The synergistic interaction between oxygen vacancies in Ni single atoms/TiO2 support and adjacent NiO nanoparticles boosts the CO2 methanation process.
Abstract
Integrating multiple active sites withi...
Von Wiley-VCH zur Verfügung gestellt
Efficient CO2/(bi)carbonate hydrogenation to formate is achieved over Ni9Pd1 catalyst with low Pd content, even at ambient conditions, with appreciable stability over several catalytic cycles, attributed to the NiPd synergistic interactions. Further, integrating the direct air capture (DAC) with CO2/(bi)carbonate hydrogenation makes it a more sustainable CCU process.
The urgent need for sustainable CO2 management has driven the development of efficient catalytic systems capable of converting CO2 into value-added chemicals under mild conditions. Herein, we report a Ni9Pd1 catalyst with a low Pd content (Ni/Pd = 9:1) for the selective CO2 hydrogenation to formate at low temperatures. Remarkably, this catalyst exhibits exceptional versatility, efficiently hydrogenating both aqueous (bi)carbonate and CO2 captured from air (as carbonate) to formate. Moreover, this catalyst shows appreciable robustness by achieving cumulative formate yields of 770.5 mmol gPd −1 (TON of 82, STY of 32.18 mmolformate gPd −1 h−1 at 28 °C) and 1371.9 mmol gPd −1 (TON of 146, STY of 57.16 mmolformate gPd −1 h−1 at 80 °C) over multiple cycles. The synergistic Ni-to-Pd interaction in this catalyst leads to the efficient CO2 activation and H2 dissociation, enabling operation under mild conditions. This study demonstrates an integrated and sustainable approach where CO2 captured from air can be hydrogenated to formate at low temperature.
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