Solid-oxide fuel cells (SOFCs) are electricity generators that can convert the chemical energy in various fuels directly to the electric power with high efficiency. Recent advances in materials and related key components for SOFCs operating at ≈500 °C are summarized here, with a focus on the materials, structures, and techniques development for low-temperature SOFCs, including the analysis of most of the critical parameters affecting the electrochemical performance of the electrolyte, anode, and cathode. New strategies, such as thin-film deposition, exsolution of nanoparticles from perovskites, microwave plasma heating, and finger-like channeled electrodes, are discussed. These recent developments highlight the need for electrodes with higher activity and electrolytes with greater conductivity to generate a high electrochemical performance at lower temperatures.

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An ideal solid oxide fuel cell (SOFC) cathode should meet multiple requirements, i.e., high activity for oxygen reduction reaction (ORR), good conductivity, favorable stability, and sound thermo‐mechanical/chemical compatibility with electrolyte, while it is very challenging to achieve all these requirements based on a single‐phase material. Herein, a cost‐effective multi‐phase nanocomposite, facilely synthesized through smart self‐assembly at high temperature, is developed as a near‐ideal cathode of intermediate‐temperature SOFCs, showing high ORR activity (an area‐specific resistance of ≈0.028 Ω cm2 and a power output of 1208 mW cm−2 at 650 °C), affordable conductivity (21.5 S cm−1 at 650 °C), favorable stability (560 h operation in single cell), excellent chemical compatibility with Sm0.2Ce0.8O1.9 electrolyte, and reduced thermal expansion coefficient (≈16.8 × 10−6 K−1). Such a nanocomposite (Sr0.9Ce0.1Fe0.8Ni0.2O3–δ) is composed of a single perovskite main phase (77.2 wt%), a Ruddlesden–Popper (RP) second phase (13.3 wt%), and surface‐decorated NiO (5.8 wt%) and CeO2 (3.7 wt%) minor phases. The RP phase promotes the oxygen bulk diffusion while NiO and CeO2 nanoparticles facilitate the oxygen surface process and O2− migration from the surface to the main phase, respectively. The strong interaction between four phases in nanodomain creates a synergistic effect, leading to the superior ORR activity.

A solid oxide fuel cell (SOFC) is a highly efficient device for converting chemical energy to electrical energy. In addition to the efforts to reduce the operating temperature of SOFCs to below 600 °C, research studies of the basic mechanism of CO2 poisoning on cathode materials are envisioned to improve the operation of dual-chamber SOFCs using ambient air. In this work, we comparatively studied the CO2 poisoning effect on two highly active perovskites SrSc(0.175)Nb(0.025)Co(0.8)O(3-δ) (SSNC) and Ba(0.5)Sr(0.5)Co(0.8)Fe(0.2)O(3-δ) (BSCF), using complementary characterization techniques, e.g., powder X-ray diffraction (XRD), Fourier transform-infrared (FT-IR) spectroscopy, atomic force microscopy (AFM), scanning electron microscopy (SEM), CO2-temperature-programmed desorption (CO2-TPD), and electrochemical impedance spectroscopy (EIS). The SSNC cathode shows better tolerance to CO2 as compared with BSCF, which is attributed to the absence of Ba, higher average metal-oxygen bond energy (ABE) of SSNC, and the higher acidity of Nb(5+) cations, whereas the oxygen vacancy concentration plays a less important role.

Electrochemical synthesis of NH3 is a carbon-free alternative to the traditional Haber-Bosch process. The challenge with nitrogen reduction reaction (NRR) to NH3 is cleavage of the inert N≡N triple bond of nitrogen gas. Obtaining NH3 from environmental pollutants, such as nitrates or nitrites, is a more practical route than NRR. However, reduction of nitrates or nitrites to ammonia is currently hampered by modest Faradaic efficiencies, typically below 10 %. Here, we report a novel heterogeneous catalyst based on iron (Fe) single-atoms supported on two-dimensional MoS2 (Fe-MoS2) for the nitrate reduction reaction (NO3RR). We have found that Fe-MoS2 exhibits remarkable performance with a maximum Faradaic efficiency of 98 % for NO3RR to NH3 at an overpotential of -0.48 V vs. the reversible hydrogen electrode (RHE) as confirmed by our isotopic nuclear magnetic resonance (NMR) analyses. Density function theory (DFT) calculations reveal that the enhanced selectivity for the production of NH3 from single Fe atoms supported on MoS2 is attributed to a reduced energy barrier of 0.38 eV associated with de-oxidation of *NO to *N -the usual potential limiting step in NO3RR. We assembled our catalyst in a two-electrode electrolyzer coupled to an InGaP/GaAs/Ge triple-junction solar cell to demonstrate a solar-to-ammonia (STA) conversion efficiency of 3.4 % and a yield rate of 0.03 mmol h -1 cm -2 equivalent to 510 µg h -1 cm -2 . Our results open new avenues for design of single-atom catalysts (SAC) for the realization of solar-driven ammonia production.

Hierarchically porous Fe3O4/C microspheres, with complex microstructures and excellent electrochemical performances as anode materials in LIBs, have been successfully prepared thanks to the self-aggregation of CO2 nano-bubbles confined by PVP and Fe(OH)3 nanoparticles decorated by citrate groups via the molecular chain entanglements during the condensation and carbonization of glucose.

Studies of stable catalysts for non-oxidative dehydrogenation of ethane (NDE) have been challenged by coke deposition from side reactions and thermal sintering of active species. Herein, we report a catalyst mechanism that overcomes both challenges to enable highly stable, active, and selective NDE. The catalyst is made of subnanometric platinum (Pt) species (i.e., single atoms and clusters) habituated on a two-dimensional (2D) multilamellar titanium silicalite-1 (M-TS-1) zeolite nanosheet support (i.e., Pt/M-TS-1). The ultrathin (∼3 nm) M-TS-1 nanosheets provide high external surface areas, high terminal silanol/titanol (−OH) groups, and weak Lewis acid sites. The first two characteristics enhance molecular transport and Pt dispersion in the catalyst support. The third characteristic prohibits side reactions to avoid coking and create strong Pt–support interaction, leading to well-dispersed Pt species against thermal sintering. The M-TS-1 nanosheet-supported Pt catalyst exhibited durable catalytic activity and high ethylene selectivity in the NDE.