Krateeka Madan, H. Seshagiri Rao, R.B. Harikrishna, G. Ranga Rao
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引用次数: 0
Abstract
In this work, hydrothermally synthesized SrTiO3 (STO) is subjected to ammonia reduction for 15 h and 45 h at 1000 ℃ under controlled conditions. The ammonia treatment reduced the band gap of SrTiO3 from 3.2 eV to 2.8 eV in ammonia-treated SrTiO3 samples (STON). XRD and Raman analysis confirm the presence of cubic phase in the STO and ammonia-treated STON-15 and STON-45 samples. Additionally, the presence of N due to ammonia reduction in STON-15 and STON-45 samples is verified by XPS analysis. In addition, XPS data shows an increase in the Ti3+ concentration in the STON-15 sample relative to the STON-45 sample when N is incorporated. STON-15 showed higher photocurrent density throughout the potential range of water splitting. An increase from 98 μA/cm2 to 250 μA/cm2 in the cathodic photocurrent density at 0 VRHE is obtained for STON-15 sample compared to STO sample. In contrast to STO, which only displayed a photocurrent density of 4.97 μA/cm2, STON-15 showed an anodic photocurrent density of 140 μA/cm2 at 1.23 VRHE. All the photoelectrochemical studies were carried out without using co-catalysts and sacrificial agents.
期刊介绍:
Catalysis Today focuses on the rapid publication of original invited papers devoted to currently important topics in catalysis and related subjects. The journal only publishes special issues (Proposing a Catalysis Today Special Issue), each of which is supervised by Guest Editors who recruit individual papers and oversee the peer review process. Catalysis Today offers researchers in the field of catalysis in-depth overviews of topical issues.
Both fundamental and applied aspects of catalysis are covered. Subjects such as catalysis of immobilized organometallic and biocatalytic systems are welcome. Subjects related to catalysis such as experimental techniques, adsorption, process technology, synthesis, in situ characterization, computational, theoretical modeling, imaging and others are included if there is a clear relationship to catalysis.