The integration of catalytic methane decomposition (CMD) with CO2 gasification (Reverse Boudouard Reaction) offers a promising chemical looping route for carbon-negative hydrogen and syngas production. This work systematically investigates the gasification reactivity of six carbon morphologies, CNTs, CNFs, activated carbon, graphite, graphene, and CMD-derived carbon, with and without Ni addition. First, activity tests and characterization (XRD, XPS, Raman) revealed that CMD-derived carbon outperformed all other benchmarks due to its highly amorphous nature (sp3/sp2 = 0.98), which provides a high density of reactive sites. Second, kinetic analysis showed that the incorporation of 5 wt% Ni on CMD carbon reduced the activation energy (Ea) from 435.3 kJ mol−1 to 114.6 kJ/mol, the lowest among all samples. This 74% reduction confirms that structural defects in CMD carbon act as anchoring sites for Ni, facilitating a strong metal–support interaction (MSI) that promotes CO2 activation. Third, an investigation into structural synergy revealed that higher Ni loadings (>5 wt%) increased the activation energy (up to 171.2 kJ mol−1). This trend is attributed to Ni agglomeration and weakened MSI, which reduces the active catalytic interface. These findings demonstrate that the efficiency of CO2 valorization is highly sensitive to carbon morphology, providing a clear optimization strategy for integrated chemical looping methane-to-syngas energy cycles.
Soliman et al. (Tue,) studied this question.