4.6 Article

Tunable Emission Properties of Manganese Chloride Small Single Crystals by Pyridine Incorporation

Journal

ACS OMEGA
Volume 4, Issue 5, Pages 8039-8045

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsomega.8b03661

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Funding

  1. 973 project [2014CB920903]
  2. MOST

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Pure transition-metal compounds seldom produce luminescence because of electron correlation and spin-spin coupling. The Pb-free perovskite materials, C10H12N2MnCl4 and C5H6NMnCl3 center dot H2O, were obtained by using pyridine-implanted manganese chloride lattices. The single-crystal X-ray diffraction indicates their different crystal structures. In C10H12N2MnCl4, MnCl4 cocoordinated with two pyridine molecules forms a lattice composed of independent mononuclear structures with paramagnetic behavior, which shows a clear emission band at 518 nm from the lowest d-d transition of a single Mn(II) ion in the octahedral crystal field. In C5H6NMnCl5 center dot H2O crystal, MnCl5 center dot(H2O)(x) octahedron-cocoordinated with less pyridine molecules than 2 lead to formation arris-share linear chains of Mn-ion octahedra, which give emission band at 620 nm due to the ferromagnetic Mn pair, and ferromagnetism. Pyridine incorporations in the transition-metal halide lattice provide a new channel to modulate the electron correlation and obtain materials with both luminescence and ferromagnetic properties.

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