Diglio Matteo, Contento Irene, Impemba Salvatore, Berretti Enrico, Della Sala Paolo, Oliva Giuseppina, Naddeo Vincenzo, Caporali Stefano, Primo Ana, Talotta Carmen, Gaeta Carmine, Capacchione Carmine, Grassi Alfonso, Buonerba Antonio
Department of Chemistry and Biology "Adolfo Zambelli", University of Salerno, Via Giovanni Paolo II, 132, 84084 Fisciano (SA), Italy.
Interuniversity Consortium of Chemical Reactivity and Catalysis (CIRCC), Via Celso Ulpiani, 27, 70126 Bari, Italy.
Energy Fuels. 2025 Jul 10;39(29):14320-14329. doi: 10.1021/acs.energyfuels.5c01537. eCollection 2025 Jul 24.
Formic acid (FA) is considered one of the most promising carriers of clean and safe dihydrogen. This study highlights the potential of using poly-(2,6-dimethyl-1,4-phenylene oxide) (PPO) as a support for AuNPs to produce H through formic acid dehydrogenation (FAD). The developed synthesis method allows for precise control over the gold content by completely encapsulating AuNPs (4-6 nm) within the PPO matrix, ensuring a uniform distribution of nanoparticles with an active cubic morphology. In an aqueous solution (or a water/DMAc mixture), the catalyst exhibited high activity, generating H without producing CO, underscoring its high selectivity for dehydrogenation. At 105 °C, the catalyst showed a TOF of 360 mol·mol ·h and an activation energy of 39.3 ± 2.6 kJ·mol. By optimizing the formic acid concentration and gold loading, the system achieved an impressive TOF of 600 mol·mol ·h, comparable to the best values reported in the literature. Notably, the AuNPs-PPO system facilitates the FAD reaction without requiring additional bases or modified supports. The reaction order of 0.81 ± 0.04 with respect to FA concentration indicates the rapid diffusion of the reagent within the polymer matrix without limiting its reactivity. Lastly, the AuNPs-PPO catalytic system has been demonstrated to be reusable.
甲酸(FA)被认为是最有前途的清洁安全的二氢载体之一。本研究强调了使用聚(2,6 - 二甲基 - 1,4 - 亚苯基氧化物)(PPO)作为金纳米颗粒(AuNPs)的载体以通过甲酸脱氢(FAD)产生氢气的潜力。所开发的合成方法通过将AuNPs(4 - 6纳米)完全封装在PPO基质中,实现了对金含量的精确控制,确保具有活性立方形态的纳米颗粒均匀分布。在水溶液(或水/二甲基乙酰胺混合物)中,该催化剂表现出高活性,产生氢气而不产生一氧化碳,突出了其对脱氢的高选择性。在105℃下,该催化剂的转化频率(TOF)为360 mol·mol⁻¹·h,活化能为39.3±2.6 kJ·mol⁻¹。通过优化甲酸浓度和金负载量,该体系实现了高达600 mol·mol⁻¹·h的令人印象深刻的TOF,与文献报道的最佳值相当。值得注意的是,AuNPs - PPO体系促进FAD反应,无需额外的碱或改性载体。相对于FA浓度的反应级数为0.81±0.04,表明试剂在聚合物基质中快速扩散,而不会限制其反应活性。最后,已证明AuNPs - PPO催化体系可重复使用。