Hai Nguyen Duy, Tran Nhat Duy, Tran Thuy Tien Nguyen, Yu Jianmin, Peng Lishan, Le Thi Anh, Tran Phuong Dung Ngoc, Tran Nhu Hoa Thi, Phan Thang Bach, Tran Ngoc Quang
Center for Innovative Materials and Architectures, Ho Chi Minh City 700000, Viet Nam; Vietnam National University, Ho Chi Minh City 700000, Viet Nam.
Center for Innovative Materials and Architectures, Ho Chi Minh City 700000, Viet Nam; Vietnam National University, Ho Chi Minh City 700000, Viet Nam; Faculty of Materials Science and Technology, University of Science, Ho Chi Minh City 700000, Viet Nam.
J Colloid Interface Sci. 2025 Dec 15;700(Pt 3):138618. doi: 10.1016/j.jcis.2025.138618. Epub 2025 Aug 5.
Metal-organic frameworks have been widely considered a potential alternative for noble metal catalysts for green hydrogen from seawater electrolysis, yet their performance is often limited by low activity and poor stability. Here, we propose a linker engineering strategy to optimize the phase composition of ultrathin Ni-MOF nanosheet arrays, aiming to enhance both activity and stability. We found that partial substitution of terephthalic acid (BDC) with electron-withdrawing tetrafluoroterephthalate (TFBDC) ligand alters the electronic structure and significantly promotes the formation of the catalytically active γ-NiOOH phase in Ni-TFBDC-2. This results in a 90 mV reduction in the overpotential for the oxygen evolution reaction at 50 mA cm, surpassing the performance of a state-of-the-art RuO catalyst, and is accompanied by an increased corrosion potential in seawater. Furthermore, the enrichment of the γ-NiOOH phase in Ni-TFBDC-2 effectively suppresses the passivation during urea oxidation reaction (UOR) in a seawater electrolyte, enabling the achievement of an industrially relevant current density of 0.8 A cm. Operando characterizations reveal that Ni-TFBDC-2 undergoes an electrooxidation process to form Ni species, which subsequently act as the active catalytic sites for the OER. Additionally, the urea-assisted natural seawater electrolyzer assembled with Ni-TFBDC-2 requires a low voltage of 1.76 V at 400 mA cm and demonstrates excellent durability over 170 h of continuous operation. This work offers a novel strategy to enrich the catalytically active phase in MOF-based electrocatalysts, aiming to achieve high activity and long-term stability during urea-assisted natural seawater electrolysis. It is noteworthy that different notable aspects, such as the durability of the materials after prolonged reaction, should be more thoroughly considered for practical applications on larger scales.
金属有机框架已被广泛认为是用于海水电解制绿氢的贵金属催化剂的一种潜在替代品,但其性能往往受到低活性和稳定性差的限制。在此,我们提出一种连接体工程策略来优化超薄镍基金属有机框架纳米片阵列的相组成,旨在提高活性和稳定性。我们发现用吸电子的四氟对苯二甲酸酯(TFBDC)配体部分取代对苯二甲酸(BDC)会改变电子结构,并显著促进Ni-TFBDC-2中催化活性γ-NiOOH相的形成。这使得在50 mA cm时析氧反应的过电位降低了90 mV,超过了最先进的RuO催化剂的性能,并且在海水中的腐蚀电位增加。此外,Ni-TFBDC-2中γ-NiOOH相的富集有效地抑制了海水电解质中尿素氧化反应(UOR)过程中的钝化现象,能够实现0.8 A cm的工业相关电流密度。原位表征表明,Ni-TFBDC-2经历电氧化过程形成镍物种,随后这些镍物种作为析氧反应的活性催化位点。此外,用Ni-TFBDC-2组装的尿素辅助天然海水电解槽在400 mA cm时需要1.76 V的低电压,并在连续运行170 h以上表现出优异的耐久性。这项工作提供了一种在基于金属有机框架的电催化剂中富集催化活性相的新策略,旨在在尿素辅助天然海水电解过程中实现高活性和长期稳定性。值得注意的是,对于更大规模的实际应用,应更全面地考虑不同的显著方面,例如长时间反应后材料的耐久性。