光催化
二氧化钛
离子
吸附
化学
乙烯
硫氰酸盐
无机化学
猝灭(荧光)
光化学
选择性
亲核细胞
材料科学
催化作用
有机化学
冶金
物理化学
物理
量子力学
荧光
作者
Lina Zhang,Tongling Liu,Taifeng Liu,Sajjad Hussain,Qiuye Li,Jianjun Yang
标识
DOI:10.1016/j.cej.2023.142358
摘要
Titanium dioxide (TiO2) with defects is a promising semiconductor photocatalyst for photoreduction CO2, due to its unique electronic properties. However, defective TiO2 is difficult to achieve a high yield of CO2 photoreduction, especially the high-value-added C2+ hydrocarbons, due to the slow transfer of multielectron/proton and sluggish C-C coupling kinetics. Here, we combine the photoinduced deposition of copper (Cu) nanoparticle on defective titania (TiO2-SBO) with thiocyanate anion (SCN-, KSCN) surface modification via impregnation route to prepare a series of high performance photocatalysts (SCN-Cu/TiO2-SBO). It was found that the production rate and selectivity of C2H4 of CO2 over sample SCN-Cu/TiO2-SBO-3 as a representative are 4.7 μmol·g−1·h−1 and 40%, while the CO and CH4 yields rise by 2 times and 5 times as compared with those over bare TiO2-SBO. This is because the Cu cocatalyst can serve as the active site for C-C coupling (via intermediate *CO-COH) and the SCN-induced surface dipole effect can enhance the carrier's dynamic behavior and accelerate the multielectron transfer, while the SCN- ions with nucleophilicity are conducive to CO2 adsorption as well as CO hydrogenation and the multi-proton coupling process of C2+ products. Furthermore, first principle calculations illustrate that the Cu species can effectively reduce the reaction energy of the key intermediate *CO-COH of ethylene, and SCN- ions benefit to the adsorption of CO2 molecules, and thereby being favor for the generation of ethylene.
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