Photocatalytic Hydrogen Evolution over Exfoliated Rh-Doped Titanate Nanosheets

ACS Omega. 2020 Apr 22;5(17):9929-9936. doi: 10.1021/acsomega.0c00204. eCollection 2020 May 5.

Abstract

Various amounts of Rh-doped titanate nanosheets (Ti3NS:Rh(x), where x is doped amount) were prepared to develop a new nanostructured photocatalyst based on metal oxide compounds that can split water to produce H2 under sunlight. Ti3NS:Rh(x) was obtained by acid exchange, intercalation, and exfoliation of Rh-doped layered sodium titanate compound (Na2Ti3-x Rh x O7). A new energy gap was found in the diffuse reflection spectrum of the Ti3NS:Rh(x) colloidal suspension solution; this new energy gap corresponds to electrons in the 4d level of Rh3+ or Rh4+, which are doped in the Ti4+ site. A photocatalyst activity of Ti3NS:Rh(x) for H2 evolution in water with triethylamine (TEA) as an electron donor was investigated. The appropriate amount of Rh doping can improve the photocatalytic activity of Ti3NS for H2 evolution from water using triethylamine (TEA) as a sacrifice agent. The reason was related to the rich state of Rh3+ or Rh4+ doped in the Ti4+ site of Ti3NS. Doping Rh 1 mol % of Ti, Ti3NS:Rh(0.03) shows the H2 evolution rates up to 1040 nmol/h, which is about 25 times larger than that of nondoped Ti3NS under UV irradiation (>220 nm) and 302 nmol/h under near-UV irradiation (>340 nm). These results show that the development of new nanostructured photocatalyst based on Rh-doped titanate compounds that can produce H2 under near-UV irradiation present in sunlight was a success.