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高温下金/钇稳定氧化锆界面上的析氧反应

Oxygen Evolution Reaction over the Au/YSZ Interface at High Temperature.

作者信息

Song Yuefeng, Zhou Si, Dong Qiao, Li Yangsheng, Zhang Xiaomin, Ta Na, Liu Zhi, Zhao Jijun, Yang Fan, Wang Guoxiong, Bao Xinhe

机构信息

State Key Laboratory of Catalysis, CAS Center for Excellence in Nanoscience, Dalian National Laboratory for Clean Energy, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Zhongshan Road 457, Dalian, 116023, China.

University of Chinese Academy of Sciences, Beijing, 100039, China.

出版信息

Angew Chem Int Ed Engl. 2019 Mar 26;58(14):4617-4621. doi: 10.1002/anie.201814612. Epub 2019 Mar 4.

Abstract

The oxygen evolution reaction (OER) is a sluggish electrocatalytic reaction in solid oxide electrolysis cells (SOECs) at high temperatures (600-850 °C). Perovskite oxide has been widely investigated for catalyzing the OER; however, the formation of cation-enriched secondary phases at the oxide/oxide interface blocks the active sites and decreases OER performance. Herein, we show that the Au/yttria-stabilized zirconia (YSZ) interface possesses much higher OER activity than the lanthanum strontium manganite/YSZ anode. Electrochemical characterization and density functional theory calculations suggest that the Au/YSZ interface provides a favorable path for OER by triggering interfacial oxygen spillover from the YSZ to the Au surface. In situ X-ray photoelectron spectroscopy results confirm the existence of spillover oxygen on the Au surface. This study demonstrates that the Au/YSZ interface possesses excellent catalytic activity for OER at high temperatures in SOECs.

摘要

析氧反应(OER)在高温(600 - 850 °C)的固体氧化物电解槽(SOECs)中是一种缓慢的电催化反应。钙钛矿氧化物已被广泛研究用于催化OER;然而,在氧化物/氧化物界面处富阳离子的第二相的形成会阻塞活性位点并降低OER性能。在此,我们表明金/氧化钇稳定的氧化锆(YSZ)界面比镧锶锰氧化物/YSZ阳极具有更高的OER活性。电化学表征和密度泛函理论计算表明,金/YSZ界面通过触发从YSZ到金表面的界面氧溢流为OER提供了一条有利的途径。原位X射线光电子能谱结果证实了金表面存在溢流氧。这项研究表明,金/YSZ界面在SOECs中高温下对OER具有优异的催化活性。

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