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Journal ArticleDOI

Photocatalytic reduction of dinitrogen to ammonia over noble-metal-loaded TiO2

TLDR
The photocatalytic reduction of dinitrogen to ammonia is influenced by the nature and amount of metal loading on TiO2 and the optimum metal content varies depending on the nature of the metal as mentioned in this paper.
Abstract
The photocatalytic reduction of dinitrogen to ammonia is influenced by the nature and amount of metal loading on TiO2. The optimum metal content varies depending on the nature of the metal. A correlation between the ammonia yield and the intermediary MH bond strength is established (low bond strength gives rise to low ammonia yield).

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Citations
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Journal ArticleDOI

A surface science perspective on TiO2 photocatalysis

TL;DR: The field of surface science provides a unique approach to understand bulk, surface and interfacial phenomena occurring during TiO2 photocatalysis as mentioned in this paper, including photon absorption, charge transport and trapping, electron transfer dynamics, adsorbed state, mechanisms, poisons and promoters, and phase and form.
Journal ArticleDOI

Photo-illuminated diamond as a solid-state source of solvated electrons in water for nitrogen reduction

TL;DR: It is demonstrated that illuminated hydrogen-terminated diamond yields facile electron emission into water, thus inducing reduction of N₂ to NH₃ at ambient temperature and pressure.
Journal ArticleDOI

Photocatalytic Conversion of Nitrogen to Ammonia with Water on Surface Oxygen Vacancies of Titanium Dioxide

TL;DR: It is reported that a commercially available TiO2 with a large number of surface oxygen vacancies, when photoirradiated by UV light in pure water with N2, successfully produces NH3.
Journal ArticleDOI

Photocatalytic fixation of nitrogen to ammonia: state-of-the-art advancements and future prospects

TL;DR: In this paper, the state-of-the-art engineering of efficient photocatalysts for dinitrogen (N2) fixation toward NH3 synthesis is reviewed and the challenges, outlooks and future prospects at the forefront of this research platform are presented.
Journal ArticleDOI

Photon-Driven Nitrogen Fixation: Current Progress, Thermodynamic Considerations, and Future Outlook

TL;DR: In this article, the authors review the history of the photocatalytic nitrogen fixation and examine current progress toward understanding and improving photofixation of nitrogen, supplemented by a quantitative review of the thermodynamic considerations and limitations for various reaction mechanism.
References
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Journal ArticleDOI

Investigation of the mechanism of hydrogen evolution during photocatalytic water decomposition on metal-loaded semiconductor powders

TL;DR: In this article, the active sites for photocatalytic hydrogen evolution were identified for some noble metals deposited on TiO/sub 2/ particles by measuring the hydrogen isotope effect of the gases produced by the photodecomposition of water using a series of metal-loaded TiO-sub 2 / suspensions (separation factor analysis).
Journal ArticleDOI

Heterogeneous photocatalytic synthesis of ammonia from water and nitrogen

TL;DR: In this paper, a photocatalytic synthesis of ammonia from water and nitrogen was performed using binary wafered catalysts prepared with semiconductor powder (TiO2, SrTiO3, CdS or GaP).
Journal ArticleDOI

Hydrogen evolution from water using solid carbon and light energy

Tomoji Kawai, +1 more
- 01 Nov 1979 - 
TL;DR: In this article, the photocatalytic decomposition of water on TiO2 using solid carbon was examined and the free energies were increased by 63 and 92 kJ mol−1 respectively, utilising light energy.
Journal ArticleDOI

Photocatalytically induced fixation of molecular nitrogen by near UV radiation

TL;DR: In this article, the results of some recent experiments in which molecular nitrogen has been fixed, at room temperaure in oxidising conditions, on the surface of rutile (TiO2) by low-energy UV photons are reported.
Journal ArticleDOI

Photocatalytic reduction of nitrogen over (Fe, Ru or Os)/TiO2 catalysts

TL;DR: In this article, the order of catalytic activity was found to be Ru > Fe > Os, while reverse order was found for the stability of the catalysts with respect to ammonia formation.
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