The structural, electronic, phonon dispersion and thermodynamic properties of MHCO 3 (M = Li, Na, K) solids were investigated using density functional theory. The calculated bulk properties for both their ambient and the high-pressure phases are in good agreement with available experimental measurements. Solid phase LiHCO 3 has not yet been observed experimentally. We have predicted several possible crystal structures for LiHCO 3 using crystallographic database searching and prototype electrostatic ground state modeling. Our total energy and phonon free energy (F PH ) calculations predict that LiHCO 3 will be stable under suitable conditions of temperature and partial pressures of CO 2 and H 2 O. Our calculations indicate that the HCO − 3 groups in LiHCO 3 and NaHCO 3 form an infinite chain structure through O · · · H · · · O hydrogen bonds. In contrast, the HCO − 3 anions form dimers, (HCO − 3 ) 2 , connected through double hydrogen bonds in all phases of KHCO 3 . Based on density functional perturbation theory, the Born effective charge tensor of each atom type was obtained for all phases of the bicarbonates. Their phonon dispersions with the longitudinal optical-transverse optical splitting were also investigated. Based on lattice phonon dynamics study, the infrared spectra and the thermodynamic properties of these bicarbonates were obtained. Over the temperature range 0-900 K, the F PH and the entropies (S) of MHCO 3 (M = Li, Na, K) systems vary as F PH (LiHCO 3 ) > F PH (NaHCO 3 ) > F PH (KHCO 3 ) and S(KHCO 3 ) > S(NaHCO 3 ) > S(LiHCO 3 ), respectively, in agreement with the available experimental data. Analysis of the predicted thermodynamics of the CO 2 capture reactions indicates that the carbonate/bicarbonate transition reactions for Na and K could be used for CO 2 capture technology, in agreement with experiments.