TY - JOUR
T1 - Controlled Solvation Structure of a Zn Ion in an Aqueous Electrolyte by Amine Additives for Long Cycle Life of a Large Capacity Zn-Air Rechargeable Battery
AU - Ishihara, Tatsumi
AU - Inoishi, Yuiko
AU - Kim, Sun
AU - Staykov, Aleksandar
AU - Watanabe, Motonori
AU - Naohara, Nao
AU - Takahashi, Kimiko
AU - Itoh, Takashi
N1 - Publisher Copyright:
© 2023 American Chemical Society.
PY - 2023/4/13
Y1 - 2023/4/13
N2 - A rechargeable Zn-air battery is expected as a large capacity battery alternative to the Li ion battery; however, short cycle life is the current issue. In this study, it was found that the addition of 3,3-diaminodipropylamine was effective for preventing the formation of a Zn dendrite in the anode resulting in a long cycle life with more than 300 cycles and a discharge capacity larger than 700 mAh/g (>85% Zn used for discharge) when Ni0.8Fe0.2Co2O4 and 8 M KOH-H2O were used for the air electrode and electrolyte, respectively. The increased cycle stability could be assigned to the change in the solvated structure of Zn2+ in the electrolyte by the strong interaction between 3,3-diaminodipropylamine and solvated water, which is suggested by Raman and Fourier transform infrared spectroscopic analyses. Ab initio molecular dynamics simulations suggest that the amine is strongly interacted with OH of solvated water molecules and changes the coordination number of Zn2+, and as result, the size of the solvated Zn2+ cluster was increased, resulting in enhanced Zn2+ mobility in the electrolyte for the uniform deposition of Zn on the anode during charge by increased mobility.
AB - A rechargeable Zn-air battery is expected as a large capacity battery alternative to the Li ion battery; however, short cycle life is the current issue. In this study, it was found that the addition of 3,3-diaminodipropylamine was effective for preventing the formation of a Zn dendrite in the anode resulting in a long cycle life with more than 300 cycles and a discharge capacity larger than 700 mAh/g (>85% Zn used for discharge) when Ni0.8Fe0.2Co2O4 and 8 M KOH-H2O were used for the air electrode and electrolyte, respectively. The increased cycle stability could be assigned to the change in the solvated structure of Zn2+ in the electrolyte by the strong interaction between 3,3-diaminodipropylamine and solvated water, which is suggested by Raman and Fourier transform infrared spectroscopic analyses. Ab initio molecular dynamics simulations suggest that the amine is strongly interacted with OH of solvated water molecules and changes the coordination number of Zn2+, and as result, the size of the solvated Zn2+ cluster was increased, resulting in enhanced Zn2+ mobility in the electrolyte for the uniform deposition of Zn on the anode during charge by increased mobility.
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U2 - 10.1021/acs.jpcc.2c08682
DO - 10.1021/acs.jpcc.2c08682
M3 - Article
AN - SCOPUS:85152204932
SN - 1932-7447
VL - 127
SP - 6619
EP - 6628
JO - Journal of Physical Chemistry C
JF - Journal of Physical Chemistry C
IS - 14
ER -