Modified electrodes and electrocatalytic reduction method of CO2
A technology for modifying electrodes and electrodes, which is applied in the direction of electrodes, electrolysis processes, electrolysis components, etc., and can solve problems such as difficult separation of catalysts, large amount of catalysts, limitations, etc.
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[0171] The present invention will be described in detail below by examples and examples, but the present invention is not limited to the examples and examples.
[0172] If not otherwise stated, the various raw materials used in the following examples are all commercially available:
[0173] Glassy carbon electrodes were purchased from Tianjin Aida Hengsheng Technology Development Co., Ltd.;
Synthetic example 1
[0174] Tetraaminophthalocyanine cobalt is synthesized according to Synthesis Example 1;
[0175] Cobalt phthalocyanine (CoPc) was purchased from Strem Chemicals;
[0176] Tetrabutylammonium perchlorate (TBAP) was purchased from Shanghai Xiyu Electromechanical System Co., Ltd.;
[0177] Single-walled carbon nanotubes were obtained from East China Normal University;
[0178] N 2 , CO 2 Purchased from Shanghai Dumaoai Purification Gas Co., Ltd., all of which are 99.995% high-purity gases;
[0179] Lithium perchlorate (LiClO 4 ), acetonitrile (ACN), and tetrahydrofuran (THF) were all purchased from Sinopharm Chemical Reagent Co., Ltd., all of which were analytically pure and used directly without treatment;
[0180] 4-Nitrophthalic acid (Shanghai Linqing Chemical Technology Co., Ltd.), urea (Shanghai Zhanyun Chemical Co., Ltd.), cobalt chloride hexahydrate (Sinopharm Chemical Reagent Co., Ltd.), ammonium molybdate (Shanghai Shangsi Fine Chemical Co., Ltd.), hydrochloric acid...
Synthetic example 1 4
[0182] The synthesis of synthetic example 1 tetraamino phthalocyanine cobalt
[0183] Tetraaminophthalocyanine cobalt is synthesized according to the following synthetic method:
[0184]
[0185]
[0186] The first step is to synthesize cobalt tetranitrophthalocyanine:
[0187] 4-Nitrophthalic acid (12.66g, 0.06mol), 30g (0.5mol) of urea, 4.27g (0.0152mmol) of cobalt chloride hexahydrate, and ammonium molybdate (0.15g as a catalyst) are respectively ground evenly, placed in 500mL volumetric flask. The temperature was slowly raised to 180°C and kept for 5h. After the reaction, the product was washed with 1.0M hydrochloric acid and 1.0M sodium hydroxide, filtered with suction, and then washed with water repeatedly until neutral, and dried in a vacuum oven at a constant temperature of 80°C. The final product is cobalt tetranitrophthalocyanine (CoTNPc).
[0188] The second step is to synthesize cobalt tetraaminophthalocyanine:
[0189] 9.193g CoTNPc and 33.73g Na 2 S.H...
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