Tag Archives: Kaixiang Lin

Vitamin-inspired batteries

Vitamin-inspired batteries from Harvard University? According to a July 18, 2016 news item on ScienceDaily that’s exactly the case,

Harvard researchers have identified a whole new class of high-performing organic molecules, inspired by vitamin B2, that can safely store electricity from intermittent energy sources like solar and wind power in large batteries.

The development builds on previous work in which the team developed a high-capacity flow battery that stored energy in organic molecules called quinones and a food additive called ferrocyanide. That advance was a game-changer, delivering the first high-performance, non-flammable, non-toxic, non-corrosive, and low-cost chemicals that could enable large-scale, inexpensive electricity storage.

While the versatile quinones show great promise for flow batteries, Harvard researchers continued to explore other organic molecules in pursuit of even better performance. But finding that same versatility in other organic systems has been challenging.

“Now, after considering about a million different quinones, we have developed a new class of battery electrolyte material that expands the possibilities of what we can do,” said Kaixiang Lin, a Ph.D. student at Harvard and first author of the paper. “Its simple synthesis means it should be manufacturable on a large scale at a very low cost, which is an important goal of this project.”

A July 18, 2016 Harvard University John A. Paulson School of Engineering and Applied Sciences press release (also on EurekAlert) by Leah Burrows, which originated the news item, expands on the theme,

Flow batteries store energy in solutions in external tanks — the bigger the tanks, the more energy they store. In 2014, Michael J. Aziz, the Gene and Tracy Sykes Professor of Materials and Energy Technologies at the Harvard John A. Paulson School of Engineering and Applied Sciences (SEAS), Roy Gordon, the Thomas Dudley Cabot Professor of Chemistry and Professor of Materials Science, Alán Aspuru-Guzik, Professor of Chemistry and their team at Harvard replaced metal ions used as conventional battery electrolyte materials in acidic electrolytes with quinones, molecules that store energy in plants and animals. In 2015, they developed a quinone that could work in alkaline solutions alongside a common food additive.

In this most recent research, the team found inspiration in vitamin B2, which helps to store energy from food in the body. The key difference between B2 and quinones is that nitrogen atoms, instead of oxygen atoms, are involved in picking up and giving off electrons.

“With only a couple of tweaks to the original B2 molecule, this new group of molecules becomes a good candidate for alkaline flow batteries,” said Aziz.

“They have high stability and solubility and provide high battery voltage and storage capacity. Because vitamins are remarkably easy to make, this molecule could be manufactured on a large scale at a very low cost.”

“We designed these molecules to suit the needs of our battery, but really it was nature that hinted at this way to store energy,” said Gordon, co-senior author of the paper. “Nature came up with similar molecules that are very important in storing energy in our bodies.”

The team will continue to explore quinones, as well as this new universe of molecules, in pursuit of a high-performing, long-lasting and inexpensive flow battery.

Here’s a link to and a citation for the paper,

A redox-flow battery with an alloxazine-based organic electrolyte by Kaixiang Lin, Rafael Gómez-Bombarelli, Eugene S. Beh, Liuchuan Tong, Qing Chen, Alvaro Valle, Alán Aspuru-Guzik, Michael J. Aziz, & Roy G. Gordon.  Nature Energy 1, Article number: 16102 (2016)  doi:10.1038/nenergy.2016.102 Published online: 18 July 2016

This paper is behind a paywall.

A bioinspired approach to self-healing materials

Scientists have been working to develop self-healing materials for a while now and a Jan. 8, 2016 news item on Nanowerk chronicles a relatively recent attempt,

Inspired by healing wounds in skin, a new approach protects and heals surfaces using a fluid secretion process. In response to damage, dispersed liquid-storage droplets are controllably secreted. The stored liquid replenishes the surface and completes the repair of the polymer in seconds to hours …

The fluid secretion approach to repair the material has also been demonstrated in fibers and microbeads. This bioinspired approach could be extended to create highly desired adaptive, resilient materials with possible uses in heat transfer, humidity control, slippery surfaces, and fluid delivery.

A December ??, 2015 US Department of Energy (DOE) news release, which originated the news item, expands on the theme,

A polymer that secretes stored liquid in response to damage has been designed and created to function as a self-healing material. While human-made material systems can trigger the release of stored contents, the ability to continuously self-adjust and monitor liquid supply in these compartments is a challenge. In contrast, biological systems manage complex protection and healing functions by having individual components work in concert to initiate and self-regulate a coordinated response. Inspired by biological wound-healing, this new process, developed by researchers at Harvard University, involves trapping and dispersing liquid-storage droplets within a reversibly crosslinked polymer gel network topped with a thin liquid overlayer. This novel approach allows storage of the liquid, yet is reconfigurable to induce finely controlled secretion in response to polymer damage. When the gel was damaged by slicing, the ruptured droplets in the immediate vicinity of the damage released oil and the gel network was squeezed. This squeezing allowed oil to be pushed out from neighboring droplets and the polymer network linkages to unzip and rezip rapidly, allowing just enough oil to flow to the damaged region. Healing occurred at ambient temperature within seconds to hours as fluid was secreted into the crack, severed polymer ends diffused across the gap, and new network linkages were created. Droplet-embedded polymers repaired faster or at lower temperatures than polymers without oil droplets. Also, the repaired droplet-embedded materials were much stronger than the repaired networks that did not contain the droplets. This dynamic liquid exchange to repair the material has also been demonstrated in other forms, showing the potential to extend this bioinspired approach for fabricating highly desired adaptive, resilient materials to a wide range of polymeric structures.

Here’s a link to and a citation for the paper,

Dynamic polymer systems with self-regulated secretion for the control of surface properties and material healing by Jiaxi Cui, Daniel Daniel, Alison Grinthal, Kaixiang Lin, & Joanna Aizenberg. Nature Materials 14,  790–795 (2015) doi:10.1038/nmat4325 Published online 22 June 2015

I’m not sure what occasioned a late push to promote this particular piece of research but if you are interested, the paper is behind a paywall.