TY - JOUR
T1 - Solid-State Hydroxide Ion Conductivity in Silver(I) Oxide, Ag2O
AU - Schulte, Leanna
AU - Qin, Shihan
AU - Jung, Wonil
AU - George, Christy
AU - Dillenburger, Jarrett D.
AU - Venkatesh, Akshay
AU - Ishak, Muhammad K.
AU - Wonderling, Nichole M.
AU - Marth, Sariah
AU - Park, Heemin
AU - Bae, Chulsung
AU - Rappe, Andrew M.
AU - Mallouk, Thomas E.
N1 - Publisher Copyright:
© 2024 American Chemical Society.
PY - 2024/12/10
Y1 - 2024/12/10
N2 - Silver(I) oxide, Ag2O, precipitated as microcrystals by combining aqueous silver(I) nitrate and KOH solutions, was found to be a solid-state hydroxide ion conductor with ionic conductivity on the order of 10-3 S/cm. The proton chemical shifts at 4.87 and −7.35 ppm measured by solid-state 1H NMR experiments are attributed to water molecules and in-lattice OH- coordinated to silver, respectively. The lack of spinning sidebands around the 4.87 ppm peak indicates rapid reorientation on the NMR time scale, suggesting that the water molecules are adsorbed to the surface of the Ag2O crystals. Pulsed field gradient measurements gave similar diffusion coefficients (2 × 10-7 cm2/s at 298 K) for all three proton environments, indicating chemical exchange between sites on the millisecond time scale. The activation energy for OH- diffusion measured by NMR (0.18 eV) was comparable to that obtained by conductivity measurements and density functional theory (DFT) electronic structure calculations. The calculated Pourbaix diagram of Ag2O is consistent with the slightly lower sample density observed in He pycnometry and thermogravimetric measurements.
AB - Silver(I) oxide, Ag2O, precipitated as microcrystals by combining aqueous silver(I) nitrate and KOH solutions, was found to be a solid-state hydroxide ion conductor with ionic conductivity on the order of 10-3 S/cm. The proton chemical shifts at 4.87 and −7.35 ppm measured by solid-state 1H NMR experiments are attributed to water molecules and in-lattice OH- coordinated to silver, respectively. The lack of spinning sidebands around the 4.87 ppm peak indicates rapid reorientation on the NMR time scale, suggesting that the water molecules are adsorbed to the surface of the Ag2O crystals. Pulsed field gradient measurements gave similar diffusion coefficients (2 × 10-7 cm2/s at 298 K) for all three proton environments, indicating chemical exchange between sites on the millisecond time scale. The activation energy for OH- diffusion measured by NMR (0.18 eV) was comparable to that obtained by conductivity measurements and density functional theory (DFT) electronic structure calculations. The calculated Pourbaix diagram of Ag2O is consistent with the slightly lower sample density observed in He pycnometry and thermogravimetric measurements.
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U2 - 10.1021/acs.chemmater.4c02082
DO - 10.1021/acs.chemmater.4c02082
M3 - Article
AN - SCOPUS:85210272015
SN - 0897-4756
VL - 36
SP - 11440
EP - 11448
JO - Chemistry of Materials
JF - Chemistry of Materials
IS - 23
ER -