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Highlights Ordered intermetallic pallium-zinc (PdZn) electrocatalyst comprising a high density of PdZn pairs is synthesized for achieving co-adsorption and co-activation carbon dioxide and nitrate. Both operando measurements and theoretical calculations reveal that the PdZn pairs provide a dual-site geometric structure conducive to the key C–N coupling with a low kinetical barrier. The intermetallic PdZn displays excellent performance for the co-reduction of nitrate (NO3 –) and carbon dioxide (CO2) toward urea, with a maximum FEurea of 62.78% at a small potential of – 0.4 V versus RHE.

Abstract Designing dense thick sulfur cathodes to gain high‐volumetric/areal‐capacity lithium–sulfur batteries (LSBs) in lean electrolytes is extremely desired. Nevertheless, the severe Li2S clogging and unclear mechanism seriously hinder its development. Herein, an integrated strategy is developed to manipulate Li2S redox kinetics of CoP/MXene catalyst via electron‐donor Cu doping. Meanwhile a dense S/Cu0.1Co0.9P/MXene cathode (density = 1.95 g cm−3) is constructed, which presents a large volumetric capacity of 1664 Ah L−1 (routine electrolyte) and a high areal capacity of ≈8.3 mAh cm−2 (lean electrolyte of 5.0 µL mgs−1) at 0.1 C. Systematical thermodynamics, kinetics, and theoretical simulation confirm that electron‐donor Cu doping induces the charge accumulation of Co atoms to form more chemical bonding with polysulfides, whereas weakens CoS bonding energy and generates abundant lattice vacancies and active sites to facilitate the diffusion and catalysis of polysulfides/Li2S on electrocatalyst surface, thereby decreasing the diffusion energy barrier and activation energy of Li2S nucleation and dissolution, boosting Li2S redox kinetics, and inhibiting shuttling in the dense thick sulfur cathode. This work deeply understands the atomic‐level manipulation mechanism of Li2S redox kinetics and provides dependable principles for designing high‐volumetric‐energy‐density, lean‐electrolyte LSBs through integrating bidirectional electro‐catalysts with manipulated Li2S redox and dense‐sulfur engineering.

Euodia ruticarpa is a medicinal plant recorded in in Chinese Pharmacopeia. Here we report on the complete chloroplast genome sequence of Euodia ruticarpa. The chloroplast genome is 158,762 bp in size and includes two inverted repeat regions of 54,230 bp, which is separated by a large single-copy region of 86,267 bp and a small single copy region of 18,265 bp. A total of 131 genes were predicted, including 37 tRNA, 8 rRNA, and 86 protein-coding genes. Phylogenetic analysis placed Euodia ruticarpa under the family Rutaceae.