Perera S Sameera, Munasinghe Hashini N, Yatooma Emily N, Rabuffetti Federico A
Department of Chemistry, Wayne State University, Detroit, MI 48202, USA.
Dalton Trans. 2020 Jun 16;49(23):7914-7919. doi: 10.1039/d0dt00999g.
A synthetic method was developed to enable the microwave-assisted solid-state preparation of double molybdate and double tungstate scheelite-type phosphors of formula NaRE(MO4)2 (RE = La, Pr, Eu, Dy; M = Mo, W). Starting from subgram-scale stoichiometric mixtures of metal carbonates and oxides and with the aid of granular activated charcoal as a microwave susceptor, ternary (NaEu(MO4)2), quaternary (NaLa0.95Eu0.05(MO4)2), and quinary phosphors (NaLa0.95Pr0.025Dy0.025(MO4)2) were obtained upon heating in a countertop microwave oven. The synthesis of crystalline and phase-pure materials required heating times ranging from 18 to 27 min, significantly shorter than those typically encountered in solid-state reactions assisted by conventional heating. Depending on chemical composition, the speed-up factor ranged from 30 to 40. More importantly, photoluminescence studies performed on the compositionally complex quinary molybdate NaLa0.95Pr0.025Dy0.025(MoO4)2 showed that phosphors synthesized using microwave and conventional heating have nearly identical luminescence responses. The synthetic method described in this contribution is robust, fast, simple, and ideally suited for exploratory synthesis and rapid screening of group VI metalate phosphors, as well as for the preparation of binary precursors to these materials (e.g., Na2MoO4 and Na2WO4).
开发了一种合成方法,用于通过微波辅助固态制备化学式为NaRE(MO4)2(RE = La、Pr、Eu、Dy;M = Mo、W)的钼酸双盐和钨酸双盐白钨矿型磷光体。从亚克级的金属碳酸盐和氧化物的化学计量混合物开始,并借助粒状活性炭作为微波感受器,在台式微波炉中加热后,获得了三元(NaEu(MO4)2)、四元(NaLa0.95Eu0.05(MO4)2)和五元磷光体(NaLa0.95Pr0.025Dy0.025(MO4)2)。合成结晶且相纯的材料所需的加热时间为18至27分钟,明显短于传统加热辅助的固态反应中通常遇到的时间。根据化学成分,加速因子在30至40之间。更重要的是,对成分复杂的五元钼酸盐NaLa0.95Pr0.025Dy0.025(MoO4)2进行的光致发光研究表明,使用微波和传统加热合成的磷光体具有几乎相同的发光响应。本论文中描述的合成方法稳健、快速、简单,非常适合用于第VI族金属酸盐磷光体的探索性合成和快速筛选,以及制备这些材料的二元前体(例如Na2MoO4和Na2WO4)。