scholarly journals Operando X-ray Absorption Spectroscopy (XAS) Observation of Photoinduced Oxidation in FeNi (Oxy)hydroxide Overlayers on Hematite (α-Fe2O3) Photoanodes for Solar Water Splitting

Langmuir ◽  
2020 ◽  
Vol 36 (39) ◽  
pp. 11564-11572
Author(s):  
Anton Tsyganok ◽  
Paolo Ghigna ◽  
Alessandro Minguzzi ◽  
Alberto Naldoni ◽  
Vadim Murzin ◽  
...  
2020 ◽  
Vol 234 (5) ◽  
pp. 867-885 ◽  
Author(s):  
Swati Kumari ◽  
Chinmay Khare ◽  
Fanxing Xi ◽  
Mona Nowak ◽  
Kirill Sliozberg ◽  
...  

AbstractIn order to identify new solar water splitting photoanodes, Fe–Ti–W–O materials libraries were fabricated by combinatorial reactive co-sputtering and investigated by high-throughput characterization methods to elucidate compositional, thickness, and structural properties. In addition, photoelectrochemical measurements such as potentiodynamic photocurrent determination and open circuit potential measurements were performed using an automated scanning droplet cell. In the thin-film library, a quaternary photoactive region Fe30–49Ti29–55W13–22Ox was identified as a hit composition region, comprising binary and ternary phases. The identified region shows a distinct surface morphology with larger grains (∼200 nm) being embedded into a matrix of smaller grains (∼80–100 nm). A maximum photocurrent density of 117 μA/cm2 at a bias potential of 1.45 V vs. RHE in NaClO4 as an electrolyte under standard solar simulating conditions was recorded. Additional samples with compositions from the hit region were fabricated by reactive co-sputtering and spin coating followed by annealing. Synchrotron X-ray diffraction of sputtered Fe32Ti52W16Ox thin-films, annealed in air (600 °C, 700 °C, 800 °C) revealed the presence of the phases FeTiO3 and Ti0.54W0.46O2. The composition Fe48Ti30W22Ox from the hit region was fabricated by spin coating and subsequent annealing for a detailed investigation of its structure and photoactivity. After annealing the spin-coated sample at 650 °C for 6 h, X-ray diffraction results showed a dominant pattern with narrow diffraction lines belonging to a distorted FeWO4 (ferberite) phase along with broad diffraction lines addressed as Fe2TiO5 and in a small fraction also, Fe1.7Ti0.23O3. In hematite, Fe can be substituted by Ti, therefore we suggest that in the newfound ferberite-type phase, Ti partially substitutes for Fe leading to a small lattice distortion and a doubling of the monoclinic unit cell. In addition, Na from the substrate stabilizes the new phase: its tentative chemical formula is NaxFe0.33Ti0.67W2O8. A maximum photocurrent density of around 0.43 mA/cm2 at 1.45 V vs. RHE in 1M NaOH (pH ∼ 13.6) as an electrolyte was measured. Different aspects of the dependence of annealing and precursor solution concentration on phase transformation and photoactivity are discussed.


2016 ◽  
Vol 50 (2) ◽  
pp. 024002 ◽  
Author(s):  
J J Velasco-Vélez ◽  
Travis E Jones ◽  
Verena Pfeifer ◽  
Chung-Li Dong ◽  
Yu-Xun Chen ◽  
...  

Author(s):  
Takafumi Miura ◽  
Shun Tsunekawa ◽  
Sho Onishi ◽  
Toshiaki Ina ◽  
Kehsuan Wang ◽  
...  

The role of diamines incorporated in a nickel oxide electrocatalyst for water splitting was examined using operando UV/XAFS spectroscopic techniques.


Author(s):  
Craig Lawley ◽  
Zahra Pourmand Tehrani ◽  
Adam Hugh Clark ◽  
Olga V. Safonova ◽  
Max Döbeli ◽  
...  

Oxynitrides have been shown to be promising visible light water splitting photocatalysts, but rapidly degrade under operating conditions. With a custom designed photoelectrochemical cell, we perform operando grazing incidence X-ray...


2017 ◽  
Vol 5 (1) ◽  
pp. 20-26 ◽  
Author(s):  
Emiliana Fabbri ◽  
Daniel F. Abbott ◽  
Maarten Nachtegaal ◽  
Thomas J. Schmidt

2019 ◽  
Vol 31 (3) ◽  
pp. 559-565
Author(s):  
K. Kathiresan ◽  
P. Elangovan ◽  
M.S.S. Saravanakumaar

Herein, we report the fabrication of titanium dioxide nanotubes via anodization technique through with and without hydrofluoric acid . The impact of hydrofluoric acid followed by annealing effect on TiO2 nanotubes for the solar water splitting performance was examined. Prepared TiO2 samples exhibited a diameter of about 50 to 100 nm sized nanotubes and hierarchical structures and they subjected to annealing. Synthesis and annealing effects on chemical, physical and photoelectrochemical water splitting activity of TiO2 samples were scrutinized. The crystalline nature, structure and surface morphologies of prepared TiO2 photocatalysts were explored by X-ray diffraction, scanning electron microscope, and the oxidation states of both titanium and oxygen was determined by X-ray photoelectron spectroscopy. As a consequence, after annealing at 500 ºC, TiO2 thin films treated with hydrofluoric acid solution (HF-TiO2) were found to exhibit a remarkable photoelectrochemical performance than bare TiO2 nanotubes under UV light irradiation. Moreover, the mechanistic insights acquired in the current research would be beneficial to design a novel and highly efficient photocatalyst for solar water splitting systems.


ACS Catalysis ◽  
2021 ◽  
pp. 12324-12335
Author(s):  
Ahmed S. M. Ismail ◽  
Ivan Garcia-Torregrosa ◽  
Jeroen C. Vollenbroek ◽  
Laura Folkertsma ◽  
Johan G. Bomer ◽  
...  

2002 ◽  
Vol 10 (1) ◽  
pp. 76-85 ◽  
Author(s):  
Holger Dau ◽  
Michael Haumann

Understanding structure–function relations is one of the main interests in the molecular biosciences. X-ray absorption spectroscopy of biological samples (BioXAS) has gained the status of a useful tool for characterization of the structure of protein-bound metal centers with respect to the electronic structure (oxidation states, orbital occupancies) and atomic structure (arrangement of ligand atoms). Owing to progress in the performance characteristics of synchrotron radiation sources and of experimental stations dedicated to the study of (ultra-dilute) biological samples, it is now possible to carry out new types of BioXAS experiments, which have been impracticable in the past. Of particular interest are approaches to follow biological catalysis at metal sites by characterization of functionally relevant structural changes. In this article, the first steps towards the use of BioXAS to `watch' biological catalysis are reviewed for the water-splitting reactions occurring at the manganese complex of photosynthesis. The following aspects are considered: the role of BioXAS in life sciences; methodological aspects of BioXAS; catalysis at the Mn complex of photosynthesis; combination of EXAFS and crystallographic information; the freeze-quench technique to capture semi-stable states; time-resolved BioXAS using a freeze-quench approach; room-temperature experiments and `real-time' BioXAS; tasks and perspectives.


2020 ◽  
Author(s):  
Anton Tsyganok ◽  
Paolo Ghigna ◽  
Alessandro Minguzzi ◽  
Alberto Naldoni ◽  
Vadim Murzin ◽  
...  

A FeNi (oxy)hydroxide co-catalyst overlayer was photoelectrochemically deposited on a thin film hematite (α-Fe2O3) photoanode, leading to a cathodic shift of ~100 mV in the photocurrent onset potential. Operando X-ray absorption spectroscopy (XAS) at the Fe and Ni K-edges was used to study the changes in the overlayer with potential, in dark and under illumination conditions. Potential or illumination only had a minor effect on the Fe oxidation state, suggesting that Fe atoms do not accumulate significant amount of charge over the whole potential range. In contrast, the Ni K-edge spectra showed pronounced dependence on potential in dark and under illumination. The effect of illumination is to shift the onset for the Ni oxidation because of the generated photovoltage, and suggests that holes which are photogenerated in hematite are transferred mainly to the Ni atoms in the overlayer. The increase in the oxidation state of Ni proceeds at potentials corresponding to the redox wave of Ni, which occurs immediately prior to the onset of the oxygen evolution reaction (OER). Linear fitting analysis of the obtained spectra suggests that the overlayer does not have to be fully oxidized to promote oxygen evolution. Cathodic discharge measurements show that the photogenerated charge is stored almost exclusively in the Ni atoms within the volume of the overlayer. <br>


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