CAS: Collaborative Research: Steering Proton-Coupled Electron Transfer Processes for Energy Conversion at the Metal Electrode/Porous 3D Material Interface

CAS：合作研究：引导质子耦合电子转移过程在金属电极/多孔 3D 材料界面进行能量转换

• 批准号: 2154919
• 负责人: Michelle Foster
• 金额: $ 22.1万
• 依托单位: University of Massachusetts Boston
• 依托单位国家: 美国
• 项目类别: Standard Grant
• 财政年份: 2022
• 资助国家: 美国
• 起止时间: 2022-05-01 至 2025-04-30
• 项目状态: 未结题
• 来源: https://www.nsf.gov/awardsearch/showAward?AWD_ID=2154919&HistoricalAwards=false
• 关键词: CAS; Collaborative; Research; Steering; Proton

With the support of the Chemical Catalysis program in the Division of Chemistry, Professors Matthias Waegele and Junwei (Lucas) Bao of Boston College, and Professor Mariam Ismail of the University of Massachusetts, Boston are studying how to precisely modify electrodes to control electrocatalytic reactions for energy storage. Electrocatalytic processes can store electrical energy from renewable energy sources in the form of liquid or gaseous fuels from abundant, renewable feedstocks such as carbon dioxide or biomass. A principal hurdle for the adoption of this technology is the poor product selectivity of these reactions. These reactions are complex and occur at an interface involving a liquid (the electrolyte) and a solid (the electrode). In this work, the project team will modify this interface, and thus the electrocatalytic activity, by coating the electrodes with a special class of porous material known as metal-organic frameworks (MOFs). The project team will use spectroscopy and advanced computer simulations to gain molecular-level insights into the effects of the MOF overlayers on three model reactions that are central for renewable fuel synthesis: The conversion of water to hydrogen, the conversion of carbon dioxide to carbon monoxide, and conversion of biomass to valuable chemicals and fuels. The results of this research will provide insight into the control of selectivity of electrocatalytic reaction. Further, the team will engage in synergistic activities aimed at promoting the recruitment and retention of underrepresented groups in STEM. Specifically, the team will involve female high-school students and underrepresented undergraduate minority students in this research as part of a summer program, which will expose the participants to state-of-the-art renewable energy research in the areas of synthesis, analytical chemistry, and simulation techniques.On this project, Matthias Waegele and Junwei (Lucas) Bao of Boston College and Mariam Ismail of the University of Massachusetts, Boston are studying and designing 3D active sites at the metal electrode/porous 3D material interface to facilitate desirable reaction pathways of proton-coupled electron transfer (PCET) processes for energy storage and conversion. To this end, the team will coat metal electrodes (Pt and Au) with crystalline metal-organic framework (MOF) overlayers and investigate the effects of the MOF overlayers on PCET processes. Through systematic variation of the inorganic nodes and organic linkers of the MOFs, the team will aim to understand the effect of the MOF’s chemical and physical properties on PCET. The project will focus on the hydrogen evolution reaction (HER) and the reduction of carbon dioxide to carbon monoxide. Vibrational and Raman spectroscopies will be used to characterize the metal electrode/MOF interface under catalytic conditions. Key properties to be extracted from these measurements will include the interfacial pH, electric double layer charging, MOF-intermediate interactions, interfacial water structure, and local structure of the MOF at the metal surface. Computer simulations will map minimum-energy reaction pathways. On the basis of these investigations, the project aims to establish robust interfacial property-reactivity relationships. Such design rules would serve to guide the choice of synergistic 3D material, electrolyte, and reaction conditions to steer PCET reactions in aqueous electrolytes, and thereby also support the discovery of efficient and selective pathways for renewable fuels formation.This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.

在化学系化学催化项目的支持下，波士顿学院的Matthias Waegele教授和Junwei（Lucas）Bao教授以及波士顿马萨诸塞州大学的Mariam Ismail教授正在研究如何精确修饰电极以控制用于能量存储的电催化反应。电催化过程可以以来自丰富的可再生原料（例如二氧化碳或生物质）的液体或气体燃料的形式存储来自可再生能源的电能。采用这种技术的主要障碍是这些反应的产物选择性差。这些反应是复杂的，并且发生在涉及液体（电解质）和固体（电极）的界面处。在这项工作中，项目团队将通过用一类特殊的多孔材料（称为金属有机框架（MOFs））涂覆电极来修改这种界面，从而改变电催化活性。该项目团队将使用光谱学和先进的计算机模拟来获得分子水平的见解，以了解MOF覆盖层对可再生燃料合成的三个核心模型反应的影响：水转化为氢气，二氧化碳转化为一氧化碳，以及生物质转化为有价值的化学品和燃料。本研究结果将为电催化反应选择性的控制提供参考。此外，该团队将参与协同活动，旨在促进STEM中代表性不足的群体的招聘和保留。具体来说，该团队将让高中女生和少数民族本科生参与这项研究，作为暑期项目的一部分，这将使参与者接触到合成，分析化学和模拟技术领域最先进的可再生能源研究。在这个项目中，波士顿学院的Matthias Waegele和Junwei（Lucas）Bao以及马萨诸塞州大学的Mariam Ismail，波士顿正在研究和设计金属电极/多孔3D材料界面上的3D活性位点，以促进质子耦合电子转移（PCET）过程的理想反应途径，用于能量存储和转换。为此，该团队将在金属电极（Pt和Au）上涂覆晶体金属有机框架（MOF）覆盖层，并研究MOF覆盖层对PCET过程的影响。通过MOF的无机节点和有机连接体的系统变化，该团队的目标是了解MOF的化学和物理性质对PCET的影响。该项目将侧重于析氢反应（HER）和将二氧化碳还原为一氧化碳。振动和拉曼光谱将用于表征催化条件下的金属电极/MOF界面。从这些测量中提取的关键属性将包括界面pH值，双电层充电，MOF-中间体相互作用，界面水结构和金属表面处的MOF局部结构。计算机模拟将绘制出最小能量反应路径。在这些研究的基础上，该项目旨在建立稳健的界面性能-反应性关系。这样的设计规则将有助于指导选择协同3D材料，电解质和反应条件，以引导PCET反应在水性电解质，从而也支持发现有效的和选择性的途径，可再生燃料的形成。这个奖项反映了NSF的法定使命，并已被认为是值得通过使用基金会的智力价值和更广泛的影响审查标准进行评估的支持。