Understanding the Impact of Hydrogen Activation by SrCe0.8Zr0.2O3−δ Perovskite Membrane Material on Direct Non-Oxidative Methane Conversion

Direct non-oxidative methane conversion (DNMC) converts methane (CH4) in one step to olefin and aromatic hydrocarbons and hydrogen (H2) co-product. Membrane reactors comprising methane activation catalysts and H2-permeable membranes can enhance methane conversion by in situ H2 removal via Le Chatelier's principle. Rigorous description of H2 kinetic effects on both membrane and catalyst materials in the membrane reactor, however, has been rarely studied. In this work, we report the impact of hydrogen activation by hydrogen-permeable SrCe0.8Zr0.2O3−δ (SCZO) perovskite oxide material on DNMC over an iron/silica catalyst. The SCZO oxide has mixed ionic and electronic conductivity and is capable of H2 activation into protons and electrons for H2 permeation. In the fixed-bed reactor packed with a mixture of SCZO oxide and iron/silica catalyst, stable and high methane conversion and low coke selectivity in DNMC was achieved by co-feeding of H2 in methane stream. The characterizations show that SCZO activates H2 to favor “soft coke” formation on the catalyst. The SCZO could absorb H2in situ to lower its local concentration to mitigate the reverse reaction of DNMC in the tested conditions. The co-existence of H2 co-feed, SCZO oxide, and DNMC catalyst in the present study mimics the conditions of DNMC in the H2-permeable SCZO membrane reactor. The findings in this work offer the mechanistic understanding of and guidance for the design of H2-permeable membrane reactors for DNMC and other alkane dehydrogenation reactions.

A-site management and oxygen-deficient regulation strategy with perovskite oxide electrocatalyst for oxygen evolution reaction

Perovskite oxides (ABO3) as electrocatalysts applied for oxygen evolution reaction (OER) have been studied for decades due to its high flexibility and adjustability for electronic structures. Herein, a series of...

Application of Electrochemical Deposition in Solid Oxide Fuel Cell Technology

This review paper describes the principle of electrochemical deposition and introduces recent studies applying it to the electrode fabrication of a solid oxide fuel cell (SOFC), a next-generation energy conversion device. Electrochemical deposition can easily control the structure and morphology of the deposition layer according to the applied bias/time/temperature, etc., and the process is very simple and possible even at low temperatures. In addition, deposition of cerium-based oxides, which are the representative ion-conductors or mixed-conductors widely used for SOFCs, is also possible <i>via</i> electrochemical deposition. To elucidate the effectiveness/novelty of electrochemical deposition, we present examples of the application of electrochemical deposition in SOFCs. Moreover, examples of using this method to study the properties of a material and/or to fabricate perovskite oxide-based electrodes are included.

Perovskite-Based Nanocomposite Electrocatalysts: An Alternative to Platinum ORR Catalyst in Microbial Fuel Cell Cathodes

Microbial fuel cells (MFCs) are biochemical systems having the benefit of producing green energy through the microbial degradation of organic contaminants in wastewater. The efficiency of MFCs largely depends on the cathode oxygen reduction reaction (ORR). A preferable ORR catalyst must have good oxygen reduction kinetics, high conductivity and durability, together with cost-effectiveness. Platinum-based electrodes are considered a state-of-the-art ORR catalyst. However, the scarcity and higher cost of Pt are the main challenges for the commercialization of MFCs; therefore, in search of alternative, cost-effective catalysts, those such as doped carbons and transition-metal-based electrocatalysts have been researched for more than a decade. Recently, perovskite-oxide-based nanocomposites have emerged as a potential ORR catalyst due to their versatile elemental composition, molecular mechanism and the scope of nanoengineering for further developments. In this article, we discuss various studies conducted and opportunities associated with perovskite-based catalysts for ORR in MFCs. Special focus is given to a basic understanding of the ORR reaction mechanism through oxygen vacancy, modification of its microstructure by introducing alkaline earth metals, electron transfer pathways and the synergistic effect of perovskite and carbon. At the end, we also propose various challenges and prospects to further improve the ORR activity of perovskite-based catalysts.

Piezoelectric Voltage Constant and Sensitivity Enhancements Through Phase Boundary Structure Control of Lead-free (K,Na)NbO3-based ceramics

The piezoelectric voltage constant (g33) is a material parameter critical to piezoelectric voltage-type sensors for detecting vibrations or strains. Here, we report a lead-free (K,Na)NbO3 (KNN)-based piezoelectric accelerometer with voltage sensitivity enhanced by taking advantage of a high g33. To achieve a high g33, the magnitudes of piezoelectric charge constant d33 and dielectric permittivity er of KNN were best coupled by manipulating the intrinsic polymorphic phase boundaries effectively with the help of Bi-based perovskite oxide additives. For the KNN composition that derives benefit from the combination of er and d33, the value of g33 was found to be 46.9 ´ 10-3 V·m/N, which is significantly higher than those (20 - 30 ´ 10−3 V·m/N) found in well-known polycrystalline lead-based ceramics including commercial Pb(Zr,Ti)O3 (PZT). Finally, the accelerometer sensor prototype built using the modified KNN composition demonstrated higher voltage sensitivity (183 mV/g) when measuring vibrations, showing a 29% increase against the PZT-based sensor (142 mV/g).