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用于长时析氧催化的结构扭曲的钌铱基纳米框架

Structurally-Distorted RuIr-Based Nanoframes for Long-Duration Oxygen Evolution Catalysis.

作者信息

Liu Shangheng, Tan Huang, Huang Yu-Cheng, Zhang Qiaobao, Lin Haiping, Li Ling, Hu Zhiwei, Huang Wei-Hsiang, Pao Chih-Wen, Lee Jyh-Fu, Kong Qingyu, Shao Qi, Xu Yong, Huang Xiaoqing

机构信息

State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, 361005, China.

Guangzhou Key Laboratory of Low-Dimensional Materials and Energy Storage Devices, Collaborative Innovation Center of Advanced Energy Materials, School of Materials and Energy, Guangdong University of Technology, Guangzhou, 510006, China.

出版信息

Adv Mater. 2023 Oct;35(42):e2305659. doi: 10.1002/adma.202305659. Epub 2023 Sep 20.

Abstract

Oxygen evolution reaction (OER) plays a key role in proton exchange membrane water electrolysis (PEMWE), yet the electrocatalysts still suffer from the disadvantages of low activity and poor stability in acidic conditions. Here, a new class of CdRu IrO nanoframes with distorted structure for acidic OER is successfully fabricated. Impressively, CdRu IrO displays an ultralow overpotential of 189 mV and an ultralong stability of 1500 h at 10 mA cm⁻ toward OER in 0.5 M H SO . Moreover, a PEMWE using the distorted CdRu IrO can be steadily operated at 0.1 A cm⁻ for 90 h. Microstructural analyses and X-ray absorption spectroscopy (XAS) demonstrate that the synergy between Ru and Ir in CdRu IrO induces the distortion of Ru-O, Ir-O, and Ru-M (M = Ru, Ir) bonds. In situ XAS indicates that the applied potential leads to the deformation octahedral structure of RuO /IrO and the formation of stable Ru species for OER. Theoretical calculations also reveal that the distorted structures can reduce the energy barrier of rate-limiting step during OER. This work provides an efficient strategy for constructing structural distortion to achieve significant enhancement on the activity and stability of OER catalysts.

摘要

析氧反应(OER)在质子交换膜水电解(PEMWE)中起着关键作用,但电催化剂在酸性条件下仍存在活性低和稳定性差的缺点。在此,成功制备了一类新型的具有扭曲结构的用于酸性OER的CdRu IrO纳米框架。令人印象深刻的是,CdRu IrO在0.5 M H₂SO₄中对OER在10 mA cm⁻²时显示出189 mV的超低过电位和1500 h的超长稳定性。此外,使用扭曲的CdRu IrO的PEMWE可以在0.1 A cm⁻²稳定运行90 h。微观结构分析和X射线吸收光谱(XAS)表明,CdRu IrO中Ru和Ir之间的协同作用导致Ru-O、Ir-O和Ru-M(M = Ru、Ir)键的扭曲。原位XAS表明,施加的电位导致RuO₂/IrO₂的八面体结构变形并形成用于OER的稳定Ru物种。理论计算还表明,扭曲结构可以降低OER过程中速率限制步骤的能量势垒。这项工作为构建结构扭曲以显著提高OER催化剂的活性和稳定性提供了一种有效策略。

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