Using commercially activated carbon, we developed a simple and effective direct chemical oxidation route to prepare good biocompatible multicolor photoluminescent carbon dots.
Metallic zinc (Zn) is one of the most attractive multivalent-metal anode materials in post-lithium batteries because of its high abundance, low cost and high theoretical capacity. However, it usually suffers from large voltage polarization, low Coulombic efficiency and high propensity for dendritic failure during Zn stripping/plating, hindering the practical application in aqueous rechargeable zinc-metal batteries (AR-ZMBs). Here we demonstrate that anionic surfactant-assisted in situ surface alloying of Cu and Zn remarkably improves Zn reversibility of 3D nanoporous Zn electrodes for potential use as high-performance AR-ZMB anode materials. As a result of the zincophilic ZnxCuy alloy shell guiding uniform Zn deposition with a zero nucleation overpotential and facilitating Zn stripping via the ZnxCuy/Zn galvanic couples, the self-supported nanoporous ZnxCuy/Zn electrodes exhibit superior dendrite-free Zn stripping/plating behaviors in ambient aqueous electrolyte, with ultralow polarizations under current densities up to 50 mA cm‒2, exceptional stability for 1900 h and high Zn utilization. This enables AR-ZMB full cells constructed with nanoporous ZnxCuy/Zn anode and KzMnO2 cathode to achieve specific energy of as high as ~ 430 Wh kg‒1 with ~ 99.8% Coulombic efficiency, and retain ~ 86% after long-term cycles for > 700 h.
Designing robust and cost‐effective electrocatalysts based on Earth‐abundant elements is crucial for large‐scale hydrogen production through electrochemical water splitting. Here, nitrogen‐doped carbon engrafted Mo2N/CoN hybrid nanosheets that are seamlessly oriented on hierarchical nanoporous Cu scaffold (Mo‐/Co‐N‐C/Cu), as highly efficient electrocatalysts for alkaline hydrogen evolution reaction are reported. The constituent heterostructured Mo2N/CoN nanosheets work as bifunctional electroactive sites for both water dissociation and adsorption/desorption of hydrogen intermediates while the nitrogen‐doped carbon bridges electron transfers between electroactive sites and interconnective Cu current collectors by making use of Mo‐/Co‐N‐C bonds and intimate C/Cu contacts at interfaces. As a consequence of unique architecture having electroactive sites to be sufficiently accessible, self‐supported nanoporous Mo‐/Co‐N‐C/Cu hybrid electrodes exhibit outstanding electrocatalysis in 1 m KOH, with a negligible onset overpotential and a low Tafel slope of 47 mV dec−1. They only take overpotential of as low as 230 mV to reach current density of 1000 mA cm−2. When coupled with their electro‐oxidized derivatives that mediate efficiently the oxygen evolution reaction, the alkaline water electrolyzer can achieve ≈100 mA cm−2 at 1.622 V in 1 m KOH electrolyte, ≈0.343 V lower than the device constructed with commercially available Pt/C and Ir/C nanocatalysts immobilized on nanoporous Cu electrodes.
The recently emerged single-atom alloy (SAA) catalysts have assembled the merits of the single atom catalysts (SACs) and the alloy catalysts, showing a great potential for driving nitrogen reduction reaction...
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