催化层介孔碳载体结构对质子交换膜燃料电池多相反应输运影响的LB模拟研究

Lattice Boltzmann Simulation of Mesoporous Carbon Support Structure Effects on Multiphase Transport in PEMFC Catalyst Layers

  • 摘要: 阴极催化层是质子交换膜燃料电池发生氧还原反应的关键场所,优化其碳载体结构对提升质子交换膜燃料电池性能至关重要。基于Shan-Chen伪势格子玻尔兹曼方法建立了耦合氧还原反应和组分传输的两相流模型,研究了质子交换膜燃料电池中具有连通孔与梯度孔的介孔碳载体结构对阴极催化层内的氧还原反应与输运过程的影响。结果表明,相比非连通孔结构,连通孔介孔碳结构提供了充分的氧传输通道和排水路径。对于孔径深度为外6 nm里8 nm的梯度孔介孔碳载体催化层,随着外部孔径深度增加,氧还原反应速率先增大后减小,当外部孔深为3 nm时,氧还原反应速率最大;而孔为外8 nm里6 nm的梯度孔的氧还原反应速率均随着离聚物侵入比例增加而降低。因此,设计具有连通孔、并采用外小内大且外孔深度约3 nm的梯度孔介孔碳载体结构,可优化催化层内氧气传输、液态水排出,有效提升质子交换膜燃料电池性能。

     

    Abstract: The cathode catalytic layer serves as the critical site for oxygen reduction reactions within proton exchange membrane fuel cells, and optimising its carbon carrier structure is paramount for enhancing fuel cell performance. A Shan-Chen pseudopotential lattice Boltzmann method is employed to establish a coupled two-phase flow model that integrates oxygen reduction reaction and mass transport. It investigates the influence of mesoporous carbon carrier structures—featuring interconnected pores and gradient pores—on both the oxygen reduction reaction and transport processes within the cathode catalytic layer of proton exchange membrane fuel cells. Results indicate that, compared to non-interconnected pore structures, interconnected mesoporous carbon structures provide ample oxygen transport pathways and drainage routes. For mesoporous carbon catalyst layers with gradient pores (outer depth 6 nm, inner depth 8 nm), the oxygen reduction reaction rate initially increases, then decreases with increasing outer pore depth, reaching a maximum at an outer depth of 3 nm. In contrast, for mesoporous carbon carriers with gradient pores (outer 8 nm, inner 6 nm), the oxygen reduction reaction rate decreased with increasing polymer intrusion ratio. Therefore, designing mesoporous carbon carriers with interconnected pores and employing a gradient pore structure (outer small, inner large, with an outer pore depth of approximately 3 nm) can optimise oxygen transport and liquid water drainage within the catalytic layer, effectively enhancing the performance of proton exchange membrane fuel cells.

     

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