Research News:Porous Silicon Oxide Electrodes: A Breakthrough Towards Sustainable Energy Storage

Researchers investigate a promising strategy for fixing durability issues in all-solid-state batteries

All-solid-state batteries are safer and more durable alternatives to traditional lithium-ion batteries, but the cracking anddetaching of silicon-based electrodes due to expansion and contraction limits their potential. In a recent study, researchers from Japan developed porous silicon oxide electrodes to address this issue. The pores helped reduce the stress at the electrode-electrolyte interface, vastly improving performance, durability, and capacity. These findings bring us closer to long-lasting all-solid-state batteries for renewable energy and electric vehicles.

Batteries have become an integral component of modern technology. Lithium-ion batteries (LIBs) can be found virtually everywhere, from handheld electronic devices and electric vehicles to the large power banks used in renewable energy generation systems. However, current LIB designs suffer from some crippling drawbacks, including low durability and the use of toxic liquid electrolytes.

To address these limitations, scientists have been studying all-solid-state batteries for over a decade. Although silicon-based all-solid-state batteries should be theoretically more durable than conventional LIBs, an unsolved challenge still stands before this becomes a reality. When a Si-based all-solid-state battery undergoes charge/discharge cycles, the negative Si electrode repeatedly expands and contracts. This puts a lot of mechanical stress on the interface between the electrode and the stiff solid electrolyte, causing the former to ultimately crack, detach, and suffer an irreversible dip in performance.

Against this backdrop, a research team led by Professor Takayuki Doi from Doshisha University, Japan, explored a promising solution for all-solid-state batteries. As explained in their latest paper, which was made available online and published in ACS Applied Materials & Interfaces on October 29, 2024, the researchers investigated whether adding pores to a silicon oxide (SiO_x) electrode could prevent the cracking and peeling problems caused by the expansion and contraction seen in Si electrodes. This study was co-authored by Dr. Kohei Marumoto from Doshisha University, Japan, and Dr. Kiyotaka Nakano from Hitachi High-Tech Corporation, Japan.

To test their hypothesis, the researchers synthesized porous SiO_x electrodes via radiofrequency sputtering and used them to fabricate various all-solid-state cells, using Li-La-Zr-Ta-O (LLZTO) as a solid electrolyte. They analyzed the obtained pore structures in detail using advanced scanning electron microscopy techniques and investigated their correlation with the overall performance of the cells after repeated charge/discharge cycles.

Interestingly, the highly porous SiO_x electrodes offered much better cycling performance compared to non-porous SiO_x, which suffered from a massive capacity drop after cycling. Microscopy observations clearly explained what was going on at the nanometer scale. “Non-porous SiO_x partially exfoliated from the LLZTO electrolyte by the 20^th cycle, which was consistent with the drastic decline in capacity and rise in internal resistance we observed,” says Dr. Doi. Adding further, he says, “In contrast, though the initially observed pore structure of porous SiO_x collapsed through repeated expansion and contraction, the remaining pores still served as a buffer against the internal and interfacial stresses. This ultimately helped maintain the interfacial joint between the electrode and the electrolyte.”

One pressing limitation of both Si and SiO_x electrodes in all-solid-state batteries is that their thickness must be kept extremely low (less than a micrometer) to prevent cracking and exfoliation. However, after adding pores to SiO_x, stable charge-discharge cycles could be obtained even in SiO_x films as thick as 5 µm. This translates to a massive boost in terms of space efficiency, as more energy can be stored per unit volume. “The thicker SiO_x films we achieved resulted in an energy density of the negative electrode approximately 17 times higher than that of conventional non-porous silicon electrodes,” highlights Dr. Doi.

Taken together, the findings of this study shed light on how porous structures can be leveraged to unlock the true potential of all-solid-state batteries. Such energy-storing devices will play a crucial role in charting our path towards sustainable societies, given their promising applications in domestic and industrial-scale energy generation. Moreover, thanks to their enhanced safety profile and longer lives, all-solid-state batteries could make electric vehicles a much more attractive option for consumers. “We expect the results of our research to make a multifaceted contribution towards sustainable development goals, not only in terms of climate change countermeasures based on the reduction of carbon emissions, but also in terms of economic growth and urban development,” adds Dr. Doi, while sharing his concluding thoughts.

Further studies will be needed to fully optimize the porous structure of solid SiO_x electrolytes to achieve maximum performance in all-solid-state batteries. With much luck, future developments in this exciting field will lead to a much-needed breakthrough in energy storage.

Reference

Title of original paper	Tailored Design of a Nanoporous Structure Suitable for Thick Si Electrodes on a Stiff Oxide-Based Solid Electrolyte
Journal	ACS Applied Materials & Interfaces
DOI	10.1021/acsami.4c15894

Funding information

This work was supported by the Japan Society for the Promotion of Science (JSPS) Grants-in-Aid for Scientific Research (KAKENHI) 22H04624, Grant-in-Aid for Scientific Research on Innovation Areas “Interface Ionics.”

EurekAlert!

https://www.eurekalert.org/news-releases/1068170

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Takayuki Doi

Professor, Faculty of Science and Engineering Department of Molecular Chemistry and Biochemistry

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Organization for Research Initiatives & Development
Doshisha University
Kyotanabe, Kyoto 610-0394, JAPAN
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