Solid oxide fuel cells (SOFCs) have the promise to improve energy efficiency and to provide society with a clean energy producing technology. The high temperature of operation (500−1000 °C) enables the solid oxide fuel cell to operate with existing fossil fuels and to be efficiently coupled with turbines to give very high efficiency conversion of fuels to electricity. Solid oxide fuel cells are complex electrochemical devices that contain three basic components, a porous anode, an electrolyte membrane, and a porous cathode. In this short review, a survey of the types and properties of materials that have been considered for each of these components is presented with an emphasis on the requirements for operation at intermediate temperature (500−800 °C). Some directions for future research are discussed.

Materials for Solid Oxide Fuel Cells

Progress in material selection for solid oxide fuel cell technology: A review

An insight into the analogies, state-of-the-art technologies, concepts, and prospects under the umbrella of perovskite materials (both inorganic-organic hybrid halide perovskites and ferroelectric perovskites) for future multifunctional energy conversion and storage devices is provided. Often, these are considered entirely different branches of research; however, considering them simultaneously and holistically can provide several new opportunities. Recent advancements have highlighted the potential of hybrid perovskites for high-efficiency solar cells. The intrinsic polar properties of these materials, including the potential for ferroelectricity, provide additional possibilities for simultaneously exploiting several energy conversion mechanisms such as the piezoelectric, pyroelectric, and thermoelectric effect and electrical energy storage. The presence of these phenomena can support the performance of perovskite solar cells. The energy conversion using these effects (piezo-, pyro-, and thermoelectric effect) can also be enhanced by a change in the light intensity. Thus, there lies a range of possibilities for tuning the structural, electronic, optical, and magnetic properties of perovskites to simultaneously harvest energy using more than one mechanism to realize an improved efficiency. This requires a basic understanding of concepts, mechanisms, corresponding material properties, and the underlying physics involved with these effects.

Mutual Insight on Ferroelectrics and Hybrid Halide Perovskites: A Platform for Future Multifunctional Energy Conversion.

Solid oxide fuel cells (SOFCs) have the potential to be one of the cleanest and most efficient energy technologies for direct conversion of chemical fuels to electricity. Economically competitive SOFC systems appear poised for commercialization, but widespread market penetration will require continuous innovation of materials and fabrication processes to enhance system lifetime and reduce cost. One early technical opportunity is minimization of resistance to the oxygen reduction reaction (ORR) at the cathode, which contributes the most to performance degradation and efficiency loss in the existing SOFCs, especially at temperatures <700 °C. Detailed study over the past 15 years has revealed the positive impact of catalyst infiltration on SOFC cathode performance, both in power density and durability metrics. However, realizable performance improvements rely upon strongly-coupled relationships in materials and morphology between the infiltrate and the backbone, and therefore efficacious systems cannot be simply generated with a set of simple heuristics. This article reviews recent progress in enhancing SOFC cathode performance by surface modification through a solution-based infiltration process, focusing on two backbone architectures – inherently functional and skeletal – infiltrated using wet-chemistry processes. An efficient cathode consists of a porous mixed-conducting backbone and an active coating catalyst; the porous backbone provides excellent ionic and electronic conductivity, while the infiltrated surface coating possesses high catalytic activity and stability. As available, performance comparisons are emphasized and reaction schematics for specific infiltrate/backbone systems are summarized. While significant progress has been achieved in enhancing surface catalytic activity and durability, the detailed mechanisms of performance enhancement are insufficiently understood to obtain critical insights and a scientific basis for rational design of more efficient catalysts and novel electrode architectures. Recent progress in characterization of surfaces and interfaces is briefly discussed with challenges and perspectives in surface modification of SOFC electrodes. Surface modification through infiltration is expected to play an increasingly important role in current and next-generation commercial SOFC development, and this review illustrates the sophisticated technical considerations required to inform judicious selection of an infiltrate for a given SOFC system.

Enhancing SOFC cathode performance by surface modification through infiltration

Lead halide perovskites have attracted considerable interest as photoabsorbers in PV-applications over the last few years. The most studied perovskite material achieving high photovoltaic performance has been methyl ammonium lead iodide, CH3NH3PbI3. Recently the highest solar cell efficiencies have, however, been achieved with mixed perovskites where iodide and methyl ammonium partially have been replaced by bromide and formamidinium. In this work, the mixed perovskites were explored in a systematic way by manufacturing devices where both iodide and methyl ammonium were gradually replaced by bromide and formamidinium. The absorption and the emission behavior as well as the crystallographic properties were explored for the perovskites in this compositional space. The band gaps as well as the crystallographic structures were extracted. Small changes in the composition of the perovskite were found to have a large impact on the properties of the materials and the device performance. In the investigated compositional space, cell efficiencies, for example, vary from a few percent up to 20.7%. From the perspective of applications, exchanging iodide with bromide is especially interesting as it allows tuning of the band gap from 1.5 to 2.3 eV. This is highly beneficial for tandem applications, and an empirical expression for the band gap as a function of composition was determined. Exchanging a small amount of iodide with bromide is found to be highly beneficial, whereas a larger amount of bromide in the perovskite was found to cause intense sub band gap photoemission with detrimental results for the device performance. This could be caused by the formation of a small amount of an iodide rich phase with a lower band gap, even though such a phase was not observed in diffraction experiments. This shows that stabilizing the mixed perovskites will be an important task in order to get the bromide rich perovskites, which has a higher band gap, to reach the same high performance obtained with the best compositions.

Exploration of the compositional space for mixed lead halogen perovskites for high efficiency solar cells

Electrical properties of GdBaCo2O5+x for ITSOFC applications

Highly enhanced low temperature discharge capacity of LiNi1/3Co1/3Mn1/3O2 with lithium boron oxide glass modification

We reported a facile single-solution fabrication method to grow large-scale CH3NH3PbBr3 hybrid perovskite single crystal at room temperature. The obtained single crystal in this experiment was 14 × 14 mm. The sample's in situ photophysics properties under dark and illumination, including the surface morphology, work function, surface current distribution, microcosmic I-V curves, as well as the polarization behavior, were in situ characterized by integrated utilization of a scanning probe microscopy, respectively. Piezoresponse force microscopy (PFM) phase angles indicated the existence of "polarization" in CH3NH3PbBr3 lattice. Interestingly, the "polarization effect" was enhanced by the plus light source. Moreover, a surface potential shift as large as 200 mV was observed under the condition of the illumination on and off. This research is proposed to provide an opportunity to take a fresh look at the architectural design and photovoltaic performance origin of the hybrid perovskite solar cells.

Large-Size CH3NH3PbBr3 Single Crystal: Growth and In Situ Characterization of the Photophysics Properties

synthesis of bifeo3 nanoparticles by a low-heating temperature solid-state precursor method

We investigated the structural, elastic, and electronic properties of the cubic perovskite-type BaHfO3 using a first-principles method based on the plane-wave basis set. Analysis of the band structure shows that perovskite-type BaHfO3 is a wide gap indirect semiconductor. The band-gap is predicted to be 3.94 eV within the screened exchange local density approximation (sX-LDA). The calculated equilibrium lattice constant of this compound is in good agreement with the available experimental and theoretical data reported in the literatures. The independent elastic constants (C-11, C-12, and C-44), bulk modules B and its pressure derivatives B', compressibility beta, shear modulus G, Young's modulus Y, Poisson's ratio nu, and Lame constants (mu, lambda) are obtained and analyzed in comparison with the available theoretical and experimental data for both the singlecrystalline and polycrystalline BaHfO3. The bonding-charge density calculation make it clear that the covalent bonds exist between the Hf and 0 atoms and the ionic bonds exist between the Ba atoms and HfO3 ionic groups in BaHfO3. (C) 2009 Elsevier B.V. All rights reserved.

Aimin Chang

Papers

Electrical properties of GdBaCo2O5+x for ITSOFC applications

Highly enhanced low temperature discharge capacity of LiNi1/3Co1/3Mn1/3O2 with lithium boron oxide glass modification

Large-Size CH3NH3PbBr3 Single Crystal: Growth and In Situ Characterization of the Photophysics Properties

synthesis of bifeo3 nanoparticles by a low-heating temperature solid-state precursor method

Structural, elastic, and electronic properties of cubic perovskite BaHfO3 obtained from first principles