Another Stunning Graphene Experimental Surprise

Graphene, the extraordinary form of carbon that consists of a single layer of carbon atoms, has produced another in a long list of experimental surprises. In the current issue of the journal Science, a multi-institutional team of researchers headed by Michael Crommie, a faculty senior scientist in the Materials Sciences Division at the U.S. Department of Energy’s Lawrence Berkeley National Laboratory and a professor of physics at the University of California at Berkeley, reports the creation of pseudo-magnetic fields far stronger than the strongest magnetic fields ever sustained in a laboratory – just by putting the right kind of strain onto a patch of graphene.

“We have shown experimentally that when graphene is stretched to form nanobubbles on a platinum substrate, electrons behave as if they were subject to magnetic fields in excess of 300 tesla, even though no magnetic field has actually been applied,” says Crommie. “This is a completely new physical effect that has no counterpart in any other condensed matter system.”

Crommie notes that “for over 100 years people have been sticking materials into magnetic fields to see how the electrons behave, but it’s impossible to sustain tremendously strong magnetic fields in a laboratory setting.” The current record is 85 tesla for a field that lasts only thousandths of a second. When stronger fields are created, the magnets blow themselves apart. The ability to make electrons behave as if they were in magnetic fields of 300 tesla or more – just by stretching graphene – offers a new window on a source of important applications and fundamental scientific discoveries going back over a century. This is made possible by graphene’s electronic behavior, which is unlike any other material’s.

A carbon atom has four valence electrons; in graphene (and in graphite, a stack of graphene layers), three electrons bond in a plane with their neighbors to form a strong hexagonal pattern, like chicken-wire. The fourth electron sticks up out of the plane and is free to hop from one atom to the next. The latter pi-bond electrons act as if they have no mass at all, like photons. They can move at almost one percent of the speed of light. The idea that a deformation of graphene might lead to the appearance of a pseudo-magnetic field first arose even before graphene sheets had been isolated, in the context of carbon nanotubes (which are simply rolled-up graphene). In early 2010, theorist Francisco Guinea of the Institute of Materials Science of Madrid and his colleagues developed these ideas and predicted that if graphene could be stretched along its three main crystallographic directions, it would effectively act as though it were placed in a uniform magnetic field. This is because strain changes the bond lengths between atoms and affects the way electrons move between them. The pseudo-magnetic field would reveal itself through its effects on electron orbits.

In classical physics, electrons in a magnetic field travel in circles called cyclotron orbits. These were named following Ernest Lawrence’s invention of the cyclotron, because cyclotrons continuously accelerate charged particles (protons, in Lawrence’s case) in a curving path induced by a strong field. Viewed quantum mechanically, however, cyclotron orbits become quantized and exhibit discrete energy levels. Called Landau levels, these correspond to energies where constructive interference occurs in an orbiting electron’s quantum wave function. The number of electrons occupying each Landau level depends on the strength of the field – the stronger the field, the more energy spacing between Landau levels, and the denser the electron states become at each level – which is a key feature of the predicted pseudo-magnetic fields in graphene.

Describing their experimental discovery, Crommie says, “We had the benefit of a remarkable stroke of serendipity.”

Continue reading the press release Graphene Under Strain Creates Gigantic Pseudo-Magnetic Fields at Lawrence Berkeley National Laboratory’s News Center.

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