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A NOVEL CATALYST WITH HIGHLY STABLE
                                              AND ATOMICALLY DISPERSED COBALT

                                              AND MANGANESE NITRIDE NANOCLUSTER
                                              ACTIVE SITES FOR HYDROLYTIC RELEASE

                                              OF HYDROGEN FROM AMMONIA BORANE



                                                                                                         Poster
                                              YAN Yujie
                                              BSc (Hons) in Green Engineering and Sustainability
                                              Department of Construction, Environment and Engineering





    OBJECTIVES                                RESEARCH BACKGROUND

    •   Develop a novel catalyst with         Hydrogen (H2) is a promising green energy carrier, but its storage and release
       atomically dispersed cobalt and        pose  significant  challenges.  Ammonia  borane  (AB)  is  a  high-capacity  H2
       manganese nitride nanoclusters for     storage material, but its practical use requires efficient catalysts for controlled
       Ammonia Borane (AB) hydrolysis.        H2 release.  Traditional precious metal catalysts are expensive and scarce,
    •   Enhance the stability and reactivity   which has prompted research into non-precious metal alternatives. This study
       of the catalyst to achieve high H2     aims to develop a stable and efficient catalyst for AB hydrolysis to improve H2
       generation rates.                      generation.
    •   Investigate the synergistic effects
       of cobalt and manganese in the         METHODOLOGY
       catalyst for improved performance.     The study involved synthesizing a novel catalyst, Co/Mn4N-CNT-33-800, with
    •   Evaluate the long-term durability     atomically dispersed cobalt and manganese nitride nanoclusters on carbon
       and recyclability of the catalyst for   nanotubes. Characterization techniques such as X-ray diffraction (XRD),
       practical applications.                Raman spectroscopy, and X-ray photoelectron spectroscopy (XPS) were used
    •   Provide insights for designing        to analyze the catalyst's structure and composition. Catalytic performance
       advanced non-precious metal catalysts   was  assessed  through  hydrolysis  experiments,  measuring  H2  release  rates
       for energy-related applications.       and catalyst stability over multiple cycles. Kinetic studies were conducted to
                                              determine reaction orders and activation energies, providing insights into the
                                              catalytic mechanism.

    ABOUT THE INVESTIGATOR                    FINDINGS


    I am a dedicated and passionate           The synthesized  Co/Mn4N-CNT-33-800 catalyst demonstrated exceptional
    researcher with a keen interest in        stability and reactivity, achieving high H2 generation rates and maintaining over
    green engineering and sustainability.     50% of its initial activity after 50 cycles. The catalyst's atomically dispersed
    My academic journey has been marked       active sites facilitated efficient AB hydrolysis, with a peak H2 generation rate
    by a strong commitment to advancing       of 8372 mLH2·gCoMn ¹·min ¹. The study highlighted the synergistic effects of
                                                                -
                                                                     -
    renewable energy solutions. I aim         cobalt and manganese, enhancing the catalyst's durability and performance.
    to pursue a career in research            These  findings  contribute  to  the  development  of  sustainable  H2 generation
    and development, focusing on              technologies.
    innovative catalysts for clean energy
    applications. My goal is to contribute
    to the global effort in reducing carbon
    emissions and promoting sustainable
    practices.
    FYP Supervisor: Ir Dr Alex TSANG





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