Possible mechanisms of water splitting reaction based on proton and electron release pathways revealed for CaMn4O5 cluster of PSII refined to 1.9 Å X-ray resolution

2011 ◽  
Vol 112 (1) ◽  
pp. 253-276 ◽  
Author(s):  
T. Saito ◽  
S. Yamanaka ◽  
K. Kanda ◽  
H. Isobe ◽  
Y. Takano ◽  
...  
2020 ◽  
Vol 2020 ◽  
pp. 1-11 ◽  
Author(s):  
Nur Aimi Jani ◽  
Choonyian Haw ◽  
Weesiong Chiu ◽  
Saadah Abdul Rahman ◽  
Poisim Khiew ◽  
...  

Current work reports the study of Ag nanocrystals (NCs) decorated doubly anodized (DA) TiO2 nanotubes (NTs) thin film as an efficient photoelectrode material for water splitting and photocatalytic hydrogen gas production. DA process has been shown to be capable of producing less defective NTs and creating additional spacious gaps in between NT bundles to allow efficient and uniform integration of Ag NCs. By employing photoreduction method, Ag NCs can be deposited directly onto NTs, where the size and density of coverage can be maneuvered by merely varying the concentration of Ag precursors. Field emission scanning electron microscope (FESEM) images show that the Ag NCs with controllable size are homogeneously decorated onto the walls of NTs with random yet uniform distribution. X-ray diffraction (XRD) results confirm the formation of anatase TiO2 NTs and Ag NCs, which can be well indexed to standard patterns. The decoration of metallic Ag NCs onto the surface of NTs demonstrates a significant enhancement in the photoconversion efficiency as compared to that of pristine TiO2 NTs. Additionally, the as-prepared nanocomposite film also shows improved efficiency when used as a photocatalyst platform in the production of hydrogen gas. Such improvement in the performance of water splitting and photocatalytic hydrogen gas production activity can be credited to the surface plasmonic resonance of Ag NCs present on the surface of the NTs, which renders improved light absorption and better charge separation. The current work can serve as a model of study for designing more advanced nanoarchitecture photoelectrode for renewable energy application.


2013 ◽  
Vol 594-595 ◽  
pp. 73-77 ◽  
Author(s):  
Sze Mei Chin ◽  
Suriati Sufian ◽  
Jeefferie Abd Razak

This paper highlights on the hydrogen production through photocatalytic activity by using hematite nanoparticles synthesized from self-combustion method based on different stirring period. The morphologies and microstructures of the nanostructures were determined using Field-Emission Scanning Electron Microscope (FESEM), X-Ray Diffractometer (XRD) and Particle Size Analyser (PSA). Besides that, surface area analyser was used to determine the BET surface area of the hematite samples. The hematite nanocatalyst as-synthesized are proven to be rhombohedral crystalline hematite (α-Fe2O3) with particle diameters ranging from 60-140 nm. The BET specific surface area of hematite samples increased from 5.437 to 7.6425 m2/g with increasing stirring period from 1 to 4 weeks. This caused the amount of hydrogen gas produced from photocatalytic water splitting to increase as well.


2021 ◽  
Author(s):  
Xunliang Hu ◽  
Irshad Hussain ◽  
Bien Tan

Abstract Covalent triazine frameworks (CTFs) have recently been demonstrated as promising materials for photocatalytic water splitting and are usually used in the form of suspended powder. From a practical point of view, immobilized CTFs materials are more suitable for large-scale water splitting applications, owing to their convenient separation and recycling potential. However, existing synthetic approaches mainly result in insoluble and unprocessable powders, which makes their future device application still a huge challenge. Herein, we report an aliphatic amine-assisted interfacial polymerization method to obtain free-standing, crystalline CTFs film with excellent photoelectric performance. The lateral size of the film was up to 250 cm2, the average thickness can be regulated from 30-500 nm. The crystalline structure was confirmed by high-resolution transmission electron microscope (HR-TEM), powder X-ray diffraction (PXRD), and small-angle X-ray scattering (SAXS) analysis. Intrigued by the good light absorption, crystalline structure, and big lateral size of the film, it was immobilized on a glass support that exhibited good photocatalytic hydrogen evolution performance (5.4 mmol h-1 m-2) and was easy to recycle.


2011 ◽  
Vol 135 (11) ◽  
pp. 114703 ◽  
Author(s):  
Matthew Weston ◽  
Thomas J. Reade ◽  
Andrew J. Britton ◽  
Karsten Handrup ◽  
Neil R. Champness ◽  
...  

Materials ◽  
2020 ◽  
Vol 13 (3) ◽  
pp. 744 ◽  
Author(s):  
Jinyu Huang ◽  
Feifei Li ◽  
Baozhong Liu ◽  
Peng Zhang

The hydrogen generated via the water splitting method is restricted by the high level of theoretical potential exhibited by the anode. The work focuses on synthesizing a bifunctional catalyst with a high efficiency, that is, a nickel phosphide doped with the reduced graphene oxide nanosheets supported on the Ni foam (Ni2P/rGO/NF), via the hydrothermal approach together with the calcination approach specific to the hydrogen evolution reaction (HER) and the oxygen evolution reaction (OER). The Raman, X-Ray Diffraction (XRD), X-ray Photoelectron Spectroscopy (XPS), Transmission Electron Microscope (TEM), Scanning Electron Microscopy (SEM), High-Resolution Transmission Electron Microscopy (HRTEM), as well as elemental mapping, are adopted to study the composition and morphology possessed by Ni2P/rGO/NF. The electrochemical testing is performed by constructing a parallel two-electrode electrolyzer (Ni2P/rGO/NF||Ni2P/rGO/NF). Ni2P/rGO/NF||Ni2P/rGO/NF needs a voltage of only 1.676 V for driving 10 mA/cm2, which is extremely close to Pt/C/NF||IrO2/NF (1.502 V). It is possible to maintain the current density for no less than 30 hours. It can be demonstrated that Ni2P/rGO/NF||Ni2P/rGO/NF has commercial feasibility, relying on the strong activity and high stability.


Catalysts ◽  
2020 ◽  
Vol 10 (2) ◽  
pp. 261 ◽  
Author(s):  
Van Nghia Nguyen ◽  
Minh Vuong Nguyen ◽  
Thi Hong Trang Nguyen ◽  
Minh Thuy Doan ◽  
Loan Le Thi Ngoc ◽  
...  

High-stability, high-efficiency, and low-cost solar photoelectrochemical (PEC) water splitting has great potential for hydrogen-energy applications. Here, we report on gold/titanium dioxide (Au/TiO2) nanofiber structures grown directly on a conductive indium tin oxide substrate, and used as photoelectrodes in PEC cells for hydrogen generation. The titanium dioxide nanofibers (TiO2 NFs) are synthesized using electrospinning, and are surface-modified by the deposition of gold nanoparticles (Au NPs) using a simple photoreduction method. The structure and morphology of the materials were characterized by field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). The surface plasmon resonance (SPR) of the Au NPs was investigated by ultraviolet-visible (UV-Vis) diffuse reflectance spectroscopy. The PEC properties of the as-prepared photoelectrodes were measured. The obtained photoconversion efficiency of 0.52% under simulated-sunlight illumination by a 150 W xenon lamp of the Au/TiO2 NFs structure with 15 min UV irradiation for Au NP deposition was the highest value from comparable structures. Working photoelectrode stability was tested, and the mechanism of the enhanced PEC performance is discussed.


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.


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