Our Group organises 3000+ Global Conferenceseries Events every year across USA, Europe & Asia with support from 1000 more scientific Societies and Publishes 700+ Open Access Journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.
Electrochemically fabricated substrate dependent smart electrocatalysts Ni-Fe double and Ni-Co-Fe triple hydroxides for efficient water splitting to oxygen and hydrogen
21st International Conference on Advanced Energy Materials and Research
Water electrolysis is a significant method that can utilize renewable energy to produce hydrogen; a fuel that can
transform earth towards a clean energy future. Activity of electrocatalysts for water oxidation is fundamental
for energy conversion technologies including integrated solar power generating devices and water electrolyzers.
In this study we have electrochemically fabricated the naturally abundant and stable electrocatalysts Ni-Fedouble
hydroxides, Ni-Fe-Co-triple hydroxides, for efficient splitting of water to oxygen and clean fuel hydrogen.
Oxygen-evolution activities of these electrocatalysts were examined in an alkaline solution of KOH. We focused in
determining electro-catalytic activity of these double and triple hydroxides electrodeposited on different substrates
such as Ni-foam, electrodeposited Ni-Co-oxide on Ni-foam and pressed porous Ni-Co oxide under varying
electrodeposition bath composition, electrodeposition time and electrodeposition current and potentials. We found
that Ni-Fe-Co triple hydroxide electrodeposited for total of 10 min on pressed porous Ni-Co-oxide sheet acted as a
superior electrocatalyst for oxygen evolution reaction during water splitting reaction. This electrocatalyst generated
a current density of ~ 100.0 mA cm-2 at an oxygen overpotential of 0.270 volt (= 1.5-volt vs RHE) in 1.0 M KOH at
electrolyte temperature of 25°C. However, this triple hydroxide deposited for 7 min generated 81.0 mA cm-2 at the
same overpotential, electrolyte concentration and temperature. The synergetic effect of multiple hydroxides and
the substrates was mostly responsible for such enhanced electro-catalytic activity. The effect of higher electrolyte
temperature was also found to have important role in enhancing the current density because of exponential
dependence of reaction rate on temperature. The surface morphology and the composition of these electrocatalysts
were determined using the scanning electron microscope (SEM) and energy dispersive spectroscopic (EDS) data.
Recent Publications
1. Khan S U M, Al-Shahry M and Ingler Jr W B (2002) Efficient Photochemical Water-splitting by Chemically
Modified n-TiO2. Science 297:2243-2245.
2. Shabana Y A, El-Sayed M A, El-Maradny A A, Al-Farawati R K, Al-Zobidi M I and Khan S U M (2016)
Photocatalytic removal of polychlorinated biphenyls (PCBs) using carbon- modified titanium oxide
nanoparticles. Applied Surface Science 365:108–113.
3. Kavil Y N, Shaban Y A, Orif M I, Al-Farawati R, Zobidi M Khan and S U M (2018) Production of methanol
as a fuel energy from CO2 present in polluted seawater - a photocatalytic outlook. Open Chem., 16:1089-1098.
4. Frites M, Ingler W B and Khan S U M (2014) A single chip standalone water splitting photoelectrochemical cell.
J. Technol. Innov. in Renewable Ener., 3:6-11.
Biography
Shahed U M Khan has his expertise in the synthesis of materials for the electrochemical and photoelectrochemical splitting of water. He published more than 140 papers in various journals including some top ones such “Journal of Physical Chemistry”, “Journal of American Chemical Society”, “Journal of Electrochemical Society”, “Chemical Physics, Applied Physics and Science”. He co-authored books entitled “Quantum Electrochemistry”, “Surface Electrochemistry” and coedited volume 7 of “Comprehensive Treatise of Electrochemistry.” The focus of his research is to synthesize highly stable energy materials based on naturally abundant sources for efficient splitting of water to oxygen and hydrogen, a clean fuel to have carbon footprint free society in the planet Earth.