Solar Energy
Low-cost imaging technique shows how smartphone batteries could charge in minutes
Researchers have developed a simple lab-based technique that allows them to look inside lithium-ion batteries and follow lithium ions moving in real time as the batteries charge and discharge, something which has not been possible until now.
Using the low-cost technique, the researchers identified the speed-limiting processes which, if addressed, could enable the batteries in most smartphones and laptops to charge in as little as five minutes.
The researchers, from the University of Cambridge, say their technique will not only help improve existing battery materials, but could accelerate the development of next-generation batteries, one of the biggest technological hurdles to be overcome in the transition to a fossil fuel-free world. The results are reported in the journal Nature.
While lithium-ion batteries have undeniable advantages, such as relatively high energy densities and long lifetimes in comparison with other batteries and means of energy storage, they can also overheat or even explode, and are relatively expensive to produce. Additionally, their energy density is nowhere near that of petrol. So far, this makes them unsuitable for widespread use in two major clean technologies: electric cars and grid-scale storage for solar power.
“A better battery is one that can store a lot more energy or one that can charge much faster – ideally both,” said co-author Dr Christoph Schnedermann, from Cambridge’s Cavendish Laboratory. “But to make better batteries out of new materials, and to improve the batteries we’re already using, we need to understand what’s going on inside them.”
To improve lithium-ion batteries and help them charge faster, researchers need to follow and understand the processes occurring in functioning materials under realistic conditions in real time. Currently, this requires sophisticated synchrotron X-ray or electron microscopy techniques, which are time-consuming and expensive.
“To really study what’s happening inside a battery, you essentially have to get the microscope to do two things at once: it needs to observe batteries charging and discharging over a period of several hours, but at the same time it needs to capture very fast processes happening inside the battery,” said first author Alice Merryweather, a PhD student at Cambridge’s Cavendish Laboratory.
The Cambridge team developed an optical microscopy technique called interferometric scattering microscopy to observe these processes at work. Using this technique, they were able to observe individual particles of lithium cobalt oxide (often referred to as LCO) charging and discharging by measuring the amount of scattered light.They were able to see the LCO going through a series of phase transitions in the charge-discharge cycle. The phase boundaries within the LCO particles move and change as lithium ions go in and out. The researchers found that the mechanism of the moving boundary is different depending on whether the battery is charging or discharging.
“We found that there are different speed limits for lithium-ion batteries, depending on whether it’s charging or discharging,” said Dr Akshay Rao from the Cavendish Laboratory, who led the research. “When charging, the speed depends on how fast the lithium ions can pass through the particles of active material. When discharging, the speed depends on how fast the ions are inserted at the edges. If we can control these two mechanisms, it would enable lithium-ion batteries to charge much faster.”
“Given that lithium-ion batteries have been in use for decades, you’d think we know everything there is to know about them, but that’s not the case,” said Schnedermann. “This technique lets us see just how fast it might be able to go through a charge-discharge cycle. What we’re really looking forward to is using the technique to study next-generation battery materials – we can use what we learned about LCO to develop new materials.”
“The technique is a quite general way of looking at ion dynamics in solid state materials, so you can use it on almost any type of battery material,” said Professor Clare Grey, from Cambridge’s Yusuf Hamied Department of Chemistry, who co-led the research.
The high throughput nature of the methodology allows many particles to be sampled across the entire electrode and, moving forward, will enable further exploration of what happens when batteries fail and how to prevent it.
“This lab-based technique we’ve developed offers a huge change in technology speed so that we can keep up with the fast-moving inner workings of a battery,” said Schnedermann. “The fact that we can actually see these phase boundaries changing in real time was really surprising. This technique could be an important piece of the puzzle in the development of next-generation batteries.”
Solar Energy
Breakthrough new material brings affordable, sustainable future within grasp
Breakthrough new material brings affordable, sustainable future within grasp
by Rashda Khan for Canepa News
Houston TX (SPX) Dec 23, 2024
While lithium-ion batteries have been the go-to technology for everything from smartphones and laptops to electric cars, there are growing concerns about the future because lithium is relatively scarce, expensive and difficult to source, and may soon be at risk due to geopolitical considerations. Scientists around the world are working to create viable alternatives.
An international team of interdisciplinary researchers, including the Canepa Research Laboratory at the University of Houston, has developed a new type of material for sodium-ion batteries that could make them more efficient and boost their energy performance – paving the way for a more sustainable and affordable energy future.
The new material, sodium vanadium phosphate with the chemical formula NaxV2(PO4)3, improves sodium-ion battery performance by increasing the energy density – the amount of energy stored per kilogram – by more than 15%. With a higher energy density of 458 watt-hours per kilogram (Wh/kg) compared to the 396 Wh/kg in older sodium-ion batteries, this material brings sodium technology closer to competing with lithium-ion batteries.
“Sodium is nearly 50 times cheaper than lithium and can even be harvested from seawater, making it a much more sustainable option for large-scale energy storage,” said Pieremanuele Canepa, Robert Welch assistant professor of electrical and computer engineering at UH and lead researcher of the Canepa Lab. “Sodium-ion batteries could be cheaper and easier to produce, helping reduce reliance on lithium and making battery technology more accessible worldwide.”
From Theory to Reality
The Canepa Lab, which uses theoretical expertise and computational methods to discover new materials and molecules to help advance clean energy technologies, collaborated with the research groups headed by French researchers Christian Masquelier and Laurence Croguennec from the Laboratoire de Rea’ctivite’ et de Chimie des Solides, which is a CNRS laboratory part of the Universite’ de Picardie Jules Verne, in Amiens France, and the Institut de Chimie de la Matie`re Condense’e de Bordeaux, Universite’ de Bordeaux, Bordeaux, France for the experimental work on the project. This allowed theoretical modelling to go through experimental validation.
The researchers created a battery prototype using the new material, NaxV2(PO4)3, demonstrating significant energy storage improvements. NaxV2(PO4)3, part of a group called “Na superionic conductors” or NaSICONs, is designed to let sodium ions move smoothly in and out of the battery during charging and discharging.
Unlike existing materials, it has a unique way of handling sodium, allowing it to work as a single-phase system. This means it remains stable as it releases or takes in sodium ions. This allows the NaSICON to remain stable during charging and discharging while delivering a continuous voltage of 3.7 volts versus sodium metal, higher than the 3.37 volts in existing materials.
While this difference may seem small, it significantly increases the battery’s energy density or how much energy it can store for its weight. The key to its efficiency is vanadium, which can exist in multiple stable states, allowing it to hold and release more energy.
“The continuous voltage change is a key feature,” said Canepa. “It means the battery can perform more efficiently without compromising the electrode stability. That’s a game-changer for sodium-ion technology.”
Possibilities for a Sustainable Future
The implications of this work extend beyond sodium-ion batteries. The synthesis method used to create NaxV2(PO4)3 could be applied to other materials with similar chemistries, opening new possibilities for advanced energy storage technologies. That could in turn, impact everything from more affordable, sustainable batteries to power our devices to help us transition to a cleaner energy economy.
“Our goal is to find clean, sustainable solutions for energy storage,” Canepa said. “This material shows that sodium-ion batteries can meet the high-energy demands of modern technology while being cost-effective and environmentally friendly.”
A paper based on this work was published in the journal Nature Materials. Ziliang Wang, Canepa’s former student and now a postdoctoral fellow at Northwestern University, and Sunkyu Park, a former student of the French researchers and now a staff engineer at Samsung SDI in South Korea, performed much of the work on this project.
Research Report:Obtaining V2(PO4)3 by sodium extraction from single-phase NaxV2(PO4)3 (1 < x < 3) positive electrode materials
Related Links
Canepa Research Laboratory at the University of Houston
Powering The World in the 21st Century at Energy-Daily.com
Solar Energy
Pioneering advancements in solid-state battery technology for energy storage
Pioneering advancements in solid-state battery technology for energy storage
by Riko Seibo
Tokyo, Japan (SPX) Dec 23, 2024
Recent strides in solid-state battery technology are setting the stage for a transformative era in energy storage. These advancements hold promise for revolutionizing electric vehicles and renewable energy systems through improved performance and safety. A focus on electrolyte innovation has been key to this progress, enabling the development of high-performance all-solid-state batteries (ASSBs).
A new review paper provides a comprehensive summary of advancements in inorganic solid electrolytes (ISEs), materials that are central to ASSBs. Researchers examined the roles of oxides, sulfides, hydroborates, antiperovskites, and halides not only as electrolytes but also as catholytes and interface layers, which collectively enhance battery performance and safety.
“We highlighted the recent breakthroughs in synthesizing these materials, honing our attention on the innovative techniques that enable the precise tuning of their properties to meet the demanding requirements of ASSBs,” said Eric Jianfeng Cheng, associate professor at Tohoku University’s Advanced Institute for Materials Research (AIMR). “Precise tuning is crucial for developing batteries with higher energy densities, longer life cycles, and better safety profiles than conventional liquid-based batteries.”
The review also delves into the electrochemical properties of ISEs, including ionic conductivity, stability, and electrode compatibility. Researchers evaluated current ASSB models and suggested emerging strategies that could drive the next generation of energy storage solutions.
However, challenges persist in the development of ASSBs, notably the limited compatibility between ISEs and electrodes, which can trigger interfacial reactions. Addressing these compatibility issues is vital to improving battery efficiency and longevity. The review outlines these challenges and provides insights into efforts aimed at overcoming them.
“Our comprehensive review underscores the importance of continued research and development in the field of solid-state batteries. By developing new materials, improving synthesis methods, and overcoming compatibility issues, current efforts are driving innovation toward practical ASSBs that could transform how we store and use energy,” Cheng added.
Research Report:Inorganic solid electrolytes for all-solid-state lithium/sodium-ion batteries: recent developments and applications
Related Links
Tohoku University
Powering The World in the 21st Century at Energy-Daily.com
Solar Energy
Buried interface engineering drives advances in tin-lead perovskite solar cell efficiency
Buried interface engineering drives advances in tin-lead perovskite solar cell efficiency
by Simon Mansfield
Sydney, Australia (SPX) Dec 20, 2024
A team led by Prof. Meng Li from Henan University’s School of Nanoscience and Materials Engineering has unveiled an innovative approach to overcoming stability and efficiency challenges in tin-lead (Sn-Pb) perovskite solar cells. The researchers’ work focuses on optimizing the buried hole-selective interface using a specially designed self-assembled material, offering major implications for single-junction and tandem solar cell technologies.
Tin-lead perovskites are valued for their narrow bandgap properties, which position them as key materials for producing high-efficiency solar cells. However, energy level mismatches and degradation at the buried interface have constrained both their performance and long-term stability. Addressing these issues, Prof. Meng’s team designed a boronic acid-anchored hole-selective contact material, 4-(9H-carbazole-9-yl)phenylboronic acid (4PBA).
Compared to conventional materials, 4PBA demonstrated superior stability and compatibility at the substrate surface. Its high adsorption energy of -5.24 eV and significant molecular dipole moment (4.524 D) improved energy level alignment between the substrate and perovskite layer, facilitating efficient charge extraction. Additionally, the interface engineered using 4PBA improved perovskite crystallization and substrate contact, reducing defects and non-radiative recombination.
These advancements enabled Sn-Pb perovskite solar cells incorporating 4PBA to achieve a power conversion efficiency (PCE) of 23.45%. The material’s reduced corrosiveness also mitigated the degradation effects typically caused by PEDOT:PSS, a widely used hole-transport material, enhancing chemical stability and storage durability. The cells retained 93.5% of their initial efficiency after 2,000 hours of shelf storage.
“This approach offers a practical path to enhancing both the efficiency and stability of Sn-Pb perovskite solar cells, addressing energy level mismatches and interfacial stability concerns,” the research team commented.
The findings provide a foundation for advancing efficient and stable Sn-Pb perovskite solar cells and highlight the importance of interface engineering in next-generation photovoltaic technologies.
Research Report:Buried Hole-Selective Interface Engineering for High-Efficiency Tin-Lead Perovskite Solar Cells with Enhanced Interfacial Chemical Stability
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