Bo Yu, Jin-Hang Liu, Shuaibiao Guo, Guanlin Huang, Shengjia Zhang, Shuangqiang Chen, Xiaopeng Li, Yong Wang and Li-Ping Lv
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The formation of a densely populated nanocrystalline RuO<small><sub>2</sub></small>/carbon heterostructure helps expose catalytic sites, accelerates the mass transfer rate, and further enhances the acid resistance of RuO<small><sub>2</sub></small> nanoparticles. The as-synthesized RuO<small><sub>2</sub></small>/PC consequently exhibits superior catalytic performance for the OER with an overpotential of 181 mV upon 10 mA cm<small><sup>−2</sup></small> compared to that of the commercial RuO<small><sub>2</sub></small> (343 mV) and a comparable performance to Pt/C for the HER (47.5 mV upon 10 mA cm<small><sup>−2</sup></small>) in 0.5 M H<small><sub>2</sub></small>SO<small><sub>4</sub></small>. The RuO<small><sub>2</sub></small>/PC shows promising stability with little degradation over ∼24 h. 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引用次数: 1
摘要
开发用于酸性介质中析氧反应(OER)和析氢反应(HER)的高活性双功能电催化剂一直是一个备受关注的课题。然而,现有的催化剂在酸性条件下通常存在催化效率低和耐腐蚀性差的问题。在此,我们报道了一种简单的熔盐方法来制备分级多孔碳负载的二氧化钌纳米颗粒(RuO2/PC),作为在强酸条件下进行全水分解的双功能电催化剂。密集分布的纳米晶体RuO2/碳异质结构的形成有助于暴露催化位点,加速传质速率,并进一步增强RuO2纳米颗粒的耐酸性。因此,与商业RuO2(343 mV)相比,合成的RuO2/PC对OER表现出优异的催化性能,在10 mA cm−2时的过电位为181 mV,在0.5 M H2SO4中对HER表现出与Pt/C相当的性能(在10 mA cm-2时为47.5 mV)。RuO2/PC显示出良好的稳定性,在约24小时内几乎没有降解。令人印象深刻的是,基于RuO2/PC的水电解槽在10 mA cm−2时显示出326 mV的过电位,远低于基于Pt/C和RuO2组合的电解槽(400 mV),这表明其在实际应用中具有巨大潜力。
Densely populated tiny RuO2 crystallites supported by hierarchically porous carbon for full acidic water splitting†
The exploitation of highly active bifunctional electrocatalysts for the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) in acidic media has been a subject receiving immense interest. However, the existing catalysts usually suffer from low catalytic efficiency and poor corrosion resistance under acidic conditions. Herein, we report a facile molten salt method to fabricate ruthenium dioxide nanoparticles supported by hierarchically porous carbon (RuO2/PC) as a bifunctional electrocatalyst for full water splitting under strong acidic conditions. The formation of a densely populated nanocrystalline RuO2/carbon heterostructure helps expose catalytic sites, accelerates the mass transfer rate, and further enhances the acid resistance of RuO2 nanoparticles. The as-synthesized RuO2/PC consequently exhibits superior catalytic performance for the OER with an overpotential of 181 mV upon 10 mA cm−2 compared to that of the commercial RuO2 (343 mV) and a comparable performance to Pt/C for the HER (47.5 mV upon 10 mA cm−2) in 0.5 M H2SO4. The RuO2/PC shows promising stability with little degradation over ∼24 h. Impressively, the water electrolyzer based on RuO2/PC shows an overpotential of 326 mV at 10 mA cm−2, much lower than that of the electrolyzer based on the combination of Pt/C and RuO2 (400 mV), indicating its great potential towards practical application.