Molybdenum sulphides on carbon supports as electrocatalysts for hydrogen evolution in acidic industrial wastewater
- 1. Laboratory for MEMS Applications, IMTEK – Department of Microsystems Engineering, University of Freiburg, Georges-Koehler-Allee 103, 79110 Freiburg (Germany)
- 2. Institute for Inorganic and Analytical Chemistry and Freiburg Materials Research Center, University of Freiburg, Albertstraße 21, 79104 Freiburg (Germany)
- 3. Hahn-Schickard, Georges-Koehler-Allee 103, 79110 Freiburg (Germany)
- 4. BIOSS – Centre for Biological Signalling Studies, University of Freiburg, 79110 Freiburg (Germany)
Description
Highlights: • MoSx is an efficient and durable catalyst for H2 evolution in acidic wastewater. • MoSx outperformed Pt as H2-catalyst in long term in acidic wastewater. • Improved activity over time was likely due to changes in MoSx structure. - Abstract: Microbial electrolysis cells (MECs) are an attractive future alternative technology to generate renewable hydrogen and simultaneously treat wastewaters. The thermodynamics of hydrogen evolution in MECs can be greatly improved by operating the cathode at acidic pH in combination with a neutral pH microbial anode. This can easily be achieved with acidic industrial wastewaters that have to be neutralised before discharge. For the hydrogen evolution reaction (HER) in acidic wastewater, efficient and inexpensive catalysts are required that are compatible with the often complex chemical composition of wastewaters. In this study, molybdenum sulphides (MoSx) on different carbon supports were successfully used for hydrogen evolution in different acidic media. At first, the cathodes were screened by linear sweep voltammetry in sulphuric acid (pH 0) or phosphate buffer (pH 2.2). After this, the overpotentials for H2 production of the best cathodes and their long term performances (⩾1 week) were determined in acidic industrial wastewater (pH 2.4) obtained from a plant mainly producing cellulose acetate. For the most promising MoSx cathodes, the overpotentials for HER (at 3 mA cm−2) were only ∼40 mV higher than for a platinum electrode. Most importantly, the catalytic efficiency of the MoSx electrodes improved in the wastewater over time (7–17 days), while Pt electrodes were found to be slowly deactivated. Thus, MoSx emerges as an affordable, efficient and especially durable electrocatalyst for HER in real acidic wastewaters and this could be an important contribution to take energy production from wastewaters in the form of hydrogen towards practical applications.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.apenergy.2016.12.097Additional details
Identifiers
- DOI
- 10.1016/j.apenergy.2016.12.097;
- PII
- S0306-2619(16)31867-0;
Publishing Information
- Journal Title
- Applied Energy
- Journal Volume
- 190
- Journal Page Range
- p. 1221-1233
- ISSN
- 0306-2619
- CODEN
- APENDX
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 48089147
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- CATHODES; ELECTROCATALYSTS; HYDROGEN; MOLYBDENUM SULFIDES; SILICON OXIDES; WASTE WATER
- Descriptors DEC
- CATALYSTS; CHALCOGENIDES; ELECTRODES; ELEMENTS; HYDROGEN COMPOUNDS; LIQUID WASTES; MOLYBDENUM COMPOUNDS; NONMETALS; OXIDES; OXYGEN COMPOUNDS; REFRACTORY METAL COMPOUNDS; SILICON COMPOUNDS; SULFIDES; SULFUR COMPOUNDS; TRANSITION ELEMENT COMPOUNDS; WASTES; WATER
Optional Information
- Copyright
- Copyright (c) 2017 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.