总可滴定胺法测定聚丙烯酰胺树脂的交联度

• Key Words:NITRIC-OXIDE REDUCTION; NITROGEN-FIXATION; HYDROGEN; PHOTOCATALYST; TRANSITION; REACTIVITY; CHEMISTRY
• Abstract:The electrochemical nitric oxide reduction reaction (NORR) is deemed to be a promising alternative to remove atmospheric pollutant NO and produce ammonia simultaneously. In this work, we systematically study the NORR catalytic performance of 9 different-ordered Mo2MC2O2-v (M = Ti, Zr, Hf, V, Nb, Ta, Cr, Mo, and W) coupling Graphene (Gr) monolayer forming the 2D/2D heterojunctions by first-principle calculations. The results demonstrated that B@Mo2MC2O2-v/Gr (M = Zr, Hf, Nb, Ta, and W) exhibit excellent NORR activity and selectivity to synthesize NH3 occurring spontaneously under low nitric oxide coverage compared to Mo2MC2O2- v/Gr heterojunctions. This phenomenon can be attributed to the synergetic effect between the interface interaction and the B atom doping suppressing the competitive hydrogen evolution reaction (HER). The interface interaction between B@Mo2MC2O2-v and Graphene enhanced the charge transfer from the Graphene to the MXene surface. The B atom doping provides the active site and acts as an electronic transmitter for rapid electron transfer to the adsorbed NO molecules promoting the cleavage of N=O and further interacting with the H+ to generate NH3. We introduce the triangle G(*NH2O) as an efficient descriptor to predict the NORR performance. Moreover, DOS, CDD and COHP analysis reveal the electron "donation/back-donation" mechanism between NO molecules and the B atom, which elaborates the activation effect of NO molecules. Furthermore, the key function of the p-band center (epsilon p) was emphasized in characterizing the activation degree of NO, which can be regulated by the chemical environment around the B atom. Finally, we testified the stability of catalysts using AIMD simulation. In addition, this work provides a theoretical foundation for future experimental research on NORR electrocatalysts to produce renewable fuels from pollutant NO molecules.
• Volume:393
• Issue:
• Translation or Not:no