Linking battery electrode science with correlated and quantum materials

Hard X-ray photoelectron spectroscopy (HAXPES) has transformed the way we probe electronic structures by extending the accessible depth far beyond that of conventional soft X-ray photoelectron spectroscopy. By using photon energies in the multi-keV range, the inelastic mean free path of photoelectrons increases to several tens of nanometers, enabling nondestructive and quantitative analysis of subsurface regions and buried interfaces. The tunability of photon energy and electron emission angle allows for controlled depth resolution, while near-total reflection and standing-wave geometries further refine probing sensitivity down to the nanometer scale. Numerical modeling, such as Yang X-ray Optics simulations, provides a powerful framework to quantitatively interpret rocking-curve measurements and reconstruct depth-dependent chemical and structural profiles. In parallel, hard X-ray angle-resolved photoemission spectroscopy extends electronic band mapping into the bulk regime, enabling momentum-resolved observation of band dispersion and charge redistribution across deeply buried interfaces. Core-hole clock spectroscopy, utilizing the intrinsic core-hole lifetime as an attosecond clock, directly measures ultrafast charge delocalization dynamics at the atomic scale. Together, these techniques bridge the spatial, momentum, and time domains of electron behavior in solids.Such high-energy photoelectron spectroscopy approaches provide universal insight into complex materials―ranging from functional oxides and correlated systems to semiconductors and electrochemical interfaces. They enable nanoscale tracking of oxidation states in battery electrodes, quantification of reaction layers in solid electrolytes, mapping of oxygen-vacancy distributions in perovskite oxides, and determination of band offsets in semiconductor heterostructures. As a result, HAXPES and its complementary variants are rapidly becoming indispensable analytical platforms for establishing structure–chemistry–function correlations in next-generation energy and electronic materials.

Cryogenic electron microscopy (cryo-EM) has emerged as a pivotal technology in materials science, particularly in characterizing electrochemical materials and interfaces. This paper delves into the recent advancements and applications of cryo-EM, underscoring its significance in understanding the intricate structures and mechanisms of materials sensitive to air and electron beams, such as lithium-ion battery electrodes. Cryo-EM's ability to capture materials in a near-natural state using vitreous ice and its compatibility with advanced imaging techniques like cryo-electron energy loss spectroscopy (cryo-EELS), cryo-electron tomography (cryo-ET), and cryo-focused ion beam (cryo-FIB) enhances our understanding of quantum and energy materials. This research will discuss the revolutionary impact of cryo-EM in areas like energy conservation and conversion, highlighting its role in visualizing sensitive materials and electrochemical reaction processes. This research addresses the need for comprehensive discussions on the characterization of quantum and energy materials through cryo-EM and related techniques, offering a thorough overview of recent advancements in this rapidly evolving field.

CoS2 enhanced SnO2@rGO heterostructure quantum dots for advanced lithium-ion battery anode