To contribute meaningfully to carbon dioxide (CO) emissions reduction, CO electrolyzer technology will need to scale immensely. Bench-scale electrolyzers are the norm, with active areas <5 cm. However, cell areas on the order of 100s or 1000s of cm will be required for industrial deployment. Here, we study the effects of increasing cell area, scaling over 2 orders of magnitude from a 5 cm lab-scale cell to an 800 cm pilot plant-scale cell. A direct scaling of the bench-scale cell architecture to the larger area results in a ∼20% drop in ethylene (CH) selectivity and an increase in the parasitic hydrogen (H) evolution reaction (HER). We instrument an 800 cm electrolyzer cell to serve as a diagnostic tool and determine that nonuniformities in electrode compression and flow-influenced local CO availability are the key drivers of performance loss upon scaling. Machining of an initial 800 cm cell results in a standard deviation in MEA compression that is 7-fold that of a similarly produced 5 cm cell (0.009 mm). Using these findings, we redesign an 800 cm cell for compression tolerance and increased CO transport and achieve an H FE in the revised 800 cm cell similar to that of the 5 cm case (16% at 200 mA cm). These results demonstrate that by ensuring uniform compression and fluid flow, the CO electrolyzer area can be scaled over 100-fold and retain CH selectivity (within 10% of small-scale selectivity).
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acsami.4c11103 | DOI Listing |
ACS Nano
January 2025
State Key Laboratory of New Ceramics and Fine Processing, School of Materials Science and Engineering, Tsinghua University, Beijing 100084, China.
The seamless integration of electrocatalysts onto the electrode is crucial for enhancing water electrolyzers, yet it is especially challenging when scaled up to large manufacturing. Despite thorough investigation, there are few reports that tackle this integration through roll-to-roll (R2R) methodology, a technique crucial for fulfilling industrial-scale demands. Here, we develop an R2R flash Joule heating (R2R-FJH) system to process catalytic electrodes with superior performance.
View Article and Find Full Text PDFEES Catal
December 2024
Department of Chemical Engineering, Delft University of Technology 2629 HZ Delft The Netherlands
Electrochemical CO reduction offers a promising method of converting renewable electrical energy into valuable hydrocarbon compounds vital to hard-to-abate sectors. Significant progress has been made on the lab scale, but scale-up demonstrations remain limited. Because of the low energy efficiency of CO reduction, we suspect that significant thermal gradients may develop in industrially relevant dimensions.
View Article and Find Full Text PDFAdv Mater
January 2025
School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, Jiangsu, 210023, China.
Hydrogen evolution reaction (HER), as one of the most advanced methods for the green production of hydrogen, is greatly impeded by inefficient mass transfer. Here we present an efficiently reactant enriched and mass traffic system by integrating high-curvature Pt nanocones with 3D porous TiAl framework to enhance mass transfer rate. Theoretical simulations, in situ Raman spectroscopy and potential-dependent Fourier transform infrared spectroscopy results disclose that the strong local electric field induced by high-curvature Pt can greatly promote the HO supply rate during HER, resulting in ∼1.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
School of Chemistry, Beijing Advanced Innovation Center for Biomedical Engineering, Key Laboratory of Bio-Inspired Smart Interfacial Science and Technology, Beihang University, Beijing 100191, China.
The dual-site synergistic catalytic mechanism on NiFeOOH suggests weak adsorption of Ni sites and strong adsorption of Fe sites limited its activity toward alkaline oxygen evolution reaction (OER). Large-scale density functional theory (DFT) calculations confirm that Co doping can increase Ni adsorption, while the metal vacancy can reduce Fe adsorption. The combined two factors can further modulate the atomic environment and optimize the free energy toward oxygen-containing intermediates, thus enhancing the OER activity.
View Article and Find Full Text PDFSmall
January 2025
Department of Urban, Energy, and Environmental Engineering, Chungbuk National University, Chungdae-ro 1, Seowon-Gu, Cheongju, Chungbuk, 28644, Republic of Korea.
Developing efficient, economical, and stable catalysts for the oxygen evolution reaction is pivotal for producing large-scale green hydrogen in the future. Herein, a vanadium-doped nickel-iron oxide supported on nickel foam (V-NiFeO/NF) is introduced, and synthesized via a facile hydrothermal method as a highly efficient electrocatalyst for water electrolysis. X-ray photoelectron and absorption spectroscopies reveal a synergistic interaction between the vanadium dopant and nickel/iron in the host material, which tunes the electronic structure of NiFeO to increase the number of electrochemically active sites.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!