Research offer direct view of tantalum oxidation that impedes qubit coherence

Scientists at the U.S. Department of Energy’s (DOE) Brookhaven National Laboratory and DOE’s Pacific Northwest National Laboratory (PNNL) have used a combination of scanning transmission electron microscopy (STEM) and computational modeling to get a closer look and deeper understanding of tantalum oxide. When this amorphous oxide layer forms on the surface of tantalum—a superconductor that shows great promise for making the “qubit” building blocks of a quantum computer—it can impede the material’s ability to retain quantum information.

Learning how the oxide forms may offer clues as to why this happens—and potentially point to ways to prevent quantum coherence loss. The research was recently published in the journal ACS Nano.

The paper builds on earlier research by a team at Brookhaven’s Center for Functional Nanomaterials (CFN), Brookhaven’s National Synchrotron Light Source II (NSLS-II), and Princeton University that was conducted as part of the Co-design Center for Quantum Advantage (C2QA), a Brookhaven-led national quantum information science research center in which Princeton is a key partner.

“In that work, we used X-ray photoemission spectroscopy at NSLS-II to infer details about the type of oxide that forms on the surface of tantalum when it is exposed to oxygen in the air,” said Mingzhao Liu, a CFN scientist and one of the lead authors on the study. “But we wanted to understand more about the chemistry of this very thin layer of oxide by making direct measurements,” he explained.

So, in the new study, the team partnered with scientists in Brookhaven’s Condensed Matter Physics & Materials Science (CMPMS) Department to use advanced STEM techniques that enabled them to study the ultrathin oxide layer directly. They also worked with theorists at PNNL who performed computational modeling that revealed the most likely arrangements and interactions of atoms in the material as they underwent oxidation.

Together, these methods helped the team build an atomic-level understanding of the ordered crystalline lattice of tantalum metal, the amorphous oxide that forms on its surface, and intriguing new details about the interface between these layers.

“The key is to understand the interface between the surface oxide layer and the tantalum film because this interface can profoundly impact qubit performance,” said study co-author Yimei Zhu, a physicist from CMPMS, echoing the wisdom of Nobel laureate Herbert Kroemer, who famously asserted, “The interface is the device.”

Emphasizing that “quantitatively probing a mere one-to-two-atomic-layer-thick interface poses a formidable challenge,” Zhu noted, “we were able to directly measure the atomic structures and bonding states of the oxide layer and tantalum film as well as identify those of the interface using the advanced electron microscopy techniques developed at Brookhaven.”

“The measurements reveal that the interface consists of a ‘suboxide’ layer nestled between the periodically ordered tantalum atoms and the fully disordered amorphous tantalum oxide. Within this suboxide layer, only a few oxygen atoms are integrated into the tantalum crystal lattice,” Zhu said.

The combined structural and chemical measurements offer a crucially detailed perspective on the material. Density functional theory calculations then helped the scientists validate and gain deeper insight into these observations.

“We simulated the effect of gradual surface oxidation by gradually increasing the number of oxygen species at the surface and in the subsurface region,” said Peter Sushko, one of the PNNL theorists.

By assessing the thermodynamic stability, structure, and electronic property changes of the tantalum films during oxidation, the scientists concluded that while the fully oxidized amorphous layer acts as an insulator, the suboxide layer retains features of a metal.

“We always thought if the tantalum is oxidized, it becomes completely amorphous, with no crystalline order at all,” said Liu. “But in the suboxide layer, the tantalum sites are still quite ordered.”

With the presence of both fully oxidized tantalum and a suboxide layer, the scientists wanted to understand which part is most responsible the loss of coherence in qubits made of this superconducting material.

“It’s likely the oxide has multiple roles,” Liu said.

First, he noted, the fully oxidized amorphous layer contains many lattice defects. That is, the locations of the atoms are not well defined. Some atoms can shift around to different configurations, each with a different energy level. Though these shifts are small, each one consumes a tiny bit of electrical energy, which contributes to loss of energy from the qubit.

“This so-called two-level system loss in an amorphous material brings parasitic and irreversible loss to the quantum coherence—the ability of the material to hold onto quantum information,” Liu said.

But because the suboxide layer is still crystalline, “it may not be as bad as people were thinking,” Liu said. Maybe the more fixed atomic arrangements in this layer will minimize two-level system loss.

Then again, he noted, because the suboxide layer has some metallic characteristics, it could cause other problems.

“When you put a normal metal next to a superconductor, that could contribute to breaking up the pairs of electrons that move through the material with no resistance,” he noted. “If the pair breaks into two electrons again, then you will have loss of superconductivity and coherence. And that is not what you want.”

Future studies may reveal more details and strategies for preventing loss of superconductivity and quantum coherence in tantalum.

More information:
Junsik Mun et al, Probing Oxidation-Driven Amorphized Surfaces in a Ta(110) Film for Superconducting Qubit, ACS Nano (2023). DOI: 10.1021/acsnano.3c10740

Provided by
Brookhaven National Laboratory

Citation:
Research offer direct view of tantalum oxidation that impedes qubit coherence (2024, February 5)

Subscribe
Don't miss the best news ! Subscribe to our free newsletter :