Готові списки джерел за темами / Metal oxide electrocatalyst

Добірка наукової літератури з теми "Metal oxide electrocatalyst"

Автор: Grafiati
Опубліковано: 14 березня 2023

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Статті в журналах з теми "Metal oxide electrocatalyst"

1

Sung, Yung-Eun, Heejong Shin, and Jae Jeong Kim. "(Digital Presentation) Design of Metal/Metal Oxide Nanomaterials for Highly Active, Selective, and Durable Electrocatalysts." ECS Meeting Abstracts MA2022-02, no. 42 (October 9, 2022): 1553. http://dx.doi.org/10.1149/ma2022-02421553mtgabs.

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Анотація:
Electrocatalysis is a key part of renewable energy conversion in the future energy system. Sustainable energy conversion and chemical production require catalyst structure with high activity, durability, and product selectivity. In general, nanoscale electrocatalysts suffer various degradation phenomena during electrocatalysis, which leads to critical performance loss. Recently, the various hybrid nanostructures (such as ordered structure, metal/carbon encapsulation, or metal/metal oxide) have been highly investigated to achieve promising catalytic performances and enhanced stabilities. In this presentation, we will cover three different types of nanomaterials as highly active and stable electrocatalysts for oxygen reduction reaction (ORR). First, the alloy nanoparticles with ordered structures exhibit novel catalytic properties from their unique electronic and geometric structures. In particular, Pt alloys with atomically ordered crystal structures have been found to largely improve both electrocatalytic activity and stability for ORR through increased electronic interaction between Pt and other transition metals. Similarly, we recently demonstrated that well-controlled Co-, Mn- and Fe-based ternary or binary oxide nanocatalysts have an exceptionally high ORR activity, in addition to the promising electrocatalytic stability. Therefore, it is very important to synthesize well-ordered alloy nanocrystals to obtain highly durable and active electrocatalysts with respect to their structural and compositional properties. Second, we will show the strategic employment of carbon shells on electrocatalyst surfaces to enhance stability in the electrochemical process. Carbon shells can beneficially shield catalyst surfaces from electrochemical degradation and physical agglomeration. Thus carbon shells can effectively preserve the initial active site structure during electrocatalysis. The carbon shell also provides a confined environment at interfaces, enabling unconventional electrochemical behaviors. Finally, we will suggest an effective strategy to construct metal/oxide interfaces, precisely modulating the metal/oxide interfacial interactions in the nanoscale. By controlling the interface and strain effect on catalytic activity, we can achieve high active and stable metal oxide systems for ORR. We would like to describe the details of the above results, for investigating structure-activity relationships in electrocatalytic processes. Only when we start to comprehend the fundamentals behind electrocatalysis on the structure and interface of metal/metal oxide nanocrystals, they can be further advanced to be sustainable in long-term device operation.
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2

Karuppiah, Chelladurai, Balamurugan Thirumalraj, Srinivasan Alagar, Shakkthivel Piraman, Ying-Jeng Jame Li, and Chun-Chen Yang. "Solid-State Ball-Milling of Co3O4 Nano/Microspheres and Carbon Black Endorsed LaMnO3 Perovskite Catalyst for Bifunctional Oxygen Electrocatalysis." Catalysts 11, no. 1 (January 7, 2021): 76. http://dx.doi.org/10.3390/catal11010076.

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Анотація:
Developing a highly stable and non-precious, low-cost, bifunctional electrocatalyst is essential for energy storage and energy conversion devices due to the increasing demand from the consumers. Therefore, the fabrication of a bifunctional electrocatalyst is an emerging focus for the promotion and dissemination of energy storage/conversion devices. Spinel and perovskite transition metal oxides have been widely explored as efficient bifunctional electrocatalysts to replace the noble metals in fuel cell and metal-air batteries. In this work, we developed a bifunctional catalyst for oxygen reduction and oxygen evolution reaction (ORR/OER) study using the mechanochemical route coupling of cobalt oxide nano/microspheres and carbon black particles incorporated lanthanum manganite perovskite (LaMnO3@C-Co3O4) composite. It was synthesized through a simple and less-time consuming solid-state ball-milling method. The synthesized LaMnO3@C-Co3O4 composite was characterized by scanning electron microscopy, energy dispersive X-ray spectroscopy, transmission electron microscopy, Brunauer-Emmett-Teller (BET) analysis, X-ray diffraction spectroscopy, and micro-Raman spectroscopy techniques. The electrocatalysis results showed excellent electrochemical activity towards ORR/OER kinetics using LaMnO3@C-Co3O4 catalyst, as compared with Pt/C, bare LaMnO3@C, and LaMnO3@C-RuO2 catalysts. The observed results suggested that the newly developed LaMnO3@C-Co3O4 electrocatalyst can be used as a potential candidate for air-cathodes in fuel cell and metal-air batteries.
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3

Karuppiah, Chelladurai, Balamurugan Thirumalraj, Srinivasan Alagar, Shakkthivel Piraman, Ying-Jeng Jame Li, and Chun-Chen Yang. "Solid-State Ball-Milling of Co3O4 Nano/Microspheres and Carbon Black Endorsed LaMnO3 Perovskite Catalyst for Bifunctional Oxygen Electrocatalysis." Catalysts 11, no. 1 (January 7, 2021): 76. http://dx.doi.org/10.3390/catal11010076.

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Анотація:
Developing a highly stable and non-precious, low-cost, bifunctional electrocatalyst is essential for energy storage and energy conversion devices due to the increasing demand from the consumers. Therefore, the fabrication of a bifunctional electrocatalyst is an emerging focus for the promotion and dissemination of energy storage/conversion devices. Spinel and perovskite transition metal oxides have been widely explored as efficient bifunctional electrocatalysts to replace the noble metals in fuel cell and metal-air batteries. In this work, we developed a bifunctional catalyst for oxygen reduction and oxygen evolution reaction (ORR/OER) study using the mechanochemical route coupling of cobalt oxide nano/microspheres and carbon black particles incorporated lanthanum manganite perovskite (LaMnO3@C-Co3O4) composite. It was synthesized through a simple and less-time consuming solid-state ball-milling method. The synthesized LaMnO3@C-Co3O4 composite was characterized by scanning electron microscopy, energy dispersive X-ray spectroscopy, transmission electron microscopy, Brunauer-Emmett-Teller (BET) analysis, X-ray diffraction spectroscopy, and micro-Raman spectroscopy techniques. The electrocatalysis results showed excellent electrochemical activity towards ORR/OER kinetics using LaMnO3@C-Co3O4 catalyst, as compared with Pt/C, bare LaMnO3@C, and LaMnO3@C-RuO2 catalysts. The observed results suggested that the newly developed LaMnO3@C-Co3O4 electrocatalyst can be used as a potential candidate for air-cathodes in fuel cell and metal-air batteries.
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Sharma, Shuchi, and Ranga Rao Gangavarapu. "(Digital Presentation) Synthesis and Promoting Activity of Gd2O3 for Methanol Electro-Oxidation on Pt/C." ECS Meeting Abstracts MA2022-02, no. 50 (October 9, 2022): 2426. http://dx.doi.org/10.1149/ma2022-02502426mtgabs.

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Анотація:
One of the challenges in electrocatalysis is to design either an efficient non-noble electrocatalyst or improve the electrocatalytic activity of Pt/C by incorporating promoters such as metal oxides, carbides and nitrides. Rare earth metal oxides such as CeO2 have been explored to promote methanol electro-oxidation on Pt/C electrocatalyst. It has been noted that the synthesis method has profound effect on the physiochemical and in turn electrochemical properties of metal oxide promoted Pt/C electrocatalysts. This concept is tested on Gd2O3 promoted Pt/C. Gd2O3 is prepared by precipitation (GdO-PC) method and polymer assisted method (GdO-PL). The oxygen storage capacity (OSC) of this oxide is correlated with the electrochemical activity of Gd2O3-Pt/C. GdO-PC has higher OSC and can release surface oxygen much easier as compared to GdO-PL for methanol electro-oxidation on Pt. The Gd2O3-Pt/C catalysts are prepared with Gd2O3, Vulcan carbon and Pt-salt (equivalent to 20 wt% Pt) using microwave assisted polyol reflux method. The electrocatalytic activity of Gd2O3-Pt/C towards methanol oxidation has been carried out by cyclic voltammetry, CO stripping experiments, chronopotentiometry, and chronoamperometry methods in acidic media. The measurements show that Pt-GdO-PC/C performs better than Pt-(GdO-PL)/C) and commercial Pt/C. This indicates that the synthesis route of Gd2O3 particles is crucial for promoting methanol electro-oxidation. The first principle calculations show that there is a charge transfer from Gd2O3 to Pt. (GdO-PC). It is concluded that higher OSC and charge transfer from Gd2O3 to Pt work in tandem to weaken the Pt-CO bond and oxidise CO to CO2, thus reducing the CO poisoning and enhancing the activity of the oxide promoted electrocatalyst. Figure 1
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Klaas, Lutho, Mmalewane Modibedi, Mkhulu Mathe, Huaneng Su, and Lindiwe Khotseng. "Electrochemical Studies of Pd-Based Anode Catalysts in Alkaline Medium for Direct Glycerol Fuel Cells." Catalysts 10, no. 9 (August 26, 2020): 968. http://dx.doi.org/10.3390/catal10090968.

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Анотація:
This study investigates the most effective electrocatalyst for glycerol oxidation reaction (GOR) in alkaline medium for five synthesized electrocatalysts, Pd, PdNi, PdNiO, PdMn3O4 and PdMn3O4NiO, supported on multi-walled carbon nanotubes (MWCNTs) prepared using the polyol method. The particle size and crystalline size of the electrocatalysts were determined using HR-TEM and XRD techniques, respectively, while EDS was used to determine the elemental composition. XRD showed crystalline sizes ranging from 3.4 to 10.1 nm, while HR-TEM revealed particle sizes within the range of 3.4 and 7.2 nm. The electroactivity, electron kinetics and stability of the electrocatalysts towards glycerol in alkaline medium was evaluated using linear sweep voltammetry (LSV), electrochemical impedance spectroscopy (EIS) and chronoamperometry (CA), respectively, while the electroactive surface area (ECSA) of the electrocatalysts was determined using cyclic voltammetry (CV). The metal oxide-based Pd electrocatalysts PdNiO and PdMn3O4 were the most electrochemically active, while the addition of the second metal oxide to the Pd electrocatalyst PdMn3O4NiO did not show any improvement. This was associated with this electrocatalyst having the highest particle and crystalline sizes.
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Luo, Hongmei, and Meng Zhou. "Oxide Films and Nanoparticles for Lithium Ion Battery and Oxygen Electrocatalyst Applications." ECS Meeting Abstracts MA2022-01, no. 38 (July 7, 2022): 1668. http://dx.doi.org/10.1149/ma2022-01381668mtgabs.

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Анотація:
The global energy crisis coupling with the consumption of fossil fuels and the associated environmental issues, has stimulated extensive interest in searching for clean, efficient and sustainable energy storage and conversion systems. In this talk we are going to introduce a novel chemical solution approach for epitaxial thin film deposition and oxide nanoparticle network synthesis. The use of water soluable polymer to bind the metal ions has several advantages. The formation of covalent complexes between the lone pairs on the nitrogen atoms of the polymer and the metal cations make it possible to prepare almost any metal polymer precursor solutions. The unique chemistry and processing design of this technique deliver stable and homogeneous solutions at a molecular level that allows epitaxial growth of high-quality thin films and oxide nanoparticle network materials. Oxygen electrocatalysis, including both oxygen reduction reaction (ORR) and oxygen evolution reaction (OER), dominates the performance of the devices. However, the sluggish kinetics of these two reactions limits their performance. Therefore, development of non-precious metal-based oxygen electrocatalysts is greatly demanded. Metal oxides have attracted extensive interest as alternative electrocatalysts due to their low price and good endurance under relatively high temperature, which can be doped with a wide range of cations attributed to their flexible compositions and structures, leading to easy manipulation of their electrocatalytic properties. We study the nanoscale engineering of perovskite oxides and layered oxides in energy conversion/storage devices and focus on the electrode catalyst design and fabrication for boosting ORR and OER electrocatalysis.
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LU, J. L., CHANGWEI XU, and SAN PING JIANG. "ELECTRO-OXIDATION OF ETHANOL ON NANOCRYSTALLINE Pd/C CATALYST PROMOTED WITH OXIDE IN ALKALINE MEDIA." International Journal of Nanoscience 08, no. 01n02 (February 2009): 203–7. http://dx.doi.org/10.1142/s0219581x09005864.

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Nanocrystalline Pd electrocatalyst promoted with transition metal oxide ( Co 3 O 4, NiO , and CoNiO x) is successfully synthesized on high surface carbon support by using intermittent microwave heating (IMH) method. The physical properties of the catalysts are characterized by XRD, TEM, and EDX. The results show that there is no significant microstructure change between Pd and Pd -oxide electrocatalysts and the particle sizes are in the range 5.8–3.9 nm. The linear sweep voltammogram and chronoamperometry results for the electro-oxidation of ethanol show that Pd -oxide/ C electrocatalysts exhibit much better electrochemical activity and stability as compared with pure Pd / C electrocatalyst. The results show that Pd – CoNiO x/ C exhibits the best stability and highest electro-oxidation activity, indicating the promising potential as an alternative electrocatalysts for the direct ethanol fuel cells.
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8

Knecht, Tawney A., Shannon W. Boettcher, and James E. Hutchison. "Electrochemistry-Induced Restructuring of Tin-Doped Indium Oxide Nanocrystal Films of Relevance to CO2 Reduction." Journal of The Electrochemical Society 168, no. 12 (December 1, 2021): 126521. http://dx.doi.org/10.1149/1945-7111/ac40ca.

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Анотація:
The electrochemical reduction of CO2 into fuels using renewable electricity presents an opportunity to utilize captured CO2. Electrocatalyst development has been a primary focus of research in this area. This is especially true at the nanoscale, where researchers have focused on understanding nanostructure-property relationships. However, electrocatalyst structure may evolve during operation. Indium- and tin-based oxides have been widely studied as electrocatalysts for CO2 reduction to formate, but evolution of these catalysts during operation is not well-characterized. Here, we report the evolution of nanoscale structure of precise tin-doped indium oxide nanocrystals under CO2 reduction conditions. We show that sparse monolayer nanocrystal films desorb from the electrode upon charging, but thicker nanocrystal films remain, likely due to an increased number of physical contacts. Upon applying a cathodic voltage of −1.0 V vs RHE or greater, the original 10-nm diameter nanocrystals are no longer visible, and instead form a larger microstructural network. Elemental analysis suggests the network is an oxygen-deficient indium-tin metal alloy. We hypothesize that this morphological evolution is the result of nanocrystal sintering due to oxide reduction. These data provide insights into the morphological evolution of tin-doped indium oxide nanocrystal electrocatalysts under reducing conditions and highlight the importance of post-electrochemical structural characterization of electrocatalysts.
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Nong, Hong Nhan, Hoang Phi Tran, Camillo Spöri, Malte Klingenhof, Lorenz Frevel, Travis E. Jones, Thorsten Cottre, et al. "The Role of Surface Hydroxylation, Lattice Vacancies and Bond Covalency in the Electrochemical Oxidation of Water (OER) on Ni-Depleted Iridium Oxide Catalysts." Zeitschrift für Physikalische Chemie 234, no. 5 (May 26, 2020): 787–812. http://dx.doi.org/10.1515/zpch-2019-1460.

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AbstractThe usage of iridium as an oxygen-evolution-reaction (OER) electrocatalyst requires very high atom efficiencies paired with high activity and stability. Our efforts during the past 6 years in the Priority Program 1613 funded by the Deutsche Forschungsgemeinschaft (DFG) were focused to mitigate the molecular origin of kinetic overpotentials of Ir-based OER catalysts and to design new materials to achieve that Ir-based catalysts are more atom and energy efficient, as well as stable. Approaches involved are: (1) use of bimetallic mixed metal oxide materials where Ir is combined with cheaper transition metals as starting materials, (2) use of dealloying concepts of nanometer sized core-shell particle with a thin noble metal oxide shell combined with a hollow or cheap transition metal-rich alloy core, and (3) use of corrosion-resistant high-surface-area oxide support materials. In this mini review, we have highlighted selected advances in our understanding of Ir–Ni bimetallic oxide electrocatalysts for the OER in acidic environments.
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10

Shinde, Pratik V., Rutuparna Samal, and Chandra Sekhar Rout. "Comparative Electrocatalytic Oxygen Evolution Reaction Studies of Spinel NiFe2O4 and Its Nanocarbon Hybrids." Transactions of Tianjin University 28, no. 1 (December 10, 2021): 80–88. http://dx.doi.org/10.1007/s12209-021-00310-x.

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AbstractElectrocatalytic oxygen evolution reaction (OER) is one of the crucial reactions for converting renewable electricity into chemical fuel in the form of hydrogen. To date, there is still a challenge in designing ideal cost-effective OER catalysts with excellent activity and robust durability. The hybridization of transition metal oxides and carbonaceous materials is one of the most effective and promising strategies to develop high-performance electrocatalysts. Herein, this work synthesized hybrids of NiFe2O4 spinel materials with two-dimensional (2D) graphene oxide and one-dimensional (1D) carbon nanotubes using a facile solvothermal approach. Electrocatalytic activities of NiFe2O4 with 2D graphene oxide toward OER were realized to be superior even to the 1D carbon nanotube-based electrocatalyst in terms of overpotential to reach a current density of 10 mA/cm2 as well as Tafel slopes. The NiFe2O4 with 2D graphene oxide hybrid exhibits good stability with an overpotential of 327 mV at a current density of 10 mA/cm2 and a Tafel slope of 103 mV/dec. The high performance of NiFe2O4 with 2D graphene oxide is mainly attributed to its unique morphology, more exposed active sites, and a porous structure with a high surface area. Thus, an approach of hybridizing a metal oxide with a carbonaceous material offers an attractive platform for developing an efficient electrocatalyst for water electrochemistry applications.
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Дисертації з теми "Metal oxide electrocatalyst"

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GUZMAN, MEDINA HILMAR DEL CARMEN. "Electrocatalytic reduction of CO2 to value-added products." Doctoral thesis, Politecnico di Torino, 2021. http://hdl.handle.net/11583/2907030.

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Gu, Yanjuan. "Nanostructure of transition metal and metal oxide for electrocatalysis." Click to view the E-thesis via HKUTO, 2006. http://sunzi.lib.hku.hk/hkuto/record/B37774396.

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Chen, Youjiang. "Fundamental Aspects of Electrocatalysis at Metal and Metal Oxide Electrodes." Case Western Reserve University School of Graduate Studies / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=case1284390270.

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4

Baez, Baez Victor Antonio. "Metal oxide coated electrodes for oxygen reduction." Thesis, University of Southampton, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.241271.

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Chen, Junsheng. "Ternary Metal Oxide/(Oxy)Hydroxide for Efficient Oxygen Evolution Reaction." Thesis, The University of Sydney, 2021. https://hdl.handle.net/2123/25536.

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Анотація:
Novel clean energy conversion and storage technologies, such as electrochemical water splitting and metal-air battery, play significant roles in the future clean energy society. Oxygen evolution reaction (OER), as the fundamental reaction of these technologies, is crucial for their practical application. However, OER process is sluggish since the complex reaction process (multi-electron and multi-intermediate involved reaction). Developing efficient and affordable OER electrocatalysts remains a great challenge. Recently, the multimetal incorporation strategy has aroused extensive research interest since it can effectively enhance the catalytic performance of the catalysts. Nevertheless, there are still many scientific questions to be answered for such materials systems, such as the reaction mechanism and the optimum element composition. In this thesis, earth-abundant transition metals Cobalt and iron were selected as the basic elements. Cheap and abundant metals Vanadium, Chromium, and Tungsten were chosen as the incorporation elements respectively because of their unique d orbital structure in oxidation state. Their oxides/(oxy)hydroxides were elaborately designed and synthesised. The OER performance of the incorporated materials display a huge improvement. A variety of characterisations were employed to investigate the electrochemical properties of the materials. Theoretical calculations were also applied and combined with the characterisation observation to explain the reaction mechanism and the role of the incorporation element. Practical electrical water electrolyser devices were built up to determine the synthesised OER electrocatalysts in a real situation. Specifically, a facile electrodeposition catalysts synthesis method was developed, which can rapidly manufacture electrodes with efficient OER electrocatalysts on a large scale.
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Gu, Yanjuan, and 谷艳娟. "Nanostructure of transition metal and metal oxide forelectrocatalysis." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2006. http://hub.hku.hk/bib/B37774396.

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7

Bateni, Fazel. "Development of Non-precious Metal and Metal Oxide Electrocatalysts for an Alkaline Lignin Electrolysis Process." Ohio University / OhioLINK, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1562674707447307.

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8

Trotochaud, Lena. "Structure-Composition-Activity Relationships in Transition-Metal Oxide and Oxyhydroxide Oxygen-Evolution Electrocatalysts." Thesis, University of Oregon, 2014. http://hdl.handle.net/1794/18312.

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Solar water-splitting is a potentially transformative renewable energy technology. Slow kinetics of the oxygen evolution reaction (OER) limit the efficiency of solar-water-splitting devices, thus constituting a hurdle to widespread implementation of this technology. Catalysts must be stable under highly oxidizing conditions in aqueous electrolyte and minimally absorb light. A grand goal of OER catalysis research is the design of new materials with higher efficiencies enabled by comprehensive understanding of the fundamental chemistry behind catalyst activity. However, little progress has been made towards this goal to date. This dissertation details work addressing major challenges in the field of OER catalysis. Chapter I introduces the current state-of-the-art and challenges in the field. Chapter II highlights work using ultra-thin films as a platform for fundamental study and comparison of catalyst activity. Key results of this work are (1) the identification of a Ni0.9Fe0.1OOH catalyst displaying the highest OER activity in base to date and (2) that in base, many transition-metal oxides transform to layered oxyhydroxide materials which are the active catalysts. The latter result is critical in the context of understanding structure-activity relationships in OER catalysts. Chapter III explores the optical properties of these catalysts, using in situ spectroelectrochemistry to quantify their optical absorption. A new figure-of-merit for catalyst performance is developed which considers both optical and kinetic losses due to the catalyst and describes how these factors together affect the efficiency of composite semiconductor/catalyst photoanodes. In Chapter IV, the fundamental structure-composition-activity relationships in Ni1-xFexOOH catalysts are systematically investigated. This work shows that nearly all previous studies of Ni-based catalysts were likely affected by the presence of Fe impurities, a realization which holds significant weight for future study of Ni-based catalyst materials. Chapter V discusses the synthesis of tin-titanium oxide nanoparticles with tunable lattice constants. These materials could be used to make high-surface-area supports for thin layers of OER catalysts, which is important for maximizing catalyst surface area, minimizing the use of precious-metal catalysts, and optimizing 3D structure for enhanced mass/bubble transport. Finally, Chapter VI summarizes this work and outlines directions for future research. This work contains previously published and unpublished co-authored material.
2015-03-29
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Xing, Shihui. "Rational design of bi-transition metal oxide electrocatalysts for hydrogen and oxygen evolutions." Thesis, Queensland University of Technology, 2021. https://eprints.qut.edu.au/209307/1/Shihui_Xing_Thesis.pdf.

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This thesis mainly focuses on the rational design and preparation of bi-transition metal oxide materials for high-performance electrochemical catalysis, such as hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). To address the challenges of sluggish kinetics and large overpotentials in HER and OER, the effective strategy of morphology engineering, introducing a secondary metal element and supporting on carbon-based materials were carried out and discussed.
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Wu, Ziyang. "Rational design of two-dimensional architectures for efficient electrocatalysis." Thesis, Queensland University of Technology, 2022. https://eprints.qut.edu.au/235888/1/ziyang%2Bwu%2Bthesis%284%29.pdf.

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In this thesis, the principal focus is the rational design and fabrication of two-dimensional (2D) nanoarchitectures, e.g., low-cost metal oxide nanosheets and earth-abundant transition metal layered double hydroxides (LDHs) for enhanced electrocatalysis. The related hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) performance not only demonstrated the advances of 2D nanomaterials, such as unique physical and mechanical properties, unprecedented electronic features, and ultrahigh surface areas but also indicated the possible mechanisms behind boosted activity and stability, e.g., phase engineering function and oxygen vacancies influence.
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Книги з теми "Metal oxide electrocatalyst"

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Graphene Oxide-Metal Oxide and Other Graphene Oxide-based Composites in Photocatalysis and Electrocatalysis. Elsevier, 2022. http://dx.doi.org/10.1016/c2020-0-01725-1.

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Korotcenkov, Ghenadii, Jiaguo Yu, Liuyang Zhang, and Panyong Kuang. Graphene Oxide-Metal Oxide and other Graphene Oxide-Based Composites in Photocatalysis and Electrocatalysis. Elsevier, 2022.

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Korotcenkov, Ghenadii, Jiaguo Yu, Liuyang Zhang, and Panyong Kuang. Graphene Oxide-Metal Oxide and Other Graphene Oxide-Based Composites in Photocatalysis and Electrocatalysis. Elsevier, 2022.

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4

Metal Oxide-Based Nanostructured Electrocatalysts for Fuel Cells, Electrolyzers, and Metal-air Batteries. Elsevier, 2021. http://dx.doi.org/10.1016/c2018-0-03980-8.

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Korotcenkov, Ghenadii, Yaovi Holade, and Teko Napporn. Metal Oxide-Based Nanostructured Electrocatalysts for Fuel Cells, Electrolyzers, and Metal-Air Batteries. Elsevier, 2021.

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6

Korotcenkov, Ghenadii, Teko W. Napporn, and Yaovi Holade. Metal Oxide-Based Nanostructured Electrocatalysts for Fuel Cells, Electrolyzers, and Metal-Air Batteries. Elsevier, 2021.

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7

Thangaraju, Mahadevan. Study of precious metal-oxide based electrocatalysts for the oxidation of methanol. 1996.

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Thangaraju, Mahadevan. Study of precious metal-oxide based electrocatalysts for the oxidation of methanol. 1996.

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Частини книг з теми "Metal oxide electrocatalyst"

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Nayak, Arpan Kumar, and Akshaya Kumar Swain. "Facile Room Temperature Synthesis of Reduced Graphene Oxide as Efficient Metal-Free Electrocatalyst for Oxygen Reduction Reaction." In Carbon Nanostructures, 259–71. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-30207-8_10.

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Chutia, Bhugendra, Chiranjita Goswami, and Pankaj Bharali. "Metal Oxide-Based Electrocatalysts for Metal-Air Batteries." In Metal-Air Batteries, 209–25. Boca Raton: CRC Press, 2023. http://dx.doi.org/10.1201/9781003295761-15.

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Hazarika, Kumar Kashyap, and Pankaj Bharali. "3d-Metal Oxide Nanostructures for Oxygen Electrocatalysis." In ACS Symposium Series, 353–72. Washington, DC: American Chemical Society, 2020. http://dx.doi.org/10.1021/bk-2020-1359.ch012.

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Prakash, Jai, Donald Tryk, Wesley Aldred, and Ernest Yeager. "Transition-Metal Oxide Electrocatalysts for O2 Electrodes: The Pyrochlores." In Electrochemistry in Transition, 93–106. Boston, MA: Springer US, 1992. http://dx.doi.org/10.1007/978-1-4615-9576-2_8.

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Ota, Ken-ichiro, and Akimitsu Ishihara. "Metal Oxide-Based Compounds as Electrocatalysts for Oxygen Reduction Reaction." In Lecture Notes in Energy, 391–416. London: Springer London, 2013. http://dx.doi.org/10.1007/978-1-4471-4911-8_13.

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Xie, Yuhua, Shuyuan Pan, Fang Luo, and Zehui Yang. "Electrocatalysts Based on Metal Oxides for Hydrogen Evolution Reaction." In ACS Symposium Series, 201–26. Washington, DC: American Chemical Society, 2022. http://dx.doi.org/10.1021/bk-2022-1431.ch008.

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Chisaka, Mitsuharu. "Transition Metal Oxide, Oxynitride, and Nitride Electrocatalysts with and without Supports for Polymer Electrolyte Fuel Cell Cathodes." In Electrocatalysts for Low Temperature Fuel Cells, 423–41. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2017. http://dx.doi.org/10.1002/9783527803873.ch14.

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Karuppasamy, Lakshmanan, Lakshmanan Gurusamy, Gang-Juan Lee, and Jerry J. Wu. "Synthesis of Metal/Metal Oxide Supported Reduced Graphene Oxide (RGO) for the Applications of Electrocatalysis and Supercapacitors." In Carbon Nanostructures, 1–48. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-32-9057-0_1.

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Ishihara, Akimitsu, Hideto Imai, and Ken-ichiro Ota. "Transition Metal Oxides, Carbides, Nitrides, Oxynitrides, and Carbonitrides for O2Reduction Reaction Electrocatalysts for Acid PEM Fuel Cells." In Non-Noble Metal Fuel Cell Catalysts, 183–204. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527664900.ch5.

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Makhafola, Mogwasha D., Mpitloane J. Hato, Kabelo E. Ramohlola, Phuti S. Ramaripa, Thabiso C. Maponya, Gobeng R. Monama, Kerileng M. Molapo, et al. "Synergetic Effect of Graphene Oxide and Metal Organic Framework Nanocomposites as Electrocatalysts for Hydrogen Evolution Reaction." In Carbon Related Materials, 23–54. Singapore: Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-7610-2_2.

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Тези доповідей конференцій з теми "Metal oxide electrocatalyst"

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El-Dera, Sandra Erfan, Ahmed Abd El Aziz, and Ahmed Abd El Moneim. "Evaluation of the Activity of Metal-Oxides as Anode Catalysts in Direct Methanol Fuel Cell." In ASME 2012 10th International Conference on Fuel Cell Science, Engineering and Technology collocated with the ASME 2012 6th International Conference on Energy Sustainability. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/fuelcell2012-91288.

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Анотація:
In the present work, pure iridium oxide (IrO2), and ternary catalysts (IrSnSb-Oxides and RuIrTi-Oxides) are investigated to be used as anode electrocatalysts in The Direct Methanol Fuel Cells (DMFC). Investigations of Methanol Oxidation and Hydrogen Evolution over the catalysts are measured in sulphuric acid as a supportive electrolyte using cyclic voltammetry technique at room temperature (25°C). A specific comparison between the electrocatalytic activities of IrSnSb-Oxides and RuIrTi-Oxides systems is conducted. A comprehensive examination of IrSnSb-Oxides and RuIrTi-Oxides catalysts containing different fractions of the alloying elements are performed to study the effect of varying Iridium Ir content (%) in IrSnSb-Oxides and Ruthenium Ru content (%) in RuIrTi-Oxides on the catalytic activity of ternary catalysts and on the performance of DMFC. It is observed that the electrocatalytic performance of ternary oxides catalysts is strongly dependent on the Ir and Ru content. The generated IrO2 and 33.36% Ru – 1%Ir – 65.64%Ti – Oxides catalysts prove high stability for oxidation of methanol and more proficient electrochemical activity as an anodic electrocatalyst in DMFC at 25°C. The electrochemical measurements of the Hydrogen Evolution Reaction (HER) for metal oxides show that 46.65%Ir – 40.78%Sn – 12.57%Sb sample and 18.75%Ru – 9.35%Ir – 71.9%Ti sample are the superior hydrogen evolution catalysts at 25°C.
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Prabu, M., and S. Shanmugam. "NiCo2O4 - Graphene oxide hybrid as a bifunctional electrocatalyst for air breathing cathode material in metal air batteries." In International Conference on Advanced Nanomaterials & Emerging Engineering Technologies (ICANMEET-2013). IEEE, 2013. http://dx.doi.org/10.1109/icanmeet.2013.6609319.

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Giménez, Sixto, Camilo Arturo Mesa, Ernest Pastor, Radeya Vasquez Romero, Eva Ng Leon, Francisco Fabregat Santiago, and Elena Mas Marzá. "In situ investigation of metal oxide electrocatalysts by impedance spectroscopy." In Materials for Sustainable Development Conference (MAT-SUS). València: FUNDACIO DE LA COMUNITAT VALENCIANA SCITO, 2022. http://dx.doi.org/10.29363/nanoge.nfm.2022.175.

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Rahman, Che Zuraini Che Ab, Kuan-Ying Kok, Khamirul Amin Matori, Nur Ubaidah Saidin, Thye-Foo Choo, Nordin Hj Sabli, Zainal Abidin Talib, and Yazid Yaakob. "Chemical synthesis and characterization of metal-oxide based electrocatalysts for fuel cell reactions." In MATERIALS CHARACTERIZATION USING X-RAYS AND RELATED TECHNIQUES. Author(s), 2019. http://dx.doi.org/10.1063/1.5089359.

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Giuffredi, Giorgio, Fabio Di Fonzo, Andrea Perego, Piero Mazzolini, Greta Tirelli, Mirko Prato, Francesco Fumagalli, et al. "Nanocrystalline, Mixed-Phase Transition Metal Oxide/Oxy-Chalcogenide Nanostructures for Efficient Hydrogen Evolution Electrocatalysis." In nanoGe Fall Meeting 2019. València: Fundació Scito, 2019. http://dx.doi.org/10.29363/nanoge.ngfm.2019.250.

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Di Fonzo, Fabio, Giorgio Giuffredi, Andrea Perego, Piero Mazzolini, Greta Tirelli, Mirko Prato, Francesco Fumagalli, et al. "Nanocrystalline, Mixed-Phase Transition Metal Oxide/Oxy-Chalcogenide Nanostructures for Efficient Hydrogen Evolution Electrocatalysis." In nanoGe Fall Meeting 2019. València: Fundació Scito, 2019. http://dx.doi.org/10.29363/nanoge.nfm.2019.250.

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Звіти організацій з теми "Metal oxide electrocatalyst"

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Nikolla, Eranda. Final Report: Nanostructured, Targeted Layered Metal Oxides as Active and Selective Heterogeneous Electrocatalysts for Oxygen Electrocatalysis. Office of Scientific and Technical Information (OSTI), January 2021. http://dx.doi.org/10.2172/1763600.

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Digby Macdonald. The Fundamental Role of Nano-Scale Oxide Films in the Oxidation of Hydrogen and the Reduction of Oxygen on Noble Metal Electrocatalysts. Office of Scientific and Technical Information (OSTI), April 2005. http://dx.doi.org/10.2172/838754.

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