Nickel–Iron Oxyhydroxide Oxygen-Evolution Electrocatalysts: The Role of Intentional and Incidental Iron Incorporation

2014 ◽  
Vol 136 (18) ◽  
pp. 6744-6753 ◽  
Author(s):  
Lena Trotochaud ◽  
Samantha L. Young ◽  
James K. Ranney ◽  
Shannon W. Boettcher
ACS Catalysis ◽  
2020 ◽  
Vol 11 (1) ◽  
pp. 264-270
Author(s):  
Junwu Xiao ◽  
Alexandra M. Oliveira ◽  
Lan Wang ◽  
Yun Zhao ◽  
Teng Wang ◽  
...  

2021 ◽  
Author(s):  
Laia Francàs ◽  
Shababa Selim ◽  
Sacha Corby ◽  
Dongho Lee ◽  
Camilo A. Mesa ◽  
...  

Elucidating the role of charge accumulation and reaction kinetics in governing the performance of Ni/Fe oxyhydroxides as electrocatalysts and as co-catalysts on BiVO4 photoanodes water oxidation.


2018 ◽  
Vol 11 (5) ◽  
pp. 1287-1298 ◽  
Author(s):  
Prashanth W. Menezes ◽  
Chakadola Panda ◽  
Stefan Loos ◽  
Florian Bunschei-Bruns ◽  
Carsten Walter ◽  
...  

The mechanistically distinct and synergistic role of phosphite anions in hydrogen evolution and nickel cations in oxygen evolution have been uncovered for active and durable overall water splitting catalysis in nickel phosphite.


2021 ◽  
Vol 5 (1) ◽  
Author(s):  
Daire Tyndall ◽  
Sonia Jaskaniec ◽  
Brian Shortall ◽  
Ahin Roy ◽  
Lee Gannon ◽  
...  

AbstractNickel–iron-layered double hydroxide (NiFe LDH) platelets with high morphological regularity and submicrometre lateral dimensions were synthesized using a homogeneous precipitation technique for highly efficient catalysis of the oxygen evolution reaction (OER). Considering edge sites are the point of activity, efforts were made to control platelet size within the synthesized dispersions. The goal is to controllably isolate and characterize size-reduced NiFe LDH particles. Synthetic approaches for size control of NiFe LDH platelets have not been transferable based on published work with other LDH materials and for that reason, we instead use postsynthetic treatment techniques to improve edge-site density. In the end, size-reduced NiFe LDH/single-wall carbon nanotube (SWCNT) composites allowed to further reduce the OER overpotential to 237 ± 7 mV (<L> = 0.16 ± 0.01 μm, 20 wt% SWCNT), which is one of the best values reported to date. This approach as well improved the long-term activity of the catalyst in operating conditions.


2021 ◽  
Vol 8 (3) ◽  
pp. 558-562
Author(s):  
Shan Chen ◽  
Shuaihu Jiang ◽  
Yuan Rao ◽  
Yi Dong ◽  
Junfei Bu ◽  
...  

2002 ◽  
Vol 29 (10) ◽  
pp. 1141 ◽  
Author(s):  
Govindjee ◽  
Manfredo J. Seufferheld

This paper deals first with the early, although incomplete, history of photoinhibition, of 'non-QA-related chlorophyll (Chl) a fluorescence changes', and the xanthophyll cycle that preceded the discovery of the correlation between non-photochemical quenching of Chl a fluorescence (NPQ) and conversion of violaxanthin to zeaxanthin. It includes the crucial observation that the fluorescence intensity quenching, when plants are exposed to excess light, is indeed due to a change in the quantum yield of fluorescence. The history ends with a novel turn in the direction of research — isolation and characterization of NPQ xanthophyll-cycle mutants of Chlamydomonas reinhardtii Dangeard and Arabidopsis thaliana (L.) Heynh., blocked in conversion of violaxanthin to zeaxanthin, and zeaxanthin to violaxanthin, respectively. In the second part of the paper, we extend the characterization of two of these mutants (npq1, which accumulates violaxanthin, and npq2, which accumulates zeaxanthin) through parallel measurements on growth, and several assays of PSII function: oxygen evolution, Chl a fluorescence transient (the Kautsky effect), the two-electron gate function of PSII, the back reactions around PSII, and measurements of NPQ by pulse-amplitude modulation (PAM 2000) fluorimeter. We show that, in the npq2 mutant, Chl a fluorescence is quenched both in the absence and presence of 3-(3,4-dichlorophenyl)-1,1-dimethylurea (DCMU). However, no differences are observed in functioning of the electron-acceptor side of PSII — both the two-electron gate and the back reactions are unchanged. In addition, the role of protons in fluorescence quenching during the 'P-to-S' fluorescence transient was confirmed by the effect of nigericin in decreasing this quenching effect. Also, the absence of zeaxanthin in the npq1 mutant leads to reduced oxygen evolution at high light intensity, suggesting another protective role of this carotenoid. The available data not only support the current model of NPQ that includes roles for both pH and the xanthophylls, but also are consistent with additional protective roles of zeaxanthin. However, this paper emphasizes that we still lack sufficient understanding of the different parts of NPQ, and that the precise mechanisms of photoprotection in the alga Chlamydomonas may not be the same as those in higher plants.


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