Hepatocellular carcinoma (HCC) is a common type of liver cancer that can be diagnosed by magnetic resonance imaging (MRI). If diagnosing HCC by basic MRI is difficult, then doctors use T 1-weighted or T 2-weighted imaging with a contrast agent that has long-term retention in the liver, such as Fe3O4 or FePt, to aid in MRI diagnosis. One challenging goal of cancer prevention is developing a method that can further treat or inhibit HCC cells at the time of diagnosis. Functionalized porous kaolinite can serve not only as a drug delivery system for treating cancer cells but also as a scaffold to carry FePt nanoparticles (FePt NPs) and drugs such as doxorubicin (Dox). FePt NPs combined with kaolinite modified with cetyltrimethylammonium bromide (CTAB) can form FePt@Kao nanocomposites. Multifunctional FePt@Kao can serve as a magnetic fluid hyperthermia (MFH) agent that can also be used to simultaneously visualize and treat HCC cancer cells. After being loaded with the chemotherapeutic drug Dox, FePt@Kao-Dox can provide both MFH treatment and chemotherapy. From the systematic analysis results, we demonstrated that this functionalized FePt@Kao-Dox nanocomposite can be successfully used as a platform to integrate MRI, magnetically guided targeting, and therapeutic treatment into a multifunctional drug delivery system.

Plasmonic photocatalyst of Au nanoparticle-decorated hollow mesoporous TiO2 with 0, 0.1, 0.25, 0.5, and 1% Au content was successfully synthesized by a hydrothermal method. Controlling the particle size of Au coated on TiO2 hollow microspheres (AuTHMSs) is expected to improve the photocatalytic ability. Our results of X-ray absorption spectroscopy (XAS) indicated that the coated Au ions are nulvalent and cause a lattice distortion as well as a variation in Ti 3d orbital orientation. It is also inferred that TiO6 octahedral symmetry is significantly affected by the Au incorporation, giving rise to an increase in the Ti 3d t2g unoccupied state. UV–visible absorption spectra and I–V measurements were performed to examine localized surface plasmon resonance (LSPR) effect and photoelectrocatalytic (PEC) ability. We present the first in situ XAS measurements on AuTHMS system, which enabled us to correlate the electronic structure and photocatalytic property of the material. An analysis of the results showed an LSPR effect triggered by the Au nanoparticles that provided a conductive path to the excited charge carriers, resulting in an enhanced photocurrent due to the charge transfer from Au 5d to Ti 3d orbitals under solar illumination. The photocurrent density of AuTHMSs showed an increase with Au content with a maximum for 0.5% Au, whereas in the case of 1% Au the photocurrent profile was similar to the 0% Au. Furthermore, a comparison of the XAS and PEC performance implied that the lattice distortion and the corresponding symmetry changes together with the size of Au particle substantially influenced the rate of hot electron charge transfer, resulting in the variation of PEC activity of AuTHMS samples with a higher activity for 0.5% Au. Our studies are expected to fabricate chemically stable innovative structures with enhanced surface area that would boost the photocatalytic efficiency, which is a vital factor for environmental and energy applications.

The intrinsic zinc oxide (ZnO) thin films with controllable crystallographic orientation have been synthesized on Si(100) substrates using plasma-enhanced chemical vapor deposition (PECVD) system without any buffer layer. Based on X-ray diffraction (XRD) results, the evolution of crystallographic orientation of ZnO thin films from polar c-plane (0002), polar c-plane and nonpolar m-plane (101̅0) coexist to nonpolar m-plane and a-plane (112̅0) coexist was achieved by a simple factor of controlling synthesized temperature. The plane-view morphological images exhibited that the surface texture and grain shape of ZnO thin films could have evolved from hexagonal to stripelike grains when the ZnO crystallographic orientation changed from perpendicular to parallel to the substrate. The characterization analysis indicated that the zinc precursor [diethylzinc (DEZn), Zn­(C2H5)2] played a key role on the crystallographic orientation evolution of ZnO thin films during the early stage of the growth process because DEZn not only can serve as Zn precursor but also can be employed as passivating agent to influence the crystal growth under different synthesized temperatures. Room-temperature Hall effect measurement showed that intrinsic ZnO thin film with stripelike grains possessed the lowest value of resistivity ∼7.11 × 102 Ω cm, which had an estimated carrier concentration and mobility of about 5.73 × 1014 cm–3 and 15.34 cm2/V s, respectively. The water contact angle (CA) measurement was also provided to determine the surface wettability and surface free energy of ZnO thin films, indicating that CA could be adjusted via different crystallographic orientation of ZnO thin film.

Gasochromic VO2 thin films were fabricated by the sol-gel spin-coating technique. The results of X-ray absorption spectroscopy and resonant inelastic X-ray scattering spectroscopy reveal that the origin of gasochromic coloration in VO2 is strongly related to the modulation of its structure and the electron-electron correlation. Upon gasochromic coloration, not only does the valence state change with the incorporation of hydrogen, but also the film undergoes the modification of the local atomic structure. The structural distortion varies the strength of hybridization of the O 2p-V 3d states and the bond distance of V-O and V-O varies. In the hydric process, the local atomic structure of VO2 changes from that of an un-symmetric to that of a symmetric V-O framework. The incorporated hydrogen adds electrons into the V 3d t2g orbital, enhancing the electron-electron correlation by reducing the V-V distance. This work presents a new physical insight in which the modulation of the electron-electron correlation is exploited to control the bleached and colored states, giving rise to the gasochromic phenomenon. The strong correlation among atomic spatial rearrangement, electronic structures, and transmittance supports a cooperative mechanism of the VO2 gasochromic transition. These results reveal a clear correlation between the dynamics of the lattice structure and the electronic properties and suggest a possible pathway to gasochromism and elucidation of its mechanism.

Si is regarded as a promising photocathode material for solar hydrogen evolution reaction (HER) because of its small band gap and highly negative conduction band edge. However, bare Si electrodes have high overpotential because of sluggish HER kinetics on the surface. In this study, molybdenum tungsten sulfide (MoS2–WS2) was decorated on Si photocathodes as the co-catalyst to accelerate HER kinetics. The catalytic performance of MoS2–WS2 was further enhanced by introducing phosphate materials. Phosphate-modified molybdenum tungsten sulfide (PO-MoWS) was deposited on Si photoabsorbers to provide an optimal current of −15.0 mA cm–2 at 0 V. Joint characterizations of X-ray photoelectron and X-ray absorption spectroscopies demonstrated that the phosphate material dominantly coordinated with the WS2 component in PO-MoWS. Moreover, this phosphate material induced a large number of sulfur vacancies in the PO-MoWS/Si electrodes that contributed to the ideal catalytic activity. Herein, TiO2 thin films were prepared as the protective layer to improve the stability of photocathodes. The PO-MoWS/2 nm TiO2/Si electrode maintained 83.8% of the initial photocurrent after chronoamperometric measurement was performed for 8000 s.

Pathogenic bacterial infection, especially in the wound, may threaten human health. Developing new antibacterial materials for wound healing is still urgent. Metal nanoclusters have been explored as a novel antibacterial agent. Herein, biomolecule gelatin was chosen as a substrate and functionalized with gold/silver clusters for bacterial killing. Through a simple amidation reaction, gold/silver clusters were successfully conjugated in a gelatin substrate to obtain a Au/Ag@gelatin sponge. The presence of gold/silver clusters modified the porous structure of the gelatin. Thus, the water absorption and water retention of the Au/Ag@gelatin sponge were enhanced. More importantly, the gold/silver clusters show aggregation-enhanced emission and strong reactive oxygen generation, that endow the Au/Ag@gelatin sponge with a good antibacterial property. The good physical performance and favorable bactericidal activity of the Au/Ag@gelatin sponge suggest its potential for application as a wound dressing.

TiO2–CdO composite rods were synthesized through a hydrothermal method and sputtering thin-film deposition. The hydrothermally derived TiO2 rods exhibited a rectangular cross-sectional crystal feature with a smooth surface, and the as-synthesized CdO thin film exhibited a rounded granular surface feature. Structural analyses revealed that the CdO thin film sputtered onto the surfaces of the TiO2 rods formed a discontinuous shell layer comprising many island-like CdO crystallites. The TiO2–CdO composite rods were highly crystalline, and their surfaces were rugged. A comparison of the NO2 gas-sensing properties of the CdO thin film, TiO2 rods, and TiO2–CdO composite rods revealed that the composite rods exhibited superior gas-sensing responses to NO2 gas than did the CdO thin film and TiO2 rods, which can be attributed to the microstructural differences and the formation of heterojunctions between the TiO2 core and CdO crystallites.

Bismuth telluride‐based thermoelectric (TE) materials are historically recognized as the best p‐type (ZT = 1.8) TE materials at room temperature. However, the poor performance of n‐type (ZT≈1.0) counterparts seriously reduces the efficiency of the device. Such performance imbalance severely impedes its TE applications either in electrical generation or refrigeration. Here, a strategy to boost n‐type Bi2Te2.7Se0.3 crystals up to ZT = 1.42 near room temperature by a two‐stage process is reported, that is, step 1: stabilizing Seebeck coefficient by CuI doping; step 2: boosting power factor (PF) by synergistically optimizing phonon and carrier transport via thermal‐driven Cu intercalation in the van der Waals (vdW) gaps. Theoretical ab initio calculations disclose that these intercalated Cu atoms act as modulation doping and contribute conduction electrons of wavefunction spatially separated from the Cu atoms themselves, which simultaneously lead to large carrier concentration and high mobility. As a result, an ultra‐high PF ≈63.5 µW cm−1 K−2 at 300 K and a highest average ZT = 1.36 at 300–450 K are realized, which outperform all n‐type bismuth telluride materials ever reported. The work offers a new approach to improving n‐type layered TE materials.