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锑锡氧化物负载铱纳米枝晶的析氧反应研究

Study on Oxygen Evolution Reaction of Ir Nanodendrites Supported on Antimony Tin Oxide.

作者信息

Chiang Yu-Chun, Pu Zhi-Hui, Wang Ziyi

机构信息

Department of Mechanical Engineering, Yuan Ze University, Taoyuan 320, Taiwan.

Fuel Cell Center, Yuan Ze University, Taoyuan 320, Taiwan.

出版信息

Nanomaterials (Basel). 2023 Aug 7;13(15):2264. doi: 10.3390/nano13152264.

Abstract

In this study, the iridium nanodendrites (Ir NDs) and antimony tin oxide (ATO)-supported Ir NDs (Ir ND/ATO) were prepared by a surfactant-mediated method to investigate the effect of ATO support and evaluate the electrocatalytic activity for the oxygen evolution reaction (OER). The nano-branched Ir ND structures were successfully prepared alone or supported on ATO. The Ir NDs exhibited major diffraction peaks of the fcc Ir metal, though the Ir NDs consisted of metallic Ir as well as Ir oxides. Among the Ir ND samples, Ir ND2 showed the highest mass-based OER catalytic activity (116 mA/mg at 1.8 V), while it suffered from high degradation in activity after a long-term test. On the other hand, Ir ND2/ATO had OER activity of 798 mA/mg, and this activity remained >99% after 100 cycles of LSV and the charge transfer resistance increased by less than 3 ohm. The enhanced durability of the OER mass activities of Ir ND2/ATO catalysts over Ir NDs and Ir black could be attributed to the small crystallite size of Ir and the increase in the ratio of Ir (III) to Ir (IV), improving the interactions between the Ir NDs and the ATO support.

摘要

在本研究中,通过表面活性剂介导的方法制备了铱纳米枝晶(Ir NDs)和锑锡氧化物(ATO)负载的Ir NDs(Ir ND/ATO),以研究ATO载体的作用并评估其对析氧反应(OER)的电催化活性。成功制备了单独的纳米分支Ir ND结构或负载在ATO上的结构。Ir NDs呈现出面心立方Ir金属的主要衍射峰,尽管Ir NDs由金属Ir以及Ir氧化物组成。在Ir ND样品中,Ir ND2表现出最高的基于质量的OER催化活性(在1.8 V时为116 mA/mg),但在长期测试后其活性降解严重。另一方面,Ir ND2/ATO的OER活性为798 mA/mg,在100次线性扫描伏安法(LSV)循环后该活性保持>99%,且电荷转移电阻增加小于3欧姆。Ir ND2/ATO催化剂的OER质量活性相对于Ir NDs和Ir黑具有更高的耐久性,这可归因于Ir的微晶尺寸小以及Ir(III)与Ir(IV)比例的增加,改善了Ir NDs与ATO载体之间的相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e075/10420946/ad800a96e4db/nanomaterials-13-02264-g001.jpg

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