Song Ziyang, Yang Rong, Liu Xinyu, Zhang Bin, Wu Yongmeng
Department of Chemistry, School of Science, Tianjin University, Tianjin, 300072, China.
Tianjin Key Laboratory of Molecular Optoelectronic Sciences, Frontiers Science Center for Synthetic Biology (Ministry of Education), Tianjin University, Tianjin, 300072, China.
Angew Chem Int Ed Engl. 2024 Oct 14;63(42):e202410200. doi: 10.1002/anie.202410200. Epub 2024 Sep 12.
The direct construction of metal-free catalysts on conductive substrates for electrocatalytic organic hydrogenation reactions is significant but still unexplored. Here, learning from the homogeneous molecular catalysts, an organic molecular mimetic metal-free heterogeneous catalyst is designed and constructed in situ on a graphite flake electrode via a mild electrochemical oxidation-reduction relay strategy. The as-prepared -COOH- and -OH-functionalized metal-free catalyst exhibits an electrocatalytic alkyne semihydrogenation performance with a 72 % Faradaic efficiency, 99 % selectivity and 96 % yield of the alkene product, which is comparable to that of noble metal catalysts. The removal of these oxygen-containing groups leads to negligible activity. The experimental and calculation results reveal that the origin of the high activity can be assigned to the -COOH and -OH groups on graphite. A flow electrolytic cell delivers ten grams of hydrogenated products with 81 % Faradaic efficiency. This metal-free catalyst is also suitable for gas-phase acetylene semihydrogenation and other electrocatalytic hydrogenation reactions.
在导电基底上直接构建用于电催化有机氢化反应的无金属催化剂具有重要意义,但仍未得到充分探索。在此,借鉴均相分子催化剂,通过温和的电化学氧化还原接力策略,在石墨片电极上原位设计并构建了一种有机分子模拟无金属多相催化剂。所制备的含-COOH和-OH官能团的无金属催化剂表现出电催化炔烃半氢化性能,法拉第效率为72%,烯烃产物的选择性为99%,产率为96%,与贵金属催化剂相当。去除这些含氧基团会导致活性可忽略不计。实验和计算结果表明,高活性的来源可归因于石墨上的-COOH和-OH基团。流动电解池以81%的法拉第效率输送了10克氢化产物。这种无金属催化剂也适用于气相乙炔半氢化和其他电催化氢化反应。