a mos 2 -rgo-nio@ni foam composite photoelectric catalytic hydrogen evolution material and preparation method
A mos2-rgo-nio, composite material technology, applied in chemical instruments and methods, physical/chemical process catalysts, electrodes, etc., can solve the problems of high hydrogen evolution overpotential and poor material cycle stability.
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Embodiment 1
[0028] (1) Dodemolybdenum phosphoric acid, methyl isothiourea and polysorbate were dissolved in 120 mL of deionized water at a weight ratio of 5:6:1 under constant stirring, and the mixed solution was transferred into polytetrafluoroethylene. lined stainless steel autoclave, hydrothermally treated at 180 °C for 24 h, the obtained MoS 2 Wash with deionized water, centrifuge, and vacuum dry for use. (2) RGO was prepared by treating natural graphite powder with a modified Hummer method. (3) Add 18g of PEG4000 to 100mL of deionized water, heat to dissolve, and dissolve the MoS obtained in step (1). 2 Take 0.4 g and 0.05 g of the RGO obtained in step (2) and disperse them in a PEG solution in turn, and ultrasonically treat them for 30 min to form a suspension sol. (4) The nickel foam was soaked in 0.2 M nitric acid solution for 30 min to obtain pre-oxidized NiO@Ni. (5) The NiO@Ni obtained in step (4) was immersed in the suspension sol obtained in step (3) for 2 min, then pulled ...
Embodiment 2
[0030] (1) Dissolve ammonium molybdate, thiourea and fatty acid glycerides in 120 mL of deionized water at a weight ratio of 4:7:1 under constant stirring, and transfer the mixed solution to a PTFE-lined stainless steel high pressure In the reaction kettle, hydrothermal treatment was performed at 160 °C for 30 h, and the obtained MoS 2 Wash with deionized water, centrifuge, and vacuum dry for use. (2) RGO was prepared by treating natural graphite powder with a modified Hummer method. (3) Add 16g PEG6000 to 100mL deionized water, heat to dissolve, and dissolve the MoS obtained in step (1). 2 Take 0.3 g and 0.06 g of the RGO obtained in step (2) and disperse them in the PEG solution in turn, and ultrasonically treat for 30 min to form a suspension sol. (4) The nickel foam was soaked in a 0.8 M hydrogen peroxide solution for 50 min to obtain pre-oxidized NiO@Ni. (5) The NiO@Ni obtained in step (4) was immersed in the suspension sol obtained in step (3) for 1 min, then pulled a...
Embodiment 3
[0032] (1) Dissolve sodium molybdate, vinyl thiourea and fatty acid sorbitan in 120 mL of deionized water at a weight ratio of 6:8:1 under constant stirring, and transfer the mixed solution into a polytetrafluoroethylene-lined In a stainless steel autoclave, the obtained MoS was hydrothermally treated at 170 °C for 26 h. 2 Wash with deionized water, centrifuge, and vacuum dry for use. (2) RGO was prepared by treating natural graphite powder with a modified Hummer method. (3) Add 20g PEG2000 to 100mL deionized water, heat to dissolve, and dissolve the MoS obtained in step (1). 2 Take 0.5 g and 0.07 g of the RGO obtained in step (2) and disperse them in the PEG solution in turn, and ultrasonically treat for 30 min to form a suspension sol. (4) The nickel foam was soaked in a solution of potassium permanganate with a concentration of 0.5 M for 40 min to obtain pre-oxidized NiO@Ni. (5) The NiO@Ni obtained in step (4) was immersed in the suspension sol obtained in step (3) for 3...
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