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In Situ Formation of AgCo Stabilized on Graphitic Carbon Nitride and Concomitant Hydrolysis of Ammonia Borane to Hydrogen

机译:石墨化氮化碳稳定的AgCo原位形成和氨硼烷同时水解为氢

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摘要

The development of highly-efficient heterogeneous supported catalysts for catalytic hydrolysis of ammonia borane to yield hydrogen is of significant importance considering the versatile usages of hydrogen. Herein, we reported the in situ synthesis of AgCo bimetallic nanoparticles supported on g-C3N4 and concomitant hydrolysis of ammonia borane for hydrogen evolution at room temperature. The as-synthesized Ag0.1Co0.9/g-C3N4 catalysts displayed the highest turnover frequency (TOF) value of 249.02 mol H2·(molAg·min)−1 for hydrogen evolution from the hydrolysis of ammonia borane, which was higher than many other reported values. Furthermore, the Ag0.1Co0.9/g-C3N4 catalyst could be recycled during five consecutive runs. The study proves that Ag0.1Co0.9/g-C3N4 is a potential catalytic material toward the hydrolysis of ammonia borane for hydrogen production.
机译:考虑到氢的多种用途,开发用于氨硼烷催化水解以产生氢的高效多相负载型催化剂具有重要意义。在这里,我们报道了在g-C3N4上原位合成AgCo双金属纳米颗粒,并伴随着氨硼烷的水解在室温下析氢。合成后的Ag0.1Co0.9 / g-C3N4催化剂显示出最高的周转率(TOF)值为249.02 mol H2·(molAg·min) −1 硼烷,高于许多其他报道的值。此外,Ag0.1Co0.9 / g-C3N4催化剂可在五个连续运行中进行循环利用。研究证明,Ag0.1Co0.9 / g-C3N4是潜在的催化材料,可催化氨硼烷的水解产生氢气。

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