Wednesday, March 4, 2026

Breakthrough Device Could Slash Ethylene’s Massive Carbon Footprint




A new electrolyzer turns waste-derived syngas into ethylene with significantly lower energy input.

Ethylene sits at the center of modern manufacturing. It is used to make plastics and many other everyday materials, but producing it often comes with a major climate penalty. For every ton of ethylene created, one ton of carbon dioxide is produced. With more than 300 million tons of ethylene produced each year, that adds up to an enormous source of emissions that researchers want to shrink and ultimately remove.

In a new study from Northwestern University, Ted Sargent’s team reports an electrolyzer designed to push ethylene production toward a cleaner model by linking waste and renewable electricity.

The device uses electricity to turn syngas into ethylene. Syngas is a mixture of carbon monoxide and hydrogen that can be made by gasifying plastic waste. That starting point matters because it can be easier to upgrade syngas into valuable chemicals than it is to build the same products directly from carbon dioxide. The researchers also introduced a new material that helps the reaction run effectively, and they built the system to cut the overall energy required.

The results, published in Nature Energy, point to a potential route for making ethylene with renewable power, reducing the need for fossil-based inputs along the supply chain.

“Our goal is to decarbonize chemicals,” Sargent said. “And this work is a big step in that direction.”

Sargent is the Lynn Hopton Davis and Greg Davis Professor of Chemistry at Northwestern’s Weinberg College of Arts and Sciences and a professor of electrical and computer engineering at Northwestern’s McCormick School of Engineering.

“We want to create a circular system that creates chemical building blocks from waste without using fossil fuels,” said Ke Xie, a research faculty member in chemistry at Weinberg. “And this system is part of that new atom-efficient and energy-efficient supply chain.”

Creating energy from waste

Today, most ethylene is made through steam cracking, a process that uses high-temperature steam to break down crude oil into smaller chemical components. While effective, this method relies heavily on fossil fuels and consumes large amounts of energy.

Scientists have been investigating ways to replace it with electricity-driven processes powered by renewable sources. One possibility is to convert carbon dioxide directly into ethylene. However, that reaction requires significant energy input, making it difficult to compete with existing industrial methods.

Instead, Sargent’s team focused on syngas, which is produced by heating plastic waste in a low-oxygen environment. Syngas contains carbon monoxide and hydrogen. Because it is chemically closer to ethylene than carbon dioxide is, transforming it into ethylene requires less electricity.

“A lot of syngas is made into chemicals, so finding a route to take the syngas to ethylene that’s both very selective and very energy efficient is of industrial interest,” Sargent said.

To make this conversion practical, the researchers needed to design a different kind of electrolyzer, a cell that uses electrical energy to drive chemical reactions. Most electrolyzers rely on liquid water mixed with dissolved salts that supply both positive and negative ions.

The team explored whether they could build a system that operates with gases on both sides of the reaction. In their design, carbon monoxide from syngas would enter on one side (the cathode), while hydrogen would be supplied on the other (the anode).

“In initial attempts, we tried to make a gas-gas electrolyzer, but it just didn’t work,” he said. “And what we realized was that we didn’t just need the water we needed the salt.”

A novel device that works with renewable energy

Salt provides the positive ions (cations) that the device’s copper catalyst needs to stabilize key intermediates in the reaction. Bosi Peng, a postdoctoral researcher in the lab and first author on the paper, searched for the right material that could trap those ions while also keeping them loose enough to react within the system.

“We needed to find a material in this Goldilocks zone to make a successful electrolyzer,” Sargent said. “And Bosi found a new way to solve this hard problem, which was really exciting.”

The material, sodium polyacrylate (PANa), creates a micro-environment within the system that mimics a liquid salt bath, while keeping the system dry of liquid water. The result is a process that is more than 60% more efficient than the most energy-efficient prior electrified processes that turn carbon dioxide into ethylene.

“Bosi significantly reduced the electricity needed by lowering the voltage we have to apply across the device,” Sargent said. Even further, the device works well with the intermittent nature of renewable energy sources.

“Solar and wind are very cheap sources of energy, but they come and go,” he said. “We needed to create a device that could deal with intermittent energy, and we found this system could do that. A key ingredient in doing so was to take out the liquid water with the high concentration salt in the electrolyte.”

Next, the team plans to try to reduce the energy consumption of the device even further, so it’s on par with energy used in steam cracking. They are also using artificial intelligence and machine learning tools to find catalysts that would make the device even more efficient.

Ultimately, the goal is to create a device that can scale up to be used in industry to continue to reduce ethylene’s carbon footprint.

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Tuesday, March 3, 2026

Quantum Chemistry Meets Pyrazole: A New Era in Energetic Materials! #worldresearchawards #chemistry

 


This research integrates quantum-chemistry calculations with Bayesian optimization to accelerate discovery of novel pyrazole-based energetic materials. By predicting performance, stability, and sensitivity, the data-driven framework efficiently guides molecular design, reducing experimental workload while enhancing safety and energetic efficiency.

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Monday, March 2, 2026

This Blue-Light Iron Breakthrough Could Make Drug Production Cheaper




A blue-light-powered iron catalyst just replaced rare metals and unlocked a milestone in precision drug synthesis.

Photocatalysts are materials that trigger chemical reactions when exposed to light. In modern organic chemistry, metal-based photocatalysts are especially valuable because they are stable and can be fine-tuned by adjusting the ligands attached to the central metal atom. These ligands influence how the catalyst behaves and what kinds of molecules it can help build.

Common photocatalyst metals such as ruthenium and iridium work well but are rare and costly. To address this, researchers at Nagoya University in Japan previously introduced an iron-based alternative. However, that earlier system depended on large quantities of expensive chiral ligands, which act as structural guides that determine the three-dimensional shape of the final chemical product.

In a new study published in the Journal of the American Chemical Society, the team reports a redesigned iron catalyst that cuts chiral ligand use by two-thirds. The catalyst also operates under energy-efficient blue LED light, making the process more practical and potentially more sustainable.

Using this improved system, the scientists completed the asymmetric total synthesis of (+)-heitziamide A. This natural compound, found in medicinal plants, is known to suppress respiratory bursts. The work was carried out by Professor Kazuaki Ishihara, Assistant Professor Shuhei Ohmura, and graduate student Hayato Akao at Nagoya University’s Graduate School of Engineering.

Iron Photocatalyst Design Improves Efficiency

In their 2023 work, the group developed an iron photocatalyst that incorporated three chiral ligands per iron atom. Yet only one of those ligands actually influenced enantioselectivity, meaning much of the material was not contributing to the desired three-dimensional control. That made the system less efficient than it could be.

The newly engineered catalyst takes a different approach. It pairs an inexpensive achiral bidentate ligand with a chiral ligand to form a specific iron(III) salt structure. The chiral ligand directs the three-dimensional arrangement of the product, while the achiral bidentate ligand adjusts and enhances the catalyst’s overall activity.

With this design, the team achieved a highly controlled radical cation (4 + 2) cyclization. In this reaction, two molecular components join to create a six-membered ring. The method allows chemists to construct 1,2,3,5-substituted adducts, structural patterns frequently seen in natural products such as heitziamide A.

“The new catalyst design represents the definitive form of chiral iron(III) photoredox catalysts,” stated Ohmura, one of the study’s corresponding authors. “We believe this achievement marks a significant milestone in advancing iron-based photocatalysis.”

First Asymmetric Synthesis of (+)-Heitziamide A

Although scientists have previously reported laboratory synthesis of heitziamide A, they had not achieved the total asymmetric synthesis of its naturally occurring enantiomer.

By using blue light to activate the iron photocatalyst and carefully controlling six membered ring formation, the researchers successfully completed the first total asymmetric synthesis of (+)-heitziamide A. The results suggest that employing the mirror image version of the catalyst could also produce (-)-heitziamide A, making it possible to selectively generate either enantiomer.

Implications for Drug Synthesis and Green Chemistry

This new iron photocatalyst provides a way to build complex molecules, including pharmaceutical precursors, using abundant iron and low energy blue LEDs instead of scarce rare metals.

“Achieving the first-ever asymmetric total synthesis of (+)-heitziamide A using this catalytic reaction is a remarkable accomplishment,” stated Ishihara, the study’s other corresponding author. “Several additional bioactive substances can be accessed through total synthesis, with enantioselective radical cation (4 + 2) cycloaddition serving as a key step. We intend to publish follow-up papers on the asymmetric total synthesis of these compounds in the near future.”

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Breakthrough Device Could Slash Ethylene’s Massive Carbon Footprint

A new electrolyzer turns waste-derived syngas into ethylene with significantly lower energy input. Ethylene sits at the center of modern man...