Boosting formic acid dehydrogenation via the design of a Z-scheme heterojunction photocatalyst: The case of graphitic carbon nitride/Ag/Ag3PO4-AgPd quaternary nanocomposites
Creators
- 1. Department of Nano Technology and Advanced Materials, Institute of Science, Mersin University, Mersin 33343 (Turkey)
- 2. Department of Chemistry, Vocational School of Technical Sciences, Mersin University, Mersin 33343 (Turkey)
- 3. Department of Chemistry, College of Sciences, Koç University, 34450 Sarıyer, Istanbul (Turkey)
- 4. Koç University Surface Science and Technology Center (KUYTAM), 34450 Sarıyer, Istanbul (Turkey)
- 5. Koç University TÜPRAŞ Energy Center (KUTEM), 34450 Sarıyer, Istanbul (Turkey)
Description
Highlights: • A novel Z-scheme heterojunction photocatalyst, g-CN/Ag/Ag3PO4-AgPd, is fabricated. • Formic acid dehydrogenation is boosted by a Z-scheme heterojunction photocatalyst. • g-CN/Ag/Ag3PO4-AgPd provided a very high TOF of 2107 h−1 in the FA dehydrogenation. The development of an efficient, eco-friendly, practical, and selective way to decompose formic acid (FA) into H2 and CO2 is crucial for the utilization of FA as a chemical hydrogen storage material in hydrogen economy. In this regard, photocatalytic FA dehydrogenation attracts great attention owing to its potential to meet the above-mentioned requirements. Interestingly, there is no example of heterojunction photocatalyst that tunes the hole potential of the semiconductor, resulted in a better photocatalytic activity. We report herein for the first time the design and fabrication of a novel Z-scheme heterojunction photocatalyst for FA dehydrogenation, denoted as g-CN/Ag/Ag3PO4-AgPd comprising graphitic carbon nitride (g-CN) and Ag3PO4 semiconductors, Ag and AgPd alloy nanoparticles (NPs). The designed g-CN/Ag/Ag3PO4-AgPd photocatalysts boosted the FA dehydrogenation by creating more positive hole potential and improving the charge separation efficiency of the two distinct semiconductors. The g-CN/Ag/Ag3PO4-AgPd photocatalysts provided a very high turnover frequency (TOF) of 2107 h−1 in the FA dehydrogenation under white-LED illumination at 50 °C. This TOF is 3.2 times and 44 times greater than those of g-CN/AgPd and g-CN/Pd binary non-Z-scheme heterojunction catalysts, respectively, under the same conditions and comparable to the best photocatalysts and heterogeneous catalysts reported in the FA dehydrogenation so far.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.apsusc.2020.147740Additional details
Identifiers
- DOI
- 10.1016/j.apsusc.2020.147740;
- PII
- S0169433220324971;
Publishing Information
- Journal Title
- Applied Surface Science
- Journal Volume
- 535
- Journal Page Range
- vp.
- ISSN
- 0169-4332
- CODEN
- ASUSEE
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 54078538
- Subject category
- S75: CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY;
- Descriptors DEI
- ALLOYS; CARBON DIOXIDE; CARBON NITRIDES; DEHYDROGENATION; DESIGN; FORMIC ACID; GRAPHITE; HETEROJUNCTIONS; HYDROGEN STORAGE; NANOCOMPOSITES; NANOPARTICLES; SEMICONDUCTOR MATERIALS; SILVER PHOSPHATES
- Descriptors DEC
- CARBON; CARBON COMPOUNDS; CARBON OXIDES; CARBOXYLIC ACIDS; CHALCOGENIDES; CHEMICAL REACTIONS; ELEMENTS; MATERIALS; MINERALS; MONOCARBOXYLIC ACIDS; NANOMATERIALS; NITRIDES; NITROGEN COMPOUNDS; NONMETALS; ORGANIC ACIDS; ORGANIC COMPOUNDS; OXIDES; OXYGEN COMPOUNDS; PARTICLES; PHOSPHATES; PHOSPHORUS COMPOUNDS; PNICTIDES; SEMICONDUCTOR JUNCTIONS; SILVER COMPOUNDS; STORAGE; TRANSITION ELEMENT COMPOUNDS
Optional Information
- Copyright
- Copyright (c) 2020 Elsevier B.V. All rights reserved.