Photoelectrocatalytic Hydrogen Generation: Current Advances in Materials and Operando Characterization.

Photoelectrochemical (PEC) hydrogen generation is a promising technology for green hydrogen production yet faces difficulties in achieving stability and efficiency. The scientific community is pushing toward the development of new electrode materials and a better understanding of the underlying reactions and degradation mechanisms. Advances in photocatalytic materials are being pursued through the development of heterojunctions, tailored crystal nanostructures, doping, and modification of solid-solid and solid-electrolyte interfaces. Operando and in situ techniques are utilized to deconvolute the charge transfer mechanisms and degradation pathways. In this review, both materials development and Operando characterization are covered for advancing PEC technologies. The recent advances made in the PEC materials are first reviewed including the applied improvement strategies for transition metal oxides, nitrites, chalcogenides, Si, and group III-V semiconductor materials. The efficiency, stability, scalability, and electrical conductivity of the aforementioned materials along with the improvement strategies are compared. Next, the Operando characterization methods and cite selected studies applied for PEC electrodes are described. Operando studies are very successful in elucidating the reaction mechanisms, degradation pathways, and charge transfer phenomena in PEC electrodes. Finally, the standing challenges and the potential opportunities are discussed by providing recommendations for designing more efficient and electrochemically stable PEC electrodes.

Electrospun Nanotubular Titania and Polymeric Interfaces for High Energy Density Li-Ion Electrodes.

In the current study, for the first time, electrospinning of nanotubular structures was developed for Li-ion battery high energy density applications. For this purpose, titania-based nanotubular materials were synthesized and characterized. Before electrospinning with PVDF to obtain a self-standing electrode, the nanotubes were modified to obtain the best charge-transferring structure. In the current study, for the first time, the effects of various thermal treatment temperatures and durations under an Ar-controlled atmosphere were investigated for Li+ diffusion. Electrochemical impedance spectroscopy, cyclic voltammograms, and galvanostatic intermittent titration technique showed that the fastest charge transfer kinetics belongs to the sample treated for 10 h. After optimization of electrospinning parameters, a fully nanotube-embedded fibrous structure was achieved and confirmed by scanning electron microscopy and transmission electron microscopy. The obtained flexible electrode was pressed at ambient and 80 °C to improve the fiber volume fraction. Finally, the galvanostatic charge/discharge tests for the electrospun electrode after 100 cycles illustrated that the hot-pressed sample showed the highest capacity. The polymeric network enabled the omission of metallic current collectors, thus increasing the energy density by 14%. The results of electrospun electrodes offer a promising structure for future high-energy applications.