169 results about "Ag electrode" patented technology

The invention provides a solder paste which has a solidus temperature of 255° C. or above and is improved in the wettability between Bi and Cu or Ag electrode to attain approximately equivalent wettability to those of Pb-containing high-temperature solders even in low-temperature soldering. The solder paste comprises a metal powder component consisting of Bi or a Bi alloy, a solidus temperature lowering metal for Bi, and a solid-phase metal capable of forming an intermetallic compound with the solidus temperature lowering metal, and a flux component.

The invention discloses a preparation method of a solar cell. The method comprises the following steps: providing a plurality of polycrystalline silicon wafers for texturization; overlapping the textured silicon wafers, depositing a silicon nitride or silicon oxide masking film on the periphery of the silicon wafers, then diffusing a phosphorus doping layer on the front surface of the to-be-prepared positive electrode of the silicon wafers to form a PN junction, wherein the periphery of the silicon wafers can not form the diffusion PN junction owning to the existence of the masking film; removing the peripheral masking film and the surface phosphosilicate glass; preparing a passivation layer and an antireflection layer; and performing screen printing and sintering to form a back Ag electrode, a back Al-back surface and a front Ag electrode. In the preparation method of the solar cell provided by the invention, the masking film is formed before the impurity source diffusion used for preparing the PN junction; owning to the existence of the masking film, the periphery of the silicon wafers can not form the PN junction; and the silicon wafers after diffusion is washed with acid to remove the masking film on the periphery of the silicon wafers and the phosphosilicate glass on the diffusion surface, thus achieving the aim of replacing the etching step.

The invention discloses a low temperature co-fired microwave dielectric ceramic material and a preparation method thereof. The ceramic material comprises a main powder material Li2ZnTi3O8, an auxiliary component TiO2 and low-melting-point LZB (Li2O-ZnO-BiO2) or LBS (Li2O-B2O3-SiO2) glass powder. The preparation method comprises the following steps of: adding TiO2 and the glass powder into the Li2ZnTi3O8 powder in a powder form; and then evenly mixing in a ball mill, drying, pelleting and sintering so as to obtain the ceramic material. In the invention, based on the Li2ZnTi3O8 powder as a reference, batching is carried out according to the proportions that the mass of the glass powder is 0.5-3wt% of that of Li2ZnTi3O8 and the mass of the TiO2 powder is 0-5wt% of that of Li2ZnTi3O8; and thematerial of the invention can be obtained by a traditional solid phase reaction method. The low temperature co-fired microwave dielectric ceramic material prepared by the method of the invention has low sintering temperature (about 875 DEG C) and good microwave dielectric property, and can be well co-fired with a Ag electrode; pure silver with high electricity conductivity and low cost is used asan electrode material, thus the manufacturing cost of a device can be greatly reduced; and the low temperature co-fired microwave dielectric ceramic material can be used for a low temperature co-fired ceramic (LTCC) system and manufacturing of microwave devices such as multilayer dielectric resonators, microwave antennas, filters and the like.

The invention discloses a low-temperature co-fired Li2MgTi3O8 microwave dielectric ceramic material and a preparation method thereof. The material comprises a main powder material Li2MgTi3O8 and low-melting-point Li2O-MgO-B2O3 (LMB) glass powder. The glass powder is added into Li2MgTi3O8 powder in the form of powder and then the mixture is evenly mixed in a ball mill and is dried, granulated and fired to obtain the material. The proportions of components for preparing the material are determined by taking the Li2MgTi3O8 powder as a reference, wherein the weight of the glass powder accounts for 0.5-3 percent of the weight of Li2MgTi3O8 powder. The material can be obtained through the traditional solid-phase reaction synthesis method. The low-temperature co-fired microwave dielectric ceramic material prepared by adopting the preparation method has the advantages that the firing temperature is low (approximate 875 DEG C), the microwave dielectric performance is excellent, the dielectric constant (epsilon r) is large, the quality factor (Q-f) is high, the resonant frequency-temperature factor (tf) is close to zero, the effect of co-firing with an Ag electrode is good, high-conductivity low-cost pure silver can be used as an electrode material, the manufacturing cost of devices can be greatly reduced, and the low-temperature co-fired microwave dielectric ceramic material can be used for manufacturing microwave devices such as low-temperature co-fired ceramic (LTCC) systems, multilayer dielectric resonators, microwave antennas and filters.

The invention discloses a method for manufacturing a high-performance planar structure CH3NH3PbI3-X(SCN)x-based perovskite solar energy cell in the humid air. The method comprises steps that hydrolysis of titanium tetrachloride solution is firstly carried out to acquire TiO2 colloid, the colloid acquired through hydrolysis of the titanium tetrachloride solution is deposited on FTO electro-conductive glass to acquire a TiO2 compact layer, a CH3NH3PbI3-X(SCN)x perovskite layer is prepared on the TiO2 compact layer by employing a two-step solution method, a cavity conduction layer is coated on the perovskite layer in a spinning mode, a Ag electrode is prepared through thermal evaporation, and the perovskite cell is finally acquired. Compared with the prior art, the method is advantaged in that the production process is simple, and cost is low.

The invention provides a back surface junction N-type double-sided crystal silicon cell and a preparation method thereof. The cell comprises a front surface Ag electrode, a front surface antireflection film, a phosphorus diffusion N+ front surface field layer, an N-type substrate, a boron diffusion emission electrode P+ layer, a back surface passivation composite film and a back surface AgAl electrode. The front surface and the back surface of the cell have a textured structure. The back surface passivation composite film comprises a borosilicate glass layer and a silicon nitride layer. The borosilicate glass layer is arranged on the boron diffusion emission electrode P+ layer. The silicon nitride layer is deposited on the borosilicate glass layer. Both of the front surface and the back surface of the cell can effectively receive sunlight irradiation for power generation so that comprehensive efficiency of the cell can be enhanced; and the laminated film of the borosilicate glass layer and the silicon nitride layer through oxidation treatment is adopted to act as a boron emission electrode passivation layer and a diffusion masking layer of subsequent phosphorus diffusion so that boron emission electrode passivation and diffusion masking functions can be realized simultaneously, and the process of multiple times of etching and mask deposition in the manufacturing process can be reduced. The back surface junction N-type double-sided crystal silicon cell is simple in technology, high in production efficiency and low in production technology cost.

The invention discloses a preparation method of a selective emitter solar cell, comprising the following steps: providing a silicon wafer for carrying out surface texturization; printing a diffusion permeable membrane on the silicon wafer by a first silk-screen printing plate; covering a non-electrode region by using the diffusion permeable membrane printed by the first silk-screen printing plate, exposing an electrode region to be printed; forming a light diffusion layer for the silicon wafer in the non-electrode light-affected region with the permeable membrane, and forming a heavy diffusion layer in the electrode region without the permeable membrane to be printed; carrying out corrosion for removing peripheral PN nodes, washing the membrane, and removing phosphosilicate glasses; preparing a passivation layer and an antireflection layer; and printing by the printing screen printing plate and sintering to form a back Ag electrode, a back Al-BSF and a front Ag electrode. The preparation method for the selective emitter solar cell provided by the invention adopts one-time diffusion to form the light and heavy doping required by the selective emitter solar cell, thereby reducing one-time high-temperature diffusion process, simplifying processes of the technology, and lowering the cost.

The invention relates to a silicon solar cell and a manufacturing method thereof. the method comprises the following steps: (1) carrying out wet-type chemical cleaning on a silicon wafer, and drying; (2) carrying out single-side phosphorus source diffusion on the silicon wafer; (3) placing the silicon wafer into an oxide furnace, and forming an oxide layer; (4) carrying out primary photoetching on the frontage of the silicon wafer; (5) removing the oxide layer of the photoetching graphics part of the silicon wafer; (6) carrying out whirl coating protection on the diffusion surface of the silicon wafer, and then corroding the oxide layer at the back surface; (7) carrying out single-side phosphorus source anew partial diffusion on the silicon wafer; (8) removing the oxide layer at the back surface of the silicon wafer; (9) evaporating a Ti/Pd/Ag electrode on the back surface of the silicon wafer, and then annealing; (10) firstly carrying out whirl coating protection on the back surface of the silicon wafer, and removing an optical resist at the back surface of the silicon wafer; (11) evaporating an indium tin film at the frontage of the silicon wafer by utilizing a magnetic control sputtering device; (12) carrying out secondary photoetching on the frontage of the silicon wafer; (13) carrying out tertiary photoetching on the frontage of the silicon wafer; and (14) removing the optical resist at the frontage of the silicon wafer, and annealing. According to the invention, the cell conversion efficiency can be improved effectively; and the cell and method provided by the invention can be widely used in the field of solar cells.

The invention is related to technique of electronic material, especially, to technique of capacitor material including dopant of dielectric materials of ceramic capacitor, dielectric materials, and preparation method. The bases of dopant are composite oxides including following elements expressed in formula: aR+bA +cB+dC, where R as oxides of rare earth elements including Nd2O3; A as alkali oxide / alkaline earth including Li2O, Na2O etc.; B as oxide of transition metal including MnO2; C as non-metallic oxide including B2O3, SiO2; a, b, c, d as coefficients in weight percent. Useful effects are: easy to control agglomeration technology, good evenness of produced material, good repeatability. The disclosed material is applicable to prepare X7R type MLCC of miniaturized Pd-Ag electrode with large capability.

The invention discloses an n-type crystalline silicon PERT double-sided battery with a new structure and a preparation method of the n-type crystalline silicon PERT double-sided battery, and relates to the silicon solar cell field. A p + emitter layer, a hydrogenated silicon nitride antireflection layer and an Ag/Al electrode are sequentially formed on the front surface of a n-type crystalline silicon substrate, a p + + selective emitter region is locally formed on the p + emitter layer, and a silicon oxide layer, a p-doped polycrystalline silicon layer, a hydrogenated silicon nitride passivation layer and an Ag electrode are sequentially formed on the rear surface of the n-type crystalline silicon substrate. According to the present invention, the laser doping is carried out on the surface of the borosilicate glass subjected to conventional diffusion to reduce the carrier recombination of a metal contact area, and the devices, such as the low-pressure diffusion devices, etc., are notneeded for making high sheet resistance; an ultrathin silicon oxide layer with good performance is prepared in a simple, easy-to-control and extremely-low-cost nitric acid chemical oxidation mode; after the proper side insulation and high-temperature annealing processing, the characteristics of the front side structure and the rear side structure of the battery can be improved at the same time, the mutual interference is avoided, the follow-up lifting space is large, and the important significance is achieved.

The invention provides a preparation method of a perovskite battery with an n-type doped electron transport layer and a TiO2 layer. The method comprises the following steps of: (1) FTO transparent conductive glass substrate cleaning and TiO2 thin film preparation: an upper TiO2 layer is deposited on a treated FTO transparent conductive glass substrate, and the FTO transparent conductive glass substrate with the deposited upper TiO2 layer is arranged in a drying oven for later use; (2) Bis-PCBM and DMC composite film preparation; (3) spin coating treatment on the FTO transparent conductive glass substrate with the deposited upper TiO2 layer; (4) perovskite film preparation; (5) Spiro-OMeTAD thin film preparation: a Spiro-OMeTAD solution is spin coated on the FTO transparent conductive glass substrate in step (4); and (6) MoO3 and Ag electrode preparation: an MoO3 electrode and Ag electrode are formed on a Spiro-OMeTAD thin film through evaporation. With the method of the invention adopted, the electron mobility and conductivity of a thin film can be improved; the photoelectric conversion efficiency of a device can be improved; the surface of the thin film is smoother, so that the thin film can be used as a good substrate for the deposition and growth of a perovskite layer in subsequent processes; and the degradation process of the perovskite layer can be slowed down, and the stability of the device can be improved.

The invention discloses a resistance-changing nerve simulation device having organic biocompatibility. The resistance-changing nerve simulation device comprises an ITO glass substrate, wherein a composite organic protein film and an Ag electrode film are sequentially grown on an ITO film of the ITO glass substrate, and the composite organic protein film is composite film of silver-doped wool keratin and silk protein. The preparation method comprises the steps of a) preparing a wool keratin solution; b) preparing a silk protein solution; c) preparing the silver-doped wool keratin solution; d) preparing the composite organic protein solution; e) cleaning the substrate; f) forming the composite organic protein film; and g) growing the Ag electrode film. Moreover, the invention discloses application of the device. The device prepared by a special method shows relatively stable resistance value change, difference between a high-resistance value and a low-resistance value is relatively large, and a switch voltage is relatively concentrated; and moreover, the resistance-changing nerve simulation device has a nerve simulation function, is simple in process, is easy to operate and has a wide application prospect.

The invention relates to a solar cell structure with an anti-potential induced degradation (PID) effect and a production method of the solar cell structure. The solar cell comprises a base layer, a P+ layer, a silicon base body, a diffusion layer, a thermal oxidation SiOx layer, a dual-layer plasma enhanced chemical vapor deposition (PECVD) SiNx film and an Ag electrode, wherein the thermal oxidation SiOx layer is used for improving the anti-PID capacity of the solar cell; and the production method of the solar cell with the anti-PID effect comprises a pretreatment step, a high-temperature quartz tube cleaning saturation step, a high-temperature oxidation step, a growth step of the dual-layer PECVD SiNx film and a post-treatment step. The physical structure of SiOx is applied to the surface of the solar cell to form a stable film layer, so that the influenceon the solar cell caused by the outside iseffectively isolated; and the anti-PID effect is reached. The anti-PID effect can be realized without inputting of lot of money for equipment purchasing and gas path transformation; an oxidation layer grown by the method is good in compactness; and the anti-PID attenuation test result at an assembly end shows that the assembly power attenuation is kept at 0.5%-1.5% and bettter-than-expected anti-PID effects are achieved.

The invention discloses a low-temperature sintering temperature-stable microwave dielectric ceramic and a preparation method thereof. The composition formula of the low-temperature sintering temperature-stable microwave dielectric ceramic is Bi14W2O27. The preparation method comprises the steps of (1) weighing and batching original powder of Bi2O3 and WO3 with the purity being over 99.9% according to the chemical formula Bi14W2O27; (2) carrying out wet ball-milling and mixing on raw materials obtained in the step (1) for 12 hours, taking distilled water as a solvent, drying, and then, pre-sintering in an air atmosphere for 6 hours at the temperature of 700 DEG C; (3) adding a binder into powder prepared in the step (2), granulating, then, carrying out compression molding, and finally, sintering in the air atmosphere for 4 hours at the temperature of 800-820 DEG C, wherein a polyvinyl alcohol solution with the mass concentration of 5% is adopted as the binder, and the dosage of the binder accounts for 3% of the total mass of the powder. According to the ceramic prepared by the preparation method, the sintering at the temperature of 800-820 DEG C is good, the dielectric constant reaches 12-13, the quality factor (Qf) reaches up to 61,000-84,000GHz, the temperature coefficient of resonance frequency is small, and the ceramic can be subjected to low-temperature co-sintering together with a Ag electrode, so that the ceramic has a great application value in industries.

The invention discloses a preparation method of a ternary organic solar cell, and belongs to the field of the solar cell. The preparation method comprises the following steps of (1) configuration of an active layer material: taking CB as a solvent, taking PTB7 and a coumarin derivative as a donor material based on the mass ratio of PTB7 to the coumarin derivative of 0.7:0.1-1:0.l; taking PC71BM asan acceptor material at the mass ratio of the donor material to the acceptor material of 1:1-1:3; enabling the donor material, the acceptor material and the solvent to be mixed into an active layer solution with the concentration of 7-15mg/ml; (2) performing ZnO solution configuration; (3) performing cleaning on ITO glass, and then carrying out plasma ozone treatment; (4) spin coating the surfaceof the ITO glass with ZnO, and then carrying out heating and annealing; (5) spin coating the annealed ITO glass with the active layer material, and then carrying out heating and annealing to form anactive layer; and (6) evaporating an MoO<3> layer on the surface of the active layer and then evaporating an Ag electrode. By virtue of the preparation method, efficiency improvement of the device canbe facilitated.

The invention discloses a microwave dielectric ceramic Ba3Ti2V4O17 capable of realizing low temperature sintering and a preparation method thereof. A vanadate microwave dielectric ceramic material capable of realizing low temperature sintering has the composition of Ba3Ti2V4O17. The preparation method comprises the following steps of: (1) weighing and dosing original powder of BaCO3, TiO2 and V2O5 with the purity of over 99.9 percent according to a chemical formula of Ba3Ti2V4O17; (2) performing wet ball milling and mixing the raw materials in the step (1) for 12 hours, wherein the solvent is distilled water, and pre-sintering at the temperature of 750 DEG C in atmosphere for 6 hours after drying; and (3) adding an adhesive into the powder prepared in the step (2) and pelleting, pressing and forming, and finally, sintering at the temperature of 830-850 DEG C in atmosphere for 4 hours, wherein the adhesive is a polyvinyl alcohol solution with the mass concentration of 5 percent, and the dose accounts for 3 percent of the total mass of the powder. The prepared ceramic has good sintering performance at the temperature of 850-900 DEG C and has the dielectric constant of 15-16, quality factor Qf is up to 77000-93000GHz, the resonant frequency temperature coefficient is low, the microwave dielectric ceramic can be subjected to low-temperature co-firing with an Ag electrode, and the microwave dielectric ceramic has extremely high application value in industry.

The invention belongs to the field of photoelectric detectors, and specifically relates to a Cu2O/GaOOH nano core-shell pn junction photoelectric detector and a preparation method thereof. The Cu2O/GaOOH nano core-shell pn junction photoelectric detector comprises an Ag electrode, Cu2O nano-crystals, a GaOOH nano-column array, a Ga2O3 seed crystal layer and FTO conductive glass, and is characterized in that the Ga2O3 seed crystal layer is located on the FTO conductive glass, the Cu2O/GaOOH nano-column array is located on the Ga2O3 seed crystal layer, Cu2O/GaOOH nano-columns are formed by GaOOHnano-columns and the Cu2O nano-crystals, the GaOOH nano-column array is located on the Ga2O3 seed crystal layer, and the Cu2O nano-crystals wrap the outer periphery of the GaOOH nano-columns. The Cu2O/GaOOH nano core-shell pn junction prepared according to the invention has a large specific surface area, is strong in absorption for light, can achieve wide-spectrum detection and provides an effective method for constructing a high-performance photoelectric detector. The preparation method is simple to operate, low in cost and good in repeatability, and certainly has great application prospectsin the photoelectric field in the future.

This invention discloses a double-layer solar energy battery and its manufacturing method, in which, the structure of which includes a substrate-a Ag electrode layer, a metal oxide transparent conduction layer/ type-n micro-crystal silicon-type-I non-crystal (12)-p-micro-crystal silicon (13)/ITO transparent conduction layer, the I layer in the bottom layer p-i-n junction is formed by micro-crystal silicon to avoid decline of photoelectric performance due to the long time illumination and layer-I in the p-i-n junction at the top is plated with non-crystal silicon to strengthen the spectrum absorption.

The present invention relates to a ceramic laminated device including a dielectric ceramic and an Ag electrode. In a dielectric ceramic that can be sintered at low temperatures and has a high dielectric constant and Q value, reactivity between the ceramic and Ag during sintering is suppressed low and segregation of specific elements in the proximity of the electrode is controlled. Thus, a filter having a high Q value and low loss is produced stably. For this purpose, in a ceramic laminated body including at least a ceramic and a Si-containing glass, a ratio of A/B, i.e. a ratio of a Si element concentration (A) within a range at a distance of 5 μm or smaller from the Ag electrode to a Si element concentration (B) within a range at a distance larger than 5 μm from the Ag electrode, is set equal to or smaller than 2.

The invention provides a misunderstanding prevention resistance random access memory and a production method thereof. The structure of the resistance random access memory lies in that a resistance random medium layer and an Ag electrode membrane layer are sequentially formed on a Pt membrane layer of a Pt/Ti/SiO2/Si substrate; the resistance random medium layer comprises a first ferrite bismuth membrane layer, a second ferrite bismuth doped silver membrane layer and a third ferrite bismuth membrane layer which are sequentially formed. By the arrangement, stable resistance changes are presented, resistances of high-low resistance states are quite concentrated in distribution, and the high resistance and the low resistance are large in difference, so that confusion of the high and low resistances is less prone to occurrence, and misunderstanding is not easy to occur during data reading. The resistance random access memory is remarkable in switch effect and quite beneficial to readout of the memory. In addition, anti-fatigue performance of the resistance random access memory under the high-low resistance states is quite good.

The invention discloses a multilayer varistor and a preparation method for the same. The multilayer varistor comprises a varistor body and an internal electrode in a porcelain body, wherein the varistor body consists of a ZnO-Bi2O3-SiO2-SnO2 porcelain system; and the internal electrode is a pure Ag electrode. The varistor is high in electrical property and low in production cost.

The invention relates to a flexible ultraviolet detector based on a copper oxide/gallium oxide nanopillar array pn junction and a preparation method. The detector comprise the orderly arranged parts of a flexible copper sheet substrate, wherein at least one side of the flexible copper sheet substrate is provided with a copper oxide layer, and a beta-Ga2O3 nanorod array is arranged on the copper oxide layer positioned at one side of the copper sheet substrate; a graphene/Ag nanowire composite layer which is positioned on the beta-Ga2O3 nano column array; an Ag electrode which is located on thegraphene/Ag nanowire composite layer, wherein a copper oxide/gallium oxide nanopillar array pn junction is formed between the copper oxide and the beta-Ga2O3 nanopillar array, and the flexible coppersheet substrate serves as a copper electrode to form an access with the Ag electrode. The ultraviolet detector provided by the invention has a three-dimensional space heterojunction interface structure and a solar blind characteristic, has the excellent chemical and thermal stability, is flexible and bendable, is high in pressure resistance, low in working temperature and power consumption and good in repeatability, and can directionally identify the ultraviolet light with the wavelength of 200-280nm in a solar blind waveband.

The invention relates to a manufacturing method for a ZnO nano tree array/polymer blend conformal structure hybrid solar cell and belongs to the technical field of solar cells. The method includes the steps that (1), a ZnO nano rod trunk grows on a conducting glass substrate; (2), atmosphere atomic layer deposition is performed on a sample obtained after electrolytic deposition; (3), the sample is placed in a water solution for chemical bath deposition after seed layer deposition; (4), polymer spin coating is performed; (5), metal Ag electrodes are evaporated. According to the manufactured ZnO nano tree-based conformal structure hybrid solar cell, electrons are transmitted in the axial direction of the nano rod trunk, and the transmission direction of electron holes in polymers is perpendicular to the trunk; in this way, the advantages that in the solar cell formed by assembling nano rod arrays, electron and electron hole transmitting channels are directly connected, and permeation of the polymers is convenient can be kept, besides, the maximum thickness of the polymers can not limit the height of the nano rod arrays, the loading quantity and interface area of the polymers are effectively increased, and due to the structure, performance manifestation of the polymer solar cell is facilitated better.

The invention discloses microwave dielectric ceramic BiNbW2O10 capable of being sintered at low temperature and a preparation method thereof. The composition of the microwave dielectric ceramic capable of being sintered at low temperature is BiNbW2O10. The preparation method comprises the following steps of: (1) weighing the original powder of Bi2O3, Nb2O5 and WO3 having the purity of more than 99.9% according to the chemical formula BiNbW2O10, and mixing all the original powder together; (2) performing mixing and wet ball milling on the raw materials of the step (1) for 12 hours while taking distilled water as a solvent, and pre-sintering for 6 hours in atmosphere at 850 DEG C; (3) adding a binder to the powder obtained in the step (2) and pelleting, then carrying out compression molding, and finally sintering for 4 hours in atmosphere at the temperature ranging from 900 to 930 DEG C, wherein the binder is a polyvinyl alcohol solution having the mass concentration of 5%, and the dosage of the binder is 3% of the total weight of the powder. The ceramic prepared by the preparation method disclosed by the invention is well sintered at the temperature ranging from 900 to 930 DEG C; the dielectric constant of the ceramic is in the range from 17 to 18, the value of the quality factor Qf of the ceramic is within the range from 86000 to 98000 GHz and the temperature coefficient of resonant frequency of the ceramic is low; the ceramic can be co-sintered at the low temperature with an Ag electrode and has an enormous application value in industry.

The invention discloses low-temperature sintered vanadate microwave dielectric ceramic BaZnV2O7 and a preparation method thereof. The composition of the low-temperature sintered vanadate microwave dielectric ceramic material is BaZnV2O7. The preparation method comprises the following steps of: (1) weighting the original powder of BaCO3 with the purity of above 99.9%, ZnO with the purity of above 99.9% and V2O5 with the purity of above 99.9% according to the chemical formula of the BaZnV2O7, and burdening; (2) carrying out wet-type ball milling on the raw materials obtained in the step (1) and mixing for 12 hours, wherein distilled water is used as a solvent, drying and then presintering for 6 hours at 750 DEG C atmosphere; (3) adding a binging agent to the powder prepared in the step (2), pelleting, then carrying out compression molding, and finally sintering for 4 hours at 850-900 DEG C atmosphere, wherein a polyvinyl alcohol with the mass concentration of 5% is used as the binding agent, and the using amount of the binding agent accounts for 3% of the total mass of the powder. The ceramic prepared by the method has good sintering performance at 850-900 DEG C; the dielectric constant of the ceramic reaches 17-18, the quality factor QF value of the ceramic reaches up to 57000-83000GHz, and the temperature coefficient of resonance frequency of the ceramic is small; the low-temperature sintered vanadate microwave dielectric ceramic and an Ag electrode can be sintered together at low temperature, and therefore, the low-temperature sintered vanadate microwave dielectric ceramic has very great application value in industry.