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Article Abstract

Photocatalytic hydrogen production offers an alternative pathway to establish a sustainable energy economy, utilizing the Earth's natural sunlight and water resources to address environmental concerns associated with fossil fuel combustion. While numerous photoactive materials exhibit high potential for generating hydrogen from water, the synergy achieved by combining two different materials with complementary properties in the form of heterojunctions can significantly enhance the rate of hydrogen production and quantum efficiency. Our study describes the design and generation of the metal-organic framework-derived (MOF) metal oxide heterojunction herein referred to as RTTA, composed of RuO/N,S-TiO. The RuO/N,S-TiO is generated through the pyrolysis of MOFs, Ru-HKUST-1, and the amino-functionalized MIL-125-NH in the presence of thiourea. Among the various RTTA materials tested, RTTA-1, characterized by the lowest RuO content, exhibited the highest hydrogen evolution rate, producing 10,761 μmol ⋅ hr ⋅ g of hydrogen with an apparent quantum yield of 10.0 % in pure water containing glycerol. In addition to RTTA-1, we generated two other MOF-derived metal oxide heterojunctions, namely ZTTA-1 (ZnO/N,S-TiO) and ITTA-1 (InO/N,S-TiO). These heterojunctions were tested for their photocatalytic activity, leading to apparent quantum yields of 0.7 % and 0.3 %, respectively. The remarkable photocatalytic activity observed in RTTA-1 is thought to be attributed to the synergistic effects arising from the combination of metallic properties inherent in the metal oxides, complemented by the presence of suitable band alignment, porosity, and surface properties inherited from the parent MOFs. These properties enhance electron transfer and restrict hole movement. The photocatalytic efficiency of RTTA-1 was further demonstrated in actual water samples, producing hydrogen with a rate of 8,190 μmol ⋅ hr ⋅ g in tap water, and 6,390 μmol ⋅ hr ⋅ g in river water.

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http://dx.doi.org/10.1002/anie.202405681DOI Listing

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