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用于在酸性介质中进行高活性和稳定水氧化的分级钯催化剂。

Hierarchical palladium catalyst for highly active and stable water oxidation in acidic media.

作者信息

Peng Jing, Sun Haofeng, Ni Kun, Wu Jiajing, Sun Xinyu, Su Yueqi, Cheng Han, Liu Yuhua, Guo Yuqiao, Bi Wentuan, Zhu Yanwu, Wu Changzheng, Xie Yi

机构信息

Hefei National Laboratory for Physical Science at the Microscale, CAS Center for Excellence in Nanoscience, iChEM (Collaborative Innovation Center of Chemistry for Energy Materials), and CAS Key Laboratory of Mechanical Behavior and Design of Materials, University of Science and Technology of China, Hefei 230026, China.

Institute of Energy, Hefei Comprehensive National Science Center, Hefei 230026, China.

出版信息

Natl Sci Rev. 2022 Jun 9;10(2):nwac108. doi: 10.1093/nsr/nwac108. eCollection 2023 Feb.

Abstract

Acidic water electrolysis is of great importance for boosting the development of renewable energy. However, it severely suffers from the trade-off between high activity and long lifespan for oxygen evolution catalysts on the anode side. This is because the sluggish kinetics of oxygen evolution reaction necessitates the application of a high overpotential to achieve considerable current, which inevitably drives the catalysts far away from their thermodynamic equilibrium states. Here we demonstrate a new oxygen evolution model catalyst-hierarchical palladium (Pd) whose performance even surpasses the benchmark Ir- and Ru-based materials. The Pd catalyst displays an ultralow overpotential (196 mV), excellent durability and mitigated degradation (66 μV h) at 10 mA cm in 1 M HClO. Tensile strain on Pd (111) facets weakens the binding of oxygen species on electrochemical etching-derived hierarchical Pd and thereby leads to two orders of magnitudes of enhancement of mass activity in comparison to the parent Pd bulk materials. Furthermore, the Pd catalyst displays the bifunctional catalytic properties for both oxygen and hydrogen evolutions and can deliver a current density of 2 A cm at a low cell voltage of 1.771 V when fabricated into polymer electrolyte membrane electrolyser.

摘要

酸性水电解对于推动可再生能源的发展至关重要。然而,它在阳极侧析氧催化剂的高活性和长寿命之间面临着严峻的权衡。这是因为析氧反应的缓慢动力学需要施加高过电位才能获得可观的电流,这不可避免地使催化剂远离其热力学平衡状态。在此,我们展示了一种新型析氧模型催化剂——分级钯(Pd),其性能甚至超过了基准的铱基和钌基材料。该钯催化剂在1 M HClO中,在10 mA cm时显示出超低过电位(196 mV)、优异的耐久性和减缓的降解(66 μV h)。钯(111)晶面上的拉伸应变削弱了电化学蚀刻衍生的分级钯上氧物种的结合,从而导致与母体钯块状材料相比,质量活性提高了两个数量级。此外,该钯催化剂对析氧和析氢均表现出双功能催化特性,当制成聚合物电解质膜电解槽时,在1.771 V的低电池电压下可提供2 A cm的电流密度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01d0/10035503/cdd3ba7352ee/nwac108fig1.jpg

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