| Literature DB >> 25985060 |
Kwan Woo Nam1, Sangryun Kim1, Soyeon Lee2, Michael Salama3, Ivgeni Shterenberg3, Yossi Gofer3, Joo-Seong Kim1, Eunjeong Yang1, Chan Sun Park1, Ju-Sik Kim4, Seok-Soo Lee4, Won-Seok Chang4, Seok-Gwang Doo4, Yong Nam Jo5, Yousung Jung1, Doron Aurbach3, Jang Wook Choi1.
Abstract
Rechargeable magnesium batteries have lately received great attention for large-scale energy storage systems due to their high volumetric capacities, low materials cost, and safe characteristic. However, the bivalency of Mg(2+) ions has made it challenging to find cathode materials operating at high voltages with decent (de)intercalation kinetics. In an effort to overcome this challenge, we adopt an unconventional approach of engaging crystal water in the layered structure of Birnessite MnO2 because the crystal water can effectively screen electrostatic interactions between Mg(2+) ions and the host anions. The crucial role of the crystal water was revealed by directly visualizing its presence and dynamic rearrangement using scanning transmission electron microscopy (STEM). Moreover, the importance of lowering desolvation energy penalty at the cathode-electrolyte interface was elucidated by working with water containing nonaqueous electrolytes. In aqueous electrolytes, the decreased interfacial energy penalty by hydration of Mg(2+) allows Birnessite MnO2 to achieve a large reversible capacity (231.1 mAh g(-1)) at high operating voltage (2.8 V vs Mg/Mg(2+)) with excellent cycle life (62.5% retention after 10000 cycles), unveiling the importance of effective charge shielding in the host and facile Mg(2+) ions transfer through the cathode's interface.Entities:
Keywords: Birnessite; Magnesium batteries; aqueous batteries; charge screening; crystal water
Year: 2015 PMID: 25985060 DOI: 10.1021/acs.nanolett.5b01109
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 11.189