Strategic Design and Insights into Lanthanum and Strontium Perovskite Oxides for Oxygen Reduction and Oxygen Evolution Reactions.

Perovskite oxides exhibit bifunctional activity for both oxygen reduction (ORR) and oxygen evolution reactions (OER), making them prime candidates for energy conversion in applications like fuel cells and metal-air batteries. Their intrinsic catalytic prowess, combined with low-cost, abundance, and diversity, positions them as compelling alternatives to noble metal and metal oxides catalysts. This review encapsulates the nuances of perovskite oxide structures and synthesis techniques, providing insight into pivotal active sites that underscore their bifunctional behavior. The focus centers on the breakthroughs surrounding lanthanum (La) and strontium (Sr)-based perovskite oxides, specifically their roles in zinc-air batteries (ZABs). An introduction to the mechanisms of ORR and OER is provided. Moreover, the light is shed on strategies and determinants central to optimizing the bifunctional performance of La and Sr-based perovskite oxides.

In situ growth of copper oxide on MXene by combustion method for electrochemical ammonia production from nitrate.

The elimination of the nitrogen pollutant nitrate ions through the electrochemical synthesis of ammonia is an important and environment friendly strategy. Electrochemical nitrate reduction requires highly efficient, selective, and stable catalysts to convert nitrate to ammonia. In this work, a composite of copper oxide and MXene was synthesized using a combustion technique. As reported, nitrate ions are effectively adsorbed by CuxO (CuO & Cu2O) nanoparticles. Herein, MXene is an excellent assembly for anchoring CuxO on its layered surface because it has a strong support structure. Powder X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), and transmission electron microscopy (TEM) analyses show the presence of oxidation states of metal ions and the formation of CuxO nanofoam anchors on the surface of MXene (Ti3C2Tx). The optimized CuxO/Ti3C2Tx composite exhibits an improved nitrate reduction reaction. The electrochemical studies of CuxO/Ti3C2Tx show an interesting nitrate reduction reaction (NO3RR) with a current density of 162 mA cm-2. Further, CuxO/Ti3C2Tx shows an electrocatalytic activity with an ammonia production of 41 982 µg h-1 mcat-1 and its faradaic efficiency is 48% at -0.7 V vs. RHE. Thus, such performance by CuxO/Ti3C2Tx indicates a well-suitable candidate for nitrate ion conversion to ammonia.

In situ self-assembly of molybdenum carbide and iron carbide heterostructures on N-doped carbon for an efficient oxygen reduction reaction.

Identifying highly stable, cost-effective, platinum-free, and efficient electrocatalysts for the oxygen reduction reaction (ORR) remains a formidable challenge. The ORR is important for advancing fuel cell and zinc-air battery (ZAB) technologies towards cost-efficiency and environmental sustainability. This work presents the utilization of economically viable materials through a straightforward synthesis process, exhibiting the development of efficient Mo2C/Fe3C-NC catalysts ingeniously derived from phosphomolybdic acid (PMA) and iron phthalocyanine (FePc). The results demonstrate that the optimized Mo2C/Fe3C-NC3 catalysts exhibit remarkable electrochemical performance, evidenced by an impressive onset potential of ∼1.0 V versus RHE, a half-wave potential of 0.89 V, and a superior current density of about 6.2 mA cm-2. As for their performance in ZABs, the optimized catalysts reach a peak power density of 142 mW cm-2 at a current density of 200 mA cm-2. This synergy, coupled with the uniform distribution of Mo2C and Fe3C nanoparticles, greatly enhances the active catalytic sites and promotes electrolyte diffusion. Our approach diverges from traditional methods by employing an in situ self-assembled heterostructure of Mo2C/Fe3C on nitrogen-doped carbon tubes, avoiding the conventional high-temperature hydrogen gas reduction process. Beyond serving as feasible alternatives to commercially available Pt/C catalysts, these materials hold promise for large-scale production owing to their affordability and the simplicity of the synthesis technique. Such a breakthrough paves the way towards the realization of sustainable energy technologies and lays the groundwork for further exploration into amplifying the scalability and efficiency of ORR catalysts.

Decoration of boron nanoparticles on a graphene sheet for ammonia production from nitrate.

Clean water and sanitation are two of the most important challenges worldwide and the main source for freshwater is groundwater. Nowadays, water is polluted by human activities. Concern about the presence of nitrates (NO3-) in groundwater is increasing day-by-day due to the intensive use of fertilizers and other anthropogenic sources, such as sewage or industrial wastewater discharge. Thus, the main solution available is to remove NO3- from groundwater and transfer it back to a usable nitrogen source. Electrochemical reduction of NO3- to ammonia (NH3) under ambient conditions is a highly desirable method and it needs an efficient electrocatalyst. In this work, we synthesized a composite of amorphous boron with graphene oxide (B@GO) as an efficient catalyst for the nitrate reduction reaction. XRD and TEM analysis revealed an amorphous boron decoration on the graphene oxide sheet, and XPS confirmed that no bonding between boron and carbon occurs. In B@GO, a stronger defect carbon peak was observed than in GO and there was a random distribution of boron particles on the surface of the graphene nanosheets. Amorphous boron exhibits a higher bond energy, more reactivity, and chemical activity toward nitrate ions, which could be due to the lone pair present in the B atoms and could also be due to the edge oxidized B atoms. B@GO has a high number of active sites exposed leading to excellent nitrate reduction performance with a faradaic efficiency of 61.88% and good ammonia formation rate of 40006 µg h-1 mcat-1 at -0.8 V versus reversible hydrogen electrode.