A novel type of hyper-cross-linked organic microporous polymer (HOMP) has been successfully prepared based on the radical copolymerization of bismaleimides and divinylbenzene. In comparison with the HOMPs prepared with cross-linking techniques, the new radical strategy circumvents some intractable problems, such as low atom economy, structure irregularity and corrosive byproducts. The obtained HOMPs have defined molecular structures due to the intrinsic alternating copolymerization properties of the two monomers. A maximum BET surface area of 841 m 2 g −1 and high gas capture capacity (CO 2 , 11.22 wt %, 273 K/1.0 bar; H 2 , 0.82 wt %, 77.3 K/1.0 bar; benzene, 545 mg g −1 , room temperature/0.6 bar; and cyclohexane, 1736 mg g −1 , room temperature/0.6 bar) were achieved. In addition, the polymers also displayed good chemical and thermal stability, which is critical for the practical application.
Electrocatalytic reduction of carbon monoxide into fuels or chemicals with two or more carbons is very attractive due to their high energy density and economic value. Herein we demonstrate the synthesis of a hydrophobic Cu/Cu2O sheet catalyst with hydrophobic n-butylamine layer and its application in CO electroreduction. The CO reduction on this catalyst produces two or more carbon products with a Faradaic efficiency of 93.5% and partial current density of 151 mA cm−2 at the potential of −0.70 V versus a reversible hydrogen electrode. A Faradaic efficiency of 68.8% and partial current density of 111 mA cm−2 for ethanol were reached, which is very high in comparison to all previous reports of CO2/CO electroreduction with a total current density higher than 10 mA cm−2. The as-prepared catalyst also showed impressive stability that the activity and selectivity for two or more carbon products could remain even after 100 operating hours. This work opens a way for efficient electrocatalytic conversion of CO2/CO to liquid fuels.
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