Photocatalytic Reduction of CO2 to CO and Formate: Do Reaction Conditions or Ruthenium Catalysts Control Product Selectivity?

被引:47
|
作者
Rodrigues, Roberta R. [1 ]
Boudreaux, Chance M. [2 ]
Papish, Elizabeth T. [2 ]
Delcamp, Jared H. [1 ]
机构
[1] Univ Mississippi, Dept Chem & Biochem, Coulter Hall, University, MS 38677 USA
[2] Univ Alabama, Dept Chem & Biochem, Shelby Hall, Tuscaloosa, AL 35487 USA
来源
ACS APPLIED ENERGY MATERIALS | 2019年 / 2卷 / 01期
关键词
photocatalytic CO2 reduction; homogeneous; ruthenium catalysts; NHC pincer; photosensitized; COMPLEXES; CARBON; CONVERSION; ELECTROCATALYSTS; ACETONITRILE;
D O I
10.1021/acsaem.8b01560
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The photocatalytic reduction of CO2 can generate a number of products with CO and HCO2- being two of the most commonly observed. Frequently, the selective formation of one of these products is presumed to be the result of catalyst design. However, several common variables are present when exploring the photocatalytic CO2 reduction reaction. In order to better understand the origin of selectivity in this reaction, the choices of solvent, electron and proton source, photosensitizer (PS), and catalyst were evaluated in photocatalytic CO2 reduction reactions. Intriguingly, highly selective catalysts for CO or HCO2- under one set of conditions can be transformed by these environmental choices into becoming highly selective for the opposite product while retaining high turnover numbers. This highlights the importance of carefully considering reaction conditions before ascribing catalyst selectivity to an inherent molecular design property.
引用
收藏
页码:37 / 46
页数:19
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