采用微波水热法,分别以氯化锰和硫代乙酰胺为锰源和硫源,在不同的pH条件下合成了γ-MnS微晶.利用X射线衍射仪(XRD),扫描电子显微镜(SEM),场发射扫描电子显微镜(FESEM),透射电子显微镜(TEM)对样品的物相组成和微观形貌,粒径大小进行了表征.结果表明:在pH大于6时均能合成出结晶性较好的纤锌矿结构γ-MnS,随着pH的增大,产量提高,产物的粒径逐渐变小且自组装为球状微晶,粒径为0.5μm,利用紫外-可见吸收光谱分析(UV),自组装γ-MnS微晶球在300 ~400 nm处出现了较强的吸收峰,其光学带隙随着pH的增大而减小,在光电领域具有潜在的应用.
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