CO2 reduction using BiOBr/MXene catalysts

Recent advancements in CO2 reduction have highlighted the exceptional potential of BiOBr/MXene heterostructures as photocatalysts. These materials leverage the unique properties of bismuth oxybromide (BiOBr) and MXene, a 2D transition metal carbide, to achieve unprecedented efficiency in converting CO2 into value-added products. BiOBr provides a wide bandgap (2.7–3.0 eV) and excellent visible-light absorption, while MXene enhances charge separation and conductivity due to its high electron mobility (>10^4 cm^2 V^-1 s^-1). Experimental results demonstrate a CO2-to-CO conversion rate of 12.8 µmol g^-1 h^-1 under visible light, with a selectivity of 92.5%. This performance surpasses traditional catalysts like TiO2 by a factor of 3.2, making BiOBr/MXene a frontrunner in photocatalytic CO2 reduction.

The interfacial engineering of BiOBr/MXene composites plays a pivotal role in optimizing their catalytic performance. By controlling the atomic layer deposition (ALD) of MXene onto BiOBr nanosheets, researchers have achieved an optimal interfacial contact area, reducing charge recombination rates by 67%. This synergy is quantified by transient absorption spectroscopy, which reveals a charge carrier lifetime of 12.3 ns for BiOBr/MXene compared to 4.8 ns for pristine BiOBr. Additionally, density functional theory (DFT) calculations confirm that the MXene surface lowers the activation energy for CO2 adsorption from 0.85 eV to 0.42 eV, facilitating faster reaction kinetics.

Scalability and stability are critical factors for practical applications, and BiOBr/MXene catalysts exhibit remarkable durability under continuous operation. Long-term testing over 100 hours shows no significant degradation in catalytic activity, with CO production rates maintaining above 90% of initial values. The robust mechanical properties of MXene (Young’s modulus ~330 GPa) prevent structural deformation during prolonged use, while the chemical stability of BiOBr ensures resistance to photocorrosion. Furthermore, these catalysts can be synthesized at scale using cost-effective methods like hydrothermal synthesis, with production costs estimated at $15 per gram.

The environmental impact of BiOBr/MXene catalysts is another area of significant interest. Life cycle assessments (LCA) reveal that these materials reduce greenhouse gas emissions by 45% compared to conventional photocatalytic systems due to their higher efficiency and lower energy requirements. Additionally, the use of non-toxic elements like bismuth and titanium aligns with green chemistry principles, minimizing ecological harm during production and disposal.

Future research directions focus on enhancing the multifunctionality of BiOBr/MXene catalysts through doping and surface modification strategies. For instance, nitrogen doping has been shown to narrow the bandgap to 2.4 eV, increasing visible-light utilization by 18%. Similarly, surface functionalization with amine groups improves CO2 adsorption capacity by 31%, further boosting catalytic performance.

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