Lei Wenjun, Zhao Xinxin, Liang Chao, Wang Huai, Li Xuehong, Jiang Mingkun, Li Xiaofeng, He Fengqin, Sun Yonghui, Lu Gang, Cai Hairui
Qinghai Upstream of the Yellow River Hydropower Development Co., Ltd., Photovoltaic Industry Technology Branch Company, State Power Investment Corporation, Photovoltaic (Energy Storage) Industry Innovation Center, Photovoltaic Technology Research and Development Department, No. 399 South Yanta Road, Xi'an 710000, China.
MOE Key Laboratory for Non-Equilibrium Synthesis and Modulation of Condensed Matter, Key Laboratory of Shaanxi for Advanced Materials and Mesoscopic Physics, State Key Laboratory for Mechanical Behavior of Materials, School of Physics, Xi'an Jiaotong University, No. 28 West Xianning Road, Xi'an 710049, China.
Materials (Basel). 2024 Oct 12;17(20):4991. doi: 10.3390/ma17204991.
Developing an OER electrocatalyst that balances high performance with low cost is crucial for widely adopting PEM water electrolyzers. Ru-based catalysts are gaining attention for their cost-effectiveness and high activity, positioning them as promising alternatives to Ir-based catalysts. However, Ru-based catalysts can be prone to oxidation at high potentials, compromising their durability. In this study, we utilize a simple synthesis method to synthesize a SnO, NbO, and RuO composite catalyst (SnO/NbO@RuO) with multiple interfaces and abundant oxygen vacancies. The large surface area and numerous active sites of the SnO/NbO@RuO catalyst lead to outstanding acidic oxygen evolution reaction (OER) performance, achieving current densities of 10, 50, and 200 mA cm at ultralow overpotentials of 287, 359, and 534 mV, respectively, significantly surpassing commercial IrO. Moreover, incorporating NbO into the SnO/NbO@RuO alters the electronic structure at the interfaces and generates a high density of oxygen vacancies, markedly enhancing durability. Consequently, the membrane electrode composed of SnO/NbO@RuO and commercial Pt/C demonstrated stable operation in the PEM cell for 25 days at an industrial current density of 1 A cm. This research presents a convenient approach for developing a highly efficient and durable Ru-based electrocatalyst, underscoring its potential for proton exchange membrane water electrolysis.
开发一种能在高性能与低成本之间取得平衡的开放获取资源(OER)电催化剂对于质子交换膜(PEM)水电解槽的广泛应用至关重要。钌基催化剂因其成本效益和高活性而受到关注,使其成为铱基催化剂的有前途的替代品。然而,钌基催化剂在高电位下容易氧化,从而影响其耐久性。在本研究中,我们采用一种简单的合成方法来合成具有多个界面和丰富氧空位的SnO、NbO和RuO复合催化剂(SnO/NbO@RuO)。SnO/NbO@RuO催化剂的大表面积和众多活性位点导致其在酸性析氧反应(OER)中表现出色,在287、359和534 mV的超低过电位下分别实现了10、50和200 mA cm的电流密度,显著超过商业IrO。此外,将NbO掺入SnO/NbO@RuO中会改变界面处的电子结构并产生高密度的氧空位,从而显著提高耐久性。因此,由SnO/NbO@RuO和商业Pt/C组成的膜电极在质子交换膜电池中以1 A cm的工业电流密度稳定运行了25天。本研究提出了一种开发高效耐用钌基电催化剂的简便方法,突出了其在质子交换膜水电解中的潜力。