A kind of pyrophosphate composite electrolyte and preparation method thereof
A composite electrolyte and pyrophosphate technology, applied in the field of solid fuel cell materials, can solve problems such as difficulty in meeting the use requirements of solid fuel cells, discontinuous conduction of conductive ions, decreased electrical conductivity, etc., and achieve good electrochemical performance and enhanced mechanical strength. , easy to achieve effect
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[0038] According to another object of the present invention, a method for preparing the above-mentioned composite electrolyte is provided, the method comprising the following steps:
[0039]Step 1. Mix pyrophosphate metal source, dopant atom source, concentrated phosphoric acid and metal inorganic salt, heat treatment to obtain cured product.
[0040] The pyrophosphate metal source is selected from tetravalent metals, such as tin, titanium, germanium, zirconium, preferably tin or titanium, more preferably tin. In order to ensure the conductivity of the electrolyte, the high-temperature fuel cell must be operated at a high temperature (900-1000 ° C), so that the requirements for each component of the battery are very strict, and the cost is high. In order to reduce the operating temperature and cost, the electrolyte needs to be at a medium temperature ( (400-750°C) has excellent electrical conductivity, which can reduce the production cost while ensuring the electrical conducti...
Embodiment 1
[0079] SnO 2 , Ni(NO 3 ) 2 , 14.6mol / L concentrated H 3 PO 4 with K 2 CO 3 According to the molar ratio of 2.7:0.3:7:0.5, the SnO 2 , Ni(NO 3 ) 2 and K 2 CO 3 for pre-grinding, followed by the addition of concentrated H 3 PO 4 Grinding (final molar ratio of Sn 0.9 Ni 0.1 P 2 o 7 : KPO 3 =3:1), mix well, and completely solidify after being kept at 350°C for 30 minutes to obtain a cured product.
[0080] Put the cured product in a box-type resistance furnace and heat it at 500°C for about 1 hour. After cooling to room temperature, take it out, grind it into a fine powder, and grind it evenly to obtain a composite powder.
Embodiment 2
[0082] Under the pressure of 200MPa, the composite powder was pressed into tablets for 3 minutes.
[0083] Put the pressed disc on the gasket, cover the ceramic crucible, and burn it in an electric furnace at 700°C for 1 hour to obtain Sn 0.9 Ni 0.1 P 2 o 7 / KPO 3 , where Sn 0.9 Ni 0.1 P 2 o 7 with KPO 3 The molar ratio is 3:1.
[0084] The sample was processed into an electrolyte diaphragm with a diameter of 18.0 mm and a thickness of 1.1 mm, which was used for testing the electrical performance at medium temperature in a dry nitrogen atmosphere.
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