Hetero-Element-Doped Molybdenum Oxide Materials for Energy Storage Systems

In order to meet the growing demand for the electronics market, many new materials have been studied to replace traditional electrode materials for energy storage systems. Molybdenum oxide materials are electrode materials with higher theoretical capacity than graphene, which was originally used as anode electrodes for lithium-ion batteries. In subsequent studies, they have a wider application in the field of energy storage, such as being used as cathodes or anodes for other ion batteries (sodium-ion batteries, potassium-ion batteries, etc.), and electrode materials for supercapacitors. However, molybdenum oxide materials have serious volume expansion concerns and irreversible capacity dropping during the cycles. To solve these problems, doping with different elements has become a suitable option, being an effective method that can change the crystal structure of the materials and improve the performances. Therefore, there are many research studies on metal element doping or non-metal doping molybdenum oxides. This paper summarizes the recent research on the application of hetero-element-doped molybdenum oxides in the field of energy storage, and it also provides some brief analysis and insights.

The Mechanism of Joint Reduction of MoO3 and CuO by Combined Mg/C Reducer at High Heating Rates

Understanding of the decisive role of non-isothermal treatment on the interaction mechanism and kinetics of the MoO3-CuO-Mg-C system is highly relevant for the elaboration of optimal conditions at obtaining Mo-Cu composite powder in the combustion processes. The reduction pathway of copper and molybdenum oxides with combined Mg + C reducing agents at high heating rates from 100 to 5200 K min−1 was delivered. In particular the sequence of the reactions in all the studied binary, ternary and quaternary systems contemporaneously demonstrating the effect of the heating rate on products’ phase composition and microstructure was elucidated. The combination of two highly exothermic and speedy reactions (MoO3 + 3Mg and CuO + Mg vs. MoO3 + CuO + 4Mg) led to a slow interaction with weak self-heating (dysynergistic effect) due to a change in the reaction mechanism. Furthermore, it has been shown that upon the simultaneous utilization of the Mg and C reducing agents, the process initiates exclusively with carbothermic reduction, and at relatively high temperatures it continues with magnesiothermic reaction. The effective activation energy values of the magnesiothermic stages of the studied reactions were determined by Kissinger isoconversional method.

Formation of Solid Lubricants during High Temperature Tribology of Silver-Doped Molybdenum Nitride Coatings Deposited by dcMS and HIPIMS

The coating system MoN-Ag is an interesting candidate for industrial applications as a low friction coating at elevated temperatures, due to the formation of lubricous molybdenum oxides and silver molybdates. Film deposition was performed by high-power impulse magnetron sputtering and direct current magnetron sputtering. To facilitate a future transfer to industry Mo-Ag composite targets have been sputtered in Ar/N2 atmosphere. The chemical composition of the deposited MoN-Ag films has been investigated by wavelength dispersive X-ray spectroscopy. Morphology and crystallographic phases of the films were studied by scanning electron microscopy and X-ray diffraction. To obtain film hardness in relation to Ag content and bias voltage, the instrumented indentation test was applied. Pin-on-disc tribological tests have been performed at room temperature and at high temperature (HT, 450 °C). Samples from HT tests have been analyzed by Raman measurements to identify possible molybdenum oxide and/or silver molybdate phases. At low Ag contents (≤7 at.%), coatings with a hardness of 18–31 GPa could be deposited. Friction coefficients at HT decreased with increasing Ag content. After these tests, Raman measurements revealed the MoO3 phase on all samples and the Ag2Mo4O13 phase for the highest Ag contents (~23–26 at.%).

Electrophoretic Codeposition of MoOx/MoS2 Thin Film for Platinum-Free Counter Electrode in Quantum Dot Solar Cells

The MoOx/MoS2 thin films were manufactured on conducting glass (FTO) from the ethanolic mixture of colloidal molybdenum disulfide (MoS2) and molybdenum oxides (MoOx) by electrophoretic deposition method and were used for counter electrode of quantum dot solar cells. Different ramp-rate conditions for electrophoretic deposition as well as bias potential were investigated in an attempt to get the highest possible electrocatalytic activity of polysulfide (S2-/Sn2-) redox couple. In this research, interestingly, by simply using CdS/CdSe/ZnS photoanode and polysulfide electrolyte under 1000 W.m−2 AM 1.5 G illumination, the power conversion efficiency of MoOx/MoS2-counter-electrode-based QDSC was achieved up to 2.01%, which was double compared to platinum-based counter electrode of QDSCs.

Advanced Strategies to Improve Performances of Molybdenum-Based Gas Sensors

Molybdenum-based materials have been intensively investigated for high-performance gas sensor applications. Particularly, molybdenum oxides and dichalcogenides nanostructures have been widely examined due to their tunable structural and physicochemical properties that meet sensor requirements. These materials have good durability, are naturally abundant, low cost, and have facile preparation, allowing scalable fabrication to fulfill the growing demand of susceptible sensor devices. Significant advances have been made in recent decades to design and fabricate various molybdenum oxides- and dichalcogenides-based sensing materials, though it is still challenging to achieve high performances. Therefore, many experimental and theoretical investigations have been devoted to exploring suitable approaches which can significantly enhance their gas sensing properties. This review comprehensively examines recent advanced strategies to improve the nanostructured molybdenum-based material performance for detecting harmful pollutants, dangerous gases, or even exhaled breath monitoring. The summary and future challenges to advance their gas sensing performances will also be presented.

The Effect of Additive Chemical Structure on the Tribofilms Derived from Varying Molybdenum-Sulfur Chemistries

Molybdenum disulfide (MoS2) is an effective friction modifier that can be formed on surfaces from oil-soluble lubricant additives. Different additive chemistries can be used to form MoS2 on a surface. The tribofilms formed from three different molybdenum additives (MoDTC Dimer, MoDTC Trimer, and molybdate ester) were studied in additive monoblends and fully formulated systems. The resulting tribofilms were then characterized by Raman spectroscopic spatial mapping, XPS, and FIB-TEM. The distribution of MoS2 on the surface was much more sparse for the molybdate ester than the other additives. No crystalline molybdenum oxides were observed by Raman spectroscopy, but their presence was inferred from XPS analysis. XPS analysis showed very similar distributions of Mo oxidation states from each additive, such that the chemical nature of the films formed from all of the additives is likely similar. Each of the additive tribofilms was observed to have MoS3 vibrations in Raman and persulfide XPS peaks associated with amorphous MoS3, as such this species is presented as a common frictional decomposition product for all the additives. The MoDTC trimer is more able to produce this amorphous species on the contacting surfaces due to its structural similarities to the co-ordination polymer MoS3. Graphical Abstract