Making method of porous high-performance metal fuel cell oxygen electrode
A technology for metal fuel cells and manufacturing methods, which is applied in battery electrodes, fuel cell-type half-cells, primary battery-type half-cells, and electrode manufacturing, and can solve the problems of low porosity, poor catalytic effect of the catalytic layer, and poor battery discharge performance. advanced questions
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Embodiment 1
[0058] The manufacturing method of the porous high-performance metal fuel cell oxygen electrode of the present invention is to use a volatile dispersant to replace the pore-forming agent, and integrally form the waterproof layer, the current collector and the catalytic layer in a molding mold. The electrode material is formed through a forming die instead of being rolled and formed by a rolling machine.
[0059] Specifically include the following steps:
[0060] (1) Catalyst layer 2 materials are dispersed in dispersant, add binding agent, evenly stir and disperse; The weight volume ratio of catalytic layer material and dispersant is 20g: 1L; The weight volume ratio of catalytic layer material and binding agent is 20g: 1L;
[0061] (2) Disperse the material of the waterproof layer 1 into the dispersant, add the binder, stir and disperse evenly; the weight-to-volume ratio of the waterproof layer material to the dispersant is 60g: 1L; the weight-to-volume ratio of the waterproo...
Embodiment 2
[0068] Described dispersant is ethanol,
[0069] The ratio of the catalyst layer material and dispersant described in step (1) is 10g: 1L;
[0070] The ratio of the waterproof layer material to the dispersant in step (2) is 10g:1L.
[0071] Described binding agent is PTFE;
[0072] The ratio of the catalytic layer material and the binding agent described in step (1) is 10g: 1L;
[0073] The ratio of the waterproof layer material to the binder in step (2) is 10g:1L.
[0074] The pore diameter of the filter paper described in step (3) is 30 μm.
[0075] The short fibers are plastic fibers.
[0076] Described heat treatment comprises the following steps:
[0077] (1) Dry it on a hot press at 90°C for about 10 minutes at a pressure of 35kgf / cm 2 ;
[0078] (2) After drying, process it on a press at 250°C for 3 minutes and a pressure of 15kgf / cm 2 .
[0079] All the other are with embodiment 1.
Embodiment 3
[0081] Described dispersant is propanol,
[0082] The ratio of the catalytic layer material and dispersant described in step (1) is 150g: 1L;
[0083] The ratio of the waterproof layer material to the dispersant in step (2) is 150g: 1L.
[0084] The binder is CMC;
[0085] The ratio of the catalyst layer material described in step (1) to the binding agent is 150g: 1L;
[0086] The ratio of the waterproof layer material to the binder in step (2) is 150g: 1L.
[0087] The pore diameter of the filter paper described in step (3) is 50 μm.
[0088] The short fibers are asbestos fibers.
[0089] Described heat treatment comprises the following steps:
[0090] (1) Dry it on a hot press at 90°C for about 20 minutes at a pressure of 35kgf / cm 2 ;
[0091] (2) After drying, process it on a press at 250°C for 15 minutes at a pressure of 15kgf / cm 2 .
[0092] All the other are with embodiment 1.
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