Facile synthesis of carbon nanotube-supported NiO//Fe₂O₃ for all-solid-state supercapacitors

• Shengming Zhang,
• Xuhui Wang,
• Yan Li,
• Xuemei Mu,
• Yaxiong Zhang,
• Jingwei Du,
• Guo Liu,
• Xiaohui Hua,
• Yingzhuo Sheng,
• Erqing Xie and
• Zhenxing Zhang

Beilstein J. Nanotechnol. 2019, 10, 1923–1932, doi:10.3762/bjnano.10.188

• Education, School of Physical Science and Technology, Lanzhou University, Lanzhou 730000, China 10.3762/bjnano.10.188 Abstract We have successfully prepared iron oxide and nickel oxide on carbon nanotubes on carbon cloth for the use in supercapacitors via a simple aqueous reduction method. The obtained

• these two electrodes delivers a high energy density of 63.3 Wh·kg−1 at 1.6 kW·kg−1 and retains 83% of its initial capacitance after 5000 cycles. These results demonstrate that our simple aqueous reduction method to combine CNT and metal oxides reveals an exciting future in constructing high-performance

• supercapacitors. Keywords: aqueous reduction; carbon nanotubes; iron oxide; nickel oxide; supercapacitors; Introduction Supercapacitors offer long cycling life, superior charge–recharge ability, high power density, and wide operating temperature [1][2][3]. However, the low energy density limits their

Chemiresistive/SERS dual sensor based on densely packed gold nanoparticles

• Sanda Boca,
• Cosmin Leordean,
• Simion Astilean and
• Cosmin Farcau

Beilstein J. Nanotechnol. 2015, 6, 2498–2503, doi:10.3762/bjnano.6.259

• (C19H19N7O6) were purchased from Sigma-Aldrich. Gold interdigitated electrodes (IDE) were purchased from Dropsens. Gold nanoparticle synthesis and stabilization: Colloidal gold nanoparticles (AuNPs) were synthesized by the aqueous reduction of HAuCl4 with trisodium citrate. An amount of 100 mL of 10−3 M

Some reflections on the understanding of the oxygen reduction reaction at Pt(111)

• Ana M. Gómez-Marín,
• Ruben Rizo and
• Juan M. Feliu

Beilstein J. Nanotechnol. 2013, 4, 956–967, doi:10.3762/bjnano.4.108

• compared to the bare surface [38]. Hence, it would be possible that OOHads desorbs instead of being reduced and give rise to a soluble OOH• radical species. Following these lines, next steps in the mechanism would be the aqueous reduction of OOH• that will further reduce to water. Under this framework