Tag Archives: Lev N. Zakharov

A new, stable open-shell carbon molecule from Oregon

This discovery could one day make organic solar cells more efficient than silicon ones. Researchers at the University of Oregon announced their discovery in a June 9, 2016 news item on ScienceDaily,

University of Oregon chemists have synthesized a stable and long-lasting carbon-based molecule that, they say, potentially could be applicable in solar cells and electronic devices.

The molecule changes its bonding patterns to a magnetic biradical state when heated; it then returns to a fully bonded non-magnetic closed state at room temperature. That transition, they report, can be done repeatedly without decomposition. It remains stable in the presence of both heat and oxygen.

A June 9, 2016 University of Oregon news release on EurekAlert, which originated the news item, provides more detail,

 

Biradical refers to organic compounds, known as open-shell molecules, that have two free-flowing, non-bonding electrons. Producing them using techniques to control their electron spin, and thus provide semiconducting properties, in a heated state has been hampered by instability since the first synthetic biradical hydrocarbon was made in 1907.

“Potentially our approach could help to make organic solar cells more efficient than silicon solar cells, but that’s probably far in the future,” said UO doctoral student Gabriel E. Rudebusch, the paper’s lead author. “Our synthesis is rapid and efficient. We easily can make a gram of this compound, which is very stable when exposed to oxygen and heat. This stability has been almost unheard of in the literature about biradical compounds.”

The four-step synthesis of the compound — diindenoanthracene, or DIAn — and how it held up when tested in superconducting materials were detailed in a proof-of-principle paper published online May 23 by the journal Nature Chemistry. The UO team collaborated with experts in Japan, Spain and Sweden.

The molecular framework for the new molecule involves the hydrocarbon anthracene, which has three linearly fused hexagonal benzene rings, in combination with two five-membered pentagonal rings.

“The big difference between our new molecule and a lot of other biradical molecules that have been produced is those five-membered rings,” said co-author Michael M. Haley, who holds the UO’s Richard M. and Patricia H. Noyes Professorship in Chemistry. “They have the inherent ability to accept electrons or give up electrons. This means DIAn can move both negative and positive charges, which is an essential property for useful devices such as transistors and solar cells. Also, we can heat up our molecule to 150 degrees Celsius, bring it back to room temperature and heat it up again, repeatedly, and we see no decomposition in its reaction to oxygen. The unique features of DIAn are essential if these molecules are to have a use in the real world.”

Haley’s lab is now seeking to develop derivatives of the new molecule to help move the technology forward into potential applications.

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

Diindeno-fusion of an anthracene as a design strategy for stable organic biradicals by Gabriel E. Rudebusch, José L. Zafra, Kjell Jorner, Kotaro Fukuda, Jonathan L. Marshall, Iratxe Arrechea-Marcos, Guzmán L. Espejo, Rocío Ponce Ortiz, Carlos J. Gómez-García, Lev N. Zakharov, Masayoshi Nakano, Henrik Ottosson, Juan Casado & Michael M. Haley. Nature Chemistry (2016)  doi:10.1038/nchem.2518 Published online 23 May 2016

This paper is behind a paywall.

There is another June 9, 2016 University of Oregon news release by Jim Barlow about this discovery. It covers much of the same material but focuses more closely on Rudebusch’s perspective.

Transmetalation, substituting one set of metal atoms for another set

Transmetalation bears a resemblance of sorts to transmutation. While the chemists from the University of Oregon aren’t turning lead to gold through an alchemical process they are switching out individual metal atoms, aluminum for indium. From a July 21, 2014 news item on ScienceDaily,

The yield so far is small, but chemists at the University of Oregon have developed a low-energy, solution-based mineral substitution process to make a precursor to transparent thin films that could find use in electronics and alternative energy devices.

A paper describing the approach is highlighted on the cover of the July 21 [2014] issue of the journal Inorganic Chemistry, which draws the most citations of research in the inorganic and nuclear chemistry fields. [emphasis mine] The paper was chosen by the American Chemical Society journal as an ACS Editor’s Choice for its potential scientific and broad public interest when it initially published online.

One observation unrelated to the research, the competition amongst universities seems to be heating up. While journals often tout their impact factor, it’s usually more discreetly than in what amounts to a citation in the second paragraph of the university news release, which originated the news item.

The July 21, 2014 University of Oregon news release (also on EurekAlert), describes the work in more detail,

The process described in the paper represents a new approach to transmetalation, in which individual atoms of one metal complex — a cluster in this case — are individually substituted in water. For this study, Maisha K. Kamunde-Devonish and Milton N. Jackson Jr., doctoral students in the Department of Chemistry and Biochemistry, replaced aluminum atoms with indium atoms.

The goal is to develop inorganic clusters as precursors that result in dense thin films with negligible defects, resulting in new functional materials and thin-film metal oxides. The latter would have wide application in a variety of electronic devices.

“Since the numbers of compounds that fit this bill is small, we are looking at transmetelation as a method for creating new precursors with new combinations of metals that would circumvent barriers to performance,” Kamunde-Devonish said.

Components in these devices now use deposition techniques that require a lot of energy in the form of pressure or temperature. Doing so in a more green way — reducing chemical waste during preparation — could reduce manufacturing costs and allow for larger-scale materials, she said.

“In essence,” said co-author Darren W. Johnson, a professor of chemistry, “we can prepare one type of nanoscale cluster compound, and then step-by-step substitute out the individual metal atoms to make new clusters that cannot be made by direct methods. The cluster we report in this paper serves as an excellent solution precursor to make very smooth thin films of amorphous aluminum indium oxide, a semiconductor material that can be used in transparent thin-film transistors.”

Transmetalation normally involves a reaction done in organic chemistry in which the substitution of metal ions generates new metal-carbon bonds for use in catalytic systems and to synthesize new metal complexes.

“This is a new way to use the process,” Kamunde-Devonish said, “Usually you take smaller building blocks and put them together to form a mix of your basic two or three metals. Instead of building a house from the ground up, we’re doing some remodeling. In everyday life that happens regularly, but in chemistry it doesn’t happen very often. We’ve been trying to make materials, compounds, anything that can be useful to improve the processes to make thin films that find application in a variety of electronic devices.”

The process, she added, could be turned into a toolbox that allows for precise substitutions to generate specifically desired properties. “Currently, we can only make small amounts,” she said, “but the fact that we can do this will allow us to get a fundamental understanding of how this process happens. The technology is possible already. It’s just a matter of determining if this type of material we’ve produced is the best for the process.”

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

Transmetalation of Aqueous Inorganic Clusters: A Useful Route to the Synthesis of Heterometallic Aluminum and Indium Hydroxo—Aquo Clusters by Maisha K. Kamunde-Devonish, Milton N. Jackson, Jr., Zachary L. Mensinger, Lev N. Zakharov, and Darren W. Johnson. Inorg. Chem., 2014, 53 (14), pp 7101–7105 DOI: 10.1021/ic403121r Publication Date (Web): April 18, 2014

Copyright © 2014 American Chemical Society

This paper appears to be open access (I was able to view the HTML version when I clicked).