Solar Energy

Green battery discovery turns trash into treasure

Published

2 months ago

January 10, 2025

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Green battery discovery turns trash into treasure

by Win Reynolds for Northwestern News

Evanston IL (SPX) Jan 10, 2025

The batteries used in our phones, devices and even cars rely on metals like lithium and cobalt, sourced through intensive and invasive mining. As more products begin to depend on battery-based energy storage systems, shifting away from metal-based solutions will be critical to facilitating the green energy transition.

Now, a team at Northwestern University has transformed an organic industrial waste product into an efficient storage agent for sustainable energy solutions that can one day be applied at much larger scales. This marks the first time a waste molecule – specifically, triphenylphosphine oxide (TPPO) – has been used to power a redox flow battery.

“Battery research has traditionally been dominated by engineers and materials scientists,” said Northwestern chemist and lead author Christian Malapit. “Synthetic chemists can contribute to the field by molecularly engineering an organic waste product into an energy-storing molecule. Our discovery showcases the potential of transforming waste compounds into valuable resources, offering a sustainable pathway for innovation in battery technology.”

Malapit is an assistant professor in the department of chemistry at Northwestern’s Weinberg College of Arts and Sciences.

What are redox flow batteries?

Unlike lithium and other solid-state batteries which store energy in electrodes, redox flow batteries use a chemical reaction to pump energy back and forth between electrolytes, where their energy is stored. Though not as efficient at energy storage, redox flow batteries are thought to be much better solutions for energy storage at a grid scale. A small part of the battery market at present, the market for redox flow batteries is expected to rise by 15% between 2023 and 2030 to reach a value of 700 million euros worldwide.

Power from a common waste product

Thousands of tons of TPPO are produced each year by many organic industrial synthesis processes – including the production of some vitamins, among other things – but it is rendered useless and must be carefully discarded following production.

According to the new research, published in the Journal of the American Chemical Society, a “one-pot” reaction allows chemists to turn TPPO into a usable product with powerful potential to store energy.

“Not only can an organic molecule be used, but it can also achieve high-energy density – getting closer to its metal-based competitors – along with high stability,” said Emily Mahoney, a Ph.D. candidate in the Malapit lab and the paper’s first author. “These two parameters are traditionally challenging to optimize together, so being able to show this for a molecule that is waste-derived is particularly exciting.”

To achieve both energy density and stability, the team needed to identify a strategy that allowed electrons to pack tightly together in the solution without losing storage capacity over time. They looked to the past and found a paper from 1968 describing the electrochemistry of phosphine oxides and, according to Mahoney, “ran with it.”

Then, to evaluate the molecule’s resilience as a potential energy-storage agent, the team ran tests using static electrochemical charge and discharge experiments similar to the process of charging a battery, using the battery, and then charging it again, over and over. After 350 cycles, the battery maintained remarkable health, losing negligible capacity over time.

What’s next

“This is the first instance of utilizing phosphine oxides – a functional group in organic chemistry – as the redox-active component in battery research,” Malapit said. “Traditionally, reduced phosphine oxides are highly unstable. Our molecular engineering approach addresses this instability, paving the way for their application in energy storage.”

In the meantime, the group hopes other researchers will pick up the charge and begin to work with TPPO to further optimize and improve its potential.

Research Report:Triphenylphosphine Oxide-Derived Anolyte for Application in Nonaqueous Redox Flow BatteryClick to copy article link

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Solar Energy

Identifying Key Organic-Inorganic Interaction Sites for Enhanced Emission in Hybrid Perovskites via Pressure Engineering

Published

2 hours ago

March 14, 2025

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Identifying Key Organic-Inorganic Interaction Sites for Enhanced Emission in Hybrid Perovskites via Pressure Engineering

by Simon Mansfield

Sydney, Australia (SPX) Mar 14, 2025

A research team from Jilin University has developed a new approach using pressure engineering to pinpoint organic-inorganic interaction sites in non-hydrogen-bonded hybrid metal perovskites. This innovative method provides valuable insight into the photophysical mechanisms governing hybrid perovskites and offers guidance for designing materials with tailored optical properties.

“Previous research has primarily focused on the role of hydrogen bonding in shaping the photophysical properties of hybrid perovskites,” explained Guanjun Xiao, the study’s lead researcher. “However, the lack of investigation into the interaction mechanisms of non-hydrogen-bonded hybrid perovskites has hindered precise material design for targeted applications.”

By employing high-pressure techniques, Xiao and his team studied the specific interaction sites within the non-hydrogen-bonded hybrid perovskite (DBU)PbBr3. Their findings highlighted that the spatial arrangement of Br-N atomic pairs plays a crucial role in influencing organic-inorganic interactions.

The research was published on September 16 in *Research*, a Science Partner Journal launched by the American Association for the Advancement of Science (AAAS) in collaboration with the China Association for Science and Technology (CAST). Xiao is a professor at the State Key Laboratory of Superhard Materials at Jilin University.

The study involved synthesizing microrod (DBU)PbBr3 using the hot injection method and systematically analyzing its optical and structural properties under high pressure. The researchers observed that the material’s emission exhibited enhancement and a blue shift under pressure, with photoluminescence quantum yield reaching 86.6% at 5.0 GPa. Additionally, photoluminescence lifetime measurements indicated a suppression of non-radiative recombination under pressure.

A significant discovery was the presence of an abnormally enhanced Raman mode in the pressure range where emission enhancement occurred. “This suggests a potential connection between the two phenomena,” Xiao noted. Further analysis identified the Raman mode as being linked to organic-inorganic interactions, likely associated with N-Br bonding.

To deepen their understanding, the team conducted structural evolution studies under pressure, supported by first-principles calculations. They confirmed that the primary determinants of interaction strength were the spatial arrangement of N and Br atoms, including their distance and dihedral angle. A notable isostructural phase transition at 5.5 GPa altered the primary compression direction, initially strengthening organic-inorganic interactions before leading to a subsequent decrease-trends that aligned with observed optical property changes.

“These findings bridge a significant knowledge gap in understanding organic-inorganic interactions in non-hydrogen-bonded hybrid halides, offering valuable design principles for materials with specific optical performance targets,” Xiao stated.

Research Report:Identifying Organic-Inorganic Interaction Sites Toward Emission Enhancement in Non-Hydrogen-Bonded Hybrid Perovskite via Pressure Engineering

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Solar Energy

Groundbreaking Discovery Links Small Polaron Effect to Enhanced Spin Lifetime in 2D Lead Halide Perovskites

Published

2 hours ago

March 14, 2025

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Groundbreaking Discovery Links Small Polaron Effect to Enhanced Spin Lifetime in 2D Lead Halide Perovskites

by Simon Mansfield

Sydney, Australia (SPX) Mar 14, 2025

Two-dimensional lead halide perovskites have emerged as highly promising materials for optoelectronic applications due to their superior carrier transport and defect tolerance. However, a comprehensive understanding of charge carrier dynamics in these materials has remained elusive, primarily due to their inherently soft polar lattice and pronounced electron-phonon interactions. While extensive studies have characterized charge behavior in bulk three-dimensional perovskites, the unique carrier dynamics of their two-dimensional counterparts have yet to be fully deciphered.

A recent study employed advanced transient spectroscopic methods combined with theoretical modeling to uncover the presence of small polarons in Dion-Jacobson phase 2D perovskites, particularly in the compound (4AMP)PbI4. Researchers determined that strong charge-lattice coupling induces a substantial deformation potential of 123 eV-approximately 30 times greater than those typically observed in conventional 2D and 3D perovskites. This extraordinary interaction significantly influences carrier dynamics within the material.

Utilizing optical Kerr spectroscopy, the research team identified extended polarization response times at room temperature, surpassing 600 ps. The study attributes this prolonged response to the formation of small polarons, which span roughly two-unit cells in size due to the lattice distortions present in the material. Additional investigations involving temperature-dependent phonon studies, spin relaxation analyses, and X-ray diffraction further substantiated the presence of these small polarons. These findings highlight their role in modifying excitonic Coulomb exchange interactions, leading to an up to tenfold increase in spin lifetime.

Implications for Optoelectronic Advancements

This discovery holds considerable promise for the future of optoelectronic device engineering. By elucidating the impact of small polaron formation on spin dynamics, researchers can refine 2D perovskite materials to achieve superior carrier mobility, extended spin lifetimes, and enhanced energy conversion efficiency. Such improvements could accelerate the development of next-generation solar cells, photodetectors, and spintronic devices.

The study also paves the way for tailoring charge-lattice interactions through controlled deformation potential tuning, potentially optimizing perovskite-based device performance. Future investigations may delve deeper into fine-tuning polaronic effects to further capitalize on their benefits in commercial applications.

Future Prospects

This research provides direct evidence of small polaron formation in Dion-Jacobson phase 2D perovskites, underscoring the critical influence of lattice interactions on spin dynamics and optoelectronic efficiency. Continued exploration of these mechanisms is expected to drive the development of novel materials that could redefine perovskite-based optoelectronics. These findings mark a significant step toward realizing energy-efficient, high-performance electronic and photonic devices.

Research Report:Giant deformation potential induced small polaron effect in Dion-Jacobson two-dimensional lead halide perovskites

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Solar Energy

Cheap and environmentally friendly – the next generation LEDs may soon be here

Published

1 day ago

March 13, 2025

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Cheap and environmentally friendly – the next generation LEDs may soon be here

by Anders Torneholm

Linkoping, Sweden (SPX) Mar 13, 2025

Cost, technical performance and environmental impact – these are the three most important aspects for a new type of LED technology to have a broad commercial impact on society. This has been demonstrated by researchers at Linkoping University in a study published in Nature Sustainability.

“Perovskite LEDs are cheaper and easier to manufacture than traditional LEDs, and they can also produce vibrant and intense colours if used in screens. I’d say that this is the next generation of LED technology,” says Feng Gao, professor of optoelectronics at Linkoping University.

However, for a technological shift to take place, where today’s LEDs are replaced with those based on the material perovskite, more than just technical performance is required. That is why Feng Gao’s research group has collaborated with Professor Olof Hjelm and John Laurence Esguerra, assistant professor at LiU. They specialise in how innovations contributing to environmental sustainability can be introduced to the market.

Together, they have investigated the environmental impact and cost of 18 different perovskite LEDs, knowledge that is currently incomplete. The study was conducted using so-called life cycle assessment and techno-economic assessment.

Such analyses require a clear system definition – that is, what is included and not in terms of cost and environmental impact. Within this framework, what happens from the product being created until it can no longer be used is investigated. The life cycle of the product, from cradle to grave, can be divided into five different phases: raw material production, manufacturing, distribution, use and decommissioning.

“We’d like to avoid the grave. And things get more complicated when you take recycling into account. But here we show that it’s most important to think about the reuse of organic solvents and how raw materials are produced, especially if they are rare materials,” says Olof Hjelm.

One example where the life cycle analysis provides guidance concerns the small amount of toxic lead found in perovskite LEDs. This is currently necessary for the perovskites to be effective. But, according to Olof Hjelm, focusing only on lead is a mistake. There are also many other materials in LEDs, such as gold.

“Gold production is extremely toxic. There are byproducts such as mercury and cyanide. It’s also very energy-consuming,” he says.

The greatest environmental gain would instead be achieved by replacing gold with copper, aluminium or nickel, while maintaining the small amount of lead needed for the LED to function optimally.

The researchers have concluded that perovskite LEDs have great potential for commercialisation in the long term. Maybe they can even replace today’s LEDs, thanks to lower costs and less environmental impact. The big issue is longevity. However, the development of perovskite LEDs is accelerating and their life expectancy is increasing. The researchers believe that it needs to reach about 10,000 hours for a positive environmental impact, something they think is achievable. Today, the best perovskite LEDs last for hundreds of hours.

Muyi Zhang, PhD student at the Department of Physics, Chemistry and Biology at LiU, says that much of the research focus so far is on increasing the technical performance of LED, something he believes will change.

“We want what we develop to be used in the real world. But then, we as researchers need to broaden our perspective. If a product has high technical performance but is expensive and isn’t environmentally sustainable, it may not be highly competitive in the market. That mindset will increasingly come to guide our research.”

Research Report:Towards sustainable perovskite light-emitting diodes