Defects, interfaces, and charge transport in functional micro/nano powder systems

This is the authors' abstract. We don't add key points for this paper.

Micro/nano powders are central to functional materials research, yet their behavior is still commonly interpreted through composition, synthesis strategy, or target application alone. Such descriptors are useful initially, but they do not explain why powders with apparently similar chemistry or architecture can exhibit markedly different functional responses under comparable conditions. The underlying difficulty is that the powder state creates a structurally and electronically heterogeneous environment in which reduced dimensions, high surface area, agglomerate porosity, defects, interfaces, and carrier pathways interact across surfaces, grain boundaries, heterointerfaces, and interparticle networks. A solid-state physics framework is developed for interpreting micro/nano powders through three coupled dimensions: defect landscapes, interfacial electrostatics, and charge-transport regimes. Rather than surveying material families descriptively, the analysis examines how defect partitioning, band-edge restructuring, trap states, space-charge formation, and transport-limited charge handling jointly define the active state of powders under operation. Particular attention is given to semiconducting and functional powder systems relevant to photocatalysis and energy conversion. The analysis shows that widely used explanations in powder literature remain incomplete when treated in isolation. On that basis, a variable-centered framework is proposed, together with an evidence hierarchy, application-level mapping, and minimum reporting logic, to support more physically grounded comparison and design of functional powders for energy-conversion technologies.