Pan Dingjie, Liu Qiming, Yu Bingzhe, DuBois Davida Briana, Tressel John, Yu Sarah, Kaleekal Noah, Trabanino Sophia, Jeon Yillin, Bridges Frank, Chen Shaowei
Department of Chemistry of Biochemistry, University of California, 1156 High Street, Santa Cruz, CA, 95064, USA.
Department of Physics, University of California, 1156 High Street, Santa Cruz, CA, 95064, USA.
Small. 2024 Nov;20(46):e2404729. doi: 10.1002/smll.202404729. Epub 2024 Aug 8.
Development of high-performance, low-cost catalysts for electrochemical water splitting is key to sustainable hydrogen production. Herein, ultrafast synthesis of carbon-supported ruthenium-copper (RuCu/C) nanocomposites is reported by magnetic induction heating, where the rapid Joule's heating of RuCl and CuCl at 200 A for 10 s produces Ru-Cl residues-decorated Ru nanocrystals dispersed on a CuCl scaffold, featuring effective Ru to Cu charge transfer. Among the series, the RuCu/C-3 sample exhibits the best activity in 1 m KOH toward both the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER), with an overpotential of only -23 and +270 mV to reach 10 mA cm, respectively. When RuCu/C-3 is used as bifunctional catalysts for electrochemical water splitting, a low cell voltage of 1.53 V is needed to produce 10 mA cm, markedly better than that with a mixture of commercial Pt/C+RuO (1.59 V). In situ X-ray absorption spectroscopy measurements show that the bifunctional activity is due to reduction of the Ru-Cl residues at low electrode potentials that enriches metallic Ru and oxidation at high electrode potentials that facilitates the formation of amorphous RuO. These findings highlight the unique potential of MIH in the ultrafast synthesis of high-performance catalysts for electrochemical water splitting.
开发用于电化学水分解的高性能、低成本催化剂是可持续制氢的关键。在此,通过磁感应加热报道了碳负载钌 - 铜(RuCu/C)纳米复合材料的超快合成,其中RuCl和CuCl在200 A下快速焦耳加热10 s产生分散在CuCl支架上的Ru - Cl残留物修饰的Ru纳米晶体,具有有效的Ru到Cu的电荷转移。在该系列中,RuCu/C - 3样品在1 m KOH中对析氢反应(HER)和析氧反应(OER)均表现出最佳活性,分别仅需 - 23和 + 270 mV的过电位即可达到10 mA cm。当RuCu/C - 3用作电化学水分解的双功能催化剂时,产生10 mA cm需要1.53 V的低电池电压,明显优于商业Pt/C + RuO混合物(1.59 V)。原位X射线吸收光谱测量表明,双功能活性归因于在低电极电位下Ru - Cl残留物的还原,这使金属Ru富集,以及在高电极电位下的氧化,这促进了非晶RuO的形成。这些发现突出了磁感应加热在超快合成用于电化学水分解的高性能催化剂方面的独特潜力。