Publications by authors named "Yongjie Ge"

Ultrafine iridium particles anchored on nitrogen-doped CNTs were obtained from Ir(ppy) and CNTs using a simple annealing method and acted as highly efficient bifunctional oxygen catalysts for Zn-air batteries. A synergistic effect, efficient *OH adsorption and rapid *OOH deprotonation were demonstrated from FTIR spectroscopy, EIS and activation energy measurements.

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Constructing three-dimensional (3D) current collectors is an effective strategy to solve the hindrance of the development of lithium metal anodes (LMAs). However, the excessive mass of the metallic scaffold structure leads to a decrease in energy density. Herein, lithiophilic graphene aerogels comprising reduced graphene oxide aerogels and silver nanowires (rGO-AgNW) are synthesized through chemical reduction and freeze-drying techniques.

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The electrocatalytic conversion of nitrate (NO ) to NH (NORR) at ambient conditions offers a promising alternative to the Haber-Bosch process. The pivotal factors in optimizing the proficient conversion of NO into NH include enhancing the adsorption capabilities of the intermediates on the catalyst surface and expediting the hydrogenation steps. Herein, the Cu/CuO/Pi NWs catalyst is designed based on the directed-evolution strategy to achieve an efficient reduction of NO‾.

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The electrocatalytic conversion of nitrate (NO ‾) to NH  (NO RR) offers a promising alternative to the Haber-Bosch process. However, the overall kinetic rate of NO RR is plagued by the complex proton-assisted multiple-electron transfer process. Herein, Ag/Co O /CoOOH nanowires (i-Ag/Co O  NWs) tandem catalyst is designed to optimize the kinetic rate of intermediate reaction for NO RR simultaneously.

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Functional carbon nanomaterials play a crucial role in the cathodic oxygen reduction reaction (ORR) for sustainable fuel cells and metal-air batteries. In this study, we propose an effective approach to immobilize iron phthalocyanines (FePc) by employing a porous N-doped carbon material, denoted as NC-1000, derived from a sheet-shaped coordination polymer. The resulting NC-1000 possesses substantial porosity and abundant pore defects.

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In alkaline solutions, the electrocatalytic conversion of nitrates to ammonia (NH) (NORR) is hindered by the sluggish hydrogenation step due to the lack of protons on the electrode surface, making it a grand challenge to synthesize NH at a high rate and selectivity. Herein, single-stranded deoxyribonucleic acid (ssDNA)-templated copper nanoclusters (CuNCs) were synthesized for the electrocatalytic production of NH. Because ssDNA was involved in the optimization of the interfacial water distribution and H-bond network connectivity, the water-electrolysis-induced proton generation was enhanced on the electrode surface, which facilitated the NORR kinetics.

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IrO as benchmark electrocatalyst for acidic oxygen evolution reaction (OER) suffers from its low activity and poor stability. Modulating the coordination environment of IrO by chemical doping is a methodology to suppress Ir dissolution and tailor adsorption behavior of active oxygen intermediates on interfacial Ir sites. Herein, the Re-doped IrO with low crystallinity is rationally designed as highly active and robust electrocatalysts for acidic OER.

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One-dimensional nanotube heterostructures with IrO-stabilized LaIrO is obtained by an electrospinning approach. The LaIrO/IrO catalyst exhibits superior catalytic activity and strong stability for the oxygen evolution reaction. The synergistic cooperation between the two types of Ir as the active sites in LaIrO/IrO is demonstrated by Raman spectrum and DFT calculation.

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Traditional lithium-sulfur battery catalysts are still facing substantial challenges in solving sulfur redox reactions, which involve multistep electron transfer and multiphase transformations. Here, inspired by the combination of iron dextran (INFeD) and ascorbic acid (VC) as a blood tonic for the treatment of anemia, a highly efficient VC@INFeD catalyst is developed in the sulfur cathode, accomplishing the desolvation and enrichment of high-concentration solvated lithium polysulfides at the cathode/electrolyte interface with the assistance of multiple H/Li-bonds and resolving subsequent sulfur transformations through gradient catalysis sites where the INFeD promotes long-chain lithium polysulfide conversions and VC accelerates short-chain lithium polysulfide conversions. Comprehensive characterizations reveal that the VC@INFeD can substantially reduce the energy barrier of each sulfur redox step, inhibit shuttle effects, and endow the lithium-sulfur battery with high sulfur utilization and superior cycling stability even under a high sulfur loading (5.

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Based on UPLC characteristic chromatogram and quantitative analysis of multi-components by single marker(QAMS), the content of seven types of ginsenosides in Ginseng Radix et Rhizoma was simultaneously determined, and the quality of Ginseng Radix et Rhizoma was evaluated by the principal component analysis(PCA). The chromatographic separation was performed on the Acquity UPLC BEH C_(18) column(2.1 mm×100 mm, 1.

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The electrocatalytic nitrogen reduction reaction (eNRR) is regarded as promising sustainable ammonia (NH) production alternative to the industrial Haber-Bosch process. However, the current electrocatalytic systems still exhibit a grand challenge to simultaneously boost their eNRR activity and selectivity under ambient conditions. Herein, we construct Pd/PdO electrocatalysts with a controlled oxygen level by a facile electrochemical deposition approach at different gas atmospheres.

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The key challenges facing the commercialization of lithium-sulfur (Li-S) batteries are shortening the lithium polysulfide (LiPS) intermediate existence time while accelerating solid-phase conversion reactions. Herein, inspired by highly efficient natural enzymes with Fe/N active sites for oxygen reduction reactions, we report a periodic expansion catalysis concept, i.e.

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The rapid and accurate identification of foodborne pathogenic bacteria is of great importance for human health. Matrix-assisted laser desorption/ionization-time of flight mass spectrometry (MALDI-TOF MS) can be used to rapidly and sensitively identify microorganisms but is limited by the expensive protein databases available. In this study, we established a whole-cell method for the identification of foodborne pathogenic bacteria, using MALDI-TOF MS and principal component analysis (PCA), which did not use protein extractions or expensive protein databases.

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Silver nanowire (Ag-NW) thin films are of considerable interest for next-generation transparent conductors (TCs). However, their carrier transport properties are largely plagued by the residual polyvinylpyrrolidone (PVP) ligands on surface that were introduced during the synthesis of the Ag-NWs. Here we report a rapid electrochemical cleaning strategy to thoroughly remove the surface PVP ligands and greatly improve the carrier transport properties of the Ag-NW thin films while not affecting their transmittance.

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Silver nanowire (Ag-NW) thin films have emerged as a promising next-generation transparent electrode. However, the current Ag-NW thin films are often plagued by high NW-NW contact resistance and poor long-term stability, which can be largely attributed to the ill-defined polyvinylpyrrolidone (PVP) surface ligands and nonideal Ag-PVP-Ag contact at NW-NW junctions. Herein, we report a room temperature direct welding and chemical protection strategy to greatly improve the conductivity and stability of the Ag-NW thin films.

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Thioredoxin reductase (TrxR) is critical for cellular redox regulation and is involved in tumor proliferation, apoptosis and metastasis. Its C-terminal redox-active center contains a cysteine (Cys497) and a unique selenocysteine (Sec498), which are exposed to solvent and easily accessible. Thus, it is becoming an important target for anticancer drugs.

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