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Hydrogen is a promising fossil-fuel alternative fuel owing to its environmentally neutral emissions and high energy density. However, the need for purified water and external power are critical hindrances to implementation of hydrogen production. The present work reveals the potential to overcome these shortcomings through piezo-photocatalysis of seawater using BaTiO3-x (BTO) nanoparticles. This material was made piezoelectrically active by annealing under different atmospheres, including O2, N2, Ar, and H2, the latter of which caused Ti4+ to Ti(4-x)+ multiple reductions and structural expansions that stabilized piezoelectric tetragonal BTO domains. The resultant defect equilibria combine ionic and electron effects, including Ti redox reactions, charge-compensating surface oxygen vacancy formation, and color centre alterations. Further, variety of experimental techniques revealed the effects of reduction on the energy band structure. A strong piezoelectric effect and the presence of self-polarization were confirmed by piezoresponse force microscopy, while simulation work clarified the role of vibration on band bending deriving from the former. The performance data contrasted H2 evolution using deionized (DI) water, simulated seawater, and natural seawater subjected to photocatalysis, piezocatalysis, and piezo-photocatalysis. An efficient H2 evolution rate of 132.4 micromol/g/h was achieved from DI water using piezo-photocatalysis for 5 h. In contrast, piezocatalysis for 2 h followed by piezo-photocatalysis for 3 h resulted in H2 evolution rates of 100.7 micromol/g/h for DI water, 63.4 micromol/g/h for simulated seawater, and 48.7 micromol/g/h for natural seawater. This work provides potential new strategies for large-scale green H2 production using abundant natural resources with conventional piezoelectric material while leveraging the effects of ions dissolved in seawater., 34 pages, 9 figures

Nano-sized perovskites were synthesized in a spray flame from nitrate precursors dissolved in ethanol and in ethanol/2-ethylhexanoic acid (2-EHA) mixtures. Experiments with ethanol led to a broad particle-size distribution and to the formation of undesired phases such as La₂CoO₄, La₂O₃, and Co₃O₄. The addition of 2-EHA can initiate micro explosions of the burning droplets and has been systematically investigated toward the formation of single-phase, high-surface-area LaCoO₃ and LaFeO₃ with a narrow size distribution. To investigate the effect of 2-EHA, temperature-dependent changes of the chemical composition of the precursor solutions were analyzed with ATR-FTIR between 23 and 70°C. In all cases, the formation of esters was identified while in the solutions containing iron, additional formation of carboxylates was observed. The synthesized materials were characterized by BET SSA, XRD, SAED and EDX-TEM and their catalytic activity was analyzed, reaching 50% CO conversion at temperatures below 160 and 300°C for LaCoO₃ and LaFeO₃, respectively.

γ-Fe2O3 catalyst showed higher catalytic activity than α-Fe2O3 in 150–300 °C. Both NH3 and NO x species adsorbed and reacted easily on γ-Fe2O3. However, NH3 adsorbed on α-Fe2O3 and then reacted with gaseous NO x . Gaseous NO x was more easily adsorbed on α-Fe2O3 than gaseous NH3, consequently, stable nitrates formed and blocked the active sites, which affected the SCR reaction badly.