Yu Jiaqi, Zhang Hongsen, Liu Qi, Yu Jing, Song Dalei, Xiong Chu-An, Li Ying, Li Rumin, Wang Jun
Key Laboratory of Superlight Materials and Surface Technology, Ministry of Education, College of Materials Science and Chemical Engineering, Harbin Engineering University, Harbin 150001, China; College of Environmental and Chemical Engineering, Heilongjiang University of Science and Technology, Harbin 150022, China.
Key Laboratory of Superlight Materials and Surface Technology, Ministry of Education, College of Materials Science and Chemical Engineering, Harbin Engineering University, Harbin 150001, China.
J Colloid Interface Sci. 2025 Apr;683(Pt 1):387-397. doi: 10.1016/j.jcis.2024.12.085. Epub 2024 Dec 14.
Electron effect regulation is a crucial factor influencing the activity and selectivity of Cu-based coordination compound catalysts in the electrochemical carbon dioxide reduction reaction (CORR). Despite significant progress, the structure-activity relationship and the underlying regulatory mechanisms warrant further in-depth investigation. In this study, three types of Cu-[ONNO] tetradentate coordination molecular catalysts with varying electron densities, namely Cu-NO, methoxy-modified Cu-NO (Cu-EDG-NO), and nitro-modified Cu-NO (Cu-EWG-NO), were prepared using a substituent regulation strategy. The prepared catalyst's micromorphology and structural characteristics were analyzed using various characterization methods. Systematic electrocatalytic CORR experiments were conducted to evaluate the performance of these catalysts. Compared to the unmodified Cu-NO, the Cu-EDG-NO catalyst exhibited superior reduction performance for CH and CH products. At an applied potential of -1.7 V vs. the reversible hydrogen electrode, the Faradaic efficiencies for CH and CH of Cu-EDG-NO were 37.8 ± 2.2 % and 25.0 ± 0.5 %, respectively. In contrast, the Cu-EWG-NO catalyst demonstrated higher activity towards the production of H as a by-product. The effects of electronic properties of substitutions on catalyst performance were revealed by combining experimental characterization and theoretical simulation. The results showed that the conjugation effect of the -OCH group facilitates faster electron transfer between Cu and CO, thereby enhancing CORR activity. Additionally, the introduction of different substituents modulates the local microenvironment around the Cu active centers, significantly influencing the catalytic performance. This study provides valuable theoretical and experimental insights into the design of efficient Cu-NO-type metal coordination electrocatalysts for CORR processes.
电子效应调控是影响铜基配位化合物催化剂在电化学二氧化碳还原反应(CORR)中活性和选择性的关键因素。尽管取得了显著进展,但结构 - 活性关系及潜在的调控机制仍有待进一步深入研究。在本研究中,采用取代基调控策略制备了三种具有不同电子密度的Cu - [ONNO]四齿配位分子催化剂,即Cu - NO、甲氧基修饰的Cu - NO(Cu - EDG - NO)和硝基修饰的Cu - NO(Cu - EWG - NO)。使用各种表征方法分析了所制备催化剂的微观形貌和结构特征。进行了系统的电催化CORR实验以评估这些催化剂的性能。与未修饰的Cu - NO相比,Cu - EDG - NO催化剂对CH和CH产物表现出优异的还原性能。在相对于可逆氢电极 - 1.7 V的外加电位下,Cu - EDG - NO对CH和CH的法拉第效率分别为37.8 ± 2.2%和25.0 ± 0.5%。相比之下,Cu - EWG - NO催化剂对副产物H的生成表现出更高的活性。通过结合实验表征和理论模拟揭示了取代基电子性质对催化剂性能的影响。结果表明, - OCH基团的共轭效应促进了Cu与CO之间更快的电子转移,从而增强了CORR活性。此外,不同取代基的引入调节了Cu活性中心周围的局部微环境,显著影响了催化性能。本研究为CORR过程中高效Cu - NO型金属配位电催化剂的设计提供了有价值的理论和实验见解。