Wu, et al (2024) Electric Field-Inducing Phosphorization to CoP@Biochar Composites for Efficient Bifunctional Oxygen Electrocatalysis. Green Chemistry. https://doi.org/10.1039/D4GC00551A


The development of Zinc-air batteries (ZABs) has historically been hindered by inefficient oxygen evolution and reduction reactions. A groundbreaking method proposed by researchers could dramatically shift this narrative by introducing a novel way to synthesize bifunctional catalysts at room temperature, promising to boost the performance and feasibility of ZABs.

This new approach utilizes an electric field to induce phosphorization, merging nitrogen-doped carbon with cobalt phosphide (CoP) nanoparticles. This method not only sidesteps the need for harsh synthesis conditions but also ensures a safe, non-toxic, and highly controllable process. The result is a catalyst that showcases a significantly narrow potential gap of just 0.65 volts between the half-wave potential for oxygen reduction reaction (ORR) and the potential for oxygen evolution reaction (OER). This performance is unparalleled, particularly among wood-derived carbon-based catalysts.

The practical applications of this technology are promising. In aqueous ZABs equipped with this optimized catalyst, a high discharge specific capacity of 805.8 mAh gZn^-1 was achieved, along with remarkable long-term cycling stability extending over 1200 cycles. Similarly, the quasi-solid-state ZABs demonstrated a robust discharge-specific capacity of 760.5 mAh gZn^-1. The catalyst’s exceptional performance is attributed to the synergistic effects between the dual active sites of CoP and nitrogen-doped wood carbon (NWC), fostered by the electric field.

This innovation not only paves the way for more efficient and sustainable battery technologies but also offers a new perspective on utilizing biomass for advanced catalysts under ambient conditions. It marks a significant stride in making zinc-air batteries a more viable and environmentally friendly option for energy storage.



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