Academic literature on the topic 'CO2 electrocatalytic reduction'
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Journal articles on the topic "CO2 electrocatalytic reduction"
Peiris, M. C. R., and M. Y. Udugala-Ganehenege. "Electrocatalytic Activity of (Bis(salicylaldehyde)ethylenediamino)Ni(II) Complex for CO2 Reduction." International Journal of Environmental Science and Development 7, no. 2 (2015): 91–94. http://dx.doi.org/10.7763/ijesd.2016.v7.747.
Full textKumagai, Hiromu, Tetsuya Nishikawa, Hiroki Koizumi, Taiki Yatsu, Go Sahara, Yasuomi Yamazaki, Yusuke Tamaki, and Osamu Ishitani. "Electrocatalytic reduction of low concentration CO2." Chemical Science 10, no. 6 (2019): 1597–606. http://dx.doi.org/10.1039/c8sc04124e.
Full textLi, Qian, Yu-Chao Wang, Jian Zeng, Xin Zhao, Chen Chen, Qiu-Mei Wu, Li-Miao Chen, Zhi-Yan Chen, and Yong-Peng Lei. "Bimetallic chalcogenides for electrocatalytic CO2 reduction." Rare Metals 40, no. 12 (July 20, 2021): 3442–53. http://dx.doi.org/10.1007/s12598-021-01772-7.
Full textHan, Peng, Xiaomin Yu, Di Yuan, Min Kuang, Yifei Wang, Abdullah M. Al-Enizi, and Gengfeng Zheng. "Defective graphene for electrocatalytic CO2 reduction." Journal of Colloid and Interface Science 534 (January 2019): 332–37. http://dx.doi.org/10.1016/j.jcis.2018.09.036.
Full textOgura, Kotaro, and Hiroaki Uchida. "Electrocatalytic reduction of CO2 to methanol." Journal of Electroanalytical Chemistry and Interfacial Electrochemistry 220, no. 2 (April 1987): 333–37. http://dx.doi.org/10.1016/0022-0728(87)85119-7.
Full textOgura, Kotaro, and Ichiro Yoshida. "Electrocatalytic reduction of CO2 to methanol." Journal of Molecular Catalysis 47, no. 1 (August 1988): 51–57. http://dx.doi.org/10.1016/0304-5102(88)85072-7.
Full textAlenezi, Khalaf M. "Iron Sulphur Cluster [Fe4S4(SPh)4]2– Catalyzed Electrochemical Reduction of CO2 on Carbon Electrodes in [Bu4N][BF4]-DMF Mixture." Current Analytical Chemistry 16, no. 7 (October 1, 2020): 854–62. http://dx.doi.org/10.2174/1573411015666191002170213.
Full textCunningham, Drew W., and Jenny Y. Yang. "Selective Electrocatalytic Reduction of CO2 to HCO2−." Trends in Chemistry 2, no. 4 (April 2020): 401–2. http://dx.doi.org/10.1016/j.trechm.2020.02.001.
Full textGe, Hongtao, Zhengxiang Gu, Peng Han, Hanchen Shen, Abdullah M. Al-Enizi, Lijuan Zhang, and Gengfeng Zheng. "Mesoporous tin oxide for electrocatalytic CO2 reduction." Journal of Colloid and Interface Science 531 (December 2018): 564–69. http://dx.doi.org/10.1016/j.jcis.2018.07.066.
Full textLee, Wonhee, Young Eun Kim, Min Hye Youn, Soon Kwan Jeong, and Ki Tae Park. "Catholyte-Free Electrocatalytic CO2 Reduction to Formate." Angewandte Chemie 130, no. 23 (May 8, 2018): 6999–7003. http://dx.doi.org/10.1002/ange.201803501.
Full textDissertations / Theses on the topic "CO2 electrocatalytic reduction"
Xue, Congcong. "Electrocatalytic and Photocatalytic CO2 Reduction by Ru-Re Bimetallic Complexes." The Ohio State University, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=osu1462205030.
Full textLi, Xiang. "Investigation of Interfacial Properties under Electrocatalytic Reduction Conditions:." Thesis, Boston College, 2021. http://hdl.handle.net/2345/bc-ir:109096.
Full textHeterogeneous electrocatalytic reduction is an environmentally friendly method for the conversion of abundant feedstock molecules into valuable products. Examples include the reduction of carbon dioxide to hydrocarbons and the reduction of nitrate to ammonia. Heterogeneous electrocatalysis occurs at the interface between an electrode and an electrolyte. Interfacial properties, such as surface morphology, interfacial electric field, interfacial water structure, and local pH, can substantially influence the activity and selectivity of electrocatalytic reduction processes. However, a comprehensive, molecular-level understanding of how these interfacial properties control electrocatalysis is still largely lacking to date. To develop such an understanding, it is essential to probe the properties of the electrocatalytic interface under operating conditions. This great experimental challenge is further compounded by the fact that the interface often undergoes dynamic changes during catalysis. In this thesis, we took a multimodal approach to characterize the aqueous electrolyte/copper interface during CO2/CO reduction and hydrogen evolution. Copper is the only pure metal that promotes the reduction of CO2/CO to hydrocarbons at significant reaction rates. The hydrogen evolution reaction is the main competing reaction in aqueous electrolytes. It is therefore essential to understand how these reactions are controlled by the properties of the interface. In the first part of this thesis, we employed in-situ surface-enhanced infrared absorption spectroscopy (SEIRAS) and surface-enhanced Raman spectroscopy (SERS) to investigate dynamic changes of the copper electrode surface. We found that the polycrystalline copper electrode surface undergoes a reconstruction process upon adsorption of CO. The formation of nanoscale metal clusters on the electrode manifests itself by the appearance of a new CO stretch band, which arises from a CO sub-population bound to undercoordinated copper atoms. The formation of these clusters is reversible, that is, they disappear upon desorption of CO. This work demonstratesthat a reaction intermediate such as CO can induce dynamic and reversible changes in the surface morphology of a heterogeneous catalyst. Because the changes are reversible, they would escape ex situ measurements. Our findings highlight the need for probing catalytic surfaces under operating conditions. In the second part of this thesis, we focused on how the electrolyte influences electrocatalysis at the aqueous electrolyte/copper electrode interface. Specifically, we explored the mechanisms by which cations of the supporting electrolyte affect the reduction of CO and the hydrogen evolution reaction on copper. With differential electrochemical mass spectrometry (DEMS), we determined to what extent the reduction of CO to ethylene is affected by the identity of the cations of the supporting electrolyte. Ethylene is produced in the presence of methyl4N+ and ethyl4N+ cations, whereas this product is not synthesized in propyl4N+- and butyl4N+-containing electrolytes. With SEIRAS, we found that an intermolecular interaction between surface-adsorbed CO and interfacial water is disrupted in the presence of the two larger cations. This observation suggests that this interaction promotes the hydrogenation of surface-bound CO to ethylene. This work illustrates that weak intermolecular interactions can substantially influence electrocatalytic processes. In a related study, we examined the effect of alkali metal cations of the supporting electrolyte on the hydrogen evolution reaction. We found that, in alkaline conditions, changing the cation from Na+ to Cs+ has no measurable effect on the HER. Because it is well-established that Cs+ promotes the reduction of CO2/CO to hydrocarbons, the results illustrate the changing the alkali cation enables the selective promotion of this pathway under alkaline conditions. Further, we found that in 0.1 M solutions of NaOH and CsOH of the highest commercially available purity grades, trace impurities of iron deposit on the copper electrode during the hydrogen evolution reaction. Because iron is a better catalyst for the hyrogen evolution reaction than copper, the rate of the hydrogen evolution reaction is enhanced by up to a factor of 5. These findings demonstrate that trace impurities of this ubiquitous metal pose a great challenge for the development of selective catalytic processes for CO2/CO reduction. This thesis provides a critical study of how the interfacial properties change under the electrocatalytic reduction of CO2/CO and hydrogen evolution conditions. The properties of both Cu electrode and the electrolyte contribute to the control of the selectivity of these complex electrocatalytic processes
Thesis (PhD) — Boston College, 2021
Submitted to: Boston College. Graduate School of Arts and Sciences
Discipline: Chemistry
Hicks, Robert Paul. "Probing Electrocatalytic and Photocatalytic Processes with Structure-Specific Spectroscopies:." Thesis, Boston College, 2019. http://hdl.handle.net/2345/bc-ir:108657.
Full textStudying the adsorption and reaction kinetics of surface-bound chemical species, on different metal catalysts or electrodes, is of paramount importance in the development of inhomogeneous catalytic methodology. Our study of the oxidation of CO on platinum was accomplished by designing a thin layer flow cell in an external reflection configuration. A charge-injection circuit was successfully implemented which decreased the time required to charge the double layer in the electrochemical cell. We were able to obtain a signal via Stark shift spectrum, of the adsorbed CO, using the thin layer cell configuration. Additionally, electrochemical impedance spectroscopy was used as a diagnostic tool to assess the effect of electrode geometry, on the voltage response, in the thin layer cell. The coupling of visible light-driven photoexciation with transition metal catalytic plat- forms is emerging as a synthetic strategy to achieve unique reactivity that has previously been inaccessible. One such example is the iridium/nickel-dipyridyl system discovered recently. Characterizing the interactions between the iridium and nickel catalysts, under reaction conditions, is important to develop a better understanding of the system. In order to apply infrared spectroscopic measurement techniques, in-situ, we made modifications to the synthetic scheme by changing the solvent and by utilizing different iridium catalysts for the synthesis of the desired methyl 4-(benzoyloxy)benzoate product. Using our trans- mission infrared setup we effectively demonstrated in-situ product detection of the aryl- ester coupled product. Additionally, after constructing a transient infrared pump-probe setup, we collected preliminary results of the triplet state lifetime of the iridium dye. The surface morphology of copper has been shown to affect the electrochemical reduction of CO2. Using surface-enhanced Raman spectroscopies, the reversible formation of nanoscale metal clusters on a copper electrode was revealed at sufficiently cathodic potentials where we observed the appearance of a new band at 2080 cm-1 corresponding to C≡O adsorbed to undercoordinated copper defect sites. The formation of new undercoordinated sites additionally resulted in the surface enhancement of the Raman scattering which amplified the intensity of the other spectral bands
Thesis (MS) — Boston College, 2019
Submitted to: Boston College. Graduate School of Arts and Sciences
Discipline: Chemistry
Berro, Patrick. "Exploring Photocatalytic and Electrocatalytic Reduction of CO2 with Re(I) and Zn(II) Complexes and Attempts to Employ a Novel Carbene Ligand to this Endeavor." Thesis, Université d'Ottawa / University of Ottawa, 2021. http://hdl.handle.net/10393/41625.
Full textLi, Dongfang. "Copper-based Metal-Organic-Framework for Electrochemical Carbon Dioxide Reduction." Thesis, The University of Sydney, 2022. https://hdl.handle.net/2123/29915.
Full textFERRI, MICHELE. "HYDROXYAPATITE-BASED MATERIALS FOR ENVIRONMENTAL PROCESSES." Doctoral thesis, Università degli Studi di Milano, 2021. http://hdl.handle.net/2434/815634.
Full textMigliaccio, Luca. "Bimetallic catalysts for CO2 electroreduction." Master's thesis, Alma Mater Studiorum - Università di Bologna, 2017. http://amslaurea.unibo.it/14470/.
Full textHernández, Ibáñez Naiara. "Exploration of novel materials in (bio)electrocatalysis: sensing in complex media and biocathodes for the CO2 reduction." Doctoral thesis, Universidad de Alicante, 2018. http://hdl.handle.net/10045/88207.
Full textKour, Gurpreet. "First principles investigations on transition metal based electrocatalysts for efficient clean energy conversion." Thesis, Queensland University of Technology, 2022. https://eprints.qut.edu.au/232798/1/Gurpreet_Kour_Thesis.pdf.
Full textZhang, Ting. "I Doctorate Program in Materials Science PhD Thesis Zn-Based Metal-Organic Frameworks Derived Materials for High-Efficient Carbon Dioxide Electrochemical Reduction." Doctoral thesis, Universitat Autònoma de Barcelona, 2021. http://hdl.handle.net/10803/673731.
Full textLa combustión excesiva de combustibles fósiles da como resultado la emisión de dióxido de carbono (CO2), que desencadenó crecientes problemas ambientales, como el calentamiento global, el aumento del nivel del mar, el clima extremo y la extinción de especies. Por lo tanto, las tecnologías para la conversión de CO2 en otros productos de valor jugaron un papel vital para eliminar la concentración de CO2 en la atmósfera. En ese sentido, la conversión electroquímica de CO2 alimentado por energía renovable en productos químicos útiles se considera una solución elegante para lograr el ciclo del carbono. Sin embargo, debido a la interioridad de las moléculas de CO2 y la reacción competitiva de evolución de hidrógeno (HER), los principales desafíos en el campo CO2 RR son el alto requerimiento de sobrepotencial que representa la termodinámica desfavorable y la baja eficiencia faradaica (FE) para los productos objetivo. Por lo tanto, la búsqueda de un electrocatalizador económico y de alta eficiencia es sensato y necesario para aplicaciones prácticas. En las últimas décadas, las estructuras organometálicas (MOF) absorbieron las enormes consideraciones en el campo de la electrocatálisis debido a su gran área de superficie específica, rica estructura de poros y sitios activos uniformemente dispersos. Aunque con grandes potenciales en electrocatálisis, la mayoría de los materiales MOF todavía sufren de actividad insuficiente, baja conductividad y poca estabilidad, lo que dificultaría sus aplicaciones prácticas. Especialmente, en el campo de CO2 RR, se deben considerar muchos parámetros importantes, incluida la alta eficiencia faradaica (FE), bajo sobrepotencial, gran densidad de corriente y estabilidad robusta, etc. Por lo tanto, el diseño racional de MOF para cumplir con los requisitos anteriores tanto como sea posible es crucial para explotar sus futuras aplicaciones de CO2 RR. Por lo tanto, en esta disertación, hicimos muchos esfuerzos para desarrollar catalizadores basados en MOFs / derivados de MOF con eficiencia, actividad y estabilidad superiores para aumentar el rendimiento de CO2 RR. Esta disertación se divide en 5 capítulos: El capítulo 1 es la información sobre los conceptos fundamentales sobre la CO2 RR electroquímico, que incluye la celda fundamental de la CO2 RR electroquímico, revisa los productos de reducción comunes y sus vías simples. Mientras tanto, la descripción general de los parámetros importantes que afectan la CO2 RR, incluidos los diferentes catalizadores en los últimos años y el electrolito, y las métricas relevantes que evalúan los electrocatalizadores. El Capítulo 2 trata de la fabricación de ZIF-8 modificado en superficie como electrodo basado en MOF para CO2 RR electroquímico para generar CO. En este trabajo, se preparó un ZIF-8 modificado en superficie mediante la introducción de una proporción muy pequeña de ácido 2,5-dihidroxitereftálico (DOBDC) en ZIF-8, logrando una densidad de corriente de CO mayor. En el Capítulo 3, se utiliza una ruta fácil para introducir grupos que contienen O con enlaces axiales en un catalizador de Fe-N-C a través de la pirólisis de estructuras orgánicas metálicas a base de Zn dopado con Fe (IRMOF-3), formando átomos únicos de Fe altamente dispersos con sitios activos HO-FeN4. Debido a la modulación del ambiente local inducida por tales grupos -OH, el catalizador D-Fe-N-C exhibe una actividad CO2 RR mejorada, incluida una alta selectividad con alta eficiencia Faradaica de CO y una estabilidad sólida. En el capítulo 4, proponemos que la introducción de átomos de Fe en catalizadores de Ni-N-C fabrica catalizadores de un solo átomo de metal doble (Ni/Fe-N-C) hacia CO2 RR para lograr una alta selectividad y actividad simultáneamente. El catalizador de doble metal optimizado mostró excelentes rendimientos, obteniendo una alta selectividad con eficiencia faradaica CO a un bajo sobrepotencial, superior a las contrapartes de un solo metal. Finalmente, el Capítulo 5 resume las conclusiones generales.
The excessive combustion of fossil fuels results in the emission of carbon dioxide (CO2), which triggers increasing environmental problems, such as, global warming, rising sea levels, extreme weather, and species extinction. Therefore, the technologies for conversion of CO2 into other value products plays a vital role in order to eliminate the CO2 concentration in atmosphere. Thereinto, electrochemical conversion of CO2 powered by renewable energy to useful chemicals is considered as an elegant solution to achieve the carbon cycle. However, due to the innerness of CO2 molecules and competitive hydrogen evolution reaction (HER), the main challenges in the field CO2 RR are the high overpotential requirement that represents the unfavourable thermodynamics and low Faradaic efficiency (FE) for the target products. Therefore, searching for a high-efficient and cost-friendly electrocatalyst is sensible and necessary for practical applications. In the past decades, metal-organic frameworks (MOFs) engrossed the enormous considerations in the field of electrocatalysis because of their large specific surface area, rich pore structure, and uniformly dispersed active sites. Although they have a great potential in electrocatalysis, most MOFs materials still suffer from insufficient activity, low conductivity, and poor stability, which would hinder their practical applications. Especially, in the field of CO2 RR, many important parameters, including high FE, low overpotential, large current density and robust stability among others, should be considered. Thus, the rational design of MOFs to fulfil the above requirements as much as possible is crucial for exploiting their future in CO2 RR applications. Therefore, in this dissertation, we made many efforts to develop MOFs-based/derived catalysts with superior efficiency, activity, and stability for boosting the CO2 RR performance. This dissertation is divided into 5 chapters: Chapter 1 is the insights on the fundamental concepts about electrochemical CO2 RR, which includes the fundamental cell of electrochemical CO2 RR, reviews the common reduction products and their simple pathways. Meanwhile, the overview of important parameters affecting CO2 RR, including different catalysts over the past years, electrolyte, and the relevant metrics evaluating the electrocatalysts as well as limitations of electrochemical CO2 reduction are also presented in this chapter. In addition, this chapter summarizes the fundamental concepts about MOFs materials and their high-temperature pyrolysis derived materials as the electrocatalysts. Chapter 2 deals with the fabrication of surface modified ZIF-8 as MOFs-based electrode for electrochemical CO2 RR to generate CO. In this work, a surface modified ZIF-8 has been prepared through introducing a very small proportion 2,5-dihidroxyterephthalic acid (DOBDC) into ZIF-8, achieving a higher current density of CO and a boosted Faradaic efficiency. In Chapter 3, a facile route is used to introduce axial bonded O-containing groups into a Fe-N-C catalyst through pyrolysis of Fe-doped Zn-based metal organic frameworks (IRMOF-3), forming highly dispersed Fe single atoms with HO-FeN4 active sites. Due to the local environment modulation induced by such -OH groups, the D-Fe-N-C catalyst exhibits an enhanced CO2 RR activity, including a high selectivity with CO Faradaic efficiency, and a robust stability, which is higher than that of the reported normal FeN4 sites without -OH groups. In Chapter 4, we proposed that introducing Fe atoms into Ni-N-C catalysts fabricates double metal (bimetallic) single-atom catalysts (Ni/Fe-N-C) towards CO2 RR to achieve a high selectivity and activity simultaneously. The optimized double-metal Ni/Fe-N-C catalyst showed an excellent performance, obtaining a high selectivity with a high CO Faradaic efficiency at a low overpotential. The performance obtained is superior to both single metal counterparts and other state-of-the-art M-N-C catalysts, proving that regulating single active sites with a second metal site potentially breaks the single metal-based activity benchmark to obtain the high selectivity and activity in CO2 RR, simultaneously. Finally, Chapter 5 summarizes the general conclusions.
Universitat Autònoma de Barcelona. Programa de Doctorat en Ciència de Materials
Book chapters on the topic "CO2 electrocatalytic reduction"
Goddard, William A. "Electrocatalytic CO2 Reduction." In Computational Materials, Chemistry, and Biochemistry: From Bold Initiatives to the Last Mile, 1265–79. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-18778-1_66.
Full textSimakov, David S. A. "Electrocatalytic Reduction of CO2." In Renewable Synthetic Fuels and Chemicals from Carbon Dioxide, 27–42. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-61112-9_2.
Full textLi, Fengwang, and Jie Zhang. "Electrocatalytic Reduction of CO2 in Ionic Liquid-Based Electrolytes." In Encyclopedia of Ionic Liquids, 1–15. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-10-6739-6_85-1.
Full textLi, Fengwang, and Jie Zhang. "Electrocatalytic Reduction of CO2 in Ionic Liquid-Based Electrolytes." In Encyclopedia of Ionic Liquids, 343–57. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-33-4221-7_85.
Full textOgura, Kotaro. "Electrocatalytic Reduction of CO2 on the Dual-Film Electrodes Modified with Various Metal Complexes." In Novel Trends in Electroorganic Synthesis, 197–200. Tokyo: Springer Japan, 1998. http://dx.doi.org/10.1007/978-4-431-65924-2_60.
Full textJeong, Hui-Yun, Mani Balamurugan, Chang Hyuck Choi, and Ki Tae Nam. "Chapter 6. Bridging Homogeneous and Heterogeneous Systems: Atomically Dispersed Metal Atoms in Carbon Matrices for Electrocatalytic CO2 Reduction." In Carbon Dioxide Electrochemistry, 226–86. Cambridge: Royal Society of Chemistry, 2020. http://dx.doi.org/10.1039/9781788015844-00226.
Full textFRESE, K. W. "ELECTROCHEMICAL REDUCTION OF CO2 AT SOLID ELECTRODES." In Electrochemical and Electrocatalytic Reactions of Carbon Dioxide, 145–216. Elsevier, 1993. http://dx.doi.org/10.1016/b978-0-444-88316-2.50010-3.
Full text"Mechanism of Catalytic and Electrocatalytic CO2 Reduction to Fuels and Chemicals." In Electrochemical Reduction of Carbon Dioxide, 281–306. CRC Press, 2016. http://dx.doi.org/10.1201/b20177-14.
Full textKumari, Neetu, M. Ali Haider, and Suddhasatwa Basu. "Mechanism of Catalytic and Electrocatalytic CO2 Reduction to Fuels and Chemicals." In Electrochemical Reduction of Carbon Dioxide, 267–92. CRC Press, 2016. http://dx.doi.org/10.1201/b20177-7.
Full textSánchez-Sánchez, C. M. "Electrocatalytic Reduction of CO2 in Imidazolium-Based Ionic Liquids." In Encyclopedia of Interfacial Chemistry, 539–51. Elsevier, 2018. http://dx.doi.org/10.1016/b978-0-12-409547-2.13377-3.
Full textConference papers on the topic "CO2 electrocatalytic reduction"
Ishitani, Osamu. "Photocatalytic and Electrocatalytic Reduction of Low Concentration of CO2." In nanoGe Fall Meeting 2019. València: Fundació Scito, 2019. http://dx.doi.org/10.29363/nanoge.ngfm.2019.054.
Full textIshitani, Osamu. "Photocatalytic and Electrocatalytic Reduction of Low Concentration of CO2." In nanoGe Fall Meeting 2019. València: Fundació Scito, 2019. http://dx.doi.org/10.29363/nanoge.nfm.2019.054.
Full textAlbero, Josep, Enrico Lepre, Julian Heske, Michal Nowakowski, Ernesto Scoppola, Ivo Zizak Zizak, Tobias Heil Heil, Thomas D. Kühne, Markus Antonietti, and Nieves López-Salas. "Ni-Based Electrocatalysts for Unconventional CO2 Reduction Reaction to Formic Acid." In International Conference on Frontiers in Electrocatalytic Transformations. València: Fundació Scito, 2021. http://dx.doi.org/10.29363/nanoge.interect.2021.002.
Full textGonell Gómez, Sergio, Julio Lloret-Fillol, and Alexander J. M. Miller. "Mechanistic comparisons on Ru and Fe carbene-supported complexes for electrocatalytic CO2 reduction." In International Conference on Frontiers in Electrocatalytic Transformations. València: Fundació Scito, 2021. http://dx.doi.org/10.29363/nanoge.interect.2021.034.
Full textChai, Rukaun, Yuetian Liu, Qianjun Liu, Xuan He, and Pingtian Fan. "Effect and Mechanism of CO2 Electrochemical Reduction for CCUS-EOR." In SPE Annual Technical Conference and Exhibition. SPE, 2021. http://dx.doi.org/10.2118/206135-ms.
Full textBrückner, Sven, Wen Ju, and Peter Strasser. "Efficient NiNC-GDEs for Near Neutral and Acidic CO2 Reduction in a Zero-Gap Configuration." In International Conference on Frontiers in Electrocatalytic Transformations. València: FUNDACIO DE LA COMUNITAT VALENCIANA SCITO, 2022. http://dx.doi.org/10.29363/nanoge.interect.2022.006.
Full textHod, Idan, Ran Shimoni, and Subhabrata Mukhopadhyay. "Molecular Manipulation of Heterogeneous Electrocatalytic CO2 Reduction Using Metal-Organic Frameworks." In Materials for Sustainable Development Conference (MAT-SUS). València: FUNDACIO DE LA COMUNITAT VALENCIANA SCITO, 2022. http://dx.doi.org/10.29363/nanoge.nfm.2022.047.
Full textPopovic, Stefan, Nejc Hodnik, and Marjan Bele. "Reconstruction of Copper Nanoparticles at Electrochemical CO2 Reduction Conditions: Identical Location Scanning Electron Microscopy (IL-SEM) Study." In International Conference on Frontiers in Electrocatalytic Transformations. València: Fundació Scito, 2021. http://dx.doi.org/10.29363/nanoge.interect.2021.017.
Full textHod, Idan, Ran Shimoni, Itamar Liberman, Raya Ifraemov, Wenhui He, and Chanderpratap Singh. "Metal-Organic Frameworks as a Heterogeneous Platform for (Photo)-Electrocatalytic CO2 Reduction." In nanoGe Fall Meeting 2019. València: Fundació Scito, 2019. http://dx.doi.org/10.29363/nanoge.ngfm.2019.122.
Full textHod, Idan, Ran Shimoni, Itamar Liberman, Raya Ifraemov, Wenhui He, and Chanderpratap Singh. "Metal-Organic Frameworks as a Heterogeneous Platform for (Photo)-Electrocatalytic CO2 Reduction." In nanoGe Fall Meeting 2019. València: Fundació Scito, 2019. http://dx.doi.org/10.29363/nanoge.nfm.2019.122.
Full textReports on the topic "CO2 electrocatalytic reduction"
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 text