Yang Haozhou, Guo Na, Xi Shibo, Yin Jiaxi, Song Tao, Xiao Yukun, Duan Lele, Zhang Chun, Wang Lei
Department of Chemical and Biomolecular Engineering, National University of Singapore, 4 Engineering Drive 4, Singapore, Singapore.
Department of Physics, National University of Singapore, Science Drive 4, Singapore, Singapore.
Angew Chem Int Ed Engl. 2025 Aug 4;64(32):e202509079. doi: 10.1002/anie.202509079. Epub 2025 Jun 3.
The production of hydrogen peroxide (HO) via the two-electron oxygen reduction reaction (ORR) has emerged as a promising alternative to the conventional anthraquinone process. However, achieving selective HO production at practically relevant current densities (i.e., ampere-level) remains challenging due to significant selectivity deterioration at high rates. In this study, we develop a composite catalyst by immobilizing vanadyl phthalocyanine (VOPc) on carbon nanotube (CNT) substrates and evaluate its performance under conditions relevant to practical ORR electrolysis. Encouragingly, the VOPc/CNT catalyst composite achieves a high ORR current density of up to 3.5 A cm with over 90% selectivity toward HO in acidic media. Through various in situ characterizations and theoretical calculations, we reveal that the structural integrity of the vanadium catalytic center in VOPc plays a pivotal role in stabilizing *OOH adsorption and impeding O─O cleavage under high cathodic potentials, which is critical for achieving high H₂O₂ selectivity at elevated current densities.
通过双电子氧还原反应(ORR)生产过氧化氢(HO)已成为传统蒽醌法的一种有前景的替代方法。然而,由于在高电流密度下选择性显著下降,在实际相关电流密度(即安培级)下实现选择性HO生产仍然具有挑战性。在本研究中,我们通过将钒酞菁(VOPc)固定在碳纳米管(CNT)基底上开发了一种复合催化剂,并在与实际ORR电解相关的条件下评估其性能。令人鼓舞的是,VOPc/CNT催化剂复合材料在酸性介质中实现了高达3.5 A cm的高ORR电流密度,对HO的选择性超过90%。通过各种原位表征和理论计算,我们揭示了VOPc中钒催化中心的结构完整性在高阴极电位下稳定*OOH吸附和阻碍O─O裂解方面起着关键作用,这对于在升高的电流密度下实现高过氧化氢选择性至关重要。