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Challenging thermodynamics: combining immiscible elements in a single-phase nano-ceramic.
Liu, Shuo; Dun, Chaochao; Jiang, Qike; Xuan, Zhengxi; Yang, Feipeng; Guo, Jinghua; Urban, Jeffrey J; Swihart, Mark T.
Affiliation
  • Liu S; Department of Chemical and Biological Engineering, University at Buffalo, The State University of New York, Buffalo, NY, 14260, USA.
  • Dun C; The Molecular Foundry, Lawrence Berkeley National Laboratory, Berkeley, CA, 94720, USA. cdun@lbl.gov.
  • Jiang Q; Instrumentation and Service Center for Physical Sciences, Westlake University, Hangzhou, Zhejiang, 310024, China.
  • Xuan Z; Department of Chemical and Biological Engineering, University at Buffalo, The State University of New York, Buffalo, NY, 14260, USA.
  • Yang F; RENEW Institute, University at Buffalo, The State University of New York, Buffalo, NY, 14260, USA.
  • Guo J; Advanced Light Source, Lawrence Berkeley National Laboratory, Berkeley, CA, 94720, USA.
  • Urban JJ; Advanced Light Source, Lawrence Berkeley National Laboratory, Berkeley, CA, 94720, USA.
  • Swihart MT; The Molecular Foundry, Lawrence Berkeley National Laboratory, Berkeley, CA, 94720, USA. jjurban@lbl.gov.
Nat Commun ; 15(1): 1167, 2024 Feb 07.
Article in En | MEDLINE | ID: mdl-38326434
ABSTRACT
The Hume-Rothery rules governing solid-state miscibility limit the compositional space for new inorganic material discovery. Here, we report a non-equilibrium, one-step, and scalable flame synthesis method to overcome thermodynamic limits and incorporate immiscible elements into single phase ceramic nanoshells. Starting from prototype examples including (NiMg)O, (NiAl)Ox, and (NiZr)Ox, we then extend this method to a broad range of Ni-containing ceramic solid solutions, and finally to general binary combinations of elements. Furthermore, we report an "encapsulated exsolution" phenomenon observed upon reducing the metastable porous (Ni0.07Al0.93)Ox to create ultra-stable Ni nanoparticles embedded within the walls of porous Al2O3 nanoshells. This nanoconfined structure demonstrated high sintering resistance during 640 h of catalysis of CO2 reforming of methane, maintaining constant 96% CH4 and CO2 conversion at 800 °C and dramatically outperforming conventional catalysts. Our findings could greatly expand opportunities to develop novel inorganic energy, structural, and functional materials.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Nat Commun Journal subject: BIOLOGIA / CIENCIA Year: 2024 Document type: Article Affiliation country: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Nat Commun Journal subject: BIOLOGIA / CIENCIA Year: 2024 Document type: Article Affiliation country: Estados Unidos
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