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Characterization, kinetics and redox properties of lanthanum chromium nickel oxide perovskites: Implications for combustion and solid oxide fuel cells.

机译:镧铬镍氧化物钙钛矿的表征,动力学和氧化还原特性:对燃烧和固体氧化物燃料电池的影响。

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LaCr1−xNixO3 perovskite oxides (x = 0, 0.25, 0.50, 0.75, 1.00) were investigated as possible materials for combustion of exhaust gases and as a potential solid oxide fuel cell (Sore) anode. This involved the determination of surface cation composition, kinetics of methane oxidation, catalyst stability under reducing conditions (P(O 2) 1.10−6 atm), and redox properties.; XPS investigation to obtain surface cation compositions showed that surface and bulk compositions are indistinguishable. The methane oxidation rate depended on catalyst composition, and the highest activity was measured with LaNiO 3. Ni-O-Ni ensembles in the nickel-containing materials are good candidates for the reactive species since a local defect can be formed without cation migration. A random population of B sites by Ni ions would produce a surface density of Ni-O-Ni ensembles proportional to x2 (x in LaCr 1−xNixO3), in agreement with the dependence found in this study. During transient methane reduction (0.21 kPa ≤ P(CH 4) ≤ 1.4 kPa and no gas phase oxygen), initial catalyst activities were comparable to rates in the presence of gas phase oxygen, indicating the same initial reaction pathways. The materials with high Cr (x ≥ 0.5) content are capable of preserving the perovskite lattice even after complete reduction of Ni3+ Ni2+ in methane or hydrogen and subsequent reoxidation in the oxygen/argon mixture. Oxygen mobility studies showed that at least three distinct oxygen pools exist in these catalysts at lower temperatures (50°–300°C): adsorbed CO2; easily accessed sites associated with Ni; less accessible sites that become involved at higher temperatures (≥300°C). LaCr1−xNixO3 materials have a better oxygen ion mobility than La(Sr)MnO3−δ perovskites and are comparable to (LaCa)(CoFe)O3−δ materials. LaCr0.75Ni0.25O3 oxygen ion diffusion coefficient at 300°C is 4.1010 cm 2/s. In summary: LaCr0.5Ni0.5O3 is a potential combustion catalyst due to its high hydrocarbon oxidation rate, good performance during upset conditions (oxygen lean atmosphere), and material stability to reduction/reoxidation cycles. LACr1−xNi xO3 materials are possible anodes for solid oxide fuel cells, because they provide a substantial increase in the number of active surface sites over standard anode materials.
机译:研究了LaCr 1-x Ni x O 3 钙钛矿氧化物(x = 0、0.25、0.50、0.75、1.00)作为可能的材料燃烧废气并作为潜在的固体氧化物燃料电池(Sore)阳极。这涉及测定表面阳离子组成,甲烷氧化动力学,还原条件(P(O 2 )<1 10 −6 atm)和氧化还原特性。为获得表面阳离子成分而进行的XPS研究表明,表面成分与本体成分是无法区分的。甲烷的氧化速率取决于催化剂的组成,并以LaNiO 3 测得最高的活性。含镍材料中的Ni-O-Ni集成体是反应性物种的良好候选者,因为可以形成局部缺陷而无需阳离子迁移。 Ni离子随机分布的B位置会产生与x 2 (x在LaCr 1-x Ni 中的x成正比)的Ni-O-Ni集成体的表面密度x O 3 ),与本研究中发现的依赖性一致。在短暂的甲烷还原过程中(0.21 kPa≤P(CH 4 )≤1.4 kPa且无气相氧),初始催化剂活性与存在气相氧的速率相当,表明相同的初始反应途径。 Cr(x≥0.5)含量高的材料即使完全还原Ni 3 + Ni <也能保留钙钛矿晶格。甲烷或氢气中的super> 2 + ,然后在氧气/氩气混合物中再氧化。氧迁移率研究表明,这些催化剂在较低的温度(50°-300°C)下至少存在三个不同的氧气池:吸附的CO 2 ;吸附的CO 2 。与Ni相关的易于访问的站点;进入较高温度(≥300°C)的交通不便的地点。 LaCr 1-x Ni x O 3 材料的氧离子迁移率比La(Sr)MnO 3-δ钙钛矿,可与(LaCa)(CoFe)O 3-δ材料媲美。 LaCr 0.75 Ni 0.25 O 3 在300°C时的氧离子扩散系数为4 10 10 cm 2 / s。综上所述:LaCr 0.5 Ni 0.5 O 3 是潜在的燃烧催化剂,因为它具有较高的烃类氧化速率,在不正常条件下(氧气)性能良好。稀气氛),以及对还原/再氧化循环的材料稳定性。 LACr 1-x Ni x O 3 材料可能是固体氧化物燃料电池的阳极,因为它们大大增加了活性物质的数量标准阳极材料上的表面位置。

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