2013
DOI: 10.1039/c3cc45795h
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Nanoporous Sr-rich strontium titanate: a stable and superior photocatalyst for H2 evolution

Abstract: A synthetic route to prepare nanoporous Sr-rich strontium titanate (Sr : Ti ≈ 1.03) with a high surface area is reported. The as-obtained porous nanomaterial serves as a stable and superior photocatalyst for H2 evolution.

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Cited by 33 publications
(23 citation statements)
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“…Among perovskite oxides, the alkaline earth metal titanate, SrTiO 3 has been extensively explored experimentally and theoretically for vacancy engineering by different methods. [ 97 ] In addition, SrTiO 3 ‐based materials have also been reported for benchmark water splitting performance. [ 98 ] Feng et al.…”
Section: Vacancy Engineered Materials For Photocatalytic H2 Evolution and N2 Fixationmentioning
confidence: 99%
“…Among perovskite oxides, the alkaline earth metal titanate, SrTiO 3 has been extensively explored experimentally and theoretically for vacancy engineering by different methods. [ 97 ] In addition, SrTiO 3 ‐based materials have also been reported for benchmark water splitting performance. [ 98 ] Feng et al.…”
Section: Vacancy Engineered Materials For Photocatalytic H2 Evolution and N2 Fixationmentioning
confidence: 99%
“…SrTiO 3 is well known as a photocatalyst with a potential for overall water splitting . The methods to improve its photocatalytic activity have been intensively studied so far in various aspects . Doping is one of the most important techniques to improve their activity, and the photocatalytic activity of SrTiO 3 is vastly changed by introducing impurities .…”
Section: Introductionmentioning
confidence: 99%
“…Since stability is critical for any catalyst, the time courses of photocatalytic hydrogen evolution over CuNPs from photoreduction were recorded under irradiation intermittently for 60 h, with evacuation every 12 h. Significantly, evolution rate of hydrogen shows a linear increase with the increasing of illumination time for the entire measurement, and no noticeable degradation in photocatalytic activity was observed after five sequential 12 h runs, suggesting that the catalyst is stable for at least 60 h. The total evolution of H 2 after 60 h was 0.27 mmol, far exceeding the amount of Cu precursor added (0.002 mmol). The CuNPs generated in this system showed high performance, stability, and recyclability for HER when using lactic acid as a sacrificial electron donor in the absence of air.…”
mentioning
confidence: 99%