Kamat Gaurav Ashish, Zamora Zeledón José A, Gunasooriya G T Kasun Kalhara, Dull Samuel M, Perryman Joseph T, Nørskov Jens K, Stevens Michaela Burke, Jaramillo Thomas F
Department of Chemical Engineering, Stanford University, 443 Via Ortega, Stanford, CA, 94305, USA.
SUNCAT Center for Interface Science and Catalysis, SLAC National Accelerator Laboratory, 2575 Sand Hill Road, Menlo Park, CA, 94025, USA.
Commun Chem. 2022 Feb 18;5(1):20. doi: 10.1038/s42004-022-00635-1.
Platinum is an important material with applications in oxygen and hydrogen electrocatalysis. To better understand how its activity can be modulated through electrolyte effects in the double layer microenvironment, herein we investigate the effects of different acid anions on platinum for the oxygen reduction/evolution reaction (ORR/OER) and hydrogen evolution/oxidation reaction (HER/HOR) in pH 1 electrolytes. Experimentally, we see the ORR activity trend of HClO > HNO > HSO, and the OER activity trend of HClO [Formula: see text] HNO ∼ HSO. HER/HOR performance is similar across all three electrolytes. Notably, we demonstrate that ORR performance can be improved 4-fold in nitric acid compared to in sulfuric acid. Assessing the potential-dependent role of relative anion competitive adsorption with density functional theory, we calculate unfavorable adsorption on Pt(111) for all the anions at HER/HOR conditions while under ORR/OER conditions [Formula: see text] binds the weakest followed by [Formula: see text] and [Formula: see text]. Our combined experimental-theoretical work highlights the importance of understanding the role of anions across a large potential range and reveals nitrate-like electrolyte microenvironments as interesting possible sulfonate alternatives to mitigate the catalyst poisoning effects of polymer membranes/ionomers in electrochemical systems. These findings help inform rational design approaches to further enhance catalyst activity via microenvironment engineering.
铂是一种重要材料,在氧和氢的电催化中具有应用。为了更好地理解如何通过双层微环境中的电解质效应来调节其活性,在此我们研究了不同酸根阴离子对铂在pH为1的电解质中氧还原/析出反应(ORR/OER)以及析氢/氧化反应(HER/HOR)的影响。实验上,我们观察到HClO>HNO>HSO时的ORR活性趋势,以及HClO[化学式:见原文]HNO ∼ HSO时的OER活性趋势。在所有三种电解质中HER/HOR性能相似。值得注意的是,我们证明与在硫酸中相比,在硝酸中ORR性能可提高4倍。利用密度泛函理论评估相对阴离子竞争吸附的电位依赖性作用,我们计算得出在HER/HOR条件下所有阴离子在Pt(111)上的吸附均不利,而在ORR/OER条件下[化学式:见原文]结合最弱,其次是[化学式:见原文]和[化学式:见原文]。我们结合实验与理论的工作突出了在大电位范围内理解阴离子作用的重要性,并揭示了类似硝酸盐的电解质微环境作为有趣的可能的磺酸盐替代品,以减轻电化学系统中聚合物膜/离聚物的催化剂中毒效应。这些发现有助于为通过微环境工程进一步提高催化剂活性的合理设计方法提供信息。