Enhanced Electrodes for Proton Conducting Solid Oxide Fuel Cells and Electrolyzers
用于质子传导固体氧化物燃料电池和电解槽的增强型电极
基本信息
- 批准号:0967829
- 负责人:
- 金额:$ 30.48万
- 依托单位:
- 依托单位国家:美国
- 项目类别:Standard Grant
- 财政年份:2010
- 资助国家:美国
- 起止时间:2010-04-01 至 2011-02-28
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
0967829McIntoshMatching supply with demand is a significant issue with the large-scale deployment of intermittent renewable energy systems such as wind and solar power. For example, the peak power generated when the wind blows must be matched to periods of peak demand. This necessitates the development of large and efficient means of temporary power storage. One attractive option is a high performance, reversible, and efficient fuel cell/electrolyzer system. This system would operate in electrolyzer mode to store electrical energy as chemical energy (hydrogen) during periods of plentiful power generation. Operation can then be reversed to supply electrical energy during periods of peak demand.Intellectual MeritProton conducting oxides have potential application in efficient high temperature solid oxide fuel cells and electrolyzers. While the transport properties of these materials are being studied in increasing detail, there is currently very limited knowledge regarding the catalytic and electrocatalytic activity of this class of material. Reduction and oxidation (redox) of surface oxygen sites by the Mars-van Krevelen mechanism is a central step in catalytic and electrocatalytic reaction on oxygen ion conducting materials. The central hypothesis of the proposed research is that an analogous proton-based Mars-van Krevelen mechanism will be a critical step in the catalytic cycle on proton conducting oxides. The central route to enhanced activity will be doping of transition metals both into the oxide lattice and as nanoparticles on the oxide surface. The hypothesized electrocatalytic mechanism will be validated by isotopic transient studies and the measured reaction kinetics related to proton incorporation thermodynamics, transport properties and crystal structure. Proton conducting solid oxide fuel cells and electrolyzers will be fabricated and tested to demonstrate the links between electrocatalysis and electrode function.The demonstration of a proton based Mars-van Krevelen mechanism will provide a fundamental basis from which the performance of proton conducting oxide electrodes may be interpreted and enhanced.Broader ImpactsReplacing oxygen ion conductors with proton conducting oxides can provide a new direction for heterogeneous catalyst development. The results of this multidisciplinary study will be disseminated to the catalysis, electrochemistry, and solid state ionics communities through journal publications and conference presentations. Undergraduate students will play an active role in this research through clearly identified, focused research projects. The importance and potential impact of ongoing scientific advances in the area of energy and the environment will be conveyed to the general public via "Energy days" to be held at the University of Virginia. Faculty and graduate and undergraduate students from across campus actively engaged in this field will provide technology demonstrations and discussion points. A focused approach to engaging middle school students will be developed by expanding a small existing program. The PI, as well as graduate students in the PI's laboratory, will spend a time at local middle schools introducing the concept of engineering to students through a series of hands-on projects. These will be focused on energy and sustainability concepts with learning outcomes reinforced through classroom education.
在大规模部署风能和太阳能等间歇性可再生能源系统时,供需匹配是一个重要问题。例如,刮风时产生的峰值电力必须与需求高峰期相匹配。这就需要开发大型、高效的临时储电手段。一个有吸引力的选择是高性能、可逆和高效的燃料电池/电解槽系统。该系统将在电解槽模式下运行,在发电充足的时期将电能储存为化学能(氢气)。智能质子导电氧化物在高效高温固体氧化物燃料电池和电解槽中具有潜在的应用前景。虽然这些材料的传输特性正在被越来越详细地研究,但目前关于这类材料的催化和电催化活性的知识非常有限。在氧离子导电材料的催化和电催化反应中,表面氧位的还原和氧化(氧化还原)是MARS-van Krevelen机理的核心步骤。这项拟议研究的中心假设是,类似的基于质子的火星-范克雷文机制将是质子传导氧化物催化循环的关键步骤。提高活性的中心途径是将过渡金属同时掺杂到氧化物晶格中和氧化物表面的纳米颗粒中。该假说的电催化机理将通过同位素瞬变研究以及与质子掺入热力学、传输性质和晶体结构相关的测量反应动力学来验证。质子导电固体氧化物燃料电池和电解槽将被制造和测试,以证明电催化和电极功能之间的联系。基于质子的MARS-van Krevelen机理的论证将为解释和提高质子导电氧化物电极的性能提供基本依据。这项多学科研究的结果将通过期刊出版物和会议报告向催化、电化学和固态离子社区传播。本科生将通过明确的、有重点的研究项目在这项研究中发挥积极的作用。能源和环境领域正在进行的科学进步的重要性和潜在影响将通过将在弗吉尼亚大学举行的“能源日”活动向公众传达。活跃在该领域的教师、研究生和本科生将提供技术演示和讨论点。将通过扩大现有的一个小项目来开发吸引中学生的有重点的方法。PI以及PI实验室的研究生将在当地中学度过一段时间,通过一系列实践项目向学生介绍工程的概念。这些活动将侧重于能源和可持续发展概念,并通过课堂教育加强学习成果。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
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Steven McIntosh其他文献
Revealing hidden nanoscale electrocatalysis
揭示隐藏的纳米级电催化作用
- DOI:
10.1038/s41929-025-01326-5 - 发表时间:
2025-04-25 - 期刊:
- 影响因子:44.600
- 作者:
Steven McIntosh - 通讯作者:
Steven McIntosh
Steven McIntosh的其他文献
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{{ truncateString('Steven McIntosh', 18)}}的其他基金
Collaborative Research: Electrochemical Production of NH3 Using Proton-Conducting Ceramic Electrolytes
合作研究:利用质子传导陶瓷电解质电化学生产NH3
- 批准号:
1803758 - 财政年份:2018
- 资助金额:
$ 30.48万 - 项目类别:
Standard Grant
EFRI-PSBR: Continuous Liquid Fuel Production via Scalable Biosynthesis of Enzyme-Quantum Dot Hybrid Photocatalysts
EFRI-PSBR:通过酶-量子点混合光催化剂的可扩展生物合成连续生产液体燃料
- 批准号:
1332349 - 财政年份:2013
- 资助金额:
$ 30.48万 - 项目类别:
Standard Grant
CAREER: A Novel Approach to Catalysis for Next Generation Direct-Hydrocarbon Solid Oxide Fuel Cells
职业生涯:下一代直接碳氢化合物固体氧化物燃料电池的催化新方法
- 批准号:
1101814 - 财政年份:2010
- 资助金额:
$ 30.48万 - 项目类别:
Standard Grant
Enhanced Electrodes for Proton Conducting Solid Oxide Fuel Cells and Electrolyzers
用于质子传导固体氧化物燃料电池和电解槽的增强型电极
- 批准号:
1101817 - 财政年份:2010
- 资助金额:
$ 30.48万 - 项目类别:
Standard Grant
CAREER: A Novel Approach to Catalysis for Next Generation Direct-Hydrocarbon Solid Oxide Fuel Cells
职业生涯:下一代直接碳氢化合物固体氧化物燃料电池的催化新方法
- 批准号:
0643931 - 财政年份:2007
- 资助金额:
$ 30.48万 - 项目类别:
Standard Grant
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Collaborative Research: Elucidation of the Grotthuss Topochemistry in Reticular Electrodes for Fast Proton Batteries
合作研究:阐明快速质子电池网状电极中的 Grotthuss 拓扑化学
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合作研究:阐明快速质子电池网状电极中的 Grotthuss 拓扑化学
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Enhanced Electrodes for Proton Conducting Solid Oxide Fuel Cells and Electrolyzers
用于质子传导固体氧化物燃料电池和电解槽的增强型电极
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Carbon nanotube-based three-dimensional electrodes for proton exchange membrane fuel cells
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