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Pivotal Role of Modifiable A-Site Doping in Enhancing Valence Stability and Excited State Dynamics of MnO6.
Zhang, Yaowen; Sun, Yuqi; Liu, Chanqiang; Liu, Junwei; Lu, Jiajun; Wang, Bo; Duan, Longhui; Chen, Gang; Zheng, Beining; Han, Mei; Feng, Shouhua.
Afiliación
  • Zhang Y; State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, Jilin Provincial International Cooperation Key Laboratory of Advanced Inorganic Soild Functional Materials, College of Chemistry, Jilin University, Qianjin Street 2699, Changchun, 130012, P. R. China.
  • Sun Y; State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, Jilin Provincial International Cooperation Key Laboratory of Advanced Inorganic Soild Functional Materials, College of Chemistry, Jilin University, Qianjin Street 2699, Changchun, 130012, P. R. China.
  • Liu C; State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, Jilin Provincial International Cooperation Key Laboratory of Advanced Inorganic Soild Functional Materials, College of Chemistry, Jilin University, Qianjin Street 2699, Changchun, 130012, P. R. China.
  • Liu J; State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, Jilin Provincial International Cooperation Key Laboratory of Advanced Inorganic Soild Functional Materials, College of Chemistry, Jilin University, Qianjin Street 2699, Changchun, 130012, P. R. China.
  • Lu J; State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, Jilin Provincial International Cooperation Key Laboratory of Advanced Inorganic Soild Functional Materials, College of Chemistry, Jilin University, Qianjin Street 2699, Changchun, 130012, P. R. China.
  • Wang B; State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, Jilin Provincial International Cooperation Key Laboratory of Advanced Inorganic Soild Functional Materials, College of Chemistry, Jilin University, Qianjin Street 2699, Changchun, 130012, P. R. China.
  • Duan L; State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, Jilin Provincial International Cooperation Key Laboratory of Advanced Inorganic Soild Functional Materials, College of Chemistry, Jilin University, Qianjin Street 2699, Changchun, 130012, P. R. China.
  • Chen G; State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry, Jilin University, Qianjin Street 2699, Changchun, 130012, P. R. China.
  • Zheng B; College of Physics, Jilin University, Qianjin Street 2699, Changchun, 130012, P. R. China.
  • Han M; State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, Jilin Provincial International Cooperation Key Laboratory of Advanced Inorganic Soild Functional Materials, College of Chemistry, Jilin University, Qianjin Street 2699, Changchun, 130012, P. R. China.
  • Feng S; State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, Jilin Provincial International Cooperation Key Laboratory of Advanced Inorganic Soild Functional Materials, College of Chemistry, Jilin University, Qianjin Street 2699, Changchun, 130012, P. R. China.
Small Methods ; : e2400539, 2024 Aug 30.
Article en En | MEDLINE | ID: mdl-39212198
ABSTRACT
The controlled regulation of A-site in rare earth manganate perovskites can orderly arrange the electronic states, leading to the emergence of unique transport properties. However, it is challenging to balance crystal structure stability and property variations during the multi-ion doping. In this study, a series of multivalent manganate perovskites are synthesized by hydrothermal method through the A-site multielement doping, which enables the manganese atoms with varying valence states to orderly arrange at the B site. Powder X-ray diffraction (PXRD) and X-ray absorption spectra (XAS) confirm that the splitting of the K─O hybrid orbitals in the crystal effectively prevents any distortion of the MnO6 octahedron, thereby facilitating the ordered arrangement of Mn (III) -Mn (IV) -Mn (V) at the B-site and promoting superstructure formation. The transient absorption spectra (TAS) reveals that the sequential arrangement of Mn (III) - Mn (IV) - Mn(V) better forms the charge transfer channels, and thereby makes the photodynamic properties of the sample composition-dependent. These photodynamic properties will facilitate the study of exciton-electron coupling behavior in LCKMO crystals during electrical transport.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Small Methods Año: 2024 Tipo del documento: Article Pais de publicación: Alemania
Texto completo
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Imprimir
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Small Methods Año: 2024 Tipo del documento: Article Pais de publicación: Alemania