Defects-engineered tailoring of tri-doped interlinked metal-free bifunctional catalyst with lower gibbs free energy of OER/HER intermediates for overall water splitting

Controllable tailoring of metal-free/carbon-based nanostructures tends an encouraging way to enhance the bifunctional activity of electrodes, but a great challenge owing to the sluggish kinetics of oxygen evolution reaction (OER) and hydrogen evolution reaction (HER). Herein, a facile tempted-defects assisted fractionation strategy is presented to synthesize N, S, and O tri-doped metal-free catalyst (DETDAP). Due to this effective tempted-defects and heteroatoms interlinking in DE-TDAP, it delivers the lowest overpotential toward both the OER (346 mV) and HER (154 mV) at 10 mA cm(2). Remarkably, the DE-TDAP-electrode carries only a cell voltage of 1.81 V at 10 mA cm(-2) for overall water splitting and longterm stability. Considerably, the density functional theory (DFT) calculation exposes that the tailored defects in tri-doped interlinking could enhance bifunctional catalytic performance devising from lower Gibbs free energy of OER/HER intermediates on active sites. This struggle henceforth provides a perceptive understanding of the synergetic principles of heteroatom-interlinking-tailoring nano structures in water splitting. (C) 2021 Elsevier Ltd. All rights reserved.

Automated summary

A facile tempted-defects assisted fractionation strategy was presented to synthesize N, S, and O tri-doped metal-free catalyst (DETDAP), which exhibits excellent bifunctional catalytic activity with low overpotential towards both the OER and HER. The tailored defects in tri-doped interlinking were found to enhance the bifunctional catalytic performance, providing a perceptive understanding of the synergetic principles of heteroatom-interlinking-tailoring nanostructures in water splitting.