Síntese e aplicação de nanocristais semicondutores inorgânicos ternários

Detalhes bibliográficos
Ano de defesa: 2016
Autor(a) principal: Matos, Charlene Regina Santos lattes
Orientador(a): Gimenez, Iara de Fátima
Banca de defesa: Não Informado pela instituição
Tipo de documento: Tese
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal de Sergipe
Programa de Pós-Graduação: Pós-Graduação em Ciência e Engenharia de Materiais
Departamento: Não Informado pela instituição
País: Brasil
Palavras-chave em Português:
Palavras-chave em Inglês:
Área do conhecimento CNPq:
Link de acesso: https://ri.ufs.br/handle/riufs/3465
Resumo: In this work, semiconductor nanocrystal alloys (NCs), ZnCdTe and MgCdTe were obtained by the bottom-up approach in aqueous synthesis assisted by conventional and microwave-assisted hydrothermal route. Different synthesis variables such as pH, capping agent (mercaptopropionic acid and glutathione), Zn/Cd ratio and time were used for ZnCdTe nanocrystal synthesis. For MgCdTe synthesis, pH was kept constant while time, Mg/Cd ratio and capping agent were evaluated. UV-Vis absorption and emission spectra (PL) showed composition dependence (Zn / Cd and Mg / Cd) which was altered depending on the synthesis parameter. These results were corroborated by transmission electron microscopy (TEM) as well as for chemical analysis by atomic absorption spectrometry. Cyclic voltammetry was used as a complementary technique to optical characterizations in the determination of semiconductor NCs band gap, obtaining approximate results. Novel nanocomposites of graphene derivatives (from citric acid and graphite) modified with NCs of MgCdTe were satisfactorily prepared by in situ hydrothermal synthesis and characterized by PL and TEM. Homemade modified carbon paste electrodes were built to evaluate the electrochemical behavior of the new composites, being used for the first time to the study of epinephrine and lidocaine eletrooxidation and their mixtures. The differential pulse voltammetry, proved to be a sensitive technique in both determination of electroactive species with detection limits that reached 9.2x10-8 mol.L-1, for epinephrine and 9.5x10-7 mol.L - 1 for lidocaine.