Open Research will be updating the system on Tuesday, 14 July 2026, from 8:15 to 9:00 AM. We apologise for any inconvenience caused.

Cultural advice

The Australian National University acknowledges, celebrates and pays our respects to the Ngunnawal and Ngambri people of the Canberra region and to all First Nations Australians on whose traditional lands we meet and work, and whose cultures are among the oldest continuing cultures in human history.

Aboriginal and Torres Strait Islander peoples are advised that ANU Library collections may include images, names, voices, and other representations of deceased persons.

Material in the collection may contain terms, language or views that reflect the period in which the item was created and may be considered inappropriate today.

A broad pore size distribution mesoporous SnO 2 as anode for lithium-ion batteries

Loading...
Thumbnail Image

Date

Authors

Shiva, Konda
Mangalampalli, S.R.N. Kiran
Ramamurty, U
Asokan, S
Bhattacharyya, A.J.

Journal Title

Journal ISSN

Volume Title

Publisher

Springer

Abstract

We demonstrate here that mesoporous tin dioxide (abbreviated M-SnO2) with a broad pore size distribution can be a prospective anode in lithium-ion batteries. M-SnO2 with pore size ranging between 2 and 7.5 nm was synthesized using a hydrothermal procedure involving two different surfactants of slightly different sizes, and characterized. The irreversible capacity loss that occurs during the first discharge and charge cycle is 890 mAh g-1, which is smaller than the 1,010-mAh g-1 loss recorded for mesoporous SnO2 (abbreviated S-SnO2) synthesized using a single surfactant. After 50 cycles, the discharge capacity of M-SnO2 (504 mAh g-1) is higher than that of S-SnO2 (401 mAh g-1) and solid nanoparticles of SnO2 (abbreviated nano-SnO2<4 mAh g-1) and nano-SnO2. Transmission electron microscopy revealed higher disorder in the pore arrangement in M-SnO2. This, in turn imparts lower stiffness to M-SnO2 (elastic modulus, ER≈14.5 GPa) vis-a-vis S-SnO2 (ER≈20.5 GPa), as obtained using the nanoindenta-tion technique. Thus, the superior battery performance of M-SnO2 is attributed to its intrinsic material mechanical property. The fluidity of the internal microstructure of M-SnO2 resulted in a lower degree of aggregation of Sn particles compared to S-SnO2 and nano-SnO2 structural stabilization and long-term cyclability.

Description

Citation

Source

Journal of Solid State Electrochemistry

Book Title

Entity type

Access Statement

License Rights

Restricted until

2037-12-31
abcd