Electrocatalytic Conversion of CO2 to Formic Acid: A Journey from 3d-Transition Metal-Based Molecular Catalyst Design to Electrolyzer Assembly.

IF 19.3 1区 材料科学 Q1 CHEMISTRY, PHYSICAL
ACS Energy Letters Pub Date : 2024-10-15 Epub Date: 2024-09-23 DOI:10.1021/acs.accounts.4c00418
Chandan Das, Suhana Karim, Somnath Guria, Tannu Kaushik, Suchismita Ghosh, Arnab Dutta
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引用次数: 0

Abstract

ConspectusElectrochemical CO2 reduction to obtain formate or formic acid is receiving significant attention as a method to combat the global warming crisis. Significant efforts have been devoted to the advancement of CO2 reduction techniques over the past few decades. This Account provides a unified discussion on various electrochemical methodologies for CO2 to formate conversion, with a particular focus on recent advancements in utilizing 3d-transition-metal-based molecular catalysts. This Account primarily focuses on understanding molecular functions and mechanisms under homogeneous conditions, which is essential for assessing the optimized reaction conditions for molecular catalysts. The unique architectural features of the formate dehydrogenase (FDH) enzyme provide insight into the key role of the surrounding protein scaffold in modulating the active site dynamics for stabilizing the key metal-bound CO2 intermediate. Additionally, the protein moiety also triggers a facile proton relay around the active site to drive electrocatalytic CO2 reduction forward. The fine-tuning of FDH machinery also ensures that the electrocatalytic CO2 reduction leads to the production of formic acid as the major yield without any other carbonaceous products, while limiting the competitive hydrogen evolution reaction. These lessons from the enzymes are key in designing biomimetic molecular catalysts, primarily based on multidentate ligand scaffolds containing peripheral proton relays. The subtle modifications of the ligand framework ensure the favored production of formic acid following electrocatalytic CO2 reduction in the solution phase. Next, the molecular catalysts are required to be mounted on robust electroactive surfaces to develop their corresponding heterogeneous versions. The surface-immobilization provides an edge to the molecular electrocatalysts as their reactivity can be scaled up with improved durability for long-term electrocatalysis. Despite challenges in developing high-performance, selective catalysts for the CO2 to formic acid transformation, significant progress is being made with the tactical use of graphene and carbon nanotube-based materials. To date, the majority of the research activity stops here, as the development of an operational CO2 to formic acid converting electrolyzer prototype still remains in its infancy. To elaborate on the potential future steps, this Account covers the design, scaling parameters, and existing challenges of assembling large-scale electrolyzers. A short glimpse at the utilization of electrolyzers for industrial-scale CO2 reduction is also provided here. The proper evaluation of the surface-immobilized electrocatalysts assembled in an electrolyzer is a key step for gauging their potential for practical viability. Here, the key electrochemical parameters and their expected values for industrial-scale electrolyzers have been discussed. Finally, the techno-economic aspects of the electrolyzer setup are summarized, completing the journey from tactical design of molecular catalysts to their appropriate application in a commercially viable electrolyzer setup for CO2 to formate electroreduction. Thus, this Account portrays the complete story of the evolution of a molecular catalyst to its sustainable application in CO2 utilization.

Abstract Image

二氧化碳到甲酸的电催化转化:从 3d 过渡金属分子催化剂设计到电解槽组装的历程。
Conspectus 通过电化学方法还原二氧化碳以获得甲酸或甲酸作为应对全球变暖危机的一种方法,正受到广泛关注。过去几十年来,人们一直致力于二氧化碳还原技术的发展。本鸿运国际账户登录统一讨论了将二氧化碳转化为甲酸盐的各种电化学方法,尤其关注了利用基于 3d 过渡金属的分子催化剂的最新进展。本报告主要侧重于了解均相条件下的分子功能和机理,这对于评估分子催化剂的优化反应条件至关重要。甲酸脱氢酶(FDH)的独特结构特征让我们深入了解了周围蛋白质支架在调节活性位点动力学以稳定关键的金属结合二氧化碳中间体方面的关键作用。此外,蛋白质分子还能触发活性位点周围的质子中继,推动电催化二氧化碳还原向前发展。对 FDH 机制的微调还确保了电催化二氧化碳还原能够产生甲酸作为主要产物,而不产生任何其他碳质产物,同时限制了竞争性氢进化反应。从酶中汲取的这些经验是设计仿生分子催化剂的关键,这些催化剂主要基于含有外围质子中继的多叉配体支架。配体框架的微妙变化确保了在溶液阶段电催化二氧化碳还原后甲酸的有利生产。接下来,需要将分子催化剂安装在坚固的电活性表面上,以开发相应的异质催化剂。表面固定化为分子电催化剂提供了优势,因为它们的反应活性可以放大,并提高了长期电催化的耐久性。尽管在开发用于将二氧化碳转化为甲酸的高性能、选择性催化剂方面存在挑战,但在战术性使用石墨烯和碳纳米管基材料方面正在取得重大进展。迄今为止,由于二氧化碳转化为甲酸电解槽原型的开发仍处于起步阶段,因此大部分研究活动到此为止。为了详细阐述未来可能采取的步骤,本报告将介绍组装大型电解槽的设计、扩展参数和现有挑战。此外,还简要介绍了利用电解槽进行工业规模二氧化碳还原的情况。对组装在电解槽中的表面固定电催化剂进行适当评估,是衡量其实际应用潜力的关键步骤。这里讨论了工业规模电解槽的关键电化学参数及其预期值。最后,总结了电解槽装置的技术经济方面,从而完成了从分子催化剂的战术设计到其在商业上可行的二氧化碳到甲酸酯电还原电解槽装置中的适当应用的全过程。因此,本开户绑定手机领体验金描绘了从分子催化剂的演变到其在二氧化碳利用中的可持续应用的完整故事。
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来源期刊
ACS Energy Letters
ACS Energy Letters Energy-Renewable Energy, Sustainability and the Environment
CiteScore
31.20
自引率
5.00%
发文量
469
审稿时长
1 months
期刊介绍: ACS Energy Letters is a monthly journal that publishes papers reporting new scientific advances in energy research. The journal focuses on topics that are of interest to scientists working in the fundamental and applied sciences. Rapid publication is a central criterion for acceptance, and the journal is known for its quick publication times, with an average of 4-6 weeks from submission to web publication in As Soon As Publishable format. ACS Energy Letters is ranked as the number one journal in the Web of Science Electrochemistry category. It also ranks within the top 10 journals for Physical Chemistry, Energy & Fuels, and Nanoscience & Nanotechnology. The journal offers several types of articles, including Letters, Energy Express, Perspectives, Reviews, Editorials, Viewpoints and Energy Focus. Additionally, authors have the option to submit videos that summarize or support the information presented in a Perspective or Review article, which can be highlighted on the journal's website. ACS Energy Letters is abstracted and indexed in Chemical Abstracts Service/SciFinder, EBSCO-summon, PubMed, Web of Science, Scopus and Portico.
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