Synergistic Enhancement of MgH₂ Hydrolysis via Microalloying and Precursor-Tailored g-C<sub>3</sub>N<sub>4</sub>

作者
Bo-yu Zhang,Jing Bai,Juan Wang,Qiantong Li,Shijie Cao,Zhixue Wang,Xiaowen Wang,Yunhua Xu
标识
DOI:10.20517/scierxiv202511.0692.v1
摘要

MgH2 is recognized as an excellent material for hydrogen production due to its high theoretical hydrogen production capacity, environmental friendliness, safety and ease of transport. However, during the hydrogen production process via hydrolysis, magnesium hydroxide (Mg(OH)2) is continuously generated and deposits on the surface of MgH2,inhibiting the reaction and resulting in the actual amount of H2 generated being significantly lower than the theoretical value. Additionally, the reaction is sensitive to temperature and exhibits slow kinetic. To address these challenges, we employed micro-alloying to introduce Zn elements and incorporated various g-C3N4catalysts to synergistically catalyze and modify MgH2, thereby enhancing its hydrolysis performance. The MU-C3N4/MgH2@5Zn sample demonstrated a hydrogen production capacity of 150.29 ml·0.1 g-1at room temperature (25 °C), which is 5.3 times greater than that of Pure-MgH2@5Zn (28.3 ml·0.1 g-1). Concurrently, the conversion rate reached 92%, and the reaction rate was significantly improved. The enhanced hydrolysisperformance is attributed to the synergistic effects of microalloying and the efficient catalysis of g-C3N4, which not only accelerate the hydrolysis reaction but also effectively inhibit the formation of theMg(OH)2 coating. The g-C3N4 catalyst employed in this study is characterized by its straightforward preparation, low cost, and environmental friendliness, allowing the reaction to proceed under mild conditions (25 °C). Furthermore, the microalloying process is easily achievable. Collectively, these factors underscore the potential for scalable and sustainable hydrogen production via MgH2 hydrolysis in future applications.
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