TY - JOUR
T1 - Novel magnetic and optical properties of Sn1-xZnxO2 nanoparticles
AU - Franco, Nevil A.
AU - Reddy, Kongara M.
AU - Eixenberger, Josh
AU - Tenne, Dmitri A.
AU - Hanna, Charles B.
AU - Punnoose, Alex
N1 - Publisher Copyright:
© 2015 AIP Publishing LLC.
PY - 2015/5/7
Y1 - 2015/5/7
N2 - In this work, we report on the effects of doping SnO2 nanoparticles with Zn2+ ions. A series of ∼2-3nm sized Sn1-xZnxO2 crystallite samples with 0≤x≤0.18 were synthesized using a forced hydrolysis method. Increasing dopant concentration caused systematic changes in the crystallite size, oxidation state of Sn, visible emission, and band gap of SnO2 nanoparticles. X-ray Diffraction studies confirmed the SnO2 phase purity and the absence of any impurity phases. Magnetic measurements at room temperature showed a weak ferromagnetic behavior characterized by an open hysteresis loop. Their saturation magnetization Ms increases initially with increasing Zn concentrations; however for x>0.06, Ms decreases. Samples with the highest Ms values (x=0.06) were analyzed using an Inductively Coupled Plasma Mass Spectrometer, looking for traces of any magnetic elements in the samples. Concentrations of all transition metals (Fe, Co, Mn, Cr, and Ni) in these samples were below ppb level, suggesting that the observed magnetism is not due to random inclusions of any spurious magnetic impurities and it cannot be explained by the existing models of magnetic exchange. A new visible emission near 490nm appeared in the Zn doped SnO2 samples in the photoluminescence spectra which strengthened as x increased, suggesting the formation of defects such as oxygen vacancies. X-ray Photoelectron Spectroscopy (XPS) confirmed the nominal Zn dopant concentrations and the 2+ oxidation state of Zn in the Sn1-xZnxO2 samples. Interestingly, the XPS data indicated the presence of a small fraction of Sn2+ ions in Sn1-xZnxO2 samples in addition to the expected Sn4+, and the Sn2+ concentration increased with increasing x. The presence of multi-valent metal ions and oxygen defects in high surface area oxide nanoparticles has been proposed as a potential recipe for weak ferromagnetism (Coey et al., New J. Phys. 12, 053025 (2010)).
AB - In this work, we report on the effects of doping SnO2 nanoparticles with Zn2+ ions. A series of ∼2-3nm sized Sn1-xZnxO2 crystallite samples with 0≤x≤0.18 were synthesized using a forced hydrolysis method. Increasing dopant concentration caused systematic changes in the crystallite size, oxidation state of Sn, visible emission, and band gap of SnO2 nanoparticles. X-ray Diffraction studies confirmed the SnO2 phase purity and the absence of any impurity phases. Magnetic measurements at room temperature showed a weak ferromagnetic behavior characterized by an open hysteresis loop. Their saturation magnetization Ms increases initially with increasing Zn concentrations; however for x>0.06, Ms decreases. Samples with the highest Ms values (x=0.06) were analyzed using an Inductively Coupled Plasma Mass Spectrometer, looking for traces of any magnetic elements in the samples. Concentrations of all transition metals (Fe, Co, Mn, Cr, and Ni) in these samples were below ppb level, suggesting that the observed magnetism is not due to random inclusions of any spurious magnetic impurities and it cannot be explained by the existing models of magnetic exchange. A new visible emission near 490nm appeared in the Zn doped SnO2 samples in the photoluminescence spectra which strengthened as x increased, suggesting the formation of defects such as oxygen vacancies. X-ray Photoelectron Spectroscopy (XPS) confirmed the nominal Zn dopant concentrations and the 2+ oxidation state of Zn in the Sn1-xZnxO2 samples. Interestingly, the XPS data indicated the presence of a small fraction of Sn2+ ions in Sn1-xZnxO2 samples in addition to the expected Sn4+, and the Sn2+ concentration increased with increasing x. The presence of multi-valent metal ions and oxygen defects in high surface area oxide nanoparticles has been proposed as a potential recipe for weak ferromagnetism (Coey et al., New J. Phys. 12, 053025 (2010)).
UR - http://www.scopus.com/inward/record.url?scp=84928405147&partnerID=8YFLogxK
U2 - 10.1063/1.4918341
DO - 10.1063/1.4918341
M3 - Article
AN - SCOPUS:84928405147
SN - 0021-8979
VL - 117
JO - Journal of Applied Physics
JF - Journal of Applied Physics
IS - 17
M1 - 17E515
ER -