Windle Christopher D, Wieczorek Alexander, Xiong Lunqiao, Sachs Michael, Bozal-Ginesta Carlota, Cha Hyojung, Cockcroft Jeremy K, Durrant James, Tang Junwang
Department of Chemical Engineering UCL Torrington Place London WC1E 7JE UK
Department of Chemistry and Centre for Processable Electronics, Imperial College London, White City Campus London W12 0BZ UK.
Chem Sci. 2020 Jul 24;11(32):8425-8432. doi: 10.1039/d0sc02986f.
The covalent attachment of molecules to 2D materials is an emerging area as strong covalent chemistry offers new hybrid properties and greater mechanical stability compared with nanoparticles. A nickel bis-aminothiophenol catalyst was grafted onto a range of 2D carbon nitrides (CN H ) to form noble metal-free photocatalysts for H production. The hybrids produce H beyond 8 days with turnover numbers reaching 1360 based on nickel, a more than 3 fold higher durability than reported molecular catalyst-carbon nitride mixtures, and under longer wavelengths (>475 nm). Time-resolved spectroscopy reveals sub-microsecond electron transfer to the grafted catalyst, six orders of magnitude faster compared with similar reports of non-grafted catalysts. The photoelectrons on the catalyst have a 1000 times longer half-time (7 ms) compared with bare carbon nitride (10 μs). The grafting strategy operates across a range of molecular catalyst-carbon nitride combinations, thus paving the way for robust efficient photocatalysts based on low-cost tunable components.
与纳米颗粒相比,由于强大的共价化学提供了新的混合特性和更高的机械稳定性,分子与二维材料的共价连接是一个新兴领域。一种镍双氨基硫酚催化剂被接枝到一系列二维碳氮化物(CN H )上,以形成用于制氢的无贵金属光催化剂。这些杂化物在超过8天的时间里产生氢气,基于镍的周转数达到1360,耐久性比报道的分子催化剂 - 碳氮化物混合物高出3倍以上,并且在更长波长(>475 nm)下也能产生氢气。时间分辨光谱显示向接枝催化剂的亚微秒级电子转移,与未接枝催化剂的类似报道相比快六个数量级。与裸碳氮化物(10微秒)相比,催化剂上的光电子半衰期长1000倍(7毫秒)。这种接枝策略适用于一系列分子催化剂 - 碳氮化物组合,从而为基于低成本可调组件的稳健高效光催化剂铺平了道路。