Method for constructing ruthenium terpyridyl electrochemiluminescence sensor with graphene porous material
A ruthenium terpyridine electrochemical and porous material technology, which is applied in the direction of material electrochemical variables, can solve the problems of loss of electrode surface pore structure, affecting the performance of electrochemiluminescent sensors, and increase of electrode surface resistance, so as to achieve good conductivity and prevent The effect of reduced electrode active area and good porous structure
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Embodiment 1
[0026] Measure 6mL of 2.5wt% polyvinyl alcohol solution into 35mg of graphene oxide contained in a beaker, and obtain a uniform dispersion after ultrasonic dispersion for 40min. The obtained graphene oxide dispersion was then frozen by placing the beaker in a bath filled with liquid nitrogen. After it is completely frozen, put the obtained solution into a freeze dryer whose freezing temperature has reached -60°C, turn on the vacuum mode, and operate the vacuum freeze dryer in vacuum freezing mode for 48 hours until the water in the sample is completely sublimated. A graphene oxide porous composite is obtained. Subsequently, the prepared graphene oxide porous composite was calcined in a nitrogen atmosphere at 750 °C for 2 h at a heating rate of 5 °C / min. After the calcination is completed, the sample is taken out to obtain a graphene porous material. Take PGR and ultrasonically disperse it into 1wt% Nafion solution to prepare 1.25mg mL -1 PGR. Take 5 µL of the PGR suspensi...
Embodiment 2
[0028] Measure 6mL of 2.5wt% polyvinyl alcohol solution into 35mg of graphene oxide contained in a beaker, and obtain a uniform dispersion after ultrasonic dispersion for 40min. The obtained graphene oxide dispersion was then frozen by placing the beaker in a bath filled with liquid nitrogen. After it is completely frozen, put the resulting solution into a freeze dryer whose freezing temperature has reached -60°C, turn on the vacuum mode, and operate the vacuum freeze dryer in vacuum freezing mode for 40 hours until the water in the sample is completely sublimated. The graphene oxide porous composite (PGR) is obtained. Subsequently, the prepared graphene oxide porous composite was calcined in a nitrogen atmosphere at 750° C. for 3.5 h at a heating rate of 5° C. / min. After the calcination, the sample is taken out to obtain a porous block reduced to graphene. Take a certain amount of PGR and ultrasonically disperse it into 1wt% Nafion solution to prepare 5mg mL -1 PGR.
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Embodiment 3
[0032] Measure 5mL of 2.5wt% PVA solution and add it to 35mg graphene oxide contained in a beaker, and obtain a uniform dispersion after ultrasonic dispersion for 40min. The obtained graphene oxide dispersion was then frozen by placing the beaker in a bath filled with liquid nitrogen. After it is completely frozen, put the resulting solution into a freeze dryer whose freezing temperature has reached -60°C, turn on the vacuum mode, and operate the vacuum freeze dryer in vacuum freezing mode for 55 hours until the water in the sample is completely sublimated. The graphene oxide porous composite (PGR) is obtained. Subsequently, the prepared graphene oxide porous composite was calcined in a nitrogen atmosphere at 800° C. for 1.5 h at a heating rate of 2° C. / min. After the calcination, the sample is taken out to obtain a porous block reduced to graphene. Take a certain amount of PGR and ultrasonically disperse it into 1wt% Nafion solution to prepare 2.5mg mL -1 PGR. Take 5 μl ...
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