbing coating and preparation method thereof
CN105779926B (en) Prepare the new process for being used for high temperature solar energy selective absorption coating under atmospheric environment
CN204478557U (en) A kind of double absorption layer coating for selective absorption of sunlight spectrum
CN104930735A (en) Solar absorbing film and preparation method thereof
CN104596138B (en) Solar selective absorption film system
CN201273736Y (en) Solar energy heat collecting tube

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant