多模态原位表征揭示了用于酸性可持续能源技术的钴电催化剂的意外稳定性

IF 15.6 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Ashton M. Aleman, Colin F. Crago, Gaurav A. Kamat, Aniket S. Mule, Jaime E. Avilés Acosta, Jesse E. Matthews, Nathaniel Keyes, Ryan T. Hannagan, Adam C. Nielander, Michaela Burke Stevens* and Thomas F. Jaramillo*, 
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引用次数: 0

摘要

对这些系统中非贵重材料如何降解的理解有限,往往阻碍了耐用和负担得起的可持续能源技术的加速发展。在酸性质子交换膜燃料电池和水电解槽中,金属钴(Co)被认为是一种不稳定的成分,通常与贵金属或其他稳定剂结合使用。为了了解Co不稳定性背后的机制,我们采用了一个实验平台,通过在线电感耦合等离子体质谱法和电化学体质谱法在电化学测试中定量溶解,以及非原位表征。在不同的条件下(电催化、时间、气体类型饱和度和离子浓度),观察到的Co稳定性窗口与经典化学热力学预测的不同,这表明了比以前理解的新的稳定和降解机制。值得注意的是,Co对析氢反应(HER)很活跃,其长时间稳定性比热力学预测的高~ 300 mV。此外,在含氧环境中,Co同时进行HER和氧还原反应(ORR),但经历不同的形态变化和溶解机制。有趣的是,在开路电压下,无氧环境中的溶解减少了22倍,提出了在器件关闭协议期间减少Co损失的途径。最后,在更极端的操作条件下,Co在大量溶解后变得稳定,这表明微环境中高浓度的Co2+离子诱导形成了稳定的CoHO2表面。总之,这些结果可以用来改进设计和开发更强大、更具成本效益的可持续能源技术,并促进长期材料利用的战略战略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Multimodal In Situ Characterization Uncovers Unexpected Stability of a Cobalt Electrocatalyst for Acidic Sustainable Energy Technologies

Multimodal In Situ Characterization Uncovers Unexpected Stability of a Cobalt Electrocatalyst for Acidic Sustainable Energy Technologies

An accelerated development of durable and affordable sustainable energy technologies is often hindered by a limited understanding of how nonprecious materials within these systems degrade. In acidic proton exchange membrane fuel cells and water electrolyzers, metallic cobalt (Co) is considered an unstable component that is often combined with precious metals or other stabilizers. To understand the mechanisms behind Co instability, we employ an experimental platform that quantifies dissolution with on-line inductively coupled plasma mass spectrometry and product formation with electrochemical mass spectrometry during electrochemical testing, along with ex situ characterization. Under varied conditions (electrocatalysis, time, gas-type saturation, and ion concentration), windows of Co stability are observed that are different than predicted with classical chemical thermodynamics, suggesting new stabilization and degradation mechanisms than previously understood. Notably, Co is active for the hydrogen evolution reaction (HER), with prolonged stability that is ∼300 mV greater than thermodynamically projected. Additionally, in an oxygenated environment, Co concurrently performs the HER and the oxygen reduction reaction (ORR) yet undergoes different morphology changes and dissolution mechanisms. Interestingly, at open-circuit voltage, there is a 22× decrease in dissolution in an oxygen-free environment, proposing a route to decrease Co losses during device shutdown protocols. Lastly, under more extreme operating conditions, Co becomes stable after a substantial amount of dissolution, suggesting that high concentrations of Co2+ ions in the microenvironment induce the formation of a stable CoHO2 surface. Altogether, these results can be leveraged to improve the design and development of more robust and cost-effective sustainable energy technologies, as well as promote strategic strategies for prolonged material utilization.

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来源期刊
CiteScore
24.40
自引率
6.00%
发文量
2398
审稿时长
1.6 months
期刊介绍: The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.
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