TY - JOUR
T1 - Water Photolysis by UV Irradiation of Rhodium Loaded Strontium Titanate Catalysts. Relation between Catalytic Activity and Nature of the Deposit from Combined Photolysis and ESCA Studies
AU - Lehn, J. M.
AU - Sauvage, J. P.
AU - Zlessel, R.
AU - Hilaire, L.
N1 - Publication details (e.g. title, author(s), publication statuses and dates) are captured on an “AS IS” and “AS AVAILABLE” basis at the time of record harvesting from the data source. Suggestions for further amendments or supplementary information can be sent to [email protected].
PY - 1982
Y1 - 1982
N2 - Photochemical water splitting (H2O → H2 + 1/2O2) has been shown to occur on UV irradiation of aqueous suspensions of strontium titanate, modified by surface photodeposition of rhodium species.7 Further improvement of the catalytic materials has now been achieved, using thermal deposition techniques. The most active material, prepared by heating rhodium chloride impregnated SrTiO3 powder at 500°C in air, allowed one to produce appreciable quantities of (H2 + 1/2O2) gas and to reach high turnover numbers on the catalytic material. The photolysis efficiency presents a strong pH dependence with an optimum around pH ∼ 14 and increases markedly when the wavelength of the light decreases from 400 to 300 nm. The amount of rhodium deposited also has a marked effect with an optimum at about 0.2–0.3% Rh by weight. ESCA studies have provided information about the nature of the catalytic deposit and about its relation to the activity of the materials. Catalytic efficiency and mechanistic aspects are discussed. The oxidation state of the rhodium species has a drastic influence: whereas SrTiO3 loaded with reduced rhodium shows no catalytic activity, the efficiency increases on progressive oxidation of the deposited metal to surface rhodium(III) species, as detected by ESCA. The photoactive step may involve both band‐gap excitation of the semi‐conductor support and direct UV excitation of the deposited Rh(III) species. Copyright © 1982 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim
AB - Photochemical water splitting (H2O → H2 + 1/2O2) has been shown to occur on UV irradiation of aqueous suspensions of strontium titanate, modified by surface photodeposition of rhodium species.7 Further improvement of the catalytic materials has now been achieved, using thermal deposition techniques. The most active material, prepared by heating rhodium chloride impregnated SrTiO3 powder at 500°C in air, allowed one to produce appreciable quantities of (H2 + 1/2O2) gas and to reach high turnover numbers on the catalytic material. The photolysis efficiency presents a strong pH dependence with an optimum around pH ∼ 14 and increases markedly when the wavelength of the light decreases from 400 to 300 nm. The amount of rhodium deposited also has a marked effect with an optimum at about 0.2–0.3% Rh by weight. ESCA studies have provided information about the nature of the catalytic deposit and about its relation to the activity of the materials. Catalytic efficiency and mechanistic aspects are discussed. The oxidation state of the rhodium species has a drastic influence: whereas SrTiO3 loaded with reduced rhodium shows no catalytic activity, the efficiency increases on progressive oxidation of the deposited metal to surface rhodium(III) species, as detected by ESCA. The photoactive step may involve both band‐gap excitation of the semi‐conductor support and direct UV excitation of the deposited Rh(III) species. Copyright © 1982 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim
UR - http://www.scopus.com/inward/record.url?scp=84985154116&partnerID=8YFLogxK
UR - https://www.scopus.com/record/pubmetrics.uri?eid=2-s2.0-84985154116&origin=recordpage
U2 - 10.1002/ijch.198200032
DO - 10.1002/ijch.198200032
M3 - RGC 21 - Publication in refereed journal
SN - 0021-2148
VL - 22
SP - 168
EP - 172
JO - Israel Journal of Chemistry
JF - Israel Journal of Chemistry
IS - 2
ER -