TY - JOUR
T1 - Covalent grafting of molecular catalysts on C3N: X Hy as robust, efficient and well-defined photocatalysts for solar fuel synthesis
AU - Windle, Christopher D.
AU - Wieczorek, Alexander
AU - Xiong, Lunqiao
AU - Sachs, Michael
AU - Bozal-Ginesta, Carlota
AU - Cha, Hyojung
AU - Cockcroft, Jeremy K.
AU - Durrant, James
AU - Tang, Junwang
N1 - Publisher Copyright:
© The Royal Society of Chemistry.
PY - 2020/8/28
Y1 - 2020/8/28
N2 - 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 (C3NxHy) to form noble metal-free photocatalysts for H2 production. The hybrids produce H2 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 ca. 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.
AB - 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 (C3NxHy) to form noble metal-free photocatalysts for H2 production. The hybrids produce H2 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 ca. 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.
UR - http://www.scopus.com/inward/record.url?scp=85090112610&partnerID=8YFLogxK
U2 - 10.1039/d0sc02986f
DO - 10.1039/d0sc02986f
M3 - Article
AN - SCOPUS:85090112610
SN - 2041-6520
VL - 11
SP - 8425
EP - 8432
JO - Chemical Science
JF - Chemical Science
IS - 32
ER -