微型多孔材料
选择性
材料科学
催化作用
多孔性
金属有机骨架
吸附
光催化
化学工程
产量(工程)
结晶
量子产额
选择性吸附
聚苯乙烯
Atom(片上系统)
纳米技术
化学
物理化学
有机化学
聚合物
嵌入式系统
复合材料
工程类
物理
冶金
荧光
量子力学
计算机科学
作者
Zhiguo Liu,Ziyu Chen,Mingyang Li,Jiaying Li,Weijie Zhuang,Xiao Yang,Shiqun Wu,Jinlong Zhang
标识
DOI:10.1021/acscatal.3c01118
摘要
The rational construction of single-atom-modified porous metal–organic frameworks (MOFs) for efficient CO2 photoconversion is a promising avenue, yet the one that poses a significant challenge. In this study, we demonstrate the successful construction of a Ni single-atom-immobilized ZIF-8 with an ordered hierarchical (macro–micro) pore structure for highly efficient photocatalytic CO2 reduction to CO. The interpenetrated macroporous structure in microporous ZIF-8 is built up by employing polystyrene (PS) opal as a hard template, while the high stability of the framework is achieved through the double-solvent-induced crystallization. The hierarchical porous structure enables rapid mass transport and strong adsorption of CO2, while Ni single atoms as active sites and electron-trapping sites optimize the reaction energy and hinder the competitive H2 evolution. As a result, the Ni single-atom-immobilized hierarchical porous ZIF-8 achieves high stability and an activity of 4.2 mmol g–1 h–1 for CO yield with an electronic selectivity of 94%, which shows a 47-fold CO yield of that for ZIF-8. This work highlights the significance of constructing a hierarchical porous structure of MOFs and single-atom-active sites to improve the activity and selectivity of CO2 photoreduction for realizing carbon neutralization.
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