@article {1080, title = {Addressing the Stability Gap in Photoelectrochemistry: Molybdenum Disulfide Protective Catalysts for Tandem III{\textendash}V Unassisted Solar Water Splitting}, journal = {ACS Energy Letters}, year = {2020}, month = {07/2020}, pages = {2631-2640}, doi = {10.1021/acsenergylett.0c01132}, url = {https://doi.org/10.1021/acsenergylett.0c01132}, author = {Micha Ben-Naim and Reuben J. Britto and Chase W. Aldridge and Rachel Mow and Myles A. Steiner and Adam C. Nielander and Laurie A. King and Daniel J. Friedman and Todd G. Deutsch and James L. Young and Thomas F. Jaramillo} } @article {1181, title = {Advancement of Proton-Conducting Solid Oxide Fuel Cells and Solid Oxide Electrolysis Cells at Idaho National Laboratory (INL)}, journal = {ECS Transactions}, volume = {91}, year = {2019}, month = {07/2019}, pages = {1029{\textendash}1034}, abstract = {Proton conducting ceramics have been considered as a strategic material system used in solid oxide fuel cells and solid oxide electrolysis cells for electricity generation and hydrogen production. The high proton conductivity of protonic electrolyte and rapid development of robust electrode materials have significantly promoted the reduction of feasible operating temperature to intermediate temperature range (400 600 {\textdegree}C), which can attribute to favorable technical and economic advantages when they are compared with conventional oxide-ion conducting electrolyte based solid oxide cell system. In the past few years, Idaho National Laboratory has been devoted to developing advanced electrolyte and electrode materials R\&D, diverse manufacturing capability, and expanding evaluation facility for these applications, aiming to further improve performance, stability and manufacturing cost. There are some remarkable accomplishments achieved on electrode engineering, electrolyte optimization, new material down-selection and large-scale cell fabrication in Idaho National Laboratory.}, keywords = {BCZYYb7111, HTE, NiO-BaCe0.7Zr0.1Y0.1Yb0.1O3, PrBa0.5Sr0.5Co1.5Fe0.5O3, Protonic conductor, SOEC}, doi = {10.1149/09101.1029ecst}, url = {https://doi.org/10.1149/09101.1029ecst}, author = {Hanping Ding and Wei Wu and Dong Ding} } @article {1060, title = {Approaches for co-sintering metal-supported proton-conducting solid oxide cells with Ba(Zr,Ce,Y,Yb)O3-δ electrolyte}, journal = {International Journal of Hydrogen Energy}, volume = {44}, year = {2019}, month = {05/2019}, pages = {13768-13776}, abstract = {

Published on May 21st, 2019. Proton conducting oxide electrolyte materials could potentially lower the operating temperature of metal-supported solid oxide cells (MS-SOCs) to the intermediate range 400 to 600\ {\textdegree}C. The porous metal substrate provides the advantages of MS-SOCs such as high thermal and redox cycling tolerance, low-cost of structural materials, and mechanical ruggedness. In this work, the viability of co-sintering fabrication of metal-supported proton conducting solid oxide cells using BaZr1-x-yCexYyO3-δ (BZCY) is investigated. BZCY ceramics are sintered at 1450\ {\textdegree}C in reducing environment alone and supported on FeCr alloy metal support, and key characteristics such as Ba loss, sintering behavior, and chemical compatibility with metal support are determined. Critical challenges are identified for this fabrication approach, including: Contamination of the electrolyte with Si and Cr from the metal support, incomplete electrolyte sintering, and evaporation of electrolyte constituents. Various approaches to overcome these limitations are proposed, and preliminary assessment indicates that the use of barrier layers, low-Si-content stainless steel, and sintering aids warrant further development.

}, doi = {10.1016/j.ijhydene.2019.03.181}, url = {http://www.sciencedirect.com/science/article/pii/S0360319919312108}, author = {Ruofan Wang and Grace Y. Lay and Dong Ding and Tianli Zhu} } @article {1061, title = {Assessment of co-sintering as a fabrication approach for metal-supported proton-conducting solid oxide cells}, journal = {Solid State Ionics}, volume = {332}, year = {2019}, month = {04/2019}, pages = {25-33}, abstract = {

Published on April 1st, 2019. Proton conducting oxide electrolyte materials could potentially lower the operating temperature of metal-supported solid oxide cells (MS-SOCs) to the intermediate range 400 to 600 {\textdegree}C. The porous metal substrate provides the advantages of MS-SOCs such as high thermal and redox cycling tolerance, low-cost of structural materials, and mechanical ruggedness. In this work, viability of co-sintering fabrication of metal-supported proton conducting solid oxide cells is investigated. Candidate proton conducting oxides including perovskite oxides BaZr0.7Ce0.2Y0.1O3-δ, SrZr0.5Ce0.4Y0.1O3-δ, and Ba3Ca1.18Nb1.82O9-δ, pyrochlore oxides La1.95Ca0.05Zr2O7-δ and La2Ce2O7, and acceptor doped rare-earth ortho-niobate La0.99Ca0.01NbO4 are synthesized via solid state reactive or sol-gel methods. These ceramics are sintered at 1450 {\textdegree}C in reducing environment alone and supported on Fe-Cr alloy metal support, and their key characteristics such as phase formation, sintering property, and chemical compatibility with metal support are determined. Most electrolyte candidates suffer from one or more challenges identified for this fabrication approach, including: phase decomposition in reducing atmosphere, evaporation of electrolyte constituents, contamination of the electrolyte with Si and Cr from the metal support, and incomplete electrolyte sintering. In contrast, La0.99Ca0.01NbO4 is found to be highly compatible with the metal support and co-sintering processing in reducing atmosphere. A metal-supported cell is fabricated with La0.99Ca0.01NbO4 electrolyte, ferritic stainless steel support, Pt air electrode and nanoparticulate ceria-Ni hydrogen electrocatalyst. The total resistance is 50 Ω{\textperiodcentered}cm2 at 600 {\textdegree}C. This work clearly demonstrates the challenges, opportunities, and breakthrough of metal-supported proton-conducting solid oxide cells by co-sintering fabrication.

}, issn = {0167-2738}, doi = {10.1016/j.ssi.2019.01.004}, url = {http://www.sciencedirect.com/science/article/pii/S0167273818309263}, author = {Ruofan Wang and Conor Byrne and Michael C. Tucker} } @article {777, title = {Active Site Revealed for Water Oxidation on Electrochemically Induced δ - MnO 2 : Role of Spinel-to-Layer Phase Transition}, journal = {Journal of the American Chemical Society}, volume = {140}, year = {2018}, note = {{\textquoteright}doi: 10.1021/acsenergylett.0c01132\n - I.Am.Hydrogen{\textquoteright} {\textquoteright}\n - jyoungstrom{\textquoteright} {\textquoteright}Jason thinks this is great.\n~\n - jyoungstrom{\textquoteright} {\textquoteright}\n - estechel{\textquoteright} }, pages = {1783-1792}, abstract = {Published on February 7th, 2018.}, issn = {0002-7863, 1520-5126}, doi = {10.1021/jacs.7b11393}, url = {http://pubs.acs.org/doi/10.1021/jacs.7b11393}, author = {Ye-Fei Li and Zhi-Pan Liu} } @article {990, title = {Assessing the role of hydrogen in Fermi-level pinning in chalcopyrite and kesterite solar absorbers from first-principles calculations}, journal = {Journal of Applied Physics}, volume = {123}, year = {2018}, note = {

{\textquoteright}doi: 10.1021/acsenergylett.0c01132\n - I.Am.Hydrogen{\textquoteright} {\textquoteright}\n - jyoungstrom{\textquoteright} {\textquoteright}Jason thinks this is great.\n\ \n - jyoungstrom{\textquoteright} {\textquoteright}\n - estechel{\textquoteright}

}, pages = {161408}, abstract = {

Publshed on March 7th, 2018. Understanding the impact of impurities in solar absorbers is critical to engineering high-performance in devices, particularly over extended periods of time. Here, we use hybrid functional calculations to explore the role of hydrogen interstitial (Hi) defects in the electronic properties of a number of attractive solar absorbers within the chalcopyrite and kesterite families to identify how this common impurity may influence device performance. Our results identify that Hi can inhibit the highly p-type conditions desirable for several higher-band gap absorbers and that H incorporation could detrimentally affect the open-circuit voltage (Voc) and limit device efficiencies. Additionally, we find that Hi can drive the Fermi level away from the valence band edge enough to lead to n-type conductivity in a number of chalcopyrite and kesterite absorbers, particularly those containing Ag rather than Cu. We find that these effects can lead to interfacial Fermi-level pinning that can qualitatively explain the observed performance in high-Ga content CIGSe solar cells that exhibit saturation in the Voc with increasing band gap. Our results suggest that compositional grading rather than bulk alloying, such as by creating In-rich surfaces, may be a better strategy to favorably engineering improved thin-film photovoltaics with larger-band gap absorbers.

}, issn = {0021-8979}, doi = {10.1063/1.5006272}, url = {https://aip.scitation.org/doi/10.1063/1.5006272}, author = {J. B. Varley and V. Lordi and T. Ogitsu and A. Deangelis and K. Horsley and N. Gaillard} } @article {1008, title = {Anodic Behavior of the Aluminum Current Collector in Imide-Based Electrolytes: Influence of Solvent, Operating Temperature, and Native Oxide-Layer Thickness}, journal = {ChemSusChem}, volume = {10}, year = {2017}, note = {{\textquoteright}doi: 10.1021/acsenergylett.0c01132\n - I.Am.Hydrogen{\textquoteright} {\textquoteright}\n - jyoungstrom{\textquoteright} {\textquoteright}Jason thinks this is great.\n~\n - jyoungstrom{\textquoteright} {\textquoteright}\n - estechel{\textquoteright} }, pages = {804-814}, abstract = {Published on February 22nd, 2017. The inability of imide salts to form a sufficiently effective passivation layer on aluminum current collectors is one of the main obstacles that limit their broad application in electrochemical energy-storage systems. However, under certain circumstances, the use of electrolytes with imide electrolyte salts in combination with the aluminum current collector is possible. In this contribution, the stability of the aluminum current collector in electrolytes containing either lithium bis(trifluoromethanesulfonyl) imide (LiTFSI) or lithium fluorosulfonyl-(trifluoromethanesulfonyl) imide (LiFTFSI) as conductive salt was investigated by electrochemical techniques, that is, cyclic voltammetry (CV) and chronocoulometry (CC) in either room-temperature ionic liquids or in ethyl methyl sulfone. In particular, the influence of the solvent, operating temperature, and thickness of the native oxide layer of aluminum on the pit formation at the aluminum current collector surface was studied by means of scanning electron microscopy. In general, a more pronounced aluminum dissolution and pit formation was found at elevated temperatures as well as in solvents with a high dielectric constant. An enhanced thickness of the native aluminum oxide layer increases the oxidative stability versus dissolution. Furthermore, we found a different reaction rate depending on dwell time at the upper cut-off potential for aluminum dissolution in TFSI- and FTFSI-based electrolytes during the CC measurements; the use of LiFTFSI facilitated the dissolution of aluminum compared to LiTFSI. Overall, the mechanism of anodic aluminum dissolution is based on: i) the attack of the Al2O3 surface by acidic species and ii) the dissolution of bare aluminum into the electrolyte, which, in turn, is influenced by the electrolyte{\textquoteright}s dielectric constant.}, issn = {1864-564X}, doi = {10.1002/cssc.201601636}, url = {http://onlinelibrary.wiley.com/doi/10.1002/cssc.201601636/abstract}, author = {Paul Meister and Xin Qi and Richard Kloepsch and Elisabeth Kr{\"a}mer and Benjamin Streipert and Martin Winter and Tobias Placke} } @article {871, title = {Applications and limitations of two step metal oxide thermochemical redox cycles; a review}, journal = {J. Mater. Chem. A}, volume = {5}, year = {2017}, note = {{\textquoteright}doi: 10.1021/acsenergylett.0c01132\n - I.Am.Hydrogen{\textquoteright} {\textquoteright}\n - jyoungstrom{\textquoteright} {\textquoteright}Jason thinks this is great.\n~\n - jyoungstrom{\textquoteright} {\textquoteright}\n - estechel{\textquoteright} }, pages = {18951-18966}, issn = {2050-7488, 2050-7496}, doi = {10.1039/C7TA05025A}, url = {http://xlink.rsc.org/?DOI=C7TA05025A}, author = {B. Bulfin and J. Vieten and C. Agrafiotis and M. Roeb and C. Sattler} } @article {991, title = {Acidic or Alkaline? Towards a New Perspective on the Efficiency of Water Electrolysis}, journal = {Journal of The Electrochemical Society}, volume = {163}, year = {2016}, note = {{\textquoteright}doi: 10.1021/acsenergylett.0c01132\n - I.Am.Hydrogen{\textquoteright} {\textquoteright}\n - jyoungstrom{\textquoteright} {\textquoteright}Jason thinks this is great.\n~\n - jyoungstrom{\textquoteright} {\textquoteright}\n - estechel{\textquoteright} }, pages = {F3197-F3208}, abstract = {Published on January 1st, 2016. Water electrolysis is a promising technology for enabling the storage of surplus electricity produced by intermittent renewable power sources in the form of hydrogen. At the core of this technology is the electrolyte, and whether this is acidic or alkaline affects the reaction mechanisms, gas purities and is of significant importance for the stability and activity of the electrocatalysts. This article presents a simple but precise physical model to describe the voltage-current characteristic, heat balance, gas crossover and cell efficiency of water electrolyzers. State-of-the-art water electrolysis cells with acidic and alkaline electrolyte are experimentally characterized in order to parameterize the model. A rigorous comparison shows that alkaline water electrolyzers with Ni-based catalysts but thinner separators than those typically used is expected be more efficient than acidic water electrolysis with Ir and Pt based catalysts. This performance difference was attributed mainly to a similar conductivity but approximately 38-fold higher diffusivities of hydrogen and oxygen in the acidic polymer electrolyte membrane (Nafion) than those in the alkaline separator (Zirfon filled with a 30 wt} KOH solution). With reference to the detailed analysis of the cell characteristics, perspectives for the improvement of the efficiency of water electrolyzers are discussed.}, issn = {0013-4651, 1945-7111}, doi = {10.1149/2.0271611jes}, url = {http://jes.ecsdl.org/content/163/11/F3197}, author = {Maximilian Schalenbach and Geert Tjarks and Marcelo Carmo and Wiebke Lueke and Martin Mueller and Detlef Stolten} } @article {1011, title = {An analysis of degradation phenomena in polymer electrolyte membrane water electrolysis}, journal = {Journal of Power Sources}, volume = {326}, year = {2016}, note = {{\textquoteright}doi: 10.1021/acsenergylett.0c01132\n - I.Am.Hydrogen{\textquoteright} {\textquoteright}\n - jyoungstrom{\textquoteright} {\textquoteright}Jason thinks this is great.\n~\n - jyoungstrom{\textquoteright} {\textquoteright}\n - estechel{\textquoteright} }, pages = {120-128}, abstract = {Published on September 15th, 2016. The durability of a polymer electrolyte membrane (PEM) water electrolysis single cell, assembled with regular porous transport layers (PTLs) is investigated for just over 1000~h. We observe a significant degradation rate of 194~μV~h-1 and conclude that 78\% of the detectable degradation can be explained by an increase in ohmic resistance, arising from the anodic Ti-PTL. Analysis of the polarization curves also indicates a decrease in the anodic exchange current density, j0, that results from the over-time contamination of the anode with Ti species. Furthermore, the average Pt-cathode particle size increases during the test, but we do not believe this phenomenon makes a significant contribution to increased cell voltages. To validate the anode Ti-PTL as a crucial source of increasing resistance, a second cell is assembled using Pt-coated Ti-PTLs. This yields a substantially reduced degradation rate of only 12~μV~h-1, indicating that a non-corroding anode PTL is vital for PEM electrolyzers. It is our hope that forthcoming tailored PTLs will not only contribute to fast progress on cost-efficient stacks, but also to its long-term application of PEM electrolyzers involved in industrial processes.}, issn = {0378-7753}, doi = {10.1016/j.jpowsour.2016.06.082}, url = {http://www.sciencedirect.com/science/article/pii/S0378775316307844}, author = {Christoph Rakousky and Uwe Reimer and Klaus Wippermann and Marcelo Carmo and Wiebke Lueke and Detlef Stolten} } @inbook {749, title = {Application of SR methods for the study of nanocomposite materials for Hydrogen Energy}, volume = {84}, year = {2016}, note = {{\textquoteright}doi: 10.1021/acsenergylett.0c01132\n - I.Am.Hydrogen{\textquoteright} {\textquoteright}\n - jyoungstrom{\textquoteright} {\textquoteright}Jason thinks this is great.\n~\n - jyoungstrom{\textquoteright} {\textquoteright}\n - estechel{\textquoteright} }, pages = {397-406}, publisher = {Elsevier Science Bv}, organization = {Elsevier Science Bv}, address = {Amsterdam}, abstract = {This work summarizes results of synchrotron radiation (SR) studies of the real/defect structure of nanocrystalline/nanocomposite oxide materials, which determines their functional properties in hydrogen energy field as catalysts and mixed ionic electronic conductors (cathodes and anodes of solid oxide fuel cells, oxygen separation membranes). For nanocrystalline ceria-zirconia mixed oxide prepared via modified Pechini route using ethanol solution of reagents, a high spatial uniformity of cations distribution between domains along with the oxygen sublattice deficiency revealed by full-profile Rietveld refinement of SR diffraction data provide structure disordering enhancing oxygen mobility. For PrNi0.5Co0.5O3-delta - Ce0.9Y0.1O2-delta nanocomposite extensive transfer of Pr cations into fluorite domains generates a new path of fast oxygen diffusion along chains of Pr3+ - Pr4+ cations as directly proved by analysis of the unit cell relaxation after changing pO(2) in perfect agreement with data obtained by oxygen isotope heteroexchange. (C) 2016 The Authors. Published by Elsevier B.V.}, author = {V. A. Sadykov and S. N. Pavlova and Z. S. Vinokurov and A. N. Shmakov and N. F. Eremeev and Yu E. Fedorova and E. P. Yakimchuk and V. V. Kriventsov and V. A. Bolotov and Yu Yu Tanashev and E. M. Sadovskaya and S. V. Cherepanova and K. V. Zolotarev and N. A. Vinokurov and B. A. Knyazev} } @article {929, title = {Advancing Oxide Materials for Thermochemical Production of Solar Fuels}, journal = {Energy Procedia}, volume = {49}, year = {2014}, note = {{\textquoteright}doi: 10.1021/acsenergylett.0c01132\n - I.Am.Hydrogen{\textquoteright} {\textquoteright}\n - jyoungstrom{\textquoteright} {\textquoteright}Jason thinks this is great.\n~\n - jyoungstrom{\textquoteright} {\textquoteright}\n - estechel{\textquoteright} }, pages = {2019-2026}, issn = {18766102}, doi = {10.1016/j.egypro.2014.03.214}, url = {http://linkinghub.elsevier.com/retrieve/pii/S1876610214006687}, author = {J.E. Miller and A. Ambrosini and E.N. Coker and M.D. Allendorf and A.H. McDaniel} } @article {928, title = {Annual Average Efficiency of a Solar-thermochemical Reactor}, journal = {Energy Procedia}, volume = {49}, year = {2014}, note = {{\textquoteright}doi: 10.1021/acsenergylett.0c01132\n - I.Am.Hydrogen{\textquoteright} {\textquoteright}\n - jyoungstrom{\textquoteright} {\textquoteright}Jason thinks this is great.\n~\n - jyoungstrom{\textquoteright} {\textquoteright}\n - estechel{\textquoteright} }, pages = {1932-1939}, issn = {18766102}, doi = {10.1016/j.egypro.2014.03.205}, url = {http://linkinghub.elsevier.com/retrieve/pii/S1876610214006596}, author = {I. Ermanoski and N. Siegel} } @article {838, title = {Analysis and improvement of a high-efficiency solar cavity reactor design for a two-step thermochemical cycle for solar hydrogen production from water}, journal = {Solar Energy}, volume = {97}, year = {2013}, note = {{\textquoteright}doi: 10.1021/acsenergylett.0c01132\n - I.Am.Hydrogen{\textquoteright} {\textquoteright}\n - jyoungstrom{\textquoteright} {\textquoteright}Jason thinks this is great.\n~\n - jyoungstrom{\textquoteright} {\textquoteright}\n - estechel{\textquoteright} }, pages = {26-38}, abstract = {Published in November 2013.}, issn = {0038092X}, doi = {10.1016/j.solener.2013.07.032}, url = {http://linkinghub.elsevier.com/retrieve/pii/S0038092X13003071}, author = {Anis Houaijia and Christian Sattler and Martin Roeb and Matthias Lange and Stefan Breuer and Jan Peter S{\"a}ck} } @article {816, title = {Analytical Model of CeO 2 Oxidation and Reduction}, journal = {The Journal of Physical Chemistry C}, volume = {117}, year = {2013}, note = {{\textquoteright}doi: 10.1021/acsenergylett.0c01132\n - I.Am.Hydrogen{\textquoteright} {\textquoteright}\n - jyoungstrom{\textquoteright} {\textquoteright}Jason thinks this is great.\n~\n - jyoungstrom{\textquoteright} {\textquoteright}\n - estechel{\textquoteright} }, pages = {24129-24137}, abstract = {Published on November 21st, 2013.}, issn = {1932-7447, 1932-7455}, doi = {10.1021/jp406578z}, url = {http://pubs.acs.org/doi/abs/10.1021/jp406578z}, author = {B. Bulfin and A. J. Lowe and K. A. Keogh and B. E. Murphy and O. L{\"u}bben and S. A. Krasnikov and I. V. Shvets} } @article {1029, title = {Accelerated lifetime testing and standardization of SOFC systems | Dansk Gasteknisk Center}, number = {64009-0246}, year = {2012}, note = {{\textquoteright}doi: 10.1021/acsenergylett.0c01132\n - I.Am.Hydrogen{\textquoteright} {\textquoteright}\n - jyoungstrom{\textquoteright} {\textquoteright}Jason thinks this is great.\n~\n - jyoungstrom{\textquoteright} {\textquoteright}\n - estechel{\textquoteright} }, abstract = {There is a demand for methods to evaluate or predict the lifetime of SOFC systems. The mechanisms behind cell degradation are fairly well known, but the system aspects including the effects of operating conditions are less well known. The project has shown that there exists no agreed method to predict the lifetime of an SOFC system. Even a lifetime definition does not exist.}, url = {https://www.dgc.dk/publikation/2012/accelerated-lifetime-testing-and-standardization-sofc-systems}, author = {Mikael N{\"a}slund and Henrik Iskov} } @article {999, title = {Addressing the terawatt challenge: scalability in the supply of chemical elements for renewable energy}, journal = {RSC Advances}, volume = {2}, year = {2012}, note = {{\textquoteright}doi: 10.1021/acsenergylett.0c01132\n - I.Am.Hydrogen{\textquoteright} {\textquoteright}\n - jyoungstrom{\textquoteright} {\textquoteright}Jason thinks this is great.\n~\n - jyoungstrom{\textquoteright} {\textquoteright}\n - estechel{\textquoteright} }, pages = {7933-7947}, doi = {10.1039/C2RA20839C}, url = {http://pubs.rsc.org/en/Content/ArticleLanding/2012/RA/C2RA20839C}, author = {Peter C. K.~Vesborg and Thomas F.~Jaramillo} } @article {815, title = {Atomic layer deposited thin film metal oxides for fuel production in a solar cavity reactor}, journal = {International Journal of Hydrogen Energy}, volume = {37}, year = {2012}, note = {{\textquoteright}doi: 10.1021/acsenergylett.0c01132\n - I.Am.Hydrogen{\textquoteright} {\textquoteright}\n - jyoungstrom{\textquoteright} {\textquoteright}Jason thinks this is great.\n~\n - jyoungstrom{\textquoteright} {\textquoteright}\n - estechel{\textquoteright} }, pages = {16888-16894}, abstract = {Published in November 2012.}, issn = {03603199}, doi = {10.1016/j.ijhydene.2012.08.004}, url = {http://linkinghub.elsevier.com/retrieve/pii/S0360319912017703}, author = {Paul Lichty and Xinhua Liang and Christopher Muhich and Brian Evanko and Carl Bingham and Alan W. Weimer} } @article {817, title = {Advances in hydrogen production by thermochemical water decomposition: A review}, journal = {Energy}, volume = {35}, year = {2010}, note = {{\textquoteright}doi: 10.1021/acsenergylett.0c01132\n - I.Am.Hydrogen{\textquoteright} {\textquoteright}\n - jyoungstrom{\textquoteright} {\textquoteright}Jason thinks this is great.\n~\n - jyoungstrom{\textquoteright} {\textquoteright}\n - estechel{\textquoteright} }, pages = {1068-1076}, abstract = {Published in February 2010.}, issn = {03605442}, doi = {10.1016/j.energy.2009.06.018}, url = {http://linkinghub.elsevier.com/retrieve/pii/S0360544209002345}, author = {Marc A. Rosen} } @article {1134, title = {Assessing the Oxidative Stability of Anion Exchange Membranes in Oxygen Saturated Aqueous Alkaline Solutions}, journal = {Frontiers in Energy Research}, volume = {10}, month = {2022}, keywords = {anion exchange membrane, conductivity, electrolysis, protocol and guidelines, stability}, doi = {10.3389/fenrg.2022.871851}, author = {Arges, Christopher G. and Ramani, Vijay and Wang, Zhongyang and Ouimet, Ryan J.} }