Academic literature on the topic 'Electrochemical energy storage and conversion'
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Journal articles on the topic "Electrochemical energy storage and conversion"
Li, Liang, Xueliang Andy Sun, Jiujun Zhang, and Jun Lu. "Electrochemical Energy Storage and Conversion at EEST2016." ACS Energy Letters 2, no. 1 (December 15, 2016): 151–53. http://dx.doi.org/10.1021/acsenergylett.6b00604.
Full textSuller Garcia, Marco Aurélio. "Electrochemical Energy Storage and Conversion Systems – A Short Review." Journal of Mineral and Material Science (JMMS) 3, no. 3 (August 1, 2022): 1–2. http://dx.doi.org/10.54026/jmms/1041.
Full textBaglio, Vincenzo. "Electrocatalysts for Energy Conversion and Storage Devices." Catalysts 11, no. 12 (December 6, 2021): 1491. http://dx.doi.org/10.3390/catal11121491.
Full textLiang, Xinqi, Minghua Chen, Guoxiang Pan, Jianbo Wu, and Xinhui Xia. "New carbon for electrochemical energy storage and conversion." Functional Materials Letters 12, no. 04 (August 2019): 1950049. http://dx.doi.org/10.1142/s1793604719500498.
Full textVan Vliet, Krystyn J. "(Invited) Electrochemomechanical Coupling in Functional Oxides for Energy Conversion and Storage Devices." ECS Meeting Abstracts MA2018-01, no. 32 (April 13, 2018): 1945. http://dx.doi.org/10.1149/ma2018-01/32/1945.
Full textDang, Jingshuang, and Ruyi Zhong. "Advanced Materials for Electrochemical Energy Conversion and Storage." Coatings 12, no. 7 (July 12, 2022): 982. http://dx.doi.org/10.3390/coatings12070982.
Full textHuang, Zhuojun. "Designing Polymers for Electrochemical Energy Conversion & Storage." ECS Meeting Abstracts MA2020-01, no. 43 (May 1, 2020): 2514. http://dx.doi.org/10.1149/ma2020-01432514mtgabs.
Full textBalasingam, Suresh Kannan, Karthick Sivalingam Nallathambi, Mohammed Hussain Abdul Jabbar, Ananthakumar Ramadoss, Sathish Kumar Kamaraj, and Manab Kundu. "Nanomaterials for Electrochemical Energy Conversion and Storage Technologies." Journal of Nanomaterials 2019 (April 11, 2019): 1–2. http://dx.doi.org/10.1155/2019/1089842.
Full textXia, Xinhui, Shenghui Shen, Xihong Lu, and Hui Xia. "Multiscale nanomaterials for electrochemical energy storage and conversion." Materials Research Bulletin 96 (December 2017): 297–300. http://dx.doi.org/10.1016/j.materresbull.2017.09.045.
Full textAdhikari, Santosh, Michael K. Pagels, Jong Yeob Jeon, and Chulsung Bae. "Ionomers for electrochemical energy conversion & storage technologies." Polymer 211 (December 2020): 123080. http://dx.doi.org/10.1016/j.polymer.2020.123080.
Full textDissertations / Theses on the topic "Electrochemical energy storage and conversion"
Chandrasekaran, Rajeswari. "Modeling of electrochemical energy storage and energy conversion devices." Diss., Georgia Institute of Technology, 2010. http://hdl.handle.net/1853/37292.
Full textNavarrete, Algaba Laura. "New electrochemical cells for energy conversion and storage." Doctoral thesis, Universitat Politècnica de València, 2017. http://hdl.handle.net/10251/78458.
Full textEn la presente tesis doctoral se han desarrollado materiales para su uso en celdas electroquímicas. Las celdas electroquímicas estudiadas, se podrían separar en dos grandes grupos: materiales de óxido sólido y sales ácidas. En el primer grupo, se optimizaron materiales para su uso como electrodos en pilas de combustible y electrolizadores, basados en electrolitos con conducción puramente iónica. Dentro de este grupo, se comprobó la influencia de dopar la perovskita Ba0.5Sr0.5Co0.8Fe0.2O3-d, con un 3% de Y, Zr y Sc en la posición B (ABO3-d). Esta optimización llevó a la reducción de la resistencia de polarización así como a una mejora de la estabilidad con el tiempo. Así mismo, se determinaron los mecanismos limitantes en la reacción de reducción de oxígeno, y se comprobó la influencia de la presencia de CO2 en condiciones de operación. El La2NiO4+d perteneciente a la serie de Ruddlesden-Popper, es un conductor mixto de iones oxígeno y electrones. Éste, fue dopado tanto en la posición del La (con Nd y Pr) como en la posición del Ni (con Co). Los dopantes introducidos además de producir cambios estructurales, provocaron mejoras en el rendimiento de la celda, reduciendo para alguno de ellos, como el La1.5Pr0.5Ni0.8Co0.2O4+d, en casi un orden de magnitud la resistencia de polarización del electrodo de referencia (La2NiO4+d). De la misma manera, se optimizaron las propiedades del electrodo basado en el conductor electrónico puro La0.8Sr0.2MnO3-d (LSM). La adición de una segunda fase, con conductividad iónica, permitió aumentar los puntos triples (TPB) en los que la reacción de reducción de oxígeno tiene lugar y reducir la resistencia de polarización. Con el fin de mejorar la reacción de reducción de oxígeno, se estudió la adición de nanocatalizadores mediante la técnica de infiltración. Los diferentes óxidos infiltrados produjeron el cambio de las propiedades electroquímicas del electrodo, siendo el óxido de praseodimio el catalizador que consiguió disminuir en dos órdenes de magnitud la resistencia de polarización del composite no infiltrado. De la misma manera, la mejora de la eficiencia del electrodo infiltrado con Pr, mejoró los resultados de la celda electroquímica trabajando como pila (mayores densidades de potencia) y como electrolizador (menores voltajes). En lo que respecta a los materiales seleccionados para su uso como electrodos en electrolitos con conductividad protónica, se optimizó la eficiencia del cátodo basado en LSM, mediante el uso de una segunda fase conductora protónica (La5.5WO12-d) y variando la temperatura de sinterización del electrodo. Finalmente, se mejoró la actividad catalítica mediante la infiltración de nanopartículas de ceria dopada con samario, produciendo mayores densidades de corriente de la pila de combustible. Los materiales pertenecientes a la serie de Ruddlesden-Popper y usados para cátodos en pilas iónicas, fueron empleados también para cátodos en pilas protónicas. Después de comprobar que el material electrolítico (LWO) era compatible con los compuestos de la serie de Ruddlesden-Popper, se estudió la influencia de la temperatura de sinterización de los electrodos en el rendimiento, así como de la composición de la atmosfera de aire (seca, H2O y D2O). Finalmente, se diseñó y optimizó las celdas electroquímicas basadas en sales ácidas (CsH2PO4). En este sentido, se estudiaron diferentes configuraciones de celda, que permitieran obtener un electrolito denso con el menor espesor posible y unos electrodos activos a la reacción de reducción/oxidación de hidrógeno. Se consiguió reducir el espesor del electrolito soportando la celda en discos de acero y níquel porosos. Se añadió una resina tipo epoxi al material electrolítico para aumentar sus propiedades mecánicas. De la misma manera, se cambió la configuración de los electrodos pasando por conductores electrónicos puros a electrodos compuestos por conductores
En la present tesis doctoral es van desenvolupar materials per al seu ús en cel·les electroquímiques. Les cel·les electroquímiques estudiades poden ser dividides en dos grans grups: materials d'òxid sòlid i sals àcides. En el primer grup, es van optimitzar materials per al seu ús com a elèctrodes en piles de combustible i electrolitzadors, basats en electròlits amb conducció purament iònica. Dins d'este grup, es va comprovar la influència de dopar la perovskita Ba0.5Sr0.5Co0.8Fe0.2O3-d amb un 3% de Y, Zr i Sc en la posició B (ABO3-d;). Esta optimització va portar a la reducció de la resistència de polarització així com a una millora de l'estabilitat amb el temps. Així mateix, es van determinar els mecanismes limitants en la reacció de reducció d'oxigen, i es va comprovar la influència de la presència de CO2 en condicions d'operació. El La2NiO4+d pertanyent a la sèrie de Ruddlesden-Popper, és un conductor mixt d'ions oxigen i electrons. Este, va ser dopat tant en la posició del La (amb Nd i Pr) com en la posició del Ni (amb Co). Els dopants introduïts a més de produir canvis estructurals, van provocar millores en el rendiment de la cel·la, reduint per a algun d'ells, com el La1.5Pr0.5Ni0.8Co0.2O4+d, en quasi un ordre de magnitud la resistència de polarització de l'elèctrode de referència (La2NiO4+d). De la mateixa manera, es van optimitzar les propietats de l'elèctrode basat en el conductor electrònic pur La0.8Sr0.2MnO3-d (LSM). L'addició d'una segona fase, amb conductivitat iònica, va permetre augmentar els punts triples (TPB), en els que la reacció de reducció d'oxigen té lloc, i reduir la resistència de polarització. A fi de millorar la reacció de reducció d'oxigen, es va estudiar l'adició de nanocatalitzadors per mitjà de la tècnica d'infiltració. Els diferents òxids infiltrats van produir el canvi de les propietats electroquímiques de l'elèctrode, sent l'òxid de praseodimi el catalitzador que va aconseguir disminuir en dos ordres de magnitud la resistència de polarització del composite no infiltrat. De la mateixa manera, la millora de l'eficiència de l'elèctrode infiltrat amb Pr, va millorar els resultats de la cel·la electroquímica treballant com a pila (majors densitats de potència) i com a electrolitzador (menors voltatges). Pel que fa als materials seleccionats per al seu ús com a elèctrodes en electròlits amb conductivitat protònica, es va optimitzar l'eficiència del càtode basat en LSM, per mitjà de l'ús d'una segona fase conductora protònica (La5.5WO12-d;) i variant la temperatura de sinterització de l'elèctrode. Finalment, es va millorar l'activitat catalítica mitjançant la infiltració de nanopartícules de ceria dopada amb samari, produint majors densitats de corrent de la pila de combustible. Els materials pertanyents a la sèrie de Ruddlesden-Popper i usats per a càtodes en piles iòniques, van ser empleats també per a càtodes en piles protòniques. Després de comprovar que el material electrolític (LWO) era compatible amb els compostos de la sèrie de Ruddlesden-Popper, es va estudiar la influència de la temperatura de sinterització dels elèctrodes en el rendiment, així com de la composició de l'atmosfera d'aire (seca, H2O i D2O). Finalment, es van dissenyar i optimitzar les cel·les electroquímiques basades en sals àcides (CsH2PO4). En este sentit, es van estudiar diferents configuracions de cel·la, que permeteren obtindre un electròlit dens amb el menor espessor possible i uns elèctrodes actius a la reacció de reducció/oxidació d'hidrogen. Es va aconseguir reduir l'espessor de l'electròlit suportant la cel·la en discos d'acer i níquel porosos. Es va afegir una resina tipus epoxi al material electrolític per a augmentar les seues propietats mecàniques. De la mateixa manera, es va canviar la configuració dels elèctrodes passant per conductors electrònics purs a elèctrodes compostos per conductors protònics
Navarrete Algaba, L. (2017). New electrochemical cells for energy conversion and storage [Tesis doctoral no publicada]. Universitat Politècnica de València. https://doi.org/10.4995/Thesis/10251/78458
TESIS
Jonas, Ncumisa Prudence. "Electrochemical energy conversion using metal hydrides hydrogen storage materials." Thesis, University of the Western Cape, 2010. http://etd.uwc.ac.za/index.php?module=etd&action=viewtitle&id=gen8Srv25Nme4_2992_1361369645.
Full textMetal hydrides hydrogen storage materials have the ability to reversibly absorb and release large amounts of hydrogen at low temperature and pressure. In this study, metal hydride materialsemployed as negative electrodes in Ni-MH batteries are investigated. Attention is on AB5 alloys due to their intermediate thermodynamic properties. However, AB5 alloys a have 
tendency of forming oxide film on their surface which inhibits hydrogen dissociation and penetration into interstitial sites leading to reduced capacity. To redeem this, the materials were micro-encapsulated by electroless deposition with immersion in Pd and Pt baths. PGMs were found to increase activation, electrochemical activity and H2 sorption kinetics of the MH alloys. Between the two catalysts the one which displayed better performance was chosen. The materials were characterized by X-ray difractommetry, and the alloys presented hexagonal CaCu5 &ndash
type 
structure of symmetry P6/mmm. No extra phases were found, all the modified electrodes displayed the same behavior as the parent material. No shift or change in peaks which corresponded to Pd or Pt were observed. Scanning Electron Microscopy showed surface morphology of the materials modified with Pd and Pt particles, the effect of using different reducing agents (i.e., N2H4 and NaH2PO2), and alloys functionalized with &gamma
-aminosopropyltrietheosilane solution prior to Pd deposition. From all the surface modified alloys, Pt and Pd particles were observed on the 
surface of the AB5 alloys. Surface modification without pre-functionalization had non-uniform coatings, but the prefunctionalized exhibited more uniform coatings. Energy dispersive X-ray Spectroscopy and Atomic Absorption Spectroscopy determined loading of the Pt and Pd on the surface of all the alloys, and the results were as follows: EDS ( Pt 13.41 and Pd 31.08wt%), AAS (Pt 0.11 and Pd 0.78wt%). Checking effect of using different reducing agents N2H4 and NaH2PO2 for electroless Pd plating the results were as follows: EDS (AB5_N2H4_Pd- 7.57 and AB5_NaH2PO2_Pd- 31.08wt%), AAS (AB5_N2H4_Pd- 11.27 and AB5_NaH2PO2_Pd- 0.78wt%). For the AB5 alloys pre-functionalized with &gamma
-APTES, the results were: EDS (10.24wt%) and AAS (0.34wt%). Electrochemical characterization was carried out by charge/discharge cycling controlled via potential to test the AB5 alloy. Overpotential for unmodified, Pt and Pd modified 
electrodes were -1.1V, -1.24V, and -1.60V, respectively. Both modified electrodes showed discharge overpotentials at lower values implying higher specific power for the battery in comparison with the unmodified electrodes. However, Pd electrode exhibited higher specific power than Pt. To check the effect of the reducing agent the results were as follows: AB5_ N2H4_Pd (0.4V) and AB5_NaH2PO2_Pd (-0.2V), sodium hypophosphite based alloy showing lower overpotential values, implying it had higher specific power than hydrazine based bath. Alloy prefunctionalized with &gamma
-APTES, the overpotential was (0.28V), which was higher than -0.2V of the alloy without pre-functionalization, which means pre-functionalization with &gamma
-APTES did not improve the performance of the alloy electrode. Polarization resistance of the electrodes was investigated with Electrochemical Impedance Spectroscopy. The unmodified alloy showed high resistance of 
21.6884 while, both Pt and Pd modified electrodes exhibited decrease 14.7397 and 12.1061 respectively, showing increase in charge transfer for the modified electrodes. Investigating the effect of the reducing agent, the alloys exhibited the following results: (N2H4 97.8619 and NaH2PO2 12.1061) based bath. Alloy pre-functionalized with &gamma
-APTES displayed the 
resistance of 9.3128. Cyclic Voltammetry was also used to study the electrochemical activity of the alloy electrodes. The voltammograms obtained displayed the anodic current peak at -0.64V 
o -0.65V for the Pt and Pd modified electrodes, respectively. Furthermore, the electrode which was not coated with Pt or Pd the current peak occurred at -0.59V. The Pd and Pt coated 
alloy electrodes represented lower discharge overpotentials, which are important to improve the battery performance. Similar results were also observed with alloy electrodes Pd modified 
using N2H4 (-0.64V) and NaH2PO2 (-0.65V). For the electrode modified with and without &gamma
-APTES the over potentials were the same (-0.65V). PGM deposition has shown to significantly 
improve activation and hydrogen sorption performance and increased the electro-catalytic activity of these alloy electrodes. Modified electrodes gave better performance than the unmodified 
electrodes. As a result, Pd was chosen as the better catalyst for the modification of AB5 alloy. Based on the results, it was concluded that Pd electroless plated using NaH2PO2 reducing agent 
had better performance than electroless plating using N2H4 as the reducing agent. Alloy electrode pre-functionalized with &gamma
-APTES gave inconsistent results, and this phenomenon needs to 
be further investigated. In conclusion, the alloy modified with Pd employing NaH2PO2 based electroless plating bath exhibited consistent results, and was found to be suitable candidate for 
use in Ni-MH batteries.
Aaronson, Barak D. B. "High resolution electrochemical imaging for energy conversion and storage applications." Thesis, University of Warwick, 2015. http://wrap.warwick.ac.uk/78415/.
Full textDiLeo, Roberta A. "Nanomaterial synthesis and characterization for energy storage and conversion devices /." Online version of thesis, 2008. http://hdl.handle.net/1850/7367.
Full textSheehan, Margaret K. "Enhanced Performance in Electrochemical Energy Storage and Conversion via Carbon-Integrated Nanostructures." Thesis, Boston College, 2016. http://hdl.handle.net/2345/bc-ir:107261.
Full textElectrochemical energy storage and conversion applications benefit from the integration of nanostructures into the devices, as they have many more active sites per gram which enables excellent mass utilization of the active species. By controlling the surface of fuel cell catalysts, higher activity and efficiency can be achieved as compared to the bulk counterpart, with multiple catalyst facets of varying activity and efficiency. Nanostructured electrochemical capacitors have enhanced electrolyte diffusion over the surface of the electrode, facilitating high rate capability. Nanostructured materials for energy storage and conversion devices, such as electrochemical capacitors and proton exchange membrane fuel cells, can perform even better with the incorporation of carbon. High surface area carbon can enhance the activity of electrochemical capacitors by improving the conductivity of the electrode and/or enhancing the double layer capacitance. Carbon supports for fuel cell catalysts enable proper dispersion of active material without sacrificing conductivity. The work reported in this thesis is aimed toward improving the performance of electrochemical energy storage and conversion devices through novel incorporation of carbon. Carbon was first used to enhance the performance of electrocatalysts. By wrapping fuel cell catalysts in a porous carbon shell, the activity was increased over its bare and CNT-supported counterparts. The carbon shell synthetic method reported here is a good route to the production of a conductive host for Pd electrocatalysts with good contact and in one step with the formation of the Pd nanoparticles. Carbon was also used to enhance the performance of pseudocapacitors, first by incorporating it into the precursor spray solution in the generation of mesoporous metal oxides and then as a metal-organic framework-derived carbon host with dispersed electrochemically active metal oxides. A carbon network was generated from the pyrolysis of pore directing agents during the decomposition of precursor metal nitrates in the generation of mesoporous manganese oxides in a modified spray pyrolysis approach. The addition of Super P to the precursor spray solution further enhanced the conductivity of the material, enabling the formation of high-performing pseudocapacitors. Lastly, nitrogen-doped carbon cubes produced from thermally-treated parent ZIF-8 cubes were tested as electrochemical capacitors and found to have higher specific capacitance than the nitrogen-doped carbon generated from the parent ZIF-8 rhombic dodecahedra. ZIF-67 cubes were then thermally treated to yield cubic nitrogen-doped carbon hosts for the generated cobalt nanoparticles. Once the cobalt particles were oxidized, the cobalt oxide/carbon hybrid structure exhibited the best pseudocapacitive performance of the ZIF-derived carbon materials tested, exhibiting high specific capacitance and good capacitance retention with increased scan rates and prolonged cycling. Each of the materials tested for electrochemical energy storage and conversion saw an enhancement in performance with the addition of carbon. The results reported here illustrate the importance of carbon in electrochemical cells and the importance of continuing research to modify and improve the methods for carbon production and integration
Thesis (PhD) — Boston College, 2016
Submitted to: Boston College. Graduate School of Arts and Sciences
Discipline: Chemistry
McCulloch, William David. "Electrochemical Energy Conversion and Storage through Solar Redox Flow and Superoxide Batteries." The Ohio State University, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=osu1524054086338847.
Full textFalola, Bamidele Daniel. "TRANSITION METAL COATINGS FOR ENERGY CONVERSION AND STORAGE; ELECTROCHEMICAL AND HIGH TEMPERATURE APPLICATIONS." OpenSIUC, 2017. https://opensiuc.lib.siu.edu/dissertations/1354.
Full textKim, Il Tae. "Carbon-based magnetic nanohybrid materials for polymer composites and electrochemical energy storage and conversion." Diss., Georgia Institute of Technology, 2011. http://hdl.handle.net/1853/45876.
Full textLee, Seung Woo Ph D. Massachusetts Institute of Technology. "Design of electrode for electrochemical energy storage and conversion devices using multiwall carbon nanotubes." Thesis, Massachusetts Institute of Technology, 2010. http://hdl.handle.net/1721.1/59878.
Full textCataloged from PDF version of thesis.
Includes bibliographical references.
All-multiwall carbon nanotube (MWNT) thin films are created by layer-by-layer (LbL) assembly of surface functionalized MWNTs. Negatively and positively charged MWNTs were prepared by surface functionalization, allowing the incorporation of MWNTs into highly tunable thin films via the LbL technique. The pH dependent surface charge on the MWNTs gives this system the unique characteristics of LbL assembly of weak polyelectrolytes, controlling thickness and morphology with assembly pH conditions. We demonstrate that these MWNT thin films have randomly oriented interpenetrating network structure with well developed nanopores using SEM, which is an ideal structure of functional materials for various applications. LbL-MWNT electrodes show high electronic conductivity in comparison with polymer composites with single wall nanotubes, and high capacitive behavior in aqueous electrolyte with precise control of capacity. Of significance, additive-free LbL-MWNT electrodes with thicknesses of several microns can deliver high energy density (200 Wh/kg) at an exceptionally high power of 100 kW/kg in lithium nonaqueous cells. Utilizing the redox reactions on the surface functional groups in a wide voltage window (1.5 - 4.5 V vs. lithium) in nonaqueous electrolytes, asymmetric electrochemical capacitors consisting of LbL-MWNT and either lithium or a lithium titanium oxide negative electrode exhibit gravimetric energy density -5 times higher than conventional electrochemical capacitors with comparable gravimetric power and cycle life. Thin-film LbL-MWNT electrodes could potentially lead to breakthrough power sources for microsystems and flexible electronic devices such as smart cards and ebook readers, while thicker LbL-MWNT electrodes could expand the application of electrochemical capacitors into heavy vehicle and industrial systems, where the ability to deliver high energy at high power will be an enabling technological development. Furthermore, nanoscale pseuduocapactive oxides and electrocatalysts were incorporated into LbL-MWNT electrodes for energy storage and conversion. Inorganic oxides such as MnO2 and RuO2 are incorporated to increase volumetric capacitance in LbLMWNT electrodes using electroless deposition and square wave pulse potential deposition methods. Preliminary results show that we can increase volumetric capacitance of LbLMWNT/ MnO2 and LbL-MWNT/RuO2 composite up to 1000 F/cm3 in aqueous electrolytes. In addition, Pt and Pt/Ru alloy electrocatalysts are introduced into LbL-MWNT electrodes using square wave pulse potential deposition, which show higher CO and methanol oxidation activities. Tailored incorporation of metal and oxide nanoparticles into LbLMWNT electrodes by square wave pulse potential opens a new strategy for novel energy storage and conversion electrodes with superior electrochemical properties.
by Seung Woo Lee.
Ph.D.
Books on the topic "Electrochemical energy storage and conversion"
Shi, Yixiang, Ningsheng Cai, Tianyu Cao, and Jiujun Zhang. High-Temperature Electrochemical Energy Conversion and Storage. Boca Raton : CRC Press, Taylor & Francis Group, 2018. | Series: Electrochemical energy store & conversion: CRC Press, 2017. http://dx.doi.org/10.1201/b22506.
Full textLiu, Ru-Shi, Lei Zhang, Xueliang Sun, Hansan Liu, and Jiujun Zhang, eds. Electrochemical Technologies for Energy Storage and Conversion. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2011. http://dx.doi.org/10.1002/9783527639496.
Full textManthiram, Arumugam, Prashant N. Kumta, S. K. Sundaram, and Gerbrand Ceder, eds. Materials for Electrochemical Energy Conversion and Storage. 735 Ceramic Place, Westerville, Ohio 43081: The American Ceramic Society, 2006. http://dx.doi.org/10.1002/9781118370858.
Full textHou, Junbo. Advanced Electrochemical Materials in Energy Conversion and Storage. Boca Raton: CRC Press, 2022. http://dx.doi.org/10.1201/9781003133971.
Full textFranco, Alejandro A., Marie Liesse Doublet, and Wolfgang G. Bessler, eds. Physical Multiscale Modeling and Numerical Simulation of Electrochemical Devices for Energy Conversion and Storage. London: Springer London, 2016. http://dx.doi.org/10.1007/978-1-4471-5677-2.
Full textArumugam, Manthiram, American Chemical Society, American Ceramic Society Meeting, and American Ceramic Society Meeting, eds. Materials for electrochemical energy conversion and storage: Papers from the Electrochemical Materials, Processes, and Devices symposium at the 102nd Annual Meeting of The American Ceramic Society, held April 29-May 3, 2000, in St. Louis, Missouri, and the Materials for Electrochemical Energy Conversion and Storage Symposium at the 103rd Annual Meeting of The American Ceramic Society, held April 22-25, 2001, in Indianapolis, Indiana, USA. Westerville, Ohio: The American Ceramic Society, 2002.
Find full textTarascon, Jean-Marie, and Patrice Simon. Electrochemical Energy Storage. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2015. http://dx.doi.org/10.1002/9781118998151.
Full textEichel, Rüdiger-A., ed. Electrochemical Energy Storage. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-26130-6.
Full textSoni, Amit, Dharmendra Tripathi, Jagrati Sahariya, and Kamal Nayan Sharma. Energy Conversion and Green Energy Storage. Boca Raton: CRC Press, 2022. http://dx.doi.org/10.1201/9781003258209.
Full textEuropean, Symposium on Electrical Engineering (3rd 1994 Nancy France). Electrochemical engineering and energy. New York: Plenum Press, 1994.
Find full textBook chapters on the topic "Electrochemical energy storage and conversion"
Yu, Aiping, Aaron Davies, and Zhongwei Chen. "Electrochemical Supercapacitors." In Electrochemical Technologies for Energy Storage and Conversion, 317–82. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527639496.ch8.
Full textBockris, John O’M, and Shahed U. M. Khan. "Electrochemical Conversion and Storage of Energy." In Surface Electrochemistry, 861–925. Boston, MA: Springer US, 1993. http://dx.doi.org/10.1007/978-1-4615-3040-4_9.
Full textChen, Zhongwei, Fathy M. Hassan, and Aiping Yu. "Electrochemical Engineering Fundamentals." In Electrochemical Technologies for Energy Storage and Conversion, 45–68. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527639496.ch2.
Full textChouhan, Neelu, and Ru-Shi Liu. "Electrochemical Technologies for Energy Storage and Conversion." In Electrochemical Technologies for Energy Storage and Conversion, 1–43. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527639496.ch1.
Full textCucinotta, Clotilde S., and Monica Kosa. "Electrochemical Interfaces for Energy Storage and Conversion." In Encyclopedia of Nanotechnology, 1–14. Dordrecht: Springer Netherlands, 2015. http://dx.doi.org/10.1007/978-94-007-6178-0_100941-1.
Full textLavacchi, Alessandro, Hamish Miller, and Francesco Vizza. "Electrochemical Devices for Energy Conversion and Storage." In Nanostructure Science and Technology, 63–89. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4899-8059-5_3.
Full textCucinotta, Clotilde S., and Monica Kosa. "Electrochemical Interfaces for Energy Storage and Conversion." In Encyclopedia of Nanotechnology, 983–95. Dordrecht: Springer Netherlands, 2016. http://dx.doi.org/10.1007/978-94-017-9780-1_100941.
Full textBagotsky, V. S. "Electrochemical Systems in Energy Conversion and Storage." In Electrochemistry in Research and Development, 55–68. Boston, MA: Springer US, 1985. http://dx.doi.org/10.1007/978-1-4684-5098-9_9.
Full textMillet, Pierre. "Hydrogen Compression, Purification, and Storage." In Electrochemical Technologies for Energy Storage and Conversion, 425–62. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527639496.ch10.
Full textMbam, Sylvester M., Raphael M. Obodo, Assumpta C. Nwanya, A. B. C. Ekwealor, Ishaq Ahmad, and Fabian I. Ezema. "Synthesis and Electrochemical Properties of Graphene." In Electrode Materials for Energy Storage and Conversion, 263–77. Boca Raton: CRC Press, 2021. http://dx.doi.org/10.1201/9781003145585-11.
Full textConference papers on the topic "Electrochemical energy storage and conversion"
Hill, Davion, Yumei Zhai, Arun Agarwal, Edward Rode, Francois Ayello, and Narasi Sridhar. "Energy Storage Via Electrochemical Conversion of CO2 Into Specialty Chemicals." In ASME 2011 5th International Conference on Energy Sustainability. ASMEDC, 2011. http://dx.doi.org/10.1115/es2011-54048.
Full textShao, Mingfei, Jingbin Han, Jingwen Zhao, Min Wei, David G. Evans, and Xue Duan. "Layered Double Hydroxide Materials Used in Electrochemical Energy Storage and Conversion." In Photonics for Energy. Washington, D.C.: OSA, 2015. http://dx.doi.org/10.1364/pfe.2015.pt3f.4.
Full textDing, Liang-Xin, Qi Li, An-Liang Wang, Rui Guo, Xue-Feng Lu, Han Xu, Gao-Ren Li, and Ye-Xiang Tong. "Design and synthesis of composite nanomaterials for electrochemical energy conversion and storage." In Nanophotonics, Nanoelectronics and Nanosensor. Washington, D.C.: OSA, 2013. http://dx.doi.org/10.1364/n3.2013.nsa3a.44.
Full textCapo-Misut, Ruben, Raul Santiago Munoz-Aguilar, Joan Rocabert, Jose Ignacio Candela, and Pedro Rodriguez. "Control of energy storage system integrating electrochemical batteries and SC for grid-connected applications." In 2016 IEEE Energy Conversion Congress and Exposition (ECCE). IEEE, 2016. http://dx.doi.org/10.1109/ecce.2016.7854966.
Full textPanda, Manas Ranjan, Anish Raj K., Ananta Sarkar, Qiaoliang Bao, and Sagar Mitra. "Electrochemical investigation of MoTe2/rGO composite materials for sodium-ion battery application." In INTERNATIONAL CONFERENCE ON NANOMATERIALS FOR ENERGY CONVERSION AND STORAGE APPLICATIONS: NECSA 2018. Author(s), 2018. http://dx.doi.org/10.1063/1.5035235.
Full textChavda, Arvind, Biren Patel, Priyanka Marathey Indrajit Mukhopadhyay, and Abhijit Ray. "Synthesis and characterization of spray deposited CZTS thin films for photo-electrochemical application." In INTERNATIONAL CONFERENCE ON NANOMATERIALS FOR ENERGY CONVERSION AND STORAGE APPLICATIONS: NECSA 2018. Author(s), 2018. http://dx.doi.org/10.1063/1.5035246.
Full textManzhos, Sergei. "Effects of aggregate state in atomistic modeling of materials for electrochemical energy conversion and storage devices (Conference Presentation)." In Energy Harvesting and Storage: Materials, Devices, and Applications X, edited by Achyut K. Dutta and Palani Balaya. SPIE, 2020. http://dx.doi.org/10.1117/12.2556164.
Full textSangeeta, Shruti Agnihotri, Anil Arya, and A. L. Sharma. "Improved electrochemical performance of the Cr doped cathode materials for energy storage/conversion devices." In INTERNATIONAL CONFERENCE ON CONDENSED MATTER AND APPLIED PHYSICS (ICC 2015): Proceeding of International Conference on Condensed Matter and Applied Physics. Author(s), 2016. http://dx.doi.org/10.1063/1.4946431.
Full textOrel, Boris, U. L. Stangar, and F. Svegl. "Electrochemical and structural properties of SnO2 and Sb:SnO2 transparent electrodes with mixed electronically conductive and ion-storage characteristics." In Optical Materials Technology for Energy Efficiency and Solar Energy Conversion XIII, edited by Volker Wittwer, Claes G. Granqvist, and Carl M. Lampert. SPIE, 1994. http://dx.doi.org/10.1117/12.185424.
Full textKumar, Vijay, and C. R. Mariappan. "Electrochemical performance of spinel-type Ni doped ZnCo2O4 mesoporous rods as an electrode for supercapacitors." In INTERNATIONAL CONFERENCE ON NANOMATERIALS FOR ENERGY CONVERSION AND STORAGE APPLICATIONS: NECSA 2018. Author(s), 2018. http://dx.doi.org/10.1063/1.5035232.
Full textReports on the topic "Electrochemical energy storage and conversion"
Sariciftci, Niyazi Serdar. CO2 Recycling: The Conversion of Renewable Energy into Chemical Fuels. AsiaChem Magazine, November 2020. http://dx.doi.org/10.51167/acm00011.
Full textFarmand, Maryam. X-ray Absorption Spectroscopy Characterization of Electrochemical Processes in Renewable Energy Storage and Conversion Devices. Office of Scientific and Technical Information (OSTI), May 2013. http://dx.doi.org/10.2172/1341608.
Full textAuthor, Not Given. Electrochemical Energy Storage Technical Team Roadmap. Office of Scientific and Technical Information (OSTI), June 2013. http://dx.doi.org/10.2172/1220126.
Full textCairns, E. J. Energy Conversion and Storage Program. Office of Scientific and Technical Information (OSTI), March 1992. http://dx.doi.org/10.2172/7148265.
Full textAtanassov, Plamen. Materials for Energy Conversion: Materials for Energy Conversion and Storage. Office of Scientific and Technical Information (OSTI), March 2017. http://dx.doi.org/10.2172/1349091.
Full textKinoshita, Kim, ed. Technology Base Research Project for electrochemical energy storage. Office of Scientific and Technical Information (OSTI), June 1991. http://dx.doi.org/10.2172/6014352.
Full textGreenbaum, Steven G. SPECTROSCOPIC STUDIES OF MATERIALS FOR ELECTROCHEMICAL ENERGY STORAGE. Office of Scientific and Technical Information (OSTI), March 2014. http://dx.doi.org/10.2172/1150847.
Full textKinoshita, K., ed. Technology Base Research Project for electrochemical energy storage. Office of Scientific and Technical Information (OSTI), June 1991. http://dx.doi.org/10.2172/6265242.
Full textKinoshita, Kim. Technology Base Research Project for electrochemical energy storage. Office of Scientific and Technical Information (OSTI), May 1989. http://dx.doi.org/10.2172/5428337.
Full textDurstock, Michael F. Advanced Energy Storage and Conversion Devices. Fort Belvoir, VA: Defense Technical Information Center, December 2008. http://dx.doi.org/10.21236/ada515951.
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