Metabolomics analysis of different diameter classes of Taxus chinensis reveals that the resource allocation is related to carbon and nitrogen metabolism.

Taxus chinensis (Taxus cuspidata Sieb. et Zucc.) is a traditional medicinal plant known for its anticancer substance paclitaxel, and its growth age is also an important factor affecting its medicinal value. However, how age affects the physiological and metabolic characteristics and active substances of T. chinensis is still unclear. In this study, carbon and nitrogen accumulation, contents of active substances and changes in primary metabolites in barks and annual leaves of T. chinensis of different diameter classes were investigated by using diameter classes instead of age. The results showed that leaves and barks of small diameter class (D1) had higher content of non-structural carbohydrates and C, which were effective in enhancing defense capacity, while N content was higher in medium (D2) and large diameter classes (D3). Active substances such as paclitaxel, baccatin III and cephalomannine also accumulated significantly in barks of large diameter classes. Moreover, 21 and 25 differential metabolites were identified in leaves and barks of different diameter classes, respectively. The differential metabolites were enhanced the TCA cycle and amino acid biosynthesis, accumulate metabolites such as organic acids, and promote the synthesis and accumulation of active substances such as paclitaxel in the medium and large diameter classes. These results revealed the carbon and nitrogen allocation mechanism of different diameter classes of T. chinensis, and its relationship with medicinal components, providing a guidance for the harvesting and utilization of wild T. chinensis.

Green rGO/FeNPs nanocomposites activated peroxydisulfate for the removal of mixed 17ß-estradiol and estriol.

Reduced graphene oxide/iron nanoparticles (rGO/FeNPs) synthesized by the chemical method have been used in Fenton oxidation of organic contaminants, yet little is known about biosynthesized rGO/FeNPs using green tea extract (GT) as how to activate persulfate in sulfate radical-based advanced oxidation processes. In this study, rGO/FeNPs were used to activate peroxydisulfate (PDS) for 17ß-estradiol (ßE2) and estriol (E3) removal. The rGO/FeNPs-PDS system removed 83.6% of ßE2 and 62.5% of E3 within 240 min, which was confirmed by a combination of adsorption and degradation via both radical and non-radical pathways. Four main reactive species in ßE2 and E3 degradation were observed, i.e., hydroxyl radical (·OH), sulfate radical (SO4·-), singlet oxygen (1O2) and electron transfer, with the respective contributions of ·OH (32.9 and 34.7%), SO4·- (16.1 and 19.7%), 1O2 (12.2 and 14.1%) and electron transfer (8.0 and 7.2%). Analysis of X-ray photoelectron spectroscopy (XPS), Fourier transform infrared (FTIR), Electron Paramagnetic Resonance (EPR) and electrochemical measurements all indicated that beside the well-known role of Fe, CO from rGO through the generation of ·OH, SO4·-, 1O2 and electron transfer, as well as GT through electron transfer also participated in the activation of PDS. Finally, the degradation pathways of ßE2/E3 were proposed. Overall, this study provides a new insight into the biosynthesis of rGO/FeNPs to activate PDS for the oxidation of mixed emerging contaminants.

Decoupled Water Electrolysis Driven by 1†cm2 Single Perovskite Solar Cell Yielding a Solar-to-Hydrogen Efficiency of 14.4 .

Invited for this month's cover is the group of Yubin Chen at Xi'an Jiaotong University as well as collaborators at Shanghai Jiao Tong University. The image shows a decoupled water electrolysis system driven by a single perovskite solar cell (PSC) to produce separated hydrogen and oxygen. The Research Article itself is available at 10.1002/cssc.202201689.

Decoupled Water Electrolysis Driven by 1 cm2 Single Perovskite Solar Cell Yielding a Solar-to-Hydrogen Efficiency of 14.4 .

Solar water splitting by photovoltaic (PV) electrolysis is a promising route for sustainable hydrogen production. However, multiple PV cells connected in series are generally required to fulfil the practical electrolytic voltages, which inevitably increases the system complexity and resistance. Decoupled water electrolysis for separate hydrogen and oxygen evolution needs smaller voltage to drive each half-reaction, which provides a feasibility to achieve the single PV cell driven water electrolysis. Herein, by introducing sodium nickelhexacyanoferrate (NaNiHCF) as the redox mediator, decoupled acid water electrolyzer and amphoteric water electrolyzer were respectively constructed. The required voltages for the hydrogen or oxygen evolution steps matched with the output voltages of the perovskite solar cell (PSC). Impressively, by combining one 1 cm2 FAPbI3 -based PSC (efficiency: 18.77 %) with the decoupled amphoteric water electrolyzer, a solar-to-hydrogen (STH) efficiency of 14.4 % was achieved, which outperformed previously reported PSC-driven water electrolysis cells.

Fenton-oxidation of rifampicin via a green synthesized rGO@nFe/Pd nanocomposite.

Antibiotics are an emerging class of persistent contaminants that are now of major environmental concern because they pose potential risks to both environmental and human health. Here reduced graphene oxide composited with bimetallic iron/palladium nanoparticles (rGO@nFe/Pd) was synthesized via a green tea extract and used to remove a common antibiotic, rifampicin from aqueous solution. The innate physical rifampicin removal efficiency of the composite (79.9 %) was increased to 85.7 % when combined with Fenton-oxidation. The mechanism and the main factors controlling Fenton-oxidation of rifampicin by rGO@nFe/Pd were investigated. Oxidation followed a pseudo-second-order degradation kinetic model with an activation energy of 47.3 kJ mol-1. rGO@nFe/Pd were characterized by Brunauer-Emmett-Teller (BET), fourier transform infrared (FTIR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray energy spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS), X-Ray powder diffraction (XRD), and zeta potential. Rifampicin degradation products observed by LC-UV, where subsequently confirmed to be mainly 5,6,9-trihydroxynaphtho [2,1-b] furan-1(2 H)-one, 5,6-dihydroxy-1-oxo-1,2-dihydronaphtho [2,1-b] furan-2-yl formate and (S)-5,6,9-trihydroxy-2-(3-methoxypropoxy)-2-methylnaphtho [2,1-b] furan-1(2 H)-one by LC-MS. Finally, the practical effectiveness of the composite material for antibiotic removal was demonstrated by the treatment of representative wastewaters, where rifampicin removal efficiencies of 80.4, 77.9 and 70.2 % were observed for river, aquaculture wastewater and domestic wastewater, respectively.