@article {1120,
	title = {Outstanding Properties and Performance of CaTi0.5Mn0.5O3{\textendash}δ for Solar-Driven Thermochemical Hydrogen Production},
	journal = {Matter},
	volume = {4},
	year = {2021},
	pages = {688-708},
	keywords = {inorganic perovskite, oxygen non-stoichiometry, phase transition, solar fuel, thermo-kinetic limit, thermochemical hydrogen production, thermodynamic properties},
	doi = {https://doi.org/10.1016/j.matt.2020.11.016},
	author = {X. Qian and J. He and E. Mastronardo and B. Baldassarri and W. Yuan and C. Wolverton and S. M. Haile}
}
@article {1126,
	title = {Favorable Redox Thermodynamics of SrTi0.5Mn0.5O3-δ in Solar Thermochemical Water Splitting},
	journal = {Chemistry of Materials},
	volume = {32},
	year = {2020},
	pages = {9335-9346},
	keywords = {Cubic perovskite, Modeling, Perovskite, SrTi0.5Mn0.5O3-δ},
	doi = {https://doi.org/10.1021/acs.chemmater.0c03278},
	author = {X. Qian and J. He and E. Mastronardo and B. Baldassarri and C. Wolverton and S. M. Haile}
}
@article {1172,
	title = {Highly quaternized polystyrene ionomers for high performance anion exchange membrane water electrolysers},
	journal = {Nature Energy},
	volume = {5},
	year = {2020},
	month = {3},
	keywords = {LTE; AEM electrolysis; Novel ionomer},
	doi = {10.1038/s41560-020-0577-x},
	author = {Kim, Yu Seung and Li, Dongguo and Park, Eun Joo and Wenlei, Zhu and Qiurong, Shi and Zhou, Yang and Tian, Hangyu and Lin, Yuehe and Serov, Alexey and Zulevi, Barr and Baca, Ehren Donel and Fujimoto, Cy and Chung, Hoon}
}
@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 {932,
	title = {Enhanced Oxidation Kinetics in Thermochemical Cycling of CeO <sub>2</sub> through Templated Porosity},
	journal = {The Journal of Physical Chemistry C},
	volume = {117},
	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 = {1692-1700},
	issn = {1932-7447, 1932-7455},
	doi = {10.1021/jp309247c},
	url = {http://pubs.acs.org/doi/abs/10.1021/jp309247c},
	author = {Stephen G. Rudisill and Luke J. Venstrom and Nicholas D. Petkovich and Tingting Quan and Nicholas Hein and Daniel B. Boman and Jane H. Davidson and Andreas Stein}
}
@article {774,
	title = {Valence measurement of Mn oxides using Mn K-beta emission spectroscopy},
	journal = {JOURNAL OF PHYSICS AND CHEMISTRY OF SOLIDS},
	volume = {61},
	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 = {547-460},
	abstract = {High resolution Mn K-beta emission spectra provide a direct method to probe the effective spin state and charge density on Mn sites. Direct
comparison of MnF2 and MnO reveals significant changes due to the degree of covalency. The detailed shape and energy shi  of thr spectra for the
perovskite LaMnO3 and CaMnO3 compounds are found to be very similar to Mn2O3 and MnO2, respectively. Detailed Mn K-beta X-ray emission results on
La1-xCaxMnO3 can be well fit by linear superpositions of the end member spectra. However, for x < 0.3, a retarded response is found. No evidence for Mn2+ is
found},
	author = {Q Qian and TA Tyson and CC Kao and JP Rueff and FMF deGroot and M Croft and SW Cheong and M Breenblatt and MA Subramanian}
}
