scholarly journals Selective nitration of PsbO1, PsbO2, and PsbP1 decreases PSII oxygen evolution and photochemical efficiency in intact leaves of Arabidopsis

2017 ◽  
Vol 12 (10) ◽  
pp. e1376157 ◽  
Author(s):  
Misa Takahashi ◽  
Jun Shigeto ◽  
Atsushi Sakamoto ◽  
Hiromichi Morikawa
Keyword(s):  
Oxygen Evolution ◽  
Photochemical Efficiency ◽  
Intact Leaves ◽  
Selective Nitration

The Role of D 1* in Light-Induced D 1 Protein Turnover in Leaves

1993 ◽  
Vol 48 (3-4) ◽  
pp. 246-250
Author(s):  
Anna J. Syme ◽  
Harald R . Bolhàr-N ordenkampf ◽  
Christa Critchley
Keyword(s):  
Chlorophyll Fluorescence ◽  
Photosystem Ii ◽  
Light Intensity ◽  
Protein Turnover ◽  
Photochemical Efficiency ◽  
Light Conditions ◽  
Ps Ii ◽  
Light Intensities ◽  
Intact Leaves

Abstract Light-induced degradation of the D 1 protein of photosystem II (PS II) was determined by radioactive pulse-chase labelling experiments in intact leaves of Schefflera polybotrya. PS II photochemical efficiency was monitored by measuring chlorophyll fluorescence. A significant and consistent decline in the Fv/ Fm ratio was taken to indicate photoinhibition. The formation and degradation of a modified form of the D 1 protein, D 1*, was different under photoinhibi-tory or non-photoinhibitory light conditions. At photoinhibitory irradiance greater amounts of D 1 * were formed relative to D 1, and the degradation of D 1* was slower when compared with non-photoinhibitory irradiance. The formation and degradation of D 1* were therefore shown to be at least partly light intensity dependent. Higher light intensities appeared to slow D 1* degradation, which suggests a modification in PS II turnover properties.

scholarly journals Selective nitration of PsbO1 inhibits oxygen evolution from isolated Arabidopsis thylakoid membranes

2017 ◽  
Vol 12 (4) ◽  
pp. e1304342 ◽  
Author(s):  
Misa Takahashi ◽  
Jun Shigeto ◽  
Atsushi Sakamoto ◽  
Hiromichi Morikawa
Keyword(s):  
Oxygen Evolution ◽  
Thylakoid Membranes ◽  
Selective Nitration

Rational prediction of multifunctional bilayer single atom catalysts for the hydrogen evolution, oxygen evolution and oxygen reduction reactions

Nanoscale ◽  
2020 ◽  
Vol 12 (39) ◽  
pp. 20413-20424
Author(s):  
Riming Hu ◽  
Yongcheng Li ◽  
Fuhe Wang ◽  
Jiaxiang Shang
Keyword(s):  
Oxygen Reduction ◽  
Hydrogen Evolution ◽  
Oxygen Evolution ◽  
Single Atom ◽  
Reduction Reactions ◽  
Oxygen Reduction Reactions

Bilayer single atom catalysts can serve as promising multifunctional electrocatalysts for the HER, ORR, and OER.

Towards a Design of Active Oxygen Evolution Catalysts: Insights from Automated Density Functional Theory Calculations and Machine Learning

2019 ◽  
Author(s):  
Seoin Back ◽  
Kevin Tran ◽  
Zachary Ulissi
Keyword(s):  
Machine Learning ◽  
Oxygen Evolution ◽  
Active Sites ◽  
Density Functional ◽  
Chemical Space ◽  
Density Functional Theory Calculations ◽  
Catalyst Design ◽  
Transition Metal Catalysts ◽  
Oxide Materials ◽  
Design Strategies

<div> <div> <div> <div><p>Developing active and stable oxygen evolution catalysts is a key to enabling various future energy technologies and the state-of-the-art catalyst is Ir-containing oxide materials. Understanding oxygen chemistry on oxide materials is significantly more complicated than studying transition metal catalysts for two reasons: the most stable surface coverage under reaction conditions is extremely important but difficult to understand without many detailed calculations, and there are many possible active sites and configurations on O* or OH* covered surfaces. We have developed an automated and high-throughput approach to solve this problem and predict OER overpotentials for arbitrary oxide surfaces. We demonstrate this for a number of previously-unstudied IrO2 and IrO3 polymorphs and their facets. We discovered that low index surfaces of IrO2 other than rutile (110) are more active than the most stable rutile (110), and we identified promising active sites of IrO2 and IrO3 that outperform rutile (110) by 0.2 V in theoretical overpotential. Based on findings from DFT calculations, we pro- vide catalyst design strategies to improve catalytic activity of Ir based catalysts and demonstrate a machine learning model capable of predicting surface coverages and site activity. This work highlights the importance of investigating unexplored chemical space to design promising catalysts.<br></p></div></div></div></div><div><div><div> </div> </div> </div>

S Doping Optimized Intermediate Energetics of FeCoOOh for Enhanced Oxygen Evolution Catalytic Activity

2020 ◽  
Author(s):  
Ding Yuan ◽  
Yuhai Dou ◽  
Chun-Ting He ◽  
Linping Yu ◽  
Li Xu ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Oxygen Evolution

ALGAE AND PROGRESS IN PHOTOSYNTHESIS RESEARCH I-Oxygen evolution and carbon fixation

2000 ◽  
Vol 1 (1) ◽  
pp. 235-244
Author(s):  
Ahmed Hamad ◽  
Mohamed Osman ◽  
Refaat Abdel-Basset
Keyword(s):  
Oxygen Evolution ◽  
Carbon Fixation ◽  
Photosynthesis Research

Effect of various cations on the initial rate of formation of peroxodisulphates

1980 ◽  
Vol 45 (8) ◽  
pp. 2272-2282 ◽  
Author(s):  
Jan Balej ◽  
Martin Kadeřávek
Keyword(s):  
Sulphuric Acid ◽  
Oxygen Evolution ◽  
Anodic Polarization ◽  
Initial Rate ◽  
Degree Of Conversion ◽  
Polarization Curves ◽  
Mixed Solutions ◽  
Low Degree ◽  
Partial Polarization

Preparation of peroxodisulphates by electrolysis of mixed solutions of sulphuric acid and various sulphates was studied at low degree of conversion; the partial polarization curves of peroxodisulphate formation and of oxygen evolution obtained from the overall anodic polarization curves and current yields of the principal anodic processes were examined. The mechanism of the effect of various cations on the rate of anodic formation of peroxodisulfates is discussed.

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