Sustainable method can electrosynthesize important chemical for synthetic rubber production

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Illustration of the electrocatalytic conversion of acetylene (C2H2) to 1,3-butadiene (C4H6) on copper catalysts. The process involves the adsorption of acetylene molecules onto the catalyst surface, followed by hydrogenation and coupling of *C₂H₂ and *C₂H₃ intermediates, leading to the formation of 1,3-butadiene, which is subsequently desorbed. Credit: Nature Catalysis (2024). DOI: 10.1038/s41929-024-01250-0

Chemists from the National University of Singapore (NUS) have developed a sustainable method to electrosynthesize 1,3-butadiene, a feedstock used for synthetic rubber production, from acetylene.

Lowering the energy requirements and environmental impact of producing multi-carbon molecules is critical for advancing a more sustainable chemical industry.

A key approach is electrification, which uses renewable electricity to convert simple feedstocks such as water and carbon dioxide (CO2) into valuable chemicals and fuels.

Achieving this requires identifying clear target molecules and efficient synthesis routes. One such target is 1,3-butadiene. Today, 1,3-butadiene is produced as a minor by-product alongside ethylene from the energy-intensive cracking of naphtha or ethane. Despite this, more than 18 million tons of this critical feedstock are produced annually.

A research team led by Associate Professor Yeo Boon Siang, Jason from the Department of Chemistry at NUS has found that copper catalysts, after a simple modification with iodide anions, are highly efficacious for converting acetylene to 1,3-butadiene. The findings were published in the journal Nature Catalysis.

The catalyst was able to produce 1,3-butadiene with a Faradaic efficiency of 93% at −0.85 V versus the Standard Hydrogen Electrode (SHE) and a partial current density of −75 mA cm-2 at −1.0 V versus SHE.

The partial current density of 1,3-butadiene, an indicator of catalytic activity, was at least 20 times higher than that reported in previous studies.

This research was conducted in collaboration with Dr. Federico CALLE-VALLEJO from the Basque Foundation for Science and the University of the Basque Country, both in Spain.

The team also included Dr. Wei Jie Teh from the Department of Chemistry, NUS, Mr. Eleonora Romeo and Professor Francesc Illas from the University of Barcelona, Spain, Dr. Ben Rowley from Shell Global Solutions International B.V., and Dr. Shibo Xi from the Institute of Sustainability for Chemical, Energy and Environment, Agency for Science, Technology and Research.

Extensive characterization of the catalyst using in situ spectroscopies and computational simulations using density functional theory revealed that iodide promotes stable ensembles of neutral and partially oxidized Cu sites (Cuδ+–Cu0 sites), which enhance the carbon-carbon (C–C) coupling of *C2H3 intermediates to form 1,3-butadiene.

Prof Yeo said, "This work is the fruit of an intense collaboration between experimentalists and theoreticians, together with our industrial partner, to discover how important chemicals, such as 1,3-butadiene, could be more sustainably produced."

Building on the research findings from their work, the research team plans to develop catalysts capable of coupling acetylene into longer-chain hydrocarbons, which could potentially be used as aviation fuel.

More information: Wei Jie Teh et al, Selective electroreduction of acetylene to 1,3-butadiene on iodide-induced Cuδ+–Cu0 sites, Nature Catalysis (2024). DOI: 10.1038/s41929-024-01250-0

Journal information: Nature Catalysis

Provided by National University of Singapore