Kinetics and mechanism of ionic intercalation/de-intercalation during the formation of α-cobalt hydroxide and its polymorphic transition to β-cobalt hydroxide: Reaction-diffusion framework

Handle URI:
http://hdl.handle.net/10754/562010
Title:
Kinetics and mechanism of ionic intercalation/de-intercalation during the formation of α-cobalt hydroxide and its polymorphic transition to β-cobalt hydroxide: Reaction-diffusion framework
Authors:
Rahbani, Janane; Khashab, Niveen M. ( 0000-0003-2728-0666 ) ; Patra, Digambara; Al-Ghoul, Mazen
Abstract:
We study the kinetics and mechanism of intercalation and de-intercalation of small anions during the formation of crystalline α-Co(OH) 2 and its transformation to β-Co(OH) 2 within a reaction-diffusion framework. We therein use fluorescence spectroscopy with Rhodamine 6G (Rh6G) as a probe as well as other spectroscopic and imaging techniques. The method is based on the reaction and diffusion of hydroxide ions into a gel matrix containing the Co(ii) ions, the conjugate anions to be intercalated and Rh6G. The advantage of this simple method is that it allows us to separate throughout space the various stages during the formation of α-Co(OH) 2 and its transformation to β-Co(OH) 2, thus enabling fluorescence measurements of the those stages by simply focusing on different areas of the tube. It also permits us to extract with ease the solids for characterization and image analysis. The macroscopic evolution of the system, which consists of a leading blue front designating the formation of α-Co(OH) 2 followed by a sharp blue/pink interface designating the transformation to the pink β-Co(OH) 2, exhibits different dynamics depending on the anion present in the gel. At a certain stage, the blue/pink interface stops its propagation and only the blue front continues. This represents clear evidence of the dependence of the kinetics of intercalation and de-intercalation on the nature of the anion. The coexisting polymorphs were collected and characterized using XRD, FTIR, Raman and UV-Vis. The fluorescence images of the α-Co(OH) 2 reveal clearly the presence of Rh6G between its layers, whereas images from the β polymorph indicate the opposite. Moreover, the fluorescence of Rh6G is monitored during the formation of α-Co(OH) 2 and its conversion to β-Co(OH) 2. During the formation, the fluorescence intensity and lifetime are significantly increased whereas the opposite happens during the transformation to the β phase. We are able to calculate the activation energies associated with the intercalation and de-intercalation of anions and show using SEM that the polymorphic transformation is accompanied by an Ostwald ripening mechanism whereby the smaller crystals of α-Co(OH) 2 dissolve to reappear as larger crystals of β-Co(OH) 2. We find that the activation energies of de-intercalation are systematically smaller than those of intercalation. Our results confirm many aspects of the results of Du et al. on the conversion of a chloride-intercalated α-Co(OH) 2 to β-Co(OH) 2. © The Royal Society of Chemistry 2012.
KAUST Department:
Numerical Porous Media SRI Center (NumPor); Smart Hybrid Materials (SHMs) lab; Physical Sciences and Engineering (PSE) Division; Chemical Science Program; Advanced Membranes and Porous Materials Research Center
Publisher:
Royal Society of Chemistry
Journal:
Journal of Materials Chemistry
Issue Date:
2012
DOI:
10.1039/c2jm31694c
Type:
Article
ISSN:
09599428
Appears in Collections:
Articles; Advanced Membranes and Porous Materials Research Center; Physical Sciences and Engineering (PSE) Division; Controlled Release and Delivery Laboratory; Chemical Science Program

Full metadata record

DC FieldValue Language
dc.contributor.authorRahbani, Jananeen
dc.contributor.authorKhashab, Niveen M.en
dc.contributor.authorPatra, Digambaraen
dc.contributor.authorAl-Ghoul, Mazenen
dc.date.accessioned2015-08-03T09:36:10Zen
dc.date.available2015-08-03T09:36:10Zen
dc.date.issued2012en
dc.identifier.issn09599428en
dc.identifier.doi10.1039/c2jm31694cen
dc.identifier.urihttp://hdl.handle.net/10754/562010en
dc.description.abstractWe study the kinetics and mechanism of intercalation and de-intercalation of small anions during the formation of crystalline α-Co(OH) 2 and its transformation to β-Co(OH) 2 within a reaction-diffusion framework. We therein use fluorescence spectroscopy with Rhodamine 6G (Rh6G) as a probe as well as other spectroscopic and imaging techniques. The method is based on the reaction and diffusion of hydroxide ions into a gel matrix containing the Co(ii) ions, the conjugate anions to be intercalated and Rh6G. The advantage of this simple method is that it allows us to separate throughout space the various stages during the formation of α-Co(OH) 2 and its transformation to β-Co(OH) 2, thus enabling fluorescence measurements of the those stages by simply focusing on different areas of the tube. It also permits us to extract with ease the solids for characterization and image analysis. The macroscopic evolution of the system, which consists of a leading blue front designating the formation of α-Co(OH) 2 followed by a sharp blue/pink interface designating the transformation to the pink β-Co(OH) 2, exhibits different dynamics depending on the anion present in the gel. At a certain stage, the blue/pink interface stops its propagation and only the blue front continues. This represents clear evidence of the dependence of the kinetics of intercalation and de-intercalation on the nature of the anion. The coexisting polymorphs were collected and characterized using XRD, FTIR, Raman and UV-Vis. The fluorescence images of the α-Co(OH) 2 reveal clearly the presence of Rh6G between its layers, whereas images from the β polymorph indicate the opposite. Moreover, the fluorescence of Rh6G is monitored during the formation of α-Co(OH) 2 and its conversion to β-Co(OH) 2. During the formation, the fluorescence intensity and lifetime are significantly increased whereas the opposite happens during the transformation to the β phase. We are able to calculate the activation energies associated with the intercalation and de-intercalation of anions and show using SEM that the polymorphic transformation is accompanied by an Ostwald ripening mechanism whereby the smaller crystals of α-Co(OH) 2 dissolve to reappear as larger crystals of β-Co(OH) 2. We find that the activation energies of de-intercalation are systematically smaller than those of intercalation. Our results confirm many aspects of the results of Du et al. on the conversion of a chloride-intercalated α-Co(OH) 2 to β-Co(OH) 2. © The Royal Society of Chemistry 2012.en
dc.publisherRoyal Society of Chemistryen
dc.titleKinetics and mechanism of ionic intercalation/de-intercalation during the formation of α-cobalt hydroxide and its polymorphic transition to β-cobalt hydroxide: Reaction-diffusion frameworken
dc.typeArticleen
dc.contributor.departmentNumerical Porous Media SRI Center (NumPor)en
dc.contributor.departmentSmart Hybrid Materials (SHMs) laben
dc.contributor.departmentPhysical Sciences and Engineering (PSE) Divisionen
dc.contributor.departmentChemical Science Programen
dc.contributor.departmentAdvanced Membranes and Porous Materials Research Centeren
dc.identifier.journalJournal of Materials Chemistryen
dc.contributor.institutionDepartment of Chemistry, American University of Beirut, P.O. Box 11-0236, Riad El-Solh 1107 2020, Beirut, Lebanonen
kaust.authorKhashab, Niveen M.en
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