具有单金属原子界面的非晶态 Ru 基金属,用于阴离子交换膜电解槽中的电催化氢进化

Yue Shi, Jiawei Fei, Hongdong Li, Caixia Li, Tianrong Zhan, Jianping Lai, Lei Wang
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引用次数: 0

摘要

由于无序的原子排列和丰富的缺陷/边缘,非晶态茂金属是一种前景广阔的催化剂。然而,制备具有原子界面的非晶态茂金属仍然面临挑战,这主要是由于非常规相的热力学障碍和原子界面的精确控制困难。在这里,我们通过引入痕量原子分散镓,合成了一类具有丰富原子界面的新型非晶钌镓金属(A-RuGa metallene)。在碱性氢进化反应中,Ga 配位的 Ru 与 Ru 之间的原子界面实现了单金属协同作用。在 -0.1 V RHE 条件下,A-RuGa 茂金属的翻转频率值达到 67 s。同时,A-RuGa 茂金属在阴离子交换膜电解槽中的质量活度在 2.0 V 时达到 5.2 A mg,首次超过了商用 Pt/C(1.0 A mg)。微量原子分散的 Ga 可以改变单金属 Ru 的局部价态,从而促进水的吸附和解离,优化 H* 的吸附,并在原子水平上加速 H* 的传输。
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Amorphous Ru-based metallene with monometallic atomic interfaces for electrocatalytic hydrogen evolution in anion exchange membrane electrolyzer
Amorphous metallene is a prospective catalyst due to disordered atomic arrangement and abundant defects/edges. However, challenges persist in preparing amorphous metallene with atomic interface, primarily due to thermodynamic impediment of unconventional phase and difficulty in precise controlling of atomic interface. Here, we synthesized a new class of amorphous RuGa metallene (A-RuGa metallene) with abundant atomic interface by introducing trace atomic-dispersed Ga. The atomic interface between Ga-coordinated Ru and Ru achieves monometallic synergism during alkaline hydrogen evolution reaction. The turnover frequency value of A-RuGa metallene reaches 67 s at −0.1 V RHE. Meanwhile, the mass activity of A-RuGa metallene in anion exchange membrane electrolyzer reaches 5.2 A mg at 2.0 V, firstly surpassing commercial Pt/C (1.0 A mg). The trace atomic dispersed Ga could change the local valence state of monometallic Ru, thus promoting water adsorption and dissociation, optimizing H* adsorption and accelerating H* transport at the atomic level.
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