Journal
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 46, Issue 5, Pages 3811-3820Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2020.10.177
Keywords
Hydrogen generation; Photocatalytic hydrolysis; Ammonia borane; RuP2 quantum dots; Graphite carbon nitride; In-situ phosphorization
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Funding
- Natural Science Foundation of Hebei Provence, China [B2019408018, E2020408004]
- Fundamental Research Funds for the Universities in Hebei Province, China [JYT201901, JYQ202002]
- Research Projects of Heibei Education Department, China [QN2019072]
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RuP2 quantum dots supported on g-C3N4 were prepared for efficient photocatalytic hydrolysis of ammonia borane. Visible-light irradiation significantly increased the reaction rate and reduced the activation energy. The photocatalytic hydrolysis mechanism and catalyst reusability were also investigated.
Hydrolytic dehydrogenation of ammonia borane (AB) driven by efficient catalysts has attracted considerable attention and is regarded as a promising strategy for hydrogen generation. Herein, RuP2 quantum dots supported on graphitic carbon nitride (g-C3N4) were successfully prepared by in-situ phosphorization, yielding a highly efficient photocatalyst toward AB hydrolysis. The catalysts were characterized by field-emission scanning electron microscopy, transmission electron microscopy, x-ray diffraction, x-ray photoelectron microscopy, inductively coupled plasma atomic emission spectroscopy, UV-visible diffuse reflectance spectroscopy and photoluminescence spectroscopy. A conventional waterdisplacement method was employed to record the hydrogen volume as a function of reaction time. Owing to visible-light irradiation, the initial turnover frequency of the AB hydrolysis was significantly enhanced by 110% (i.e., 134 min(-1)) at room temperature. Furthermore, the apparent activation energy decreased from 67.7 +/- 0.9 to 47.6 +/- 1.0 kJ mol(-1). The photocatalytic hydrolysis mechanism and catalyst reusability were also investigated. (C) 2020 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
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