Amorphous Nickel Hydroxide Nanosheets with Ultrahigh Activity and Super-Long-Term Cycle Stability as Advanced Water Oxidation Catalysts

2015 ◽  
Vol 15 (9) ◽  
pp. 4475-4483 ◽  
Author(s):  
Yuqian Gao ◽  
Hongbo Li ◽  
Guowei Yang
2012 ◽  
Vol 65 (6) ◽  
pp. 638 ◽  
Author(s):  
Alex Izgorodin ◽  
Orawan Winther-Jensen ◽  
Douglas R. MacFarlane

Future requirements for water splitting technologies need highly efficient water oxidation catalysts that are sufficiently stable for operation over many years. Recent research has achieved significant progress in improving the electro-catalytic activities of these catalysts. However, there has not been a strong research focus on their long-term mechanical and chemical stability, yet this is critical for commercial application. In this paper we discuss some of the chemical and thermodynamic challenges confronting this goal, as well as some of the strategies that are available to overcome them. The challenge becomes even greater in the area of photo-active electromaterials; fortunately some of the same strategies may allow progress in this area also.


Inorganics ◽  
2019 ◽  
Vol 7 (3) ◽  
pp. 29 ◽  
Author(s):  
Christos Mavrokefalos ◽  
Greta Patzke

The expected shortage of fossil fuels as well as the accompanying climate change are among the major challenges of the 21st century. A global shift to a sustainable energy landscape is, therefore, of utmost importance. Over the past few years, solar technologies have entered the energy market and have paved the way to replace fossil-based energy sources, in the long term. In particular, electrochemical solar-to-hydrogen technologies have attracted a lot of interest—not only in academia, but also in industry. Solar water splitting (artificial photosynthesis) is one of the most active areas in contemporary materials and catalysis research. The development of low-cost, efficient, and stable water oxidation catalysts (WOCs) remains crucial for artificial photosynthesis applications, because WOCs still represent a major economical and efficient bottleneck. In the following, we summarize recent advances in water oxidation catalysts development, with selected examples from 2016 onwards. This condensed survey demonstrates that the ongoing quest for new materials and informed catalyst design is a dynamic and rapidly developing research area.


2021 ◽  
Author(s):  
Venkataramanan Mahalingam ◽  
Gouri Tudu ◽  
Sourav Ghosh ◽  
Sagar Ganguli ◽  
Murthy Koppsetti ◽  
...  

Sustainable electrocatalytic water splitting stipulates development of cheap, efficient and stable electrocatalysts to promote comparatively sluggish oxygen evolution reaction. We have synthesized iron incorporated pure phase α-nickel hydroxide, Ni0.8Fe0.2(OH)2 electrocatalyst...


2021 ◽  
Vol 60 (3) ◽  
pp. 1806-1813
Author(s):  
Husain N. Kagalwala ◽  
Mahesh S. Deshmukh ◽  
Elamparuthi Ramasamy ◽  
Neelima Nair ◽  
Rongwei Zhou ◽  
...  

Solar RRL ◽  
2021 ◽  
Author(s):  
Matthew V. Sheridan ◽  
Benjamin D. Sherman ◽  
Yi Xie ◽  
Ying Wang

Inorganics ◽  
2018 ◽  
Vol 6 (4) ◽  
pp. 105 ◽  
Author(s):  
Laurent Sévery ◽  
Sebastian Siol ◽  
S. Tilley

Anchored molecular catalysts provide a good step towards bridging the gap between homogeneous and heterogeneous catalysis. However, applications in an aqueous environment pose a serious challenge to anchoring groups in terms of stability. Ultrathin overlayers embedding these catalysts on the surface using atomic layer deposition (ALD) are an elegant solution to tackle the anchoring group instability. The propensity of ALD precursors to react with water leads to the question whether molecules containing aqua ligands, such as most water oxidation complexes, can be protected without side reactions and deactivation during the deposition process. We synthesized two iridium and two ruthenium-based water oxidation catalysts, which contained an aqua ligand (Ir–OH2 and Ru–OH2) or a chloride (Ir–Cl and Ru–Cl) that served as a protecting group for the former. Using a ligand exchange reaction on the anchored and partially embedded Ru–Cl, the optimal overlayer thickness was determined to be 1.6 nm. An electrochemical test of the protected catalysts on meso-ITO showed different behaviors for the Ru and the Ir catalysts. The former showed no onset difference between protected and non-protected versions, but limited stability. Ir–Cl displayed excellent stability, whilst the unprotected catalyst Ir–OH2 showed a later initial onset. Self-regeneration of the catalytic activity of Ir–OH2 under operating conditions was observed. We propose chloride ligands as generally applicable protecting groups for catalysts that are to be stabilized on surfaces using ALD.


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