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The synergistic effect of surface oxygen vacancy with induced lattice strains on visible light-driven photocatalytic H2 evolution over black TiO2 was investigated. Experimental measurements and theoretical calculations on the lattice parameters of black TiO2 show that surface oxygen vacancies induce internal lattice strain during two-step aluminothermic reduction, which regulates the band structure and optimizes the photoinduced charge behavior of black TiO2. The hydrogen evolution rate of black TiO2 with strain modification shows a 12-fold increase to 1.882 mmol/g· h (equal to 4.705 μmol/cm2·h) under visible light illumination. The metastable state caused by the surface oxygen vacancies leads to the formation of a high-energy surface, which enhances visible light absorption and improves the photoinduced charge separation efficiency. Furthermore, the internal lattice strain provides the driving force and channel for the directional movement of photoinduced electrons from the bulk to the high-energy surface for photocatalytic H2 evolution. This strategy provides a new method for designing a high-performance photocatalyst for H2 production.

Herein, a series of HSP90 inhibitor-SN38 conjugates through ester and carbamate linkage in the 20-OH and 10-OH positions of SN38 were developed for improving the tumor-specific penetration and accumulation of SN38 via extracellular HSP90 (eHSP90)-mediated endocytosis. Mechanistic analyses confirmed that these novel conjugates could bind to eHSP90 and be selectively internalized into the tumor cells, which led to prolonged tumor regression in multiple models of cancer. Among all studied conjugates, compound 18b showed excellent in vitro activities, including acceptable HSP90α affinity and potent antitumor activity. Moreover, compound 18b exhibited superior antitumor activity and low toxicity in HCT116 and Capan-1 xenograft models. Pharmacokinetic analyses in HCT116 and Capan-1 xenografts further confirmed that compound 18b treatment could lead to effective cleavage and extended SN38 exposure at tumor sites. All these encouraging data indicate that this compound is a promising new candidate for cancer therapy and merits further chemical and biological evaluation.

Ni-rich LiNi0.8Co0.1Mn0.1O2 (NCM811) cathode is considered to be among the most promising candidates for high-energy-density lithium-ion batteries (LIBs). However, both capacity fading and structural degradation occur during long-term cycling, which extremely limit the commercial applications of NCM811, especially at a high cutoff voltage (>4.3 V). Here, we design a double-shell hybrid nanostructure consisting of a Li2SiO3 coating layer and a cation-mixed layer (Fm3m phase) to improve its electrochemical performance. Consequently, the Si-modified NCM811 electrode shows outstanding cycling stability with a 95.2% capacity retention at 4.3 V after 100 cycles and 87.3% at a 4.5 V high cutoff voltage after 100 cycles. This designed double-shell hybrid nanostructure alleviates side reactions, structural degradation, and internal cracking, effectively enhancing the surface structural stability. This efficient strategy provides a valuable step toward further commercial applications of the LiNi0.8Co0.1Mn0.1O2 cathode and enriches the fundamental understanding of layered cathode materials.

A series of bisthiazole-based hydroxamic acids as novel potent HDAC inhibitors was developed during our previous work. In the present work, a new series of highly potent bisthiazole-based compounds were designed and synthesized. Among the prepared compounds, compound H13, which contains an α-(S)-methyl-substituted benzyl group, displays potent inhibitory activity toward human HDACs and several cancer cells lines. Compound H13 has a favorable PK profile and high tissue distribution specificity in the colon, as well as good efficacy in the AOM-DSS mouse model for colitis-associated colonic tumorigenesis.

SiOx-based anode materials with high capacity and outstanding cycling performance have gained numerous attentions. Nevertheless, the poor electrical conductivity and non-negligible volume change hi...

Currently, there is an urgent demand for Ni-rich cathode materials with excellent electrochemical properties under harsh conditions; however, obtaining such materials is very challenging. Here, we propose an innovative modification strategy that combines gradient phosphate polyanion doping and dual-conductive layer (Li3PO4-PANI) coating. The phosphate polyanion gradient doping can be described as acting in a “support role” to optimize the crystal structure. Moreover, the dual-conductive (Li3PO4-PANI) layers can be described as acting in a “palisade role” to inhibit side reactions and enhance the ionic/electronic conductivity of the NCM cathode. For the NCM cathode, this strategy synergistically achieves three main objectives: enhancement of structure stability, improvement of the ionic/electronic conductivity of the interface, and reduction of residual lithium salts. The modified NCM cathode delivers superior cycling stability, with 81.4% capacity retention after 100 cycles (4.5 V/55 °C), whereas the orig...