Water Oxidation Catalysis: Electrocatalytic Response to Metal Stoichiometry in Amorphous Metal Oxide Films Containing Iron, Cobalt, and Nickel DOI
Rodney D. L. Smith, Mathieu S. Prévot,

Randal D. Fagan

et al.

Journal of the American Chemical Society, Journal Year: 2013, Volume and Issue: 135(31), P. 11580 - 11586

Published: July 24, 2013

Photochemical metal–organic deposition (PMOD) was used to prepare amorphous metal oxide films containing specific concentrations of iron, cobalt, and nickel study how composition affects heterogeneous electrocatalytic water oxidation. Characterization the by energy-dispersive X-ray spectroscopy photoelectron confirmed excellent stoichiometric control each 21 complex investigated. In studying electrochemical oxidation catalyzed respective films, it found that small iron produced a significant improvement in Tafel slopes cobalt or were critical lowering voltage at which catalysis commences. The best catalytic parameters series obtained for film a-Fe20Ni80. An extrapolation XPS data indicates optimal behavior this binary be manifestation stabilizing higher level. This work represents first mechanistic phases ternary oxides use as catalysts, provides foundation broad exploration other mixed-metal combinations.

Language: Английский

Electrocatalysis for the oxygen evolution reaction: recent development and future perspectives DOI

Nian-Tzu Suen,

Sung‐Fu Hung, Quan Quan

et al.

Chemical Society Reviews, Journal Year: 2017, Volume and Issue: 46(2), P. 337 - 365

Published: Jan. 1, 2017

We review the fundamental aspects of metal oxides, chalcogenides and pnictides as effective electrocatalysts for oxygen evolution reaction.

Language: Английский

Citations

5348

Benchmarking Hydrogen Evolving Reaction and Oxygen Evolving Reaction Electrocatalysts for Solar Water Splitting Devices DOI
Charles C. L. McCrory, Suho Jung,

Ivonne M. Ferrer

et al.

Journal of the American Chemical Society, Journal Year: 2015, Volume and Issue: 137(13), P. 4347 - 4357

Published: Feb. 10, 2015

Objective comparisons of electrocatalyst activity and stability using standard methods under identical conditions are necessary to evaluate the viability existing electrocatalysts for integration into solar-fuel devices as well help inform development new catalytic systems. Herein, we use a protocol primary screen evaluating activity, short-term (2 h) stability, electrochemically active surface area (ECSA) 18 hydrogen evolution reaction (HER) 26 oxygen (OER) relevant an integrated solar water-splitting device in aqueous acidic or alkaline solution. Our figure merit is overpotential achieve magnitude current density 10 mA cm(-2) per geometric area, approximate expected 10% efficient solar-to-fuels conversion 1 sun illumination. The specific ECSA each material also reported. Among HER catalysts, several could operate at with overpotentials <0.1 V and/or solutions. OER catalysts solution, no non-noble metal based materials showed promising whereas solution many performed similar achieving densities ~0.33-0.5 V. Most comparable better when compared Ir Ru solutions, while most much lower than Pt both For select additional secondary screening measurements were conducted including Faradaic efficiency extended measurements.

Language: Английский

Citations

3541

Earth-abundant catalysts for electrochemical and photoelectrochemical water splitting DOI
Isolda Roger, Michael Shipman, Mark D. Symes

et al.

Nature Reviews Chemistry, Journal Year: 2017, Volume and Issue: 1(1)

Published: Jan. 11, 2017

Language: Английский

Citations

3058

Solar Energy Supply and Storage for the Legacy and Nonlegacy Worlds DOI
Timothy R. Cook, Dilek K. Dogutan,

Steven Y. Reece

et al.

Chemical Reviews, Journal Year: 2010, Volume and Issue: 110(11), P. 6474 - 6502

Published: Nov. 10, 2010

ADVERTISEMENT RETURN TO ISSUEPREVReviewNEXTSolar Energy Supply and Storage for the Legacy Nonlegacy WorldsTimothy R. Cook, Dilek K. Dogutan, Steven Y. Reece, Yogesh Surendranath, Thomas S. Teets, Daniel G. Nocera*View Author Information Department of Chemistry, 6-335, Massachusetts Institute Technology, 77 Avenue, Cambridge, 02139-4307, United States* To whom correspondence should be addressed. E-mail: [email protected]Cite this: Chem. Rev. 2010, 110, 11, 6474–6502Publication Date (Web):November 10, 2010Publication History Received2 August 2010Published online10 November inissue 10 2010https://pubs.acs.org/doi/10.1021/cr100246chttps://doi.org/10.1021/cr100246creview-articleACS PublicationsCopyright © 2010 American Chemical SocietyRequest reuse permissionsArticle Views32426Altmetric-Citations2664LEARN ABOUT THESE METRICSArticle Views are COUNTER-compliant sum full text article downloads since 2008 (both PDF HTML) across all institutions individuals. These metrics regularly updated to reflect usage leading up last few days.Citations number other articles citing this article, calculated by Crossref daily. Find more information about citation counts.The Altmetric Attention Score is a quantitative measure attention that research has received online. Clicking on donut icon will load page at altmetric.com with additional details score social media presence given article. how calculated. Share Add toView InAdd Full Text ReferenceAdd Description ExportRISCitationCitation abstractCitation referencesMore Options onFacebookTwitterWechatLinked InRedditEmail Other access optionsGet e-Alertsclose SUBJECTS:Batteries,Catalysts,Electrodes,Energy storage,Solar energy Get e-Alerts

Language: Английский

Citations

2892

Recent Trends and Perspectives in Electrochemical Water Splitting with an Emphasis on Sulfide, Selenide, and Phosphide Catalysts of Fe, Co, and Ni: A Review DOI
Sengeni Anantharaj, Sivasankara Rao Ede,

K. Sakthikumar

et al.

ACS Catalysis, Journal Year: 2016, Volume and Issue: 6(12), P. 8069 - 8097

Published: Oct. 19, 2016

Increasing demand for finding eco-friendly and everlasting energy sources is now totally depending on fuel cell technology. Though it an way of producing the urgent requirements, needs to be improved make cheaper more eco-friendly. Although there are several types cells, hydrogen (H2) oxygen (O2) one with zero carbon emission water as only byproduct. However, supplying fuels in purest form (at least H2) essential ensure higher life cycles less decay efficiency. The current large-scale H2 production largely dependent steam reforming fossil fuels, which generates CO2 along source going depleted. As alternate, electrolysis has been given greater attention than reforming. reasons follows: very high purity produced, abundant source, no need high-temperature, high-pressure reactors, so on. In earlier days, noble metals such Pt (cathode) Ir Ru (anode) were used this purpose. problems employing these metals, they expensive. review, we elaborate how group VIII 3d metal sulfide, selenide, phosphide nanomaterials have arisen electrode materials (catalysts) beyond oxides hydroxides same. We also highlight evaluation perspective electrocatalysts toward detail.

Language: Английский

Citations

2211

Homogeneously dispersed multimetal oxygen-evolving catalysts DOI Open Access
Bo Zhang,

Xueli Zheng,

Oleksandr Voznyy

et al.

Science, Journal Year: 2016, Volume and Issue: 352(6283), P. 333 - 337

Published: March 25, 2016

Earth-abundant first-row (3d) transition metal-based catalysts have been developed for the oxygen-evolution reaction (OER); however, they operate at overpotentials substantially above thermodynamic requirements. Density functional theory suggested that non-3d high-valency metals such as tungsten can modulate 3d metal oxides, providing near-optimal adsorption energies OER intermediates. We a room-temperature synthesis to produce gelled oxyhydroxides materials with an atomically homogeneous distribution. These FeCoW exhibit lowest overpotential (191 millivolts) reported 10 milliamperes per square centimeter in alkaline electrolyte. The catalyst shows no evidence of degradation after more than 500 hours operation. X-ray absorption and computational studies reveal synergistic interplay between tungsten, iron, cobalt producing favorable local coordination environment electronic structure enhance energetics OER.

Language: Английский

Citations

2181

Exfoliation of layered double hydroxides for enhanced oxygen evolution catalysis DOI Open Access
Fang Song, Xile Hu

Nature Communications, Journal Year: 2014, Volume and Issue: 5(1)

Published: July 17, 2014

Language: Английский

Citations

2104

Electrodeposition of hierarchically structured three-dimensional nickel–iron electrodes for efficient oxygen evolution at high current densities DOI Creative Commons
Xunyu Lu, Chuan Zhao

Nature Communications, Journal Year: 2015, Volume and Issue: 6(1)

Published: March 17, 2015

Abstract Large-scale industrial application of electrolytic splitting water has called for the development oxygen evolution electrodes that are inexpensive, robust and can deliver large current density (>500 mA cm −2 ) at low applied potentials. Here we show an efficient electrode be developed by electrodepositing amorphous mesoporous nickel–iron composite nanosheets directly onto macroporous nickel foam substrates. The as-prepared exhibits high catalytic activity towards oxidation in alkaline solutions, which only requires overpotential 200 mV to initiate reaction, is capable delivering densities 500 1,000 overpotentials 240 270 mV, respectively. also shows prolonged stability against bulk electrolysis current. Collectively, three-dimensional structured most electrolytes reported best our knowledge, potentially scale electrolysis.

Language: Английский

Citations

1868

Engineering heterogeneous semiconductors for solar water splitting DOI
Xin Li, Jiaguo Yu, Jingxiang Low

et al.

Journal of Materials Chemistry A, Journal Year: 2014, Volume and Issue: 3(6), P. 2485 - 2534

Published: Nov. 19, 2014

Recent progress and strategies toward solar water splitting over heterogeneous semiconductors are reviewed the challenges future perspectives suggested.

Language: Английский

Citations

1761

The Artificial Leaf DOI
Daniel G. Nocera

Accounts of Chemical Research, Journal Year: 2012, Volume and Issue: 45(5), P. 767 - 776

Published: April 4, 2012

To convert the energy of sunlight into chemical energy, leaf splits water via photosynthetic process to produce molecular oxygen and hydrogen, which is in a form separated protons electrons. The primary steps natural photosynthesis involve absorption its conversion spatially electron–hole pairs. holes this wireless current are captured by evolving complex (OEC) photosystem II (PSII) oxidize oxygen. electrons produced as byproduct OEC reaction ferrodoxin I. With aid ferrodoxin–NADP+ reductase, they used hydrogen NADPH. For synthetic material realize solar function leaf, light-absorbing must capture photon generate that harnessed catalysts, drive four electron/hole fuel-forming water-splitting under benign conditions 1 sun (100 mW/cm2) illumination.This Account describes construction an artificial comprising earth-abundant elements interfacing triple junction, amorphous silicon photovoltaic with hydrogen- oxygen-evolving catalysts made from ternary alloy (NiMoZn) cobalt–phosphate cluster (Co-OEC), respectively. latter captures structural functional attributes PSII-OEC. Similar PSII-OEC, Co-OEC self-assembles upon oxidation metal ion 2+ 3+, may operate at room temperature, self-healing. also activates H2O proton-coupled electron transfer mechanism increased hole equivalents akin S-state pumping Kok cycle PSII. X-ray spectroscopy studies have established relative Mn3CaO4–Mn cubane where Co replaces Mn extended corner-sharing, head-to-tail dimer.The ability perform neutral or near-neutral has several consequences for leaf. NiMoZn be place Pt hydrogen. stabilize water, surface coated conducting oxide onto deposited. net result immersing triple-junction Si wafer holding it up can effect direct splitting. By constructing simple, stand-alone device composed materials, provides means inexpensive highly distributed solar-to-fuels system employs low-cost systems engineering manufacturing. Through type system, become viable supply those non-legacy world.

Language: Английский

Citations

1604