2017
DOI: 10.1002/asia.201701040
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Color Tuning in Garnet Oxides: The Role of Tetrahedral Coordination Geometry for 3 d Metal Ions and Ligand–Metal Charge Transfer (Band‐Gap Manipulation)

Abstract: We explored garnet-structured oxide materials containing 3d transition-metal ions (e.g., Co , Ni , Cu , and Fe ) for the development of new inorganic colored materials. For this purpose, we synthesized new garnets, Ca Sb Ga ZnO (I) and Ca Sb Fe ZnO (II), that were isostructural with Ca Te Zn O . Substitution of Co , Ni , and Cu at the tetrahedral Zn sites in I and II gave rise to brilliantly colored materials (different shades of blue, green, turquoise, and red). The materials were characterized by optical abs… Show more

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Cited by 20 publications
(31 citation statements)
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“…2.00 eV (orange region) produces the complementary blue color of the material . Thus, the triplet band centered at approximately 2.00 eV can be assigned to the tetrahedral Co 2+ [ 4 A 2 (F)→ 4 T 1 (P)] transition , , . A small band at ca.…”
Section: Resultsmentioning
confidence: 99%
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“…2.00 eV (orange region) produces the complementary blue color of the material . Thus, the triplet band centered at approximately 2.00 eV can be assigned to the tetrahedral Co 2+ [ 4 A 2 (F)→ 4 T 1 (P)] transition , , . A small band at ca.…”
Section: Resultsmentioning
confidence: 99%
“…A small band at ca. 2.56 eV may be attributed to the transitions between the octahedral and tetrahedral sites , , …”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…2 ZnO 12 garnet (Bhim et al, 2017), in keeping with a content of tetrahedral divalent cations less than 1.00 atoms pfu. The presence of measurable quantities of divalent Fe at the Z site in a garnet structure is not too common, but it has been demonstrated with spectroscopic methods, both for synthetic material (e.g.…”
Section: Crystal Chemistrymentioning
confidence: 91%
“…Protein metal binding is part of many biochemical mechanisms including signal transduction, enzyme catalysis, and protein structural integrity [35]. The local protein structure environment around bound metal ions can provide clues to the biochemical and cellular function of the binding [68] and how sequence-based structural changes modulates metal binding [9,10]. However, the quality of 3D protein structural data around metal binding sites can vary dramatically from structure to structure, and especially from region to region [8,11].…”
Section: Introductionmentioning
confidence: 99%