Towards Selective Partial Water Oxidation to Form H2O2: An Attractive Substitute for O2 Evolution in Water Splitting

2020 ◽  
Vol MA2020-01 (37) ◽  
pp. 1544-1544
Author(s):  
Bastian Timo Mei ◽  
Kasper Wenderich ◽  
Birgit Nieuweweme ◽  
Guido Mul
2020 ◽  
Vol 49 (3) ◽  
pp. 588-592 ◽  
Author(s):  
Fusheng Li ◽  
Ziqi Zhao ◽  
Hao Yang ◽  
Dinghua Zhou ◽  
Yilong Zhao ◽  
...  

A cobalt oxide catalyst prepared by a flame-assisted deposition method on the surface of FTO and hematite for electrochemical and photoelectrochemical water oxidation, respectively.


RSC Advances ◽  
2021 ◽  
Vol 11 (15) ◽  
pp. 8751-8758
Author(s):  
Xiaonong Wang ◽  
Xiaoxia Li ◽  
Jingxiang Low

Photocatalytic water splitting provides an effective way to prepare hydrogen and oxygen.


Author(s):  
Di Li ◽  
Yingying Xing ◽  
Changjian Zhou ◽  
Yikai Lu ◽  
Shengjie Xu ◽  
...  

The high reaction energy barrier of the oxygen evolution reaction (OER) extremely reduces the efficiency of water splitting, which is not conducive to large-scale production of hydrogen. Due to the...


2015 ◽  
Vol 3 (36) ◽  
pp. 18622-18635 ◽  
Author(s):  
Susanginee Nayak ◽  
Lagnamayee Mohapatra ◽  
Kulamani Parida

Dispersion of exfoliated CN over the surface of exfoliated LDH composite materials, and its photocatalytic water splitting under visible-light irradiation.


1989 ◽  
Vol 258 (2) ◽  
pp. 357-362 ◽  
Author(s):  
D J Chapman ◽  
J De Felice ◽  
K Davis ◽  
J Barber

Incubation of a membrane preparation enriched in Photosystem Two (PSII) at alkaline pH inhibited the water-splitting reactions in two distinct steps. Up to pH 8.5 the inhibition was reversible, whereas at higher alkalinities it was irreversible. It was shown that the reversible phase correlated with loss and rebinding of the 23 kDa extrinsic polypeptide. However, after mild alkaline treatments a partial recovery was possible without the binding of the 23 kDa polypeptide when the assay was at the optimal pH of 6.5 and in a medium containing excess Cl-. The irreversible phase was found to be closely linked with the removal of the 33 kDa extrinsic protein of PSII. Treatments with pH values above 8.5 not only caused the 33 kDa protein to be displaced from the PSII-enriched membranes, but also resulted in an irreversible modification of the binding sites such that the extrinsic 33 kDa protein could not reassociate with PSII when the pH was lowered to 6.5. The results obtained with these more extreme alkaline pH treatments support the notion that the 23 kDa protein cannot bind to PSII unless the 33 kDa protein is already bound. The differential effect of pH on the removal of the 23 kDa and 33 kDa proteins contrasted with the data of Kuwabara & Murata [(1983) Plant Cell Physiol. 24, 741-747], but this discrepancy was accounted for by the use of glycerol in the incubation media.


2012 ◽  
Vol 9 (75) ◽  
pp. 2383-2395 ◽  
Author(s):  
Mohammad Mahdi Najafpour ◽  
Fahimeh Rahimi ◽  
Eva-Mari Aro ◽  
Choon-Hwan Lee ◽  
Suleyman I. Allakhverdiev

There has been a tremendous surge in research on the synthesis of various metal compounds aimed at simulating the water-oxidizing complex (WOC) of photosystem II (PSII). This is crucial because the water oxidation half reaction is overwhelmingly rate-limiting and needs high over-voltage (approx. 1 V), which results in low conversion efficiencies when working at current densities required for hydrogen production via water splitting. Particular attention has been given to the manganese compounds not only because manganese has been used by nature to oxidize water but also because manganese is cheap and environmentally friendly. The manganese–calcium cluster in PSII has a dimension of about approximately 0.5 nm. Thus, nano-sized manganese compounds might be good structural and functional models for the cluster. As in the nanometre-size of the synthetic models, most of the active sites are at the surface, these compounds could be more efficient catalysts than micrometre (or bigger) particles. In this paper, we focus on nano-sized manganese oxides as functional and structural models of the WOC of PSII for hydrogen production via water splitting and review nano-sized manganese oxides used in water oxidation by some research groups.


2021 ◽  
Author(s):  
Guangjin Zhang ◽  
Victor Charles ◽  
Yong Yang ◽  
Menglei Yuan ◽  
Jitao Zhang ◽  
...  

Water oxidation reaction involves a four electron-proton coupled process that is kinetically sluggish and has hindered the widespread application of water-splitting technology. Metal-MOF-coupled heterostructures serve as good OER electrocatalysts due...


Author(s):  
Bingjun Jin ◽  
Yoonjun Cho ◽  
Cheolwoo Park ◽  
Jeehun Jeong ◽  
Sungsoon Kim ◽  
...  

The photoelectrochemical (PEC) water splitting efficiency is profoundly restricted by the limited light harvesting, rapid charge recombination, and sluggish water oxidation kinetics, in which the construction of a photoelectrode requires...


2018 ◽  
Vol 9 ◽  
pp. 2432-2442 ◽  
Author(s):  
Malkeshkumar Patel ◽  
Joondong Kim

Co3O4 has been widely studied as a catalyst when coupled with a photoactive material during hydrogen production using water splitting. Here, we demonstrate a photoactive spinel Co3O4 electrode grown by the Kirkendall diffusion thermal oxidation of Co nanoparticles. The thickness-dependent structural, physical, optical, and electrical properties of Co3O4 samples are comprehensively studied. Our analysis shows that two bandgaps of 1.5 eV and 2.1 eV coexist with p-type conductivity in porous and semitransparent Co3O4 samples, which exhibit light-induced photocurrent in photoelectrochemical cells (PEC) containing the alkaline electrolyte. The thickness-dependent properties of Co3O4 related to its use as a working electrode in PEC cells are extensively studied and show potential for the application in water oxidation and reduction processes. To demonstrate the stability, an alkaline cell was composed for the water splitting system by using two Co3O4 photoelectrodes. The oxygen gas generation rate was obtained to be 7.17 mL·h−1 cm−1. Meanwhile, hydrogen gas generation rate was almost twice of 14.35 mL·h−1·cm−1 indicating the stoichiometric ratio of 1:2. We propose that a semitransparent Co3O4 photoactive electrode is a prospective candidate for use in PEC cells via heterojunctions for hydrogen generation.


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