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The dehydration mechanism of Na and K birnessites: a comprehensive multitechnique study.
André, E; Cornu, D; Pérez Ramírez, L; Durand, P; Gallet, J-J; Bournel, F; Rochet, F; Ruby, C; Carteret, C; Coustel, R.
Affiliation
  • André E; Université de Lorraine, CNRS, LCPME, F-54000 Nancy, France.
  • Cornu D; Université de Lorraine, CNRS, LCPME, F-54000 Nancy, France.
  • Pérez Ramírez L; Sorbonne Université, CNRS (UMR 7614), Laboratoire de Chimie Physique Matière et Rayonnement, 75252 Paris Cedex 05, France.
  • Durand P; Synchrotron SOLEIL, L'Orme des Merisiers, F-91192 Gif-sur-Yvette, France.
  • Gallet JJ; Université de Lorraine, CNRS, CRM2, F-54000 Nancy, France.
  • Bournel F; Sorbonne Université, CNRS (UMR 7614), Laboratoire de Chimie Physique Matière et Rayonnement, 75252 Paris Cedex 05, France.
  • Rochet F; Synchrotron SOLEIL, L'Orme des Merisiers, F-91192 Gif-sur-Yvette, France.
  • Ruby C; Sorbonne Université, CNRS (UMR 7614), Laboratoire de Chimie Physique Matière et Rayonnement, 75252 Paris Cedex 05, France.
  • Carteret C; Synchrotron SOLEIL, L'Orme des Merisiers, F-91192 Gif-sur-Yvette, France.
  • Coustel R; Sorbonne Université, CNRS (UMR 7614), Laboratoire de Chimie Physique Matière et Rayonnement, 75252 Paris Cedex 05, France.
Dalton Trans ; 53(23): 9952-9963, 2024 Jun 10.
Article in En | MEDLINE | ID: mdl-38809151
ABSTRACT
The structural, spectroscopic and electronic properties of Na and K birnessites were investigated from ambient conditions (birA) to complete dehydration, and the involved mechanisms were scrutinized. Density Functional Theory (DFT) simulations were employed to derive structural models for lamellar A0.33MnO2·xH2O (A = Na+ or K+, x = 0 or 0.66), subsequently compared with the experimental results obtained for Na0.30MnO2·0.75H2O and K0.22MnO2·0.77H2O materials. Thermal analysis (TGA-DSC), X-ray diffraction (XRD), Fourier Transform Infrared (FTIR) spectroscopy, and Near Ambient Pressure X-ray Photoemission Spectroscopy (NAP-XPS) measurements were conducted for both birnessites. Dehydration under vacuum, annealing, or controlled relative humidity were considered. Results indicated that complete birnessite dehydration was a two-stage process. In the first stage, water removal from the interlayer of fully hydrated birnessite (birA) down to a molar H2O/A ratio of ∼2 (birB) led to the progressive shrinkage of the interlayer distance (3% for Na birnessite, 1% for K birnessite). In the second stage, water-free (birC) domains with a shorter interlayer distance (20% for Na birnessite, 10% for K birnessite) appeared and coexisted with birB domains. Then, birB was essentially transformed into birC when complete dehydration was achieved. The vibrational properties of birA were consistent with strong intermolecular interactions among water molecules, whereas partially dehydrated birnessite (birB) showed a distinct feature, with 3 (for Na-bir) and 2 (for K-bir) vibrations that were reproduced by DFT calculations for organized water into the interlayer (x = 0.66). The study also demonstrated that the electronic structure of Na birnessite depends on the interlayer water content. The external Na+ electronic level (Na 2p) was slightly destabilized (+0.3 eV binding energy) under near ambient conditions (birA) compared to drier conditions (birB and birC).

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Dalton Trans Journal subject: QUIMICA Year: 2024 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Dalton Trans Journal subject: QUIMICA Year: 2024 Document type: Article Affiliation country: