非阻塞I/O
异质结
光催化
X射线光电子能谱
材料科学
甲烷化
催化作用
化学工程
吸附
无机化学
化学
物理化学
光电子学
生物化学
工程类
作者
Yuexian Li,Wenli Su,Yusen Yang,Lianxia Bai,Jun Lu,Wenkai Zhang,Shuo Wei
标识
DOI:10.1016/j.apcatb.2023.123282
摘要
Considering that photosynthetic CH4 seems to have a high energy density, it serves as a powerful way for storing renewable energy. In this work, a potential pn-type inorganic intergrowth bulk heterojunction (pn-IIBH) NiO(Al)/CuO(Ni,Al) was designed and obtained by the precursor CuNiAl-layered double hydroxides with two-stage topological pyrolysis (TTP) method. The microstructure was investigated in detail EXAFS to understand in-situ topotactic formation of the IIBH. Then, by using ISI-XPS, and fs-TAS, the transfer mechanism of the photogenerated electrons in NiO(Al)/CuO(Ni,Al) was explored which met pn-type heterojunction. Furthermore, it was screened for CO2 photoreduction to target CH4 (86.59 μmol/g·h) and O2 (150.84 μmol/g·h) from H2O and the selectivity of CH4 reached more than 87.13%. Finally, in-situ IR and DFT calculation demonstrated that CO2 methanation by the hydrogenation pathway occurred and the Ni doping in the pn-IIBH activated CO2 adsorption more effectively. This work offers an approach to photocatalysis development in CO2 methanation.
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