Zhenhua Tao, Hongyu Zhao, Ning Lv, Xu Luo, Jun Yu, Xin Tan, Shichun Mu
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Particularly, its mass activity (0.335 A mg<sub>Ru</sub><sup>−1</sup>) is 1.5 times greater than that of Pt/C (0.224 A mg<sub>Pt</sub><sup>−1</sup>) at an overpotential of 50 mV. Also, it shows good industrial application prospects through tests under high temperature, high alkalinity, and large current conditions. Theoretical calculations unveil that there exists a charge redistribution at c/a-Ru/VO<sub>x</sub> heterointerfaces, which makes the surface of Ru takes on an electron-deficient state, resulting in optimization of adsorption and desorption for different reaction intermediates. This optimized behavior effectively reduces the thermodynamic energy barrier, allowing the catalyst with greatly enhanced HER performance. 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引用次数: 0
摘要
活性持久的氢进化反应催化剂对开发可再生氢能具有重要意义。本文构思了晶相/非晶相-Ru/VOx(c/a-Ru/VOx)异质催化剂,与晶相结构的催化剂相比,非晶相 VOx 暴露出更多的活性位点,增强了电荷传输,加强了金属与支撑物之间的电子相互作用。正如预期的那样,经 500 °C 热处理的 c/a-Ru/VOx-500 在碱性条件下表现出优异的 HER 性能,在 10 mA cm-2 时过电位仅为 33 mV,塔菲尔斜率较小(27 mV dec-1),优于商用铂/碳(Pt/C)催化剂。特别是在过电位为 50 mV 时,其质量活性(0.335 A mgRu-1)是 Pt/C 催化剂(0.224 A mgPt-1)的 1.5 倍。此外,通过高温、高碱度和大电流条件下的测试,它还显示出良好的工业应用前景。理论计算表明,c/a-Ru/VOx 异质界面存在电荷再分布,这使得 Ru 表面处于缺电子状态,从而优化了不同反应中间产物的吸附和解吸。这种优化行为有效降低了热力学能垒,使催化剂的 HER 性能大大提高。这一探索为设计高效、耐用的 HER 催化剂提供了一种可行的策略。
Crystalline/Amorphous-Ru/VOx Phase Engineering Expedites The Alkaline Hydrogen Evolution Kinetics
Active and durable catalysts for hydrogen evolution reaction (HER) are of great significance for developing renewable hydrogen energy. Herein, crystalline/amorphous-Ru/VOx (c/a-Ru/VOx) heterogeneous catalysts are conceived, in which the amorphous VOx exposes more active sites and enhances charge transport compared with the counterpart with a crystal phase structure, strengthening the electronic interaction between metal-support. As expected, c/a-Ru/VOx-500 with heat treatment at 500 °C exhibits excellent HER performance under alkaline conditions, with an overpotential of only 33 mV at 10 mA cm−2 and small Tafel slope (27 mV dec−1), superior to commercial platinum/carbon (Pt/C) catalysts. Particularly, its mass activity (0.335 A mgRu−1) is 1.5 times greater than that of Pt/C (0.224 A mgPt−1) at an overpotential of 50 mV. Also, it shows good industrial application prospects through tests under high temperature, high alkalinity, and large current conditions. Theoretical calculations unveil that there exists a charge redistribution at c/a-Ru/VOx heterointerfaces, which makes the surface of Ru takes on an electron-deficient state, resulting in optimization of adsorption and desorption for different reaction intermediates. This optimized behavior effectively reduces the thermodynamic energy barrier, allowing the catalyst with greatly enhanced HER performance. The exploration provides a promising strategy for designing efficient and durable catalysts for HER.
期刊介绍:
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