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不同燃料SOFC的理论电池电动势及其性能

         

摘要

以NH3以及3% H2O增湿的H2、CH4、C3H8和煤炭地下气化(underground coal gasification,UCG)气为燃料,用最小Gibbs自由能法计算平衡气体组分和理论电池电动势,并测试在NiO-GDC ‖ GDC ‖Ba0.9Co0.7Fe0.2Nb0.1O3-δ (B0.9CFN)阳极支撑固体氧化物燃料电池(SOFC)中的电池开路电压、电池性能和长期稳定性.结果表明,以上述气体作燃料的SOFC热力学计算理论电动势均高于1.05 V,而由于GDC电解质在还原气氛下存在电子电导,导致碳氢燃料在NiO-GDC‖GDC‖B0.9 CFN阳极支撑电池中的开路电压略小.中低温下,碳氢燃料相对缓慢的动力学过程和GDC电解质快速的氧离子传输速率,使得以UCG气、CH4和C3H8为燃料的电池实际积炭比理论预测少.以UCG气为燃料的SOFC在500、550、600和650℃的最高功率密度分别高达0.151、0.299、0.537和0.729W· cm-2,在0.6V恒压放电120 h后性能没有明显衰减,且阳极表面无积炭产生,表明直接UCG气SOFC具有广阔的应用前景.%The equilibrium species and theoretical electromotive force of cells fed with NH3 and 3% H2O humidified H2,CH4,C3H8 and underground coal gasification (UCG) gas on the basis of minimum Gibbs free energy were calculated,whilst the open circuit voltage (OCV),V-I characteristics and long-term stability of NiO-GDC ‖ GDC ‖ Ba0.9 Co0.7 Fe0.2 Nb0.1O3 δ (B0.9 CFN) anode-supported cells operated in above five fuels were evaluated.The results showed that direct utilization of hydrocarbon fuels in anode could achieve a desirable electromotive force (EMF) no less than 1.05 V,while the OCV for ceria-based cells was comparatively poorer due to the presence of electronic conductivity.Besides,the synergy effect between stagnant kinetics of hydrocarbons reforming and the relatively sufficient O2-supply due to fast migration of oxide ions suppressed carbon deposition at low operating temperatures for ceria-based SOFC.Furthermore,the UCG gas fed cell exhibited peak power densities as high as 0.151,0.2 9 9,0.5 3 7 and 0.729 W · cm-2,respectively at 500,550,600 and 650℃,and showed no evident performance decay and carbon deposition on anode after discharging at 600℃ under a constant voltage of 0.6 V for 120 h,thereby demonstrating UCG gas is a promising fuel for direct utilization in SOFC.

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