(560c) Development of Materials and Systems for Ammonia-Fueled Solid Oxide Fuel Cells

Hydrogen is the primary fuel source for fuel cells. However, the low volume density and difficulty in storage and transportation are major obstacles for the practical utilization. On-site generation of hydrogen from its carrier is an effective method for the fuel supply. Among various hydrogen carries, ammonia is one of the promising candidates. Ammonia has high hydrogen density. The boiling point of ammonia is relatively high, leading to the ease in liquefaction and transportation. Hydrogen can be produced from ammonia with a mildly endothermic process. The reaction temperature of ammonia cracking is about 600ËšC or higher which is close to the operating temperature of solid oxide fuel cells (SOFCs). The integration of these two devices is beneficial in terms of heat and energy managements and will lead to the development of simplified power generation systems. In this presentation, three types of ammonia-fueled SOFC systems have been investigated.

In the first system, dry ammonia is directly supplied to the anode chamber. Ammonia decomposes into nitrogen and hydrogen over the anode, and subsequently the produced hydrogen is electrochemically oxidized to generate steam and electrons. The second system consists of an ammonia cracker and SOFC. In this case, ammonia is catalytically decomposed in the ammonia cracker, and produced hydrogen is consumed as a fuel of SOFC. The development of the catalyst for ammonia cracking is a key process. Moreover, heat generated from SOFC can be effectively transferred to the endothermic process of ammonia cracker. The third system is composed of autothermal ammonia cracker and SOFC. In the autothermal ammonia cracker, the ammonia oxidation as well as the ammonia cracking proceed simultaneously over the catalysts. The ammonia oxidation enables the quick start-up of the autothermal cracker itself and SOFC due to its exothermic nature. It is important to develop the catalyst and control the reaction conditions. For the ammonia fueled SOFCs, previously, coin type cells have been applied. On the other hand, there have been few studies using commercial-size cells or stacks. A demonstration of the stack-level ammonia-fueled SOFC systems is an important step for the actual utilization of ammonia-fueled SOFCs. In this study, a 200 W class SOFC stack was applied for ammonia fueled SOFC systems.

First, the catalytic activity of Ni/Y₂O₃ and SrO modified Ni/Y₂O₃ for ammonia cracking was evaluated. These catalysts were reduced at 600ºC prior to the evaluation. For the Ni/Y₂O₃ catalyst, the ammonia conversion increased with temperature and achieved about 100% at 650ºC. The SrO modified Ni/Y₂O₃ catalyst showed much higher performance than Ni/Y₂O₃ and achieved about 100% at 600ºC. The addition of SrO was effective for the ammonia cracking over the Ni-based catalysts. Both catalysts could decompose almost the all ammonia below 650ºC, which is lower than the typical operating temperature of SOFCs. This means the ammonia cracking can proceed without an external heating in the integrated system with SOFCs. The durability test for SrO modified Ni/Y₂O₃ catalyst was conducted at 700ºC. The catalytic activity was evaluated at 515 and 565ºC during the test. This is because the ammonia conversion will maintain about 100% at 700ºC. So the degradation of the catalyst cannot be precisely confirmed. This figure shows the time course of ammonia conversion at 515 and 565ºC during the durability test at 700ºC for 1000 hours. This catalyst maintained high activity after 1000 h, even though the catalyst was subjected to many thermal cycles between 515 and 700ºC as well as continuous operation at 700ºC. The high activity of the catalyst for ammonia cracking was maintained at 700ºC over 1000 h.

Next, we evaluated the catalytic activity of Co-Ce-Zr composite oxide for autothermal ammonia cracking. The ammonia conversion increased with an increase in air / fuel ratio (AFR) and achieved about 98% at an AFR of 0.9. However, a large amount of ammonia and produced hydrogen should be consumed by oxygen at high AFR conditions, leading to low electrical efficiency of the ammonia fueled SOFC system. It is necessary to operate the autothermal ammonia cracker at a suitable AFR condition, considering the electrical efficiency as well as the amount of heat generated in the cracker. The autothermal ammonia cracking at about 0.45 corresponds to a thermoneutral reaction. So, more than 0.45 of AFR is required for the self-sustained operation of the cracker without an external heating. In this study, the AFR value for the supply of the autothermally cracked ammonia to the SOFC stack was set to be 0.75 because a sufficient heating value as well as a high ammonia conversion could be expected. The temperature range was within 500 to 600ºC. The temperature increased at the inlet zone of the catalyst which was ascribable to the exothermic reaction of ammonia oxidation. Then, the temperature continuously decreased in the middle and downstream zone, indicating the ammonia oxidation was gradually terminated and the ammonia cracking became dominant. The durability test for the Co–Ce–Zr composite oxide was also conducted. The time course of ammonia conversion was measured at an AFR of 0.75 for 1000 h. The ammonia conversion slightly decreased with operation time, but maintained about 80% after 1000 h of operation. One possible reason for this degradation is the sintering of the catalyst.

The ammonia fueled SOFC stack systems were evaluated. A NiO/ZrO₂-based material, ZrO₂-based material, and perovskite-type oxide material were applied for the anode layer, electrolyte, and cathode layer, respectively. The planar single cell was 120 mm in diameter. Each cell was sandwiched with metallic interconnects and sealed with a glass material. The stack was composed of 10 cells. I–V and I–P characteristics of the ammonia-fueled SOFC stack was evaluated at 770ºC. The ammonia cracker equipped with the Ni/Y₂O₃ catalyst was operated at 600ºC. The autothermal ammonia cracker equipped with the Co-Ce-Zr composite catalyst was operated at an AFR of 0.75. The mixture of hydrogen and nitrogen with a composition of 3 to 1 was also used as a fuel for comparison assuming the complete ammonia decomposition. The open circuit voltages of the direct ammonia and cracked ammonia fueled SOFC stacks were almost the same as that of hydrogen fueled stack. This means, for the direct ammonia fueled stack, the supplied ammonia was almost completely decomposed into hydrogen and nitrogen over the anode. For the cracked ammonia fueled system, the unconverted ammonia exhausted from the cracker would be almost completely decomposed over the anode. In the case of autothermally cracked ammonia, the open circuit voltage of stack was slightly lower than the other fuel supply systems. This is because the autothermally cracked ammonia fuel contains steam. The hydrogen partial pressure at the anode was lower than those of other systems. The cracked ammonia fueled SOFC stack showed comparable performance to the hydrogen fueled stack and achieved about 250 W at 36 A. The stack performance for the direct ammonia fueled stack was also comparable to that for the hydrogen fueled stack at low current region. But, the performance gap between the direct ammonia and the hydrogen fueled systems expanded with an increase in the current. One possible reason for this behavior is the inhibition of the ammonia cracking over the anode by steam produced from electrochemical hydrogen oxidation. The stack performance for the autothermally cracked ammonia fueled stack achieved 234 W at 36 A, which was comparable to that for the direct ammonia fueled one. The electrical efficiency at 36 A for the three types of ammonia fueled SOFC stack was calculated. The cracked ammonia-fueled system showed the highest electrical efficiency. However, the ammonia cracker was heated by an external heater. A hot module should be designed to effectively utilize the Joule heat generated from the cell chamber.

This work was supported by the Council for Science, Technology and Innovation (CSTI) Cross-ministerial Strategic Innovation Promotion Program (SIP) “energy carrier” (Funding agency: JST).