ABSTRACT
Self-supported electrocatalytic thin films consist 3D conducting network and well-embedded electrocatalysts, which endows the advantage in mass flow kinetics and durability for large-scale water splitting. Synthesis of such self-supported electrode still remains a big challenge due to the difficulty in the control over the 3D conducting network and the simultaneous growth of catalyst with well attachment on the conducting fibers. Herein, a self-supported Mo2C@carbon nanofibers (Mo2C@C NF) film has been successfully fabricated with outstanding electrocatalytic performance under optimized pyrolysis temperature and precursors mass ratio conditions. During the carbonation process, the Mo2C nanoparticles (â¼16 nm) were simultaneously grown and well dispersed on the inter-connected carbon nanofibers, which formed a 3D conducting network. The as-formed 3D carbon network was strong enough to support direct electrocatalytic application without additional ink or supporting substrates. This particular electrode structure facilitated easy access to the active catalytic sites, electron transfer, and hydrogen diffusion, resulting in the high hydrogen evolution reaction activity. A low overpotential of 86 mV was needed to achieve 10 mA cm-2current density with outstanding kinetics metric (Tafel 43 mV dec-1) in 1 M KOH. Additionally, the self-supported Mo2C@C NF film, a binder-free electrode, exhibited extraordinary stability of more than 340 h.
ABSTRACT
Contamination and waste heat are major issues in water pollution. Aiming at efficient synchronous recovery wastewater and waste heat, we designed a novel CaCO3-based phase-change microcapsule system with an n-docosane core and a CaCO3/Fe3O4 composite shell. The system was fabricated through an emulsion-templated in situ precipitation approach in a structure-directing mode, resulting in a controllable morphology for the resultant microcapsules, varying from a peanut hull through ellipsoid to dumbbell shapes. The system has a significantly enlarged specific surface area of approximately 55 m2·g-1 with the CaCO3 phase transition from vaterite to calcite. As a result, the microcapsule system exhibits improved adsorption capacities of 497.6 and 79.1 mg/g for Pb2+ and Rhodamine B removal, respectively, from wastewater. Moreover, increase in the specific surface area of the microcapsule system with a sufficient latent heat capacity of approximately 130 J·g-1 also resulted in an enhanced heat energy-storage capability and thermal conductance for waste-heat recovery. The microcapsule system also exhibits a good leakage-prevention capability and good multicycle reusability owing to the tight magnetic CaCO3/Fe3O4 composite shell. This study provides a promising approach for developing CaCO3-based phase-change microcapsules with enhanced thermal energy storage and adsorption capabilities for efficient synchronous recovery of wastewater and waste heat.
