Amorphous iron-nickel phosphonate with efficient photocatalysis oxygen production property and preparation method and application of amorphous iron-nickel phosphonate
A photocatalytic and amorphous technology, applied in chemical instruments and methods, organic compound/hydride/coordination complex catalysts, physical/chemical process catalysts, etc., can solve the problem of low photocatalytic oxygen production efficiency and achieve technological Simple operation, high-efficiency photocatalytic oxygen production performance, and high repeatability
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Embodiment 1
[0022] Dissolve 1 mmol of iron-nickel nitrate in 5 ml of N,N-dimethylformamide (solution A), and dissolve 1 mmol of 2-carboxyethylphosphonic acid in 10 ml of N,N-dimethylformamide (solution B). Add solution A to solution B dropwise under magnetic stirring. After reacting for 12 hours under solvothermal conditions at 140° C., the sample was washed by centrifugation and collected to obtain amorphous iron-nickel phosphonate.
[0023] The photocatalytic performance of the amorphous iron-nickel phosphonate prepared in Example 1 was measured in a closed gas circulation system, and the reaction system was kept at about 20° C. by circulating cooling water. With photocatalyst (the amorphous iron nickel phosphonate that embodiment 1 makes, nickel phosphate), [Ru(bpy) 3 ] Cl 2 ·6H 2 O and Na 2 S 2 o 8 Mix in borate buffer. A 300w xenon lamp was selected as the light source, and the reaction system was backfilled with argon several times to remove air before illumination. Determin...
Embodiment 2
[0026] Dissolve 2mmol of iron-nickel nitrate in 15ml N,N-dimethylformamide (solution A), dissolve 2mmol of 2-carboxyethylphosphonic acid in 15ml N,N-dimethylformamide (solution B), in Add solution A to solution B dropwise under magnetic stirring. After reacting for 24 hours under solvothermal conditions at 160° C., the sample was washed by centrifugation and collected to obtain amorphous iron-nickel phosphonate.
Embodiment 3
[0028] Dissolve 3mmol of iron-nickel nitrate in 25ml of N,N-dimethylformamide (solution A), and dissolve 4mmol of 2-carboxyethylphosphonic acid in 30ml of N,N-dimethylformamide (solution B). Add solution A to solution B dropwise under magnetic stirring. After reacting for 36 hours under solvothermal conditions at 200° C., the samples were washed by centrifugation and collected to obtain amorphous iron-nickel phosphonate.
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