STUDI KOMPOSISI DAN SIFAT OPTIK ZNO NANORODS YANG DISINTESIS MENGGUNAKAN METODE HIDROTERMAL

  • Novan Purwanto Program Studi Fisika, Fakultas Matematika dan Ilmu Pengetahuan Alam, Universitas Negeri Jakarta, Jl. Rawamangun Muka, Jakarta 13220, Indonesia
  • Isnaeni Isnaeni Lembaga Ilmu Pengetahuan Indonesia, Kawasan PUSPITEK Serpong, Muncul, Setu, Tangerang, Banten, 15314, Indonesia
  • Iwan Sugihartono Program Studi Fisika, Fakultas Matematika dan Ilmu Pengetahuan Alam, Universitas Negeri Jakarta, Jl. Rawamangun Muka, Jakarta 13220, Indonesia

Abstract

Abstrak

ZnO nanorods telah disintesis menggunakan teknik hidrotermal pada suhu 95 â°C selama 2 jam. Studi komposisi ZnO nanorods dilakukan menggunakan energy dispersive sinar-x (EDS). Hasil pengujian memberikan konfirmasi bahwa komposisi massa Zn lebih banyak dibandingkan komposisi massa O yaitu 69,44% dan 30,56%. Pengujian sifat optik ZnO nanorods menggunakan spektrofotometer UV-Vis memberikan informasi bahwa terdapat absorbansi tinggi di rentang panjang gelombang ultra-violet (UV) yaitu 360-390 nm.  dan absorbansi yang lebar di rentang panjang gelombang cahaya tampak.

Kata-kata kunci: ZnO nanorods, komposisi, absorbansi, band gap energy


Abstract

ZnO nanorods have been synthesized by hydrothermal method at 95 °C for 2 hours. The study composition of ZnO nanorods was performed using energy dispersive x-ray (EDS). The results confirm that elemental mass compositions of Zn and O are 69,44% and 30,56%. The optical properties of ZnO nanorods which investigated by using the UV-Vis spectrophotometer confirmed that the strong absorbance is in the range of UV wavelength (360-390 nm), and wide absorbances in the wavelength range of visible light.

Keywords: ZnO nanorods, compositions, absorbance, band gap energy

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Published
2018-10-30
How to Cite
Purwanto, N., Isnaeni, I., & Sugihartono, I. (2018). STUDI KOMPOSISI DAN SIFAT OPTIK ZNO NANORODS YANG DISINTESIS MENGGUNAKAN METODE HIDROTERMAL. PROSIDING SEMINAR NASIONAL FISIKA (E-JOURNAL), 7, SNF2018-PA. https://doi.org/10.21009/03.SNF2018.02.PA.14