SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-026-4271-5
Photocatalytic functional coatings are at a pivotal juncture where the primary research focus must transition from intrinsic material activity to a unified framework centered on surface serviceability. Surface serviceability encompasses the ability of a coating to maintain catalytic activity, interfacial integrity, multifunctional performance, safety, and manufacturability under specific service environments over its operational lifetime. Over the past three decades, photocatalytic surfaces have demonstrated potential for degrading organic pollutants, maintaining surface cleanliness, and enabling air purification, with applications in buildings, glass, highways, and infrastructure. However, high intrinsic activity alone does not guarantee stable long-term performance when the photocatalyst is immobilized as a substrate-integrated film. Performance is governed by coupled factors including interfacial adhesion, film structure, environmental aging, and functional durability. Current challenges extend beyond catalytic activity to include long-term deactivation, coating-substrate interfacial stability, trade-offs among multiple functions, adequacy of evaluation methods, and scalability of fabrication. These issues form a progressive service chain: design determines catalyst exposure and adhesion; environmental stresses induce functional or structural failure; multifunctional integration may compromise one function for another. Therefore, application-oriented evaluation is essential. This perspective advocates for a paradigm shift toward service-oriented design, requiring establishment of service-relevant evaluation protocols and development of scalable, repairable fabrication routes. Such efforts will enable photocatalytic coatings to evolve from high-activity laboratory materials into engineering surfaces that are verifiable, comparable, manufacturable, and durable in real-world applications.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-026-4322-4
Ultrafast scintillators with low-nanosecond emission are essential for next-generation high-rate X-ray and particle imaging. Although Ce3+-activated scintillators inherently exhibit fast response characteristics, conventional Ce3+-doped hosts rarely achieve low-nanosecond ultrafast decay. Here, we report a high-entropy fluoride scintillator (HEFS), Ce:LaGdCaSrBaF12 (Ce:LGCSB), in the form of bulk single crystals. The severe lattice distortion arising from multi-cation disorder induces exciton localization and effectively suppresses exciton diffusion. Through the rapid relaxation of localized excitons, the high-entropy Ce:LGCSB single crystals deliver a decay time of 1.23 ns with a 94.6% fast-component contribution and without any noticeable slow component. Through first-principles calculations, spectroscopic characterization, and transient dynamics analysis, we reveal that the ultrafast response originates from accelerated Frenkel exciton (FE) recombination enabled by the high-entropy environment. This work establishes entropy-engineered fluorides as promising ultrafast scintillator platforms and proposes a general strategy for extending sluggish diffusion effects to the excitonic scale, offering new opportunities for improving scintillation timing performance.
SCIENCE CHINA Materials•2025•DOI: 10.1007/s40843-025-3483-5
Despite advancements in lipid droplet (LD)-targeted photosensitizers (PSs), critical challenges persist in achieving deep-tissue penetration, overcoming tumor hypoxic resistance, and coordinating multimodal cell death pathways. To address these limitations, a molecular engineering strategy was introduced to construct a series of aggregation-induced emission (AIE) PSs (MOITP, MOITM, and MOITT), which exhibited near-infrared (NIR) emission. The strong electron-withdrawing capability of the acceptor moiety in MOITT resulted in a bathochromic shift in absorption (606 nm) and NIR-II emission (1080 nm). Under 808 nm laser irradiation, MOITT exhibited the strongest type I reactive oxygen species generation and the highest photothermal conversion efficiency (η = 44%). Notably, MOITT nanoparticles (NPs) showed efficient cellular internalization and selective accumulation in LDs. Upon laser irradiation, phototherapy mediated by MOITT NPs initiated lipid peroxidation, triggering ferroptosis while synergistically inducing apoptosis. In vivo studies demonstrated that MOITT NPs enabled high-resolution NIR-II fluorescence imaging of blood vessels and effective imaging-guided phototherapy to eradicate tumors. This work establishes a novel paradigm for spatiotemporal control of cancer therapy through organelle-specific multimodal cell death integration.