锌
纳米颗粒
热分解
纤锌矿晶体结构
熔点
热重分析
分解
化学
化学工程
红外光谱学
材料科学
核化学
纳米技术
有机化学
工程类
作者
Selina Ama Saah,Patrick Opare Sakyi,Nathaniel Owusu Boadi,Franklyn Addai Tieku,Ampem Kwabena Boampong
标识
DOI:10.1002/open.202400050
摘要
Abstract This study explores the synthesis of nanoparticles through the thermal decomposition of single‐source precursors, a method gaining popularity due to its low cost, minimal environmental toxicity, rapidity, scalability, and the ability to form nanoparticles with few defects. Zinc ethyl carbamate was synthesized and characterized using 1 H NMR and infrared spectroscopy. Its purity was confirmed through microelemental analysis and melting point determination. The melting point of the complex was determined to be 165 °C. The thermogravimetric analyses indicated a one‐step decomposition of zinc ethyl carbamate with a decomposition onset of of 200 °C, yielding a stable ZnS residue. Further thermal decomposition led to the formation of wurtzite phase ZnS nanoparticles, as evidenced by XRD. SEM micrographs displayed mixed spherical, and cubic unevenly sized, polydispersed nanoparticles, while EDX revealed approximately a 1 : 1 Zn to S ratio. Estimated band gap from the Tauc's plot gave 3.93 eV and 3.42 eV for the nanoparticles synthesized at 300 and 400 °C respectively. The wide difference in the band gaps may be as a result of the larger particles observed at 400 °C and the deformations in the sample as observed in the SEM.
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