使用均聚物作为固体模板合成金属和金属氧化物纳米粒子:Eu+3 纳米粒子产品的发光特性

Photochem Pub Date : 2024-07-14 DOI:10.3390/photochem4030018
María Ángeles Cortés, Carlos Díaz, R. de la Campa, A. Presa-Soto, María Luisa Valenzuela
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引用次数: 0

摘要

从聚(4-乙烯基吡啶)((P4VP)n)、聚(2-乙烯基吡啶)((P2VP)n)和[N=P(O2CH2CF3)]m-b-P2VP20 嵌段共聚物开始,产生了一系列含金属的均聚物、(P4VP)n⊕MXm, (P2VP)n⊕MXm, and [N=P(O2CH2CF3)]m-b-P2VP20]⊕MXm MXm = PtCl2, ZnCl2, and Eu(NO3)3, have been successfully prepared by using a direct and simple solution methodology.对所制备的含金属聚合物前驱体进行固态热解,可形成各种不同的金属和金属氧化物纳米粒子(Pt、ZnO、Eu2O3 和 EuPO4),具体取决于聚合物模板前驱体的成分和性质。因此,Eu2O3 纳米结构是通过含铕均聚物((P4VP)n⊕MXm 和 (P2VP)n⊕MXm)获得的,而 EuPO4 纳米结构则是通过含磷嵌段共聚物前体 [N=P(O2CH2CF3)]m-b-P2VP20]⊕MXm 获得的,其中 MXm = Eu(NO3)3。重要的是,尽管 Eu2O3 和 EuPO4 纳米结构都能发出强烈的荧光,但它们都受到含金属的大分子聚合物模板的性质和组成的强烈影响。因此,对于含铕的 P2VP 均聚物((P4VP)n⊕MXm 和 (P2VP)n⊕MXm),发射强度最高的是分子量最低的均聚物模板 [P4VP(Eu(NO3)3]6000、而使用嵌段共聚物前体 [N=P(O2CH2CF3)]m-b-P2VP20]⊕MXm MXm= Eu(NO3)3([N=P(O2CH2CF3)]100-b-[P2VP(Eu(NO3)3)x]20)时则相反([N=P(O2CH2CF3)]100-b-[P2VP(Eu(NO3)3)x]20 的发射强度最高)。发射跃迁的强度比为5D0 → 7F2/5D0 → 7F1,表明 Eu3+ 离子周围的不同对称性取决于聚合物前体的性质,这也影响了制备的 Pt°、ZnO、Eu2O3 和 EuPO4 纳米结构的尺寸。
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Synthesis of Metallic and Metal Oxide Nanoparticles Using Homopolymers as Solid Templates: Luminescent Properties of the Eu+3 Nanoparticle Products
Starting from poly(4-vinylpyridine) ((P4VP)n), poly(2-vinylpyridine) ((P2VP)n), and [N=P(O2CH2CF3)]m-b-P2VP20 block copolymers, a series of metal-containing homopolymers, (P4VP)n⊕MXm, (P2VP)n⊕MXm, and [N=P(O2CH2CF3)]m-b-P2VP20]⊕MXm MXm = PtCl2, ZnCl2, and Eu(NO3)3, have been successfully prepared by using a direct and simple solution methodology. Solid-state pyrolysis of the prepared metal-containing polymeric precursors led to the formation of a variety of different metallic and metal oxide nanoparticles (Pt, ZnO, Eu2O3, and EuPO4) depending on the composition and nature of the polymeric template precursor. Thus, whereas Eu2O3 nanostructures were obtained from europium-containing homopolymers ((P4VP)n⊕MXm and (P2VP)n⊕MXm), EuPO4 nanostructures were achieved using phosphorus-containing block copolymer precursors, [N=P(O2CH2CF3)]m-b-P2VP20]⊕MXm with MXm = Eu(NO3)3. Importantly, and although both Eu2O3 and EuPO4 nanostructures exhibited a strong luminescence emission, these were strongly influenced by the nature and composition of the macromolecular metal-containing polymer template. Thus, for P2VP europium-containing homopolymers ((P4VP)n⊕MXm and (P2VP)n⊕MXm), the highest emission intensity corresponded to the lowest-molecular-weight homopolymer template, [P4VP(Eu(NO3)3]6000, whereas the opposite behavior was observed when block copolymer precursors, [N=P(O2CH2CF3)]m-b-P2VP20]⊕MXm MXm= Eu(NO3)3, were used (highest emission intensity corresponded to [N=P(O2CH2CF3)]100-b-[P2VP(Eu(NO3)3)x]20). The intensity ratio of the emission transitions: 5D0 → 7F2/5D0 → 7F1, suggested a different symmetry around the Eu3+ ions depending on the nature of the polymeric precursor, which also influenced the sizes of the prepared Pt°, ZnO, Eu2O3, and EuPO4 nanostructures.
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