26. September 2013
Towards sodium ion batteries – understanding sodium dynamics on a microscopic levelResearch Using Neutrons Matter and Material Storage
Lithium ion batteries are highly efficient and provide electrical energy for laptops, mobile phones and lately also for the growing electric car market. But there are drawbacks to this technology: lithium is expensive and its extraction rather harmful to the environment. One possible alternative might be to substitute lithium with sodium – an element with similar chemical properties but much more abundant. Charging and discharging these batteries occurs via ion migration in and out of the battery electrodes. Therefore, to be able to develop the necessary sodium-based batteries, it is crucial to understand how sodium ions move in the relevant materials. Now, for the first time, scientists at the Paul Scherrer Institute PSI have determined the paths along which sodium ions move in a prospective battery material. They prepared the compound Na0.7CoO2 and investigated it using neutron-scattering at SINQ, the PSI’s Swiss neutron source. It turns out that the paths along which the ions move inside the electrode change with temperature and are directly connected to very small changes in the atomic structure of the material. With these results, one can now start to think of new and specific ways to manipulate the materials through slight changes to their structure or composition, for example – and thereby achieve the optimized material properties necessary for use in future batteries. The results have now been published in the journal Physical Review Letters.
Sodium as alternative to lithium in batteries
One option to avoid these drawbacks might be to replace lithium (Li) with sodium (Na) in electrode materials for rechargeable batteries. Sodium is similar to lithium in terms of its chemical properties, but approximately 1,000 times more abundant in the ground (26,000 ppm) and in the form of salt (NaCl) in normal seawater (15,000 ppm). This makes sodium-based batteries potentially more environmentally friendly and easier to recycle, as well as up to five times less expensive. However, sodium ions are bigger and heavier than lithium ions and nominally the operating voltage is somewhat lower. As a result, sodium-based batteries are initially expected to have a lower energy density (Wh/kg), making them larger than present lithium ion batteries. But this is obviously not a significant drawback for using them in stationary energy storage applications such as batteries storing excess energy at a wind turbine or solar panel.
In both types of batteries, the operating principle is that ions are shuttled between the battery’s positive and negative electrodes during charging and discharging, with an electrolyte serving as the medium for ion transport. In order to develop novel batteries, one has to study the current key-materials and understand the fundamental processes of ion movement on an atomic scale. A research team at the Paul Scherrer Institute in collaboration with researchers from ETH Zurich and Japan (Toyota Central Research and Development Laboratories Inc. and the Comprehensive Research Organization for Science and Society) has now investigated the material Na0.7CoO, which is similar to the most common Li-ion battery cathode material, but where the lithium has been replaced with sodium. It is built up from alternating atomic layers of cobalt oxide and sodium ions. The main goal was to study how the sodium ions move within their layer and how the structure of the material might change during such a process.
Small changes in structure mean big changes in dynamics
Most studies of ion conduction can only provide approximate information on how fast the ions are moving. In contrast to this, the PSI researchers used neutron-scattering, which is able to visualize the path of the ion movements on an atomic level. It turned out that the conduction path of the sodium ions depends considerably on temperature.
For temperatures below 15°C, the sodium ions can hardly move at all; for temperatures between 15°C and 130°C, they can only move in one dimension along special paths whereas at higher temperatures the ions can move freely within the whole sodium layer,explains Marisa Medarde, a materials scientist at the PSI and first author of the paper.
The changes in dynamics are connected to slight distortions in the structure of the material: above 130°C, the sodium ions have preferred positions within their layers that are arranged in a triangular pattern. Since the sides of these triangles are identical, hopping from corner to corner costs sodium ions the same energy independent of the direction of the movement. When the temperature decreases below 130°C, the thermal energy of the sodium ions is not enough for such a motion. As a wonder of nature, tiny changes occur in the arrangement of the preferred Sodium positions – one side of the triangles becomes shorter. Hopping between two corners separated by shorter distances costs less energy, so this small distortion makes sodium migration possible at unexpectedly low temperatures.
Learning to control the motion of ions in battery materials
The results give us a whole new degree of understanding of how complex the dynamics in these compounds and how small the effects needed to facilitate optimal conditions for the motion of ions are, explains Martin Månsson, a battery and materials researcher at PSI.
This understanding may enable us to learn how to control and optimize the transport of ions in battery materials. This could partly mean substituting one chemical element with another in present materials, applying external pressure or developing completely new compounds with a designed atomic structure.
Exploring materials with neutrons
In their investigations, the scientists used the Swiss neutron source of the Paul Scherrer Institute (SINQ). Such an experiment involves sending a beam of neutrons through the Na0.7CoO2 sample. Some of these neutrons interact with the sample and change their direction of flight; they are scattered. The number of neutrons deflected in each direction contains information on the inner atomic structure of the material: well-defined peaks appear for particular directions corresponding to regular arrangements of the atoms and ions in the material. In this case, one of these peaks clearly divides into two peaks below 130°C. This means that the distances between the preferred sodium positions are no longer equal and correspond to a slightly distorted triangular pattern within the ion planes. Such a subtle distortion of the atomic structure seems to be the key to opening the ion diffusion channels in this material.
About PSIThe Paul Scherrer Institute develops, builds and operates large, complex research facilities, and makes them available to the national and international research community. The Institute's own key research priorities are in the investigation of matter and material, energy and the environment; and human health. PSI is Switzerland's largest research institution, with 1500 members of staff and an annual budget of approximately 300 million CHF.
ContactDr. Marisa Medarde, Laboratory for Developments and Methods (LDM) LDM,
Paul Scherrer Institut, 5232 Villigen PSI, Switzerland;
Telephone: +41 56 310 3283; Email: firstname.lastname@example.org
Dr. Martin Månsson, Laboratory for Neutron Scattering LNS, Paul Scherrer Institut, 5232 Villigen PSI und
Laboratory for Quantum Magnetism (LQM), École polytechnique fédérale de Lausanne (EPFL), 1015 Lausanne, Switzerland;
Telephone: +41 56 310 5534; Email: email@example.com
Original Publication1D to 2D Na+ Ion Diffusion Inherently Linked to Structural Transitions in Na0.7CoO2
M. Medarde, M. Mena, J. L. Gavilano, E. Pomjakushina, J. Sugiyama, K. Kamazawa, V. Yu. Pomjakushin, D. Sheptyakov, B. Batlogg, H. R. Ott, M. Månsson, and F. Juranyi
Phys. Rev. Lett. 110, 266401 (2013),