Patent Grant
11833817
The present disclosure relates to a liquid ejection head substrate that ejects a liquid, and a liquid ejection head.
One of recording methods using a typical ink jet head as a liquid ejection head is a method in which ink is heated by a heating element to bubble and the ink is ejected using bubbles.
An example of a liquid ejection head to which the above ejection method is applied is disclosed in Japanese Patent Application Laid-Open No. 2017-43098. The liquid ejection head disclosed in Japanese Patent Application Laid-Open No. 201743098 includes a flow passage forming member including a resin layer having an ejection orifice and a flow passage, a heating resistance element for ejecting a liquid, a substrate having a portion covering the heating resistance element, and a protecting layer exposing a surface of the portion to the flow passage, and an intermediate layer provided between the resin layer and the protecting layer and containing a carbon nitride silicon material.
A wiring for driving the heating resistance element is provided on the substrate. The heating resistance element and the wiring are insulated by an insulating layer covering the heating resistance element and the wiring so that the heating resistance element can be driven.
In Japanese Patent Application Laid-Open No. 201743098, in the liquid ejection head, a carbon nitride silicon material is applied to the intermediate layer between the resin layer included in the flow passage forming member and the protecting layer. In such a liquid ejection head, when used in a state where a voltage is accidentally applied to the protecting layer, since the carbon nitride silicon applied to the intermediate layer has no insulating property, the carbon nitride silicon may be anodized and dissolved in the ink. When the intermediate layer dissolves, there is a possibility that a nozzle may be peeled off and normal ejection may not be performed. Furthermore, the ink in which the intermediate layer is dissolved may enter the inside of the liquid ejection head and dissolve the insulating layer, which may lead to corrosion of the wiring. Therefore, the corrosion may lead to a disadvantage of the entire liquid ejection head. As described above, since the reliability of the liquid ejection head is lowered due to the dissolution of the intermediate layer, it is an issue to suppress the deterioration of the reliability.
Therefore, an aspect of the present disclosure is to provide a liquid ejection head substrate and a liquid ejection head that satisfy a performance required as an intermediate layer, such as adhesion to a flow passage forming member and a protecting layer, and an ink resistance, and have long-term reliability in which dissolution of the intermediate layer due to anodization is suppressed.
According to an aspect of the present disclosure, there is provided a liquid ejection head substrate including: a flow passage forming member having an ejection orifice and a flow passage; a heating resistance element for ejecting a liquid; an insulating layer covering the heating resistance element; a protecting layer provided on the insulating layer and whose surface is exposed to the flow passage; and an intermediate layer provided between the flow passage forming member and the protecting layer, in which the intermediate layer contains a material represented by the following composition formula (I):
Siw1Ox1Cy1 (I)
In addition, according to another aspect of the present disclosure, there is provided a liquid ejection head substrate, in which the intermediate laver contains a material represented by the following composition formula (III):
Siw3Ox3Cy3Nz3 (III)
According to still another aspect of the present disclosure, there is provided a liquid ejection head including the above-described liquid ejection head substrate.
According to the present disclosure, it is possible to provide the liquid ejection head substrate and the liquid ejection head that satisfy the performance required as the intermediate layer, such as adhesion to the flow passage forming member and the protecting layer, and the ink resistance, and have long-term reliability in which dissolution of the intermediate layer due to anodization is suppressed.
Further features of the present disclosure will become apparent from the following description of exemplary embodiments with reference to the attached drawings.
A liquid ejection head can be mounted on an information output device such as a printer, a copying machine, a facsimile having a communication system, a word processor having a printer unit, and an industrial recording device complexly combined with various processing devices. By using the liquid ejection head, recording can be performed on various recording target media such as paper, thread, fiber, cloth, metal, plastic, glass, wood, and ceramics.
“Recording” used in the present specification means not only applying an image having a meaning such as characters and figures to a recording target medium, but also applying an image having no meaning such as a pattern.
In addition, “liquid” used in the present specification required to be broadly interpreted, and includes not only the ink used for the recording operation but also the following liquid. That is, the “liquid” also includes a liquid used for forming an image, a design, and a pattern, processing the recording target medium, and processing ink and the recording target medium by being applied onto the recording target medium. Here, the processing of one of the ink and the recording target medium refers to, for example, processing for improving fixability by one of solidification and insolubilization of the coloring material in the ink applied to the recording target medium, improving one of recording quality and color development, and improving image durability. Furthermore, the “liquid” used in the liquid ejection head of the present disclosure normally contains a large amount of electrolyte and has conductivity.
Hereinafter, embodiments of the present disclosure will be described with reference to the drawings with reference to
In addition, an intermediate layer 210 containing a specific silicon carbonate material (described later) is provided between the flow passage forming member 200 and the protecting layer 201.
The insulating layer 202 is normally made of SiN and has a film thickness (dimension in the T direction) of approximately 150 nm to 300 nm. The insulating layer 202 may be made of one of SiO and SiC. The insulating layer 202 is covered with the protecting layer 201. The protecting layer 201 is made of a conductive material. The protecting layer 201 is normally made of Ta (tantalum) and has a film thickness of approximately 200 nm to 300 nm. The protecting layer 201 may be made of one of Ir (iridium) and a laminated film of Ir and Ta. In addition, although the figure illustrates a case where an organic intermediate layer 211 is formed between the flow passage forming member 200 and the intermediate layer 210, the organic intermediate layer 211 may be omitted.
The intermediate layer 210 is formed of a layer containing a material represented by the following composition formula (I).
Siw1Ox1Cy1 (I)
[In the above formula (I), 39≤w1≤62 (at. %), 32≤x1≤55 (at. %), and 6≤y1≤29 (at. %), here, w1+x1+y1=100 (at %)].
When the liquid ejection head is used for a long period of time, a disadvantage may occur in the insulating layer 202 between the heating resistance element 6 and the protecting layer 201 accidentally, and the heating resistance element 6 and the protecting layer 201 may be conductive. As a result, the voltage applied to the heating resistance element 6 may be also applied to the protecting layer 201. However, even in a case where the protecting layer 201 of the liquid ejection head is used in a state where a voltage is accidentally applied, the intermediate layer 210 is formed with a layer containing a material represented by the composition formula (I) having a high insulating property. Therefore, it is possible to suppress ink dissolution of the intermediate layer 210 due to anodization. Therefore, it is possible to provide a liquid ejection head having long-term reliability.
An anodization mechanism will be described with reference to
In order to further enhance the ink resistance of the intermediate layer 210, as illustrated in
Specifically, the intermediate lower layer 210b is formed of a film containing the material represented by the composition formula (I), and the intermediate upper layer 210a is desirably formed of a film containing a material represented by the following composition formula (II).
Siw2Cy2Nz2 (II)
[In the above formula (II), 30≤w2≤59 (at. %), y2≥5 (at. %), and z2≥15 (at. %) here, w2+y2+z2=100 (at %)].
The composition formula (II) is equivalent to the composition formula (I) disclosed in Japanese Patent Application Laid-Open No. 2017-43098, and the technical significance of the composition range is understood from Japanese Patent Application Laid-Open No. 2017-43098.
With such a configuration, in addition to the effect of suppressing the ink dissolution of the intermediate layer 210 due to the anodization by the insulating material of the composition formula (I) described above, the ink resistance can be further enhanced by the film of the composition formula (II). Therefore, the long-term reliability of the liquid ejection head can be further enhanced.
In addition, the insulating layer 202 can be made thin in order to drive the liquid ejection head with energy-saving. In such a case, there is a concern that the passivation resistance is insufficient, moisture and ions easily permeate, and corrosion of the electrode wiring 207 occurs. Therefore, the intermediate layer 210 also can have passivation resistance.
For example, the intermediate layer 210 can be formed of a film containing a material represented by the following composition formula (III):
Siw3Ox3Cy3Nz3 (III)
[In the above formula (III), 37≤w3≤60 (at. %), 30≤x3≤53 (at. %), 6≤y3≤29 (at. %), and 4≤z3≤9 (at. %), here, w3+x3+y3+z3=100 (at %)].
With such a configuration, in addition to the effect of suppressing the ink dissolution of the intermediate layer 210 due to the anodization described above, the drive with energy-saving can be performed, so that the long-term reliability of the liquid ejection head driven with energy-saving can be enhanced.
In the intermediate layer 210, the film thickness of the film containing the material represented by the composition formula (I) is desirably 100 nm or more in order to ensure the insulating property. In addition, the film thickness of the film containing the material represented by the composition formula (II) is desirably 50 nm or more in order to ensure ink resistance. Furthermore, the film thickness of the layer containing the material represented by the composition formula (III) is desirably 100 nm or more in order to ensure the insulating property and the passivation resistance. However, when the protecting layer 201 is exposed to the flow passage, etching is performed to open the intermediate layer 210. Therefore, from the viewpoint of the selection ratio between the intermediate layer 210 and the protecting layer 201, the film thickness of the intermediate layer 210 is desirably 300 nm or less.
The Siw1Ox1Cy1 (I), Siw2Cy2Nz2 (II), and Siw3Ox3Cy3Nz3 (III) films constituting the intermediate layer 210 can be formed by using a plasma CVD method.
The outline of the film forming method of the Siw1Ox1Cy1 (I), Siw2Cy2Nz2 (II), and Siw3Ox3Cy3Nz3 (III) films will be described below with reference to
First, the distance (GAP) between a shower head 303 that functions as an upper electrode during plasma discharge and a sample stage 302 that functions as a lower electrode is determined by adjusting the height of the sample stage 302. In addition, the temperature of the sample stage 302 is adjusted by heating with a heater 304.
Next, various gases to be used flow into a film forming chamber 310 via the shower head 303. At that time, the flow rates of the various gases are controlled by mass flow controllers 301 attached to each of pipes 300 corresponding to each of gases. Thereafter, by opening an introduction valve 307a of the gas to be used, the gas is mixed in the pipe and supplied to the shower head 303. Subsequently, an exhaust valve 307b attached to an exhaust port 305 connected to a vacuum pump (not illustrated) is adjusted to control the amount of exhaust, thereby maintaining the pressure in the film forming chamber 310 constant. Thereafter, the two-frequency RF power supplies 308a and 308b discharge the plasma between the shower head 303 and the sample stage 302. The atoms dissociated in the plasma are accumulated on a wafer 306 to form a film.
The Siw1Ox1Cy1 (I) film according to the present disclosure can obtain Siw1Ox1Cy1 (I) having different composition ratios by appropriately adjusting the film formation conditions of a flow rate of SiH4 gas, a flow rate of O2 gas, a flow rate of CH4 gas, HRF power, LRF power, pressure, and temperature. Even when the flow rate ratio of each process gas was changed, Siw1Ox1Cy1 (I) with w1≤38 could not be prepared. In a case where stress suppression is required depending on the film composition and layout of the substrate, the stress suppression can be adjusted by raising the film formation temperature.
The Siw2Cy2Nz2 (II) film according to the present disclosure can obtain Siw2Cy2Nz2 (II) having different composition ratios by appropriately adjusting the film formation conditions of a flow rate of SiH4 gas, a flow rate of NH3 gas, a flow rate of N2 gas, a flow rate of CH4 gas, HRF power, LRF power, pressure, and temperature.
In order to obtain the Siw3Ox3Cy3Nz3 (III) film according to the present disclosure, the film formation conditions of a flow rate of SiH4 gas, a flow rate of N2O gas, a flow rate of CH4 gas, HRF power, LRF power, pressure, and temperature are appropriately adjusted. As a result, Siw3Ox3Cy3Nz3 (III) having different composition ratios can be obtained. Even when the flow rate ratio of each process gas was changed, the Siw3Ox3Cy3Nz3 (III) film with w3≤36 and the Siw3Ox3Cy3Nz3 (III) film with z3≥10 could not be prepared.
In this specification, Siw1Ox1Cy1 (I), Siw2Cy2Nz2 (II), and Siw3Ox3Cy3Nz3 (III) indicate the content ratio of each element as an atomic percentage (at. %). In addition, although hydrogen derived from the raw material gas of the CVD method described above is contained, the hydrogen content is not taken into consideration. However, the film formed by using the raw material gas described above normally contains approximately 15 to 30 (at. %) of hydrogen, and hydrogen may be contained as long as the film does not deviate significantly from the range. Hereinafter, examples for determining the performance of Siw1Ox1Cy1 (I), Siw2Cy2Nz2 (II), and Siw3Ox3Cy3Nz3 (III) are illustrated. In addition, in the following examples, the same experiment was carried outperformed using the SiO film as a reference level.
Hereinafter, the present disclosure will be further described with reference to Examples and Comparative Examples, and the present disclosure is not limited to these Examples.
The following experiment was performed to confirm the erosion resistance of the Siw1Ox1Cy1 (I) film and Siw3Ox3Cy3Nz3 (III) film to the ink in the embodiment. First, the films of Siw1Ox1Cy1 (I) and Siw3Ox3Cy3Nz3 (III) were formed on separate silicon substrates. Thereafter, the substrates were cut so as to have a size of 20 mm×20 mm.
The amount of dissolution when the individual pieces were immersed in 30 ml of pigment ink having a pH of approximately 9 heated to 60° C. and left for 72 hours was examined. At that time, in order to eliminate the influence of dissolution of Si exposed on the end surface and the rear surface of the substrate, the rear surface and the side surface of the substrate were protected with an ink-insoluble resin. The film thickness according to the experimental example was measured using a spectroscopic ellipsometer. By examining the variation in the film thickness in the experiment, the erosion resistance of the Siw1Ox1Cy1 (I) film and Siw3Ox3Cy3Nz3 (III) film to the ink was confirmed. The results are illustrated in Tables 1 and 2. The criteria for this experiment were as follows.
As a result of the determination at this time, it was assumed that A was significantly effective, B was effective. C was less effective, and D was substantially ineffective. This determination is the same as the results of the following experimental examples. Since the amount of dissolution of each sample a to k of the Siw1Ox1Cy1 (I) film tended to be substantially the same as the amount of dissolution of each sample A to K of Siw3Ox3Cy3Nz3 (III), only the determination result is illustrated in Table 1.
From the results illustrated in Table 1, it can be seen that the composition range of Siw1Ox1Cy1 (I) satisfying the erosion resistance to ink is a composition region satisfying 6≤y1 (at. %). From the results illustrated in Table 2, it can be seen that the composition range of Siw3Ox3Cy3Nz3 (III) satisfying the erosion resistance to ink is a composition region satisfying 6≤y3 (at. %). In particular, when using a pigment ink, it is effective to use Siw1Ox1Cy1 (I), and Siw3Ox3Cy3Nz3 (III) within the range of this composition region. In addition, even with a pigment ink and a dye ink having a pH of approximately 5 to 11, the same results as the above results were obtained.
The following experiments were performed to confirm the electrical insulating property of the Siw1Ox1Cy1 (I) film, and Siw3Ox3Cy3Nz3 (III) film in the embodiment. First, a metal layer having aluminum as a main material is formed with a thickness of 200 nm on a silicon substrate on which a silicon thermal oxide film having a film thickness of 1 μm is formed for use as a first electrode, and processed so as to have a size of 2.5 mm×2.5 mm. Thereafter, one film of Siw1Ox1Cy1 (I) and Siw3Ox3Cy3Nz3 (III) was formed to a thickness of 300 nm. Furthermore, a film having aluminum as a main material is processed into a film having a size of 2 mm×2 mm in the upper layer for use as a second electrode, and is formed with a thickness of 200 nm so as not to protrude directly above the first electrode. Thereafter, through-holes for making electrical contact with the first electrode were opened to the Siw1Ox1Cy1 (I) film and the Siw3Ox3Cy3Nz3 (III) film. Using such a sample, the amount of current when a voltage of 32 V was applied between the first electrode and the second electrode was measured. By measuring the amount of current in this experiment, the electrical insulating property of the Siw1Ox1Cy1 (I) film and Siw3Ox3Cy3Nz3 (III) film was confirmed. The results are illustrated in Tables 3 and 4. The criteria for this experiment were as follows.
Since the current values of each sample a to k of the Siw1Ox1Cy1 (I) film tended to be substantially the same as the current values of each sample A to K of Siw3Ox3Cy3Nz3 (III) film, only the determination result is illustrated in Table 3.
From the results illustrated in Table 3, it can be seen that the composition range of the Siw1Ox1Cy1 (I) film satisfying the electrical insulating property is a composition region satisfying 32≤x1 (at. %). From the results illustrated in Table 4, it can be seen that the composition range of Siw3Ox3Cy3Nz3 (III) satisfying the electrical insulating property is a composition region satisfying 30≤x3 (at. %).
One of the stress adjustment methods is the film formation temperature. The stress of SiOC can be suppressed by raising the film formation temperature. Since SiOCN has nitrogen to suppress stress, film formation can be performed at a film formation temperature lower than that of SiOC.
The following experiment was performed to measure the stress of the Siw3Ox3Cy3Nz3 (III) film in the present disclosure. A Siw3Ox3Cy3Nz3 (III) film was formed on a silicon substrate, and the stress was measured with a stress measuring instrument. The results are illustrated in Table 5. When the stress value is 0 or more, it represents tensile stress, and when the stress value is less than 0, it represents compressive stress. The criteria for this experiment are as follows.
The experimental results of Experimental Examples 1 to 3 described above are summarized in Tables 6 and 7. Table 6 is the experimental results of Siw1Ox1Cy1 (I), and Table 7 is the experimental results of Siw3Ox3Cy3Nz3 (III). For the comprehensive determination, the determination of the one with the lowest evaluation among the results of each experiment was used. The intermediate layer 210 of the liquid ejection head is required to have excellent performances listed in Experimental Examples 1 to 3 above.
The composition range of the Siw1Ox1Cy1 (I) film is defined as follows. An Siw1Ox1Cy1 (I) film with w1≤38 could not be prepared. From Table 6, the composition of the Siw1Ox1Cy1 (I) film is 32≤x1 (at. %), and 6≤y1 (at. %) with w1+x1+y1=100 (at %). As a result, the composition of the Siw1Ox1Cy1 (I) film is 39≤w1 (at. %), 32≤x1 (at. %), and 6≤y1 (at. %) as w1+x1+y1=100 (at %) so as to satisfy each performance. Since w1+x1+y1=100 (at %), each of the upper limits of w1, x1, and y1 is w1≤62 (at. %), x1≤55 (at %), and y1≤29 (at %). Therefore, the composition of the Siw1Ox1Cy1 (I) film capable of exhibiting the required performance is 39≤w1≤62 (at. %), 32≤x1≤55 (at. %), and 6≤y1≤29 (at. %) as w1+x1+y1=100 (at %).
In addition, the levels at which the comprehensive determination was A and B were the levels of c, d, e, f, g, and h. As a result, in Siw1Ox1Cy1 (I), a relational formula of 39≤w1≤43 (at. %), 35≤x1≤44 (at. %), and 13≤y1≤24 (at. %) can be satisfied.
The composition range of the Siw3Ox3Cy3Nz3 (III) film is defined as follows. A Siw3Ox3Cy3Nz3 film with w3≤36 and z3≥10 could not be prepared. From Table 7, the composition of the Siw3Ox3Cy3Nz3 (III) film is 30≤x3 (at. %), 6≤y3 (at. %), and 4≤z3 (at. %) as w3+x3+y3+z3=100 (at %). AS a result, the composition of the Siw3Ox3Cy3Nz3 film is 37≤w3 (at. %), 30≤x3 (at. %), 6≤y3 (at. %), and 4≤z3≤9 (at. %) as w3+x3+y3+z3=100 (at %) so as to satisfy each performance. Since w3+x3+y3+z3=100 (at %), each of the upper limits of w3, x3, and y3 is w3≤60 (at. %), x3≤53 (at %), and 3≤29 (at %). Therefore, the composition of the Siw3Ox3Cy3Nz3 film capable of exhibiting the required performance is as follows. That is, 37≤w3≤60 (at. %), 30≤x≤53 (at. %), 6≤y3≤29 (at. %), and 4≤z3≤9 (at. %) as w3+x3+y3+z3=100 (at %).
In addition, the levels at which the comprehensive determination was B or more were the levels D, F, G, and H. As a result, in Siw3Ox3Cy3Nz3, 37≤w3≤39 (at. %), a relational formula of 33≤x3≤41 (at. %), 12≤y3≤22 (at. %), and 7≤z3≤8 (at. %) can be satisfied.
The liquid was actually ejected using various liquid ejection heads prepared in the present embodiment. In this example, the intermediate layer 210 was formed of a single layer of one of Siw1Ox1Cy1 film and Siw3Ox3Cy3Nz3 film. The results are illustrated below.
The intermediate layer 210 formed of the materials of the levels b to j illustrated in Table 6 has an insulating property. Therefore, even in a case where the liquid ejection head was used in a state where a voltage was accidentally applied, it was possible to suppress the ink dissolution of the intermediate layer 210 due to anodization, and the liquid ejection head having the intermediate layer 210 formed of the materials of the levels of b to j had long-term reliability. In particular, in a case where the materials having the levels of c to h were used for the intermediate layer 210, both the erosion resistance and the insulating property were determined to be B or more, so that a liquid ejection head having higher reliability could be formed.
On the other hand, in the liquid ejection head using the materials of the levels a and l for the intermediate layer 210, when the ejection is continued for a long period of time, the intermediate layer 210 may be dissolved in the ink and the ejection performance may be lowered. Due to the dissolution of the intermediate layer 210, the nozzle was peeled off and normal ejection could not be performed, in some cases. Furthermore, the ink invades and dissolves the insulating layer 202, which leads to corrosion of the wiring 207, so that a disadvantage might occur in the entire liquid ejection head. In addition, although the liquid ejection head using the material of the k level for the intermediate layer 210 did not normally cause a defect, in a case where it was used in a state where a voltage was accidentally applied, since the insulating property of the intermediate layer 210 was poor, the intermediate layer 210 was anodized and dissolved in the ink. Due to the dissolution of the intermediate layer 210, the nozzle was peeled off and normal ejection could not be performed, in some cases. Furthermore, the ink invades and dissolves the insulating layer 202, which leads to corrosion of the wiring 207. Therefore, the corrosion may lead to a disadvantage of the entire liquid ejection head.
The intermediate layer 210 formed of the materials of the levels B, and D to J illustrated in Table 7 has an insulating property. Therefore, the liquid ejection head having the intermediate layer 210 formed of the materials of the levels B, and D to J can suppress the ink dissolution of the intermediate layer 210 due to anodization even in a case where the liquid ejection head is used in a state where a voltage is accidentally applied. Therefore, it was possible to form a liquid ejection head having long-term reliability. In particular, in a case where the materials having the levels of D. and F to H were used for the intermediate layer, the erosion resistance, the insulating property, and the stress were all B-determination or more, so that a liquid ejection head having higher reliability could be formed.
On the other hand, in the liquid ejection head using the materials of the levels A and L for the intermediate layer 210, when the ejection is continued for a long period of time, the intermediate layer 210 may be dissolved in the ink and the ejection performance may be lowered. Due to the dissolution of the intermediate layer 210, the nozzle was peeled off and normal ejection could not be performed, in some cases. Furthermore, the ink invades and dissolves the insulating layer 202, which leads to corrosion of the wiring 207, so that a disadvantage might occur in the entire liquid ejection head. Although the liquid ejection head using the material of the level C for the intermediate layer 210 did not cause a defect, the warp of the substrate was increased, and a transfer error and a suction error occurred in a part of the head manufacturing step. In addition, although the liquid ejection head using the material of level K for the intermediate layer 210 did not normally cause a defect, in a case where the liquid ejection head was used in a state where a voltage was accidentally applied, the insulating property of the intermediate layer 210 was poor. Therefore, the intermediate layer 210 was anodized and dissolved in the ink. Due to the dissolution of the intermediate layer 210, the nozzle was peeled off and normal ejection could not be performed, in some cases. Furthermore, the ink invades and dissolves the insulating layer 202, which leads to corrosion of the wiring 207, so that a disadvantage might occur in the entire head.
Next, Example 2 of the present disclosure will be described with reference to
The flow passage forming member 200 having a side wall portion and a ceiling portion of the flow passage 212 and the ejection orifice 209 was formed on the substrate as a cured product layer of the photosensitive resin material. The photosensitive resin material is not particularly limited, and can be selected and used from those used for the flow passage forming member of the recording head. A portion made of another material may be further added to the portion made of the resin layer of the flow passage forming member. For example, the surface of the ejection orifice to be opened may be surface-treated by forming a water-repellent layer.
As illustrated in
Next, Example 3 of the present disclosure will be illustrated only a portion different from that of Example 2. As illustrated in
Next, Example 4 of the present disclosure will be illustrated only a portion different from that of Example 2. In order to drive the liquid ejection head with energy-saving, the film thickness of the insulating layer 202 was reduced to 170 nm. However, there is a concern that the passivation resistance is insufficient, moisture and ions easily permeate, and the electrode wiring 207 may be corroded. Therefore, in order to impart the intermediate layer passivation resistance, the configuration of the intermediate layer 210 was changed as follows. The intermediate layer 210 was formed of a film containing a material in which w3, x3, y3, and z3 are w3=38 (at. %), x3=39 (at. %), y3=15 (at. %), z3=8 (at. %) in the composition formula (III): Siw3Ox3Cy3Nz3 (III). In the intermediate layer 210, the film thickness of the film made of the material represented by the composition formula (III) was set to 100 nm in order to ensure the insulating property and the passivation resistance. With this configuration, even in a case where the protecting layer 201 of the liquid ejection head was used in a state where a voltage was accidentally applied, the intermediate layer 210 had an insulating property. Therefore, it was possible to suppress the ink dissolution of the intermediate layer 210 due to anodization. Furthermore, the film thickness of the insulating layer 202 was reduced, so that driving can be performed with energy-saving.
Next, Comparative Example 1 of the present disclosure is illustrated only a portion different from that of Example 1. The configuration of the intermediate layer 210 was changed as follows.
The intermediate layer 210 was formed of a film made of a material in which x2, y2, and z2 are w2=47 (at. %), y2=17 (at. %), and z2=36 (at. %) in the composition formula (II): Siw2Cy2Nz2 (II). The film thickness was 100 nm.
With this configuration, in a case where the protecting layer 201 of the liquid ejection head is used in a state where a voltage is accidentally applied, the intermediate layer 210 has a poor insulating property. Therefore, the intermediate layer 210 may be anodized and dissolved in the ink. Due to the dissolution of the intermediate layer 210, the nozzle is peeled off and normal ejection cannot be performed. Furthermore, the ink invades and dissolves the insulating layer 202, which leads to corrosion of the wiring 207, so that a disadvantage was occurred in the entire head.
While the present disclosure has been described with reference to exemplary embodiments, it is to be understood that the invention is not limited to the disclosed exemplary embodiments. The scope of the following claims is to be accorded the broadest interpretation so as to encompass all such modifications and equivalent structures and functions.
This application claims the benefit of Japanese Patent Application No. 2020-189848, filed Nov. 13, 2020, which is hereby incorporated by reference herein in its entirety.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2020-189848 | Nov 2020 | JP | national |
| Number | Name | Date | Kind |
|---|---|---|---|
| 4873622 | Komuro et al. | Oct 1989 | A |
| 8721048 | Yasuda | May 2014 | B2 |
| 20130314474 | Yasuda et al. | Nov 2013 | A1 |
| 20170057228 | Oikawa et al. | Mar 2017 | A1 |
| Number | Date | Country |
|---|---|---|
| 1223932 | Jul 1999 | CN |
| 103373072 | Oct 2013 | CN |
| 109203676 | Jan 2019 | CN |
| 110869213 | Mar 2020 | CN |
| 2002-046266 | Feb 2002 | JP |
| 2017043098 | Mar 2017 | JP |
| Number | Date | Country | |
|---|---|---|---|
| 20220153026 A1 | May 2022 | US |
