A metal-free organic–inorganic aqueous flow battery
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Michael P. Marshak | Cooper J. Galvin | Alán Aspuru-Guzik | C. Suh | R. Gordon | Brian Huskinson | M. Aziz | Michael R. Gerhardt | S. Er | Xudong Chen
[1] M. Mench. Flow Batteries I , 2015 .
[2] C. Low,et al. Progress in redox flow batteries, remaining challenges and their applications in energy storage , 2012 .
[3] Zunyao Wang,et al. Investigation on Intramolecular Hydrogen Bond and Some Thermodynamic Properties of Polyhydroxylated Anthraquinones , 2012 .
[4] Michael J. Aziz,et al. A high power density, high efficiency hydrogen–chlorine regenerative fuel cell with a low precious metal content catalyst , 2012, 1206.2883.
[5] Lelia Cosimbescu,et al. Anthraquinone with tailored structure for a nonaqueous metal-organic redox flow battery. , 2012, Chemical communications.
[6] Michael J. Aziz,et al. Electricity storage for intermittent renewable sources , 2012 .
[7] M. Mench,et al. Redox flow batteries: a review , 2011 .
[8] Maria Skyllas-Kazacos,et al. Progress in Flow Battery Research and Development , 2011 .
[9] Junmei Wang,et al. Recent advances on aqueous solubility prediction. , 2011, Combinatorial chemistry & high throughput screening.
[10] Partha Sarathi Guin,et al. Electrochemical Reduction of Quinones in Different Media: A Review , 2011 .
[11] Jun Liu,et al. Electrochemical energy storage for green grid. , 2011, Chemical reviews.
[12] Tetsuo Sakai,et al. High-capacity organic positive-electrode material based on a benzoquinone derivative for use in rechargeable lithium batteries , 2010 .
[13] Garry R. Buettner,et al. Thermodynamic and kinetic considerations for the reaction of semiquinone radicals to form superoxide and hydrogen peroxide. , 2010, Free radical biology & medicine.
[14] T. Iitaka,et al. Failure of Conventional Density Functionals for the Prediction of Molecular Crystal Polymorphism: A Quantum Monte Carlo Study , 2010, The Journal of Physical Chemistry Letters.
[15] J. R. T. Johnsson Wass,et al. Quantum chemical modeling of the reduction of quinones. , 2006, The journal of physical chemistry. A.
[16] Peter E. Bl. Projector-Augmented Wave Method: An introduction , 2003 .
[17] R. Forster,et al. Protonation reactions of anthraquinone-2,7-disulphonic acid in solution and within monolayers , 2001 .
[18] G. Kresse,et al. From ultrasoft pseudopotentials to the projector augmented-wave method , 1999 .
[19] Burke,et al. Generalized Gradient Approximation Made Simple. , 1996, Physical review letters.
[20] Kresse,et al. Efficient iterative schemes for ab initio total-energy calculations using a plane-wave basis set. , 1996, Physical review. B, Condensed matter.
[21] B. Honig,et al. New Model for Calculation of Solvation Free Energies: Correction of Self-Consistent Reaction Field Continuum Dielectric Theory for Short-Range Hydrogen-Bonding Effects , 1996 .
[22] B. Honig,et al. Accurate First Principles Calculation of Molecular Charge Distributions and Solvation Energies from Ab Initio Quantum Mechanics and Continuum Dielectric Theory , 1994 .
[23] Hafner,et al. Ab initio molecular dynamics for liquid metals. , 1995, Physical review. B, Condensed matter.
[24] G. Kelsall,et al. Redox chemistry of H2S oxidation by the British Gas Stretford Process Part III: Electrochemical behaviour of anthraquinone 2,7 disulphonate in alkaline electrolytes , 1993 .
[25] Louette R. Johnson Lutjens. Research , 2006 .
[26] S. L. Mayo,et al. DREIDING: A generic force field for molecular simulations , 1990 .
[27] J. McBreen,et al. Transport Properties of Nafion Membranes in Electrochemically Regenerative Hydrogen/Halogen Cells , 1979 .
[28] N. Trinajstic,et al. Ground states of conjugated molecules—XIV: Redox potentials of quinones , 1965 .
[29] N. Trinajstic,et al. Ground states of conjugated molecules—XVIII : Azepines and oxepines , 1970 .
[30] L. Fieser,et al. AN ELECTROCHEMICAL STUDY OF THE REVERSIBLE REDUCTION OF ORGANIC COMPOUNDS1 , 1922 .
[31] M. L. Crossley. THE SEPARATION OF MONO-β-, 2,6- AND 2,7-SULFONIC ACIDS OF ANTHRAQUINONE. , 1915 .