Atomic-level tungsten doping triggered low overpotential for electrocatalytic water splitting.

The design of electrocatalysts with lower overpotential is of great significance for water splitting. Herein, cobalt hydroxide carbonate (CCH) has been used as a model to demonstrate the boost of its oxygen evolution reaction (OER) activity by atomic doping of W6+ (W-CCH). The 5 at % W doping reduced the OER overpotential of CCH by 95.3 mV at 15 mA cm-2, and increased the current density by 2.8 times at 1.65 V. 5%W-PCCH || 5%W-CCH-based electrolyzer only required a potential of 1.65 V to afford 10 mA cm-2 for full water splitting. The W6+ in CCH are active sites for O2- adsorption and induced an incesaed electron density near the Fermi level, which facilitates the charge transfer during electrocatalysis. The W6+ doping has been validated as an efficient booster for transition-metal carbonate hydroxides-based electrocatalysts, which has half or more than half-filled d-bands.

One-Step Synthesis of Monodispersed Mesoporous Carbon Nanospheres for High-Performance Flexible Quasi-Solid-State Micro-Supercapacitors.

Cost-effective synthesis of carbon nanospheres with a desirable mesoporous network for diversified energy storage applications remains a challenge. Herein, a direct templating strategy is developed to fabricate monodispersed N-doped mesoporous carbon nanospheres (NMCSs) with an average particle size of 100 nm, a pore diameter of 4 nm, and a specific area of 1093 m2 g-1 . Hexadecyl trimethyl ammonium bromide and tetraethyl orthosilicate not only play key roles in the evolution of mesopores but also guide the assembly of phenolic resins to generate carbon nanospheres. Benefiting from the high surface area and optimum mesopore structure, NMCSs deliver a large specific capacitance up to 433 F g-1 in 1 m H2 SO4 . The NMCS electrodes-based symmetric sandwich supercapacitor has an output voltage of 1.4 V in polyvinyl alcohol/H2 SO4 gel electrolyte and delivers an energy density of 10.9 Wh kg-1 at a power density of 14014.5 W kg-1 . Notably, NMCSs can be directly applied through the mask-assisted casting technique by a doctor blade to fabricate micro-supercapacitors. The micro-supercapacitors exhibit excellent mechanical flexibility, long-term stability, and reliable power output.

Co2P@N,P-Codoped Carbon Nanofiber as a Free-Standing Air Electrode for Zn-Air Batteries: Synergy Effects of CoNx Satellite Shells.

Here, a free-standing electrode composed of cobalt phosphides (Co2P) supported by cobalt nitride moieties (CoNx) and an N,P-codoped porous carbon nanofiber (CNF) in one-step electrospinning of environmentally friendly benign phosphorous precursors is reported. Physiochemical characterization revealed the symbiotic relationship between a Co2P crystal and surrounding nanometer-sized CoNx moieties embedded in an N,P-codoped porous carbon matrix. Co2P@CNF shows high oxygen reduction reaction and oxygen evolution reaction performance owing to the synergistic effect of Co2P nanocrystals and the neighboring CoNx moieties, which have the optimum binding strength of reactants and facilitate the mass transfer. The free-standing Co2P@CNF air-cathode-based Zn-air batteries deliver a power density of 121 mW cm-2 at a voltage of 0.76 V. The overall overpotential of Co2P@CNF-based Zn-air batteries can be significantly reduced, with low discharge-charge voltage gap (0.81 V at 10 mA cm-2) and high cycling stability, which outperform the benchmark Pt/C-based Zn-air batteries. The one-step electrospinning method can serve as a universal platform to develop other high-performance transition-metal phosphide catalysts benefitting from the synergy effect of transition nitride satellite shells. The free-standing and flexible properties of Co2P@CNF make it a potential candidate for wearable electronic devices.