Department of Materials and Optoelectronic Science, National Sun Yat-Sen University, Kaohsiung 80424, Taiwan.
Department of Photonics, National Sun Yat-Sen University, Kaohsiung 80424, Taiwan.
J Colloid Interface Sci. 2023 Mar;633:775-785. doi: 10.1016/j.jcis.2022.11.098. Epub 2022 Nov 24.
The efficient and selective photocatalytic CO conversion into higher-valued hydrocarbon products (e.g., methane and ethane) over covalent organic frameworks (COFs) remains a challenge, with all previously reported attempts producing carbon monoxide as the dominant product. Herein, we report a new ethene-based COF, through polycondensation of electron-rich (E)-1,2‑diphenylethene and 1,3,6,8‑tetraphenylpyrene units. The synthesized ethene-based COF functioned as an efficient metal-free photocatalyst for the conversion of CO into methane under visible light irradiation, with a selectivity of 100 %, a production rate of 14.7 µmol gh, and an apparent quantum yield of c.a. 0.99 % at 489.5 nm, which are the most promising values reported for CO conversion by a metal-free COF photocatalyst, without any support from a co-catalyst. The carbon origin of CH product is confirmed by isotope tracer CO experiment. Moreover, the photocatalytic system consistently produces methane for > 14 h with recyclability.
将 CO 高效且选择性地光催化转化为高附加值烃类产物(例如甲烷和乙烷)是共价有机框架(COFs)面临的一个挑战,所有之前报道的尝试均生成一氧化碳作为主要产物。在此,我们报告了一种新的乙烯基 COF,通过富电子(E)-1,2-二苯乙烯和 1,3,6,8-四苯基芘单元的缩聚反应得到。所合成的乙烯基 COF 在可见光照射下作为高效的无金属光催化剂,将 CO 转化为甲烷,选择性为 100%,产率为 14.7µmolgh,在 489.5nm 时的表观量子效率约为 0.99%,这是无金属 COF 光催化剂用于 CO 转化的最有前途的值,无需任何助催化剂的支持。通过同位素示踪 CO 实验证实了 CH 产物的碳源。此外,该光催化体系可连续 14 小时以上循环使用,持续生成甲烷。