Tunable Thermal Expansion from Negative, Zero, to Positive in Cubic Prussian Blue Analogues of GaFe(CN)6
Author(s) -
Qilong Gao,
Naike Shi,
Andrea Sanson,
Yu Sun,
Ruggero Milazzo,
Luca Olivi,
He Zhu,
Saul H. Lapidus,
Lirong Zheng,
Jun Chen,
Xianran Xing
Publication year - 2018
Publication title -
inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.348
H-Index - 233
eISSN - 1520-510X
pISSN - 0020-1669
DOI - 10.1021/acs.inorgchem.8b02428
Subject(s) - prussian blue , negative thermal expansion , chemistry , thermal expansion , ion , molecule , intercalation (chemistry) , phonon , thermal , blueshift , electrochemistry , inorganic chemistry , condensed matter physics , thermodynamics , electrode , organic chemistry , optoelectronics , photoluminescence , physics
The achievement of controlling thermal expansion is important for open-framework structures. The present work proposes a feasible way to adjust the coefficient of thermal expansion continuously from negative to positive via inserting guest Na + ions or H 2 O molecules into a GaFe(CN) 6 framework. The guest ions or molecules have an intense dampening effect on the transverse vibrations of CN atoms in the -Ga-N≡C-Fe- linkage, especially for the N atoms. This study demonstrates that electrochemical or redox intercalation of guest ions will be an effective way to tune thermal expansion in those negative thermal expansion open-framework materials induced by low-frequency phonons.
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