RESUMO
Precisely controlled heteroatom-doped metal-free carbon catalysts are highly desirable for use in various renewable energy conversion and storage devices. Herein, we report a nitrogen-doped metal-free carbon catalyst for the oxygen reduction reaction (ORR) using a facile and cost-effective synthetic method. The obtained catalysts (NC-1100) were synthesized in two steps via an amino-acid complex coating and high-temperature carbonization. The various physical characteristics revealed that NC-1100 has a unique morphology, a controlled nitrogen bonding configuration, and a uniform pore distribution. The resulting catalyst shows excellent catalytic performance toward direct 4-electron oxygen reduction reaction (ORR) in an alkaline electrolyte, with a high onset potential of 0.95 V versus RHE and limiting current density (4.5 mA cm-2). Furthermore, the developed catalysts showed superior long-term operating stability and methanol durability compared to those of commercial Pt/C. This study provides a promising guideline for the development of next-generation electrocatalysts for fuel cells and wider applications.
RESUMO
N-doped carbon materials have attracted considerable attention as highly functional materials because nitrogen doping distorts the carbon lattice, changes the charge density, and introduces additional defects. Among various positions of N atoms in N-doped carbon compounds, pyridinic-N, pyrrolic-N, and valley-N, which are doped at edge sites, exhibit specific electrocatalytic activities during the oxygen reduction reaction (ORR). However, it is difficult to selectively introduce these N atoms into a carbon matrix because the synthesis procedure typically includes high-temperature heat treatment. In this study, we applied a zeolite templating method to synthesize edge site-rich N-doped carbon materials. The sample fabricated using a zeolite template possessed high concentrations of pyridinic-N and valley-N atoms, demonstrating a significantly higher ORR catalytic activity than the sample synthesized without a zeolite template. Additional experiments conducted using various zeolites confirmed the positive effect of N-doped carbons on the ORR catalytic performance. This work demonstrated that the zeolite templating method not only increased the specific surface area and the number of active sites but also selectively created edge sites and improved the quality of the active sites.
RESUMO
The manufacture of efficient and low-cost hydrogen evolution reaction (HER) catalysts is regarded as a critical solution to achieve carbon neutrality. Herein, we developed an economical method to synthesize a CoP-anchored N-doped carbon catalyst via one-step pyrolysis using inexpensive starting materials (cobalt ion salt, phytic acid, and glycine). The size of the CoP nanoparticles was controlled by adjusting the Co/P ratio of the catalysts. Nanoscale CoP particles with adequate exposure to active sites were uniformly anchored on the surface of the conductive nitrogen-doped carbon substrate, ensuring the rapid transfer of electrons and species. When Co/P=0.89, the as-made catalyst exhibited outstanding HER activity, with an extraordinarily low overpotential of 202â mV at 10â mA cm-2 and long-term stability.