X-ray studies bridge the molecular and macro length scales during the emergence of CoO assemblies

Autor(es):Mostrar menos -

Grote, Lukas ^{[1, 2]} ; Zito, Cecilia A. ^{[2, 3]} ; Frank, Kilian ^{[4, 5]} ; Dippel, Ann-Christin ^[1] ; Reisbeck, Patrick ^{[4, 5]} ; Pitala, Krzysztof ^{[6, 7]} ; Kvashnina, Kristina O. ^{[8, 9]} ; Bauters, Stephen ^{[8, 9]} ; Detlefs, Blanka ^[10] ; Ivashko, Oleh ^[1] ; Pandit, Pallavi ^[1] ; Rebber, Matthias ^{[2, 11]} ; Harouna-Mayer, Sani Y. ^{[2, 11]} ; Nickel, Bert ^{[4, 5]} ; Koziej, Dorota ^{[2, 11]}

Afiliação do(s) autor(es):Mostrar menos -

^[1] Deutsch Elektronen Synchrotron DESY, Hamburg - Germany

^[2] Univ Hamburg, Inst Nanostruct & Solid State Phys, Ctr Hybrid Nanostruct, Hamburg - Germany

^[3] Sao Paulo State Univ UNESP, Sao Jose Do Rio Preto - Brazil

^[4] Ludwig Maximilians Univ Munchen, Fac Phys, Munich - Germany

^[5] Ctr NanoSci CeNS, Munich - Germany

^[6] AGH Univ Sci & Technol, Fac Phys & Appl Comp Sci, Krakow - Poland

^[7] AGH Univ Sci & Technol, Acad Ctr Mat & Nanotechnol, Krakow - Poland

^[8] European Synchrotron Radiat Facil ESRF, Rossendorf Beamline, Grenoble - France

^[9] Helmholtz Zentrum Dresden Rossendorf HZDR, Inst Resource Ecol, Dresden - Germany

^[10] European Synchrotron Radiat Facil ESRF, Grenoble - France

^[11] Hamburg Ctr Ultrafast Imaging, Hamburg - Germany

• Tipo de documento: Artigo Científico
• Fonte: NATURE COMMUNICATIONS; v. 12, n. 1 JUL 20 2021.
• Citações Web of Science: 0

Resumo

The key to fabricating complex, hierarchical materials is the control of chemical reactions at various length scales. To this end, the classical model of nucleation and growth fails to provide sufficient information. Here, we illustrate how modern X-ray spectroscopic and scattering in situ studies bridge the molecular- and macro- length scales for assemblies of polyhedrally shaped CoO nanocrystals. Utilizing high energy-resolution fluorescence-detected X-ray absorption spectroscopy, we directly access the molecular level of the nanomaterial synthesis. We reveal that initially Co(acac)(3) rapidly reduces to square-planar Co(acac)(2) and coordinates to two solvent molecules. Combining atomic pair distribution functions and small-angle X-ray scattering we observe that, unlike a classical nucleation and growth mechanism, nuclei as small as 2nm assemble into superstructures of 20nm. The individual nanoparticles and assemblies continue growing at a similar pace. The final spherical assemblies are smaller than 100nm, while the nanoparticles reach a size of 6nm and adopt various polyhedral, edgy shapes. Our work thus provides a comprehensive perspective on the emergence of nano-assemblies in solution. The understanding of nucleation and growth of nanostructures plays a key role in complex materials design. Here, the authors illustrate how X-ray in situ studies link transformation at the molecular- and macro- length scales during the emergence of cobalt oxide assemblies. (AU)

• Processo FAPESP: 18/08271-7 - Caracterização estrutural, eletrônica e química de compósitos de ácido grafênico com nanoesferas de CeO2 gema-casca e Pd-CeO2 gema-casca
• Beneficiário: Cecilia de Almeida Zito
• Modalidade de apoio: Bolsas no Exterior - Estágio de Pesquisa - Doutorado
• Processo FAPESP: 16/25267-8 - Compósitos de ácido grafênico com estruturas de CeO2 ocas e Pd-CeO2 do tipo gema-casca aplicados como sensores de compostos orgânicos voláteis
• Beneficiário: Cecilia de Almeida Zito
• Modalidade de apoio: Bolsas no Brasil - Doutorado