Highly efficient tribocatalytic nitrogen fixation of hydrothermally-synthesized Bi2S3 driven by mechanical friction
Abstract
Nitrogen (N2) fixation for ammonia (NH3) synthesis is a critical way for achieving carbon neutrality and fostering sustainable development. For the synthesis of NH3, the sustainable and environmentally-friendly strategies using renewable and clean energy under ambient condition have attracted researchers’ interest. Friction exists everywhere. As an emerging catalytic technology, tribocatalysis synergistically integrates the triboelectric effect with electrochemical processes. In this work, efficient tribocatalytic N2 fixation directly from air is obtained on the friction interface between bismuth sulfide (Bi2S3) particles with a narrow bandgap of 1.48 eV and a polytetrafluoroethylene rotary disk at a low-frequency stirring speed. In darkness at room temperature, the maximum generation rates of ammonia radicals (NH4+), after 5 h of friction, are respectively 250.45 μmol L−1 g−1 h−1 and 208.53 μmol L−1 g−1 h−1 under with and without the addition of 10 vol% methanol solution. Active radical negative charges are indispensable to the process of tribocatalytic N2 fixation based on the electron paramagnetic resonance experiment. Additionally, the factors that affect the NH4+ generation rate, such as the amount of catalyst, stirring speed, contact area and the pH of reaction solution, are explored to optimize catalytic behavior. After three cycles, the Bi2S3 catalyst can also maintain excellent performance in N2 fixation. Based on the excellent catalytic performance of the narrow bandgap Bi2S3 material, reasonable synergistic mechanisms are proposed, which provide a reference for the understanding of tribocatalytic mechanisms. This work reports that the abundant and non-toxic Bi2S3 catalyst, as a promising candidate, shows great potential for application in tribocatalytic N2 fixation through harnessing ordinary mechanical energy in nature.

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