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Nitrate and furfural are typical wastes mainly from industrialization and agriculturalization progresses, and their clean conversions are still very challenging for a sustainable future. Nevertheless, scant attention has been devoted to the core issues: the rational integration of two wastes recycling and the targeted manipulation of hydrogen (H*) transfer behaviors to address their sluggish reaction kinetics. Herein, we report an all-in-one electrochemical energy system that is thermodynamically designed by coupling nitrate reduction (NORR) and furfural oxidation reactions (FORs) together. Particularly, the poor kinetics for both electrode reactions are efficaciously optimized by the bifunctional electrocatalyst of RhCu alloy nanowires on copper foam (RhCu NW/CF) with highly improved dual-directional H*-modulation performances, thus initializing NORR for NH synthesis at +0.31 V and driving FOR for H harvest at an onset potential lower than 0 V. Eventually, such integrated "Furfural-Nitrate" system can simultaneously effectuate the electricity energy supply (10.76 mW cm), wastewater purification, cathodic hydrogen storage (NH), anodic H production, and biomass upgrading. Hence, it provides a promising perspective of "turning waste into treasure" in a rational manner, justifying its all-in-one property in addressing the global challenge of sustainable energy.
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http://dx.doi.org/10.1002/anie.202503424 | DOI Listing |
Dev Cell
September 2025
Laboratory of Biochemistry, Wageningen University and Research, Stippeneng 4, 6708 WE Wageningen, the Netherlands. Electronic address:
In this issue of Developmental Cell, Yuan et al. explores how the pathogenic bacterium Pseudomonas syringae modulates plant metabolism, particularly through methylglyoxal (MG) accumulation, to suppress immune responses in Arabidopsis. By affecting key proteins TTM2 and CAT2, the pathogen reduces hydrogen peroxide levels, weakening plant defense mechanisms and promoting infection.
View Article and Find Full Text PDFJ Colloid Interface Sci
September 2025
School of Materials, Shenzhen Campus of Sun Yat-sen University, Shenzhen 518107, China. Electronic address:
Harnessing the significant buildup of lactic acid (LA) within the tumor microenvironment (TME) for metabolic manipulation presents a promising avenue for cancer treatment. Nevertheless, single-agent therapies often fail to address the complex and varying needs of TME heterogeneity, posing a substantial scientific hurdle in oncology. In this context, we employ asymmetric mesoporous silica nanoparticles (AMS NPs) as delivery vehicles, simultaneously loading them with zinc‑cobalt‑manganese ferrite nanoparticles (ZCMF NPs), lactate oxidase (LOX), and doxorubicin (DOX).
View Article and Find Full Text PDFNucleic Acids Res
September 2025
Key Laboratory of Clinical Laboratory Diagnostics (Chinese Ministry of Education), College of Laboratory Medicine, Chongqing Medical University, Chongqing 400016, P. R. China.
Local pH variations play a pivotal role in numerous critical biological processes. However, achieving the tunability and selectivity of pH detection remains a challenge. Here, we present a DNA-based strategy that enables programmable and selective pH responses, which is termed shadow-strand hybridization-actuated displacement engineering (SHADE).
View Article and Find Full Text PDFChem Sci
September 2025
Tianjin Key Laboratory of Micro-scale Optical Information Science and Technology, Institute of Modern Optics and Centre of Single-Molecule Science, Nankai University Tianjin 300350 China
The keto-enol tautomerism, involving a reversible isomerization of the molecule, plays a critical role in organic synthesis, biological activity, and molecular-scale charge transport. It is therefore essential to manipulate the process of keto-enol tautomerism. Unlike typical ketones, β-diketones exist dominantly in the enol form and it is a great challenge to realize enol-keto tautomerism due to the formation of intramolecular hydrogen bonds in the enol form.
View Article and Find Full Text PDFOrg Lett
September 2025
School of Pharmaceutical and Chemical Engineering and Institute for Advanced Studies, Taizhou University, 1139 Shifu Road, Taizhou, Zhejiang 318000, China.
Here, intramolecular hydrogen bond (IMHBs)-induced rigidity is used for the first time to synthesize macrocyclic arenes. Calix[]azanediyldibenzoates (C[]A, where = 3, 4, or 5) are synthesized through a one-step condensation reaction between dimethyl 2,2'-azanediyldibenzoate and paraformaldehyde. Compared to the monomer, the macrocycles exhibit a fast and significant acidochromic response due to the intramolecular charge transfer that is boosted by the synergistic effect of their adsorption and protonation.
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