Intermetallic Pd-Y nanoparticles/N-doped carbon nanotubes as multi-active catalysts for oxygen reduction reaction, ethanol oxidation reaction, and zinc-air batteries.

Intermetallic nanomaterials are unique in terms of their band gap, atomic-level arrangement, and well-defined stoichiometry, which allows them to exhibit significantly enhanced catalytic performance in electrochemical applications. However, the preparation of durable intermetallic catalysts with a lower content of platinum group metals is challenging, while the lack of control over the loss of active components limits their long-term application due to weak interaction between the support and the nanostructure. Here, we have designed the intermetallic alloyed nanoparticles (NPs) of PdY on N-doped carbon nanotubes (PdY/NCNTs) as a multifunctional catalyst for the oxygen reduction reaction (ORR), the ethanol oxidation reaction (EOR), and zinc-air batteries (ZABs). The strong adhesion through nitrogen ensures the anchoring of alloyed PdY NPs on the NCNTs, which restrains atomic migration and sintering during their conversion to intermetallic phases. This study confirms that there is negligible active site leaching owing to the strong and multiple dative bonds between the NCNTs and PdY NPs. Therefore, this catalyst exhibits remarkable catalytic activity, resulting in a mass activity of 1317 and 2902 mA mgPd-1 at jk and jf for the ORR and the EOR, respectively, and remains stable for a longer period. In addition, the PdY/NCNT-containing air cathode-fabricated ZAB achieved a higher power density (0.236 W cm-2) compared to the benchmark Pt/C.

Revolutionizing energy storage: exploring the nanoscale frontier of all-solid-state batteries.

Due to their distinctive security characteristics, all-solid-state batteries are seen as a potential technology for the upcoming era of energy storage. The flexibility of nanomaterials shows enormous potential for the advancement of all-solid-state batteries' exceptional power and energy storage capacities. These batteries might be applied in many areas such as large-scale energy storage for power grids, as well as in the creation of foldable and flexible electronics, and portable gadgets. The most difficult aspect of creating a comprehensive nanoscale all-solid-state battery assembly is the task of decreasing the particle size of the solid electrolyte while maintaining its excellent ionic conductivity. Materials possessing nanoscale structural features and a substantial electrochemically active surface area have the potential to significantly enhance power characteristics and the cycle life. This might bring about substantial changes to existing energy storage models. The primary objective of this research is to summarize the latest advancements in utilizing nanomaterials for energy harvesting in various all-solid-state battery assemblies. This study examines the most complex solid-solid interfaces of all-solid-state batteries, as well as feasible methods for implementing nanomaterials in such interfaces. Currently, there is significant attention on the necessity to develop electrode-solid electrolyte interfaces that exhibit nanoscale particle articulation and other characteristics related to the behavior of lithium ions.

High-Performance Battery-Type Supercapacitors Based on Self-Oriented Growth of Nanorods/Nanospheres Composite Assembled on Self-Standing Conductive GO/CNF Frameworks.

MnOx-based materials have limited capacity and poor conductivity over various voltages, hampering their potential for energy storage applications. This work proposes a novel approach to address these challenges. A self-oriented multiple-electronic structure of a 1D-MnO2-nanorod/2D-Mn2O3-nanosphere composite was assembled on 2D-graphene oxide nanosheet/1D-carbon nanofiber (GO/CNF) hybrids. Aided by K+ ions, the MnO2 nanorods were partially converted to Mn2O3 nanospheres, while the GO nanosheets were combined with CNF through hydrogen bonds resulting in a unique double binary 1D-2D mixed morphology of MnO2/Mn2O3-GO/CNF hybrid, having a novel mechanism of multiple Mn ion redox reactions facilitated by the interconnected 3D network. The morphology of the MnO2 nanorods was controlled by regulating the potassium ion content through a rinsing strategy. Interestingly, pure MnO2 nanorods undergo air-annealing to form a mixture of nanorods and nanospheres (MnO2/Mn2O3) with a distinct morphology indicating pseudocapacitive surface redox reactions involving Mn2+, Mn3+, and Mn4+. In the presence of the GO/CNF framework, the charge storage properties of the MnO2/Mn2O3-GO/CNF composite electrode show dominant battery-type behavior because of the unique mesoporous structure with a crumpled morphology that provides relatively large voids and cavities with smaller diffusion paths to facilitate the accumulation/intercalation of charges at the inner electroactive sites for the diffusion-controlled process. The corresponding specific capacity of 800 C g-1 or 222.2 mAh g-1 at 1 A g-1 and remarkable cycling stability (95%) over 5000 cycles at 3 A g-1 were considerably higher than those of the reported electrodes of similar materials. Moreover, a hybrid supercapacitor device is assembled using MnO2/Mn2O3-GO/CNF as the positive electrode and activated carbon as the negative electrode, which exhibits a superior maximum energy density (∼25 Wh kg-1) and maximum power density (∼4.0 kW kg-1). Therefore, the as-synthesized composite highlights the development of highly active low-cost materials for next-generation energy storage applications.