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Photocatalytic water splitting is an ideal means of producing hydrogen in a sustainable manner, and developing highly efficient photocatalysts is a vital aspect of realizing this process. The photocatalyst Y2Ti2O5S2 (YTOS) is capable of absorbing at wavelengths up to 650 nm and exhibits outstanding thermal and chemical durability compared with other oxysulfides. However, the photocatalytic performance of YTOS synthesized using the conventional solid‐state reaction (SSR) process is limited owing to the large particle sizes and structural defects associated with this synthetic method. Herein, we report the synthesis of YTOS particles by a flux‐assisted technique. The enhanced mass transfer efficiency in the flux significantly reduced the preparation time compared with the SSR method. In addition, the resulting YTOS showed improved photocatalytic H2 and O2 evolution activity when loaded with Rh and Co3O4 co‐catalysts, respectively. These improvements are attributed to the reduced particle size and enhanced crystallinity of the material as well as the slower decay of photogenerated carriers on a nanosecond to sub‐microsecond time range. Further optimization of this flux‐assisted method together with suitable surface modification is expected to produce high‐quality YTOS crystals with superior photocatalytic activity. [ABSTRACT FROM AUTHOR]

Breast cancer is the most common cancer in women and the second leading cause of cancer‐related deaths after lung cancer. Metastasis of the central nervous system is a terrible event for breast cancer patients, affecting their survival and quality of life. Compared with hormone receptor‐positive/human epidermal growth factor receptor 2‐negative breast cancer patients, brain metastases are more likely to affect patients with triple‐negative breast cancer and human epidermal growth factor receptor 2‐positive breast cancer. The treatment of breast cancer has improved greatly in the last two decades. However, brain metastases from breast cancer remain the leading cause of morbidity and mortality. Patients with breast cancer brain metastasis have been in an inferior position due to the lack of clinical research in this field, and they are often explicitly excluded from almost all clinical trials. The occurrence and progression of brain metastases will result in severe cognitive impairment and adverse physical consequences, so we must have a good understanding of the molecular mechanisms of breast cancer brain metastasis. In this article, we have retrieved the latest literature of molecules and pathways associated with breast cancer brain metastasis, summarized common therapy strategies, and discussed the prospects and clinical implications of targeting the molecules involved. [ABSTRACT FROM AUTHOR]

Y2Ti2O5S2 (YTOS), an oxysulfide material, has attracted attention as a photocatalyst due to its optical absorption at wavelengths up to 650 nm, and its ability to split water into hydrogen and oxygen. However, the performance of YTOS in photocatalytic water splitting has remained low. One important factor accounting for this poor activity is the absence of highly efficient active sites. Surface modification with oxygen‐evolution co‐catalysts is indispensable for enhancing the activity and durability of non‐oxide narrow‐bandgap photocatalysts. Herein, we report the preparation of cobalt oxide (Co3O4)‐loaded YTOS for photocatalytic oxygen evolution. The Co3O4 co‐catalyst was loaded by thermal decomposition of cobalt nitrate. The as‐obtained sample showed significantly enhanced activity in the oxygen evolution reaction compared with unmodified or IrO2‐loaded YTOS. Transient absorption spectroscopy revealed that the Co3O4 co‐catalyst captured holes and promoted charge separation, which accounted for the enhanced activity. [ABSTRACT FROM AUTHOR]

The increased emission of CO2 has negative impacts on the environment. Among the strategies, photocatalytic reduction is promising to convert the CO2 into chemicals. In this report, CoOx nanoparticles were loaded in the channels of MIL‐101(Cr), a kind of metal‐organic frameworks (MOF), to construct a novel CoOx/MIL‐101(Cr) system to facilitate CO2 photoreduction. Under the optimal conditions, the CoOx/MIL‐101(Cr) showed a significantly enhanced performance for photocatalytic CO2 reduction compared with bare CoOx and MIL‐101(Cr). Our findings provide a pathway for a rational design of efficient MOF systems for the photocatalytic reduction of CO2. [ABSTRACT FROM AUTHOR]

Abstract: Polymeric carbon nitride (PCN) photosensitizers are proposed replacements for their inorganic counterparts in solar‐to‐fuel conversion via photoelectrochemical water splitting. However, intense charge recombination, primarily because of surface defects, limits the use of PCN in PEC systems. Now, photoanodes are designed by coating PCN films onto highly conductive yttrium‐doped zinc oxide (Y:ZnO) nanorods (NRs) serving as charge collectors. The generation of charge carriers can therefore be promoted by this type II alignment. The charge collectors would be kept nearby for charge separation and transport to be used in the interfacial redox reactions. The photocurrent density of the polymer electrode is improved to 0.4 mA cm−2 at 1.23 V vs. the reversible hydrogen electrode in a Na2SO4 electrolyte solution under AM 1.5 illumination. The result reveals a more than 50‐fold enhancement over the PCN films achieved by powder; the efficiency can be preserved at 95 % for 160 minutes. [ABSTRACT FROM AUTHOR]

Emission Spectroscopy: Amplified Emissions Spectroscopy for Sensing Applications (Ann. The theme of amplified emission, which involves complicated chemical reactions and physical processes, such as spontaneous emission, stimulation, and variation of potential energy surface is visualized here. As reviewed in article number 1900210 by Zhenhui Du and co-workers, it potentially indicates the amplified emission spectroscopy developing to a new generation of promising analytical techniques and remote sensing. [Extracted from the article]

Amplified emission spectroscopy is promising for applications of qualitative and quantitative sensing of elements and their states. This technique has the characteristics of a narrow spectral line, high spectral resolution, and high signal‐to‐noise ratio. Recently, this technology has advanced tremendously with progress in excitation methods, that is, resonance multiphoton absorption and filamentation with ultrafast lasers. The mechanism, conditions, excitation, signal processing, and applications of amplified emission spectroscopy are reviewed herein. In particular, the different formation patterns of the amplified emission spectra produced by an ultrafast laser are analyzed in detail. In addition, a brief introduction is given to the existing applications of amplified emission. Finally, both a conclusion and a perspective of the future for amplified emission are presented. [ABSTRACT FROM AUTHOR]