Biowaste-Derived Heteroatom-Doped Porous Carbon as a Sustainable Electrocatalyst for Hydrogen Evolution Reaction

Heteroatom-doped porous carbon material (H-PCM) was synthesized using Anacardium occidentale (cashew) nut's skin by a simple pyrolysis route. The resulting H-PCM was thoroughly characterized by various analytical techniques such as field emission scanning electron microscopy (FE-SEM) with energy-dispersive X-ray (EDX) spectroscopy, high-resolution transmittance electron microscopy (HRTEM), X-ray diffraction (XRD), Raman spectroscopy, nitrogen adsorption-desorption isotherms, X-ray photoelectron spectroscopy (XPS), and attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy. The obtained results strongly demonstrated that the synthesized H-PCM exhibited a porous nature, continuous sponge-like and sheet-like smooth morphology, and a moderate degree of graphitization/crystallinity with oxygen-, nitrogen-, and sulfur-containing functionalities in the carbon matrix. After the structural confirmation, as-prepared H-PCM has used a sustainable electrocatalyst for hydrogen evolution reaction (HER) because the metal-free carbonaceous catalysts are one of the most promising candidates. The H-PCM showed excellent HER activities with a lowest Tafel slope of 75 mV dec(-1) and durable stability in 0.5 M H2SO4 aqueous solution. Moreover, this work provides a versatile and effective strategy for designing excellent metal-free electrocatalysts from the cheapest biowaste/biomass for large-scale production of hydrogen gas through electrochemical water splitting.

Automated summary

Heteroatom-doped porous carbon material (H-PCM) was synthesized from cashew nut's skin through a simple pyrolysis route. The synthesized H-PCM exhibited a porous structure with sponge-like and sheet-like morphology, as well as a moderate degree of graphitization/crystallinity and various functionalities. The as-prepared H-PCM showed excellent electrocatalytic activity for hydrogen evolution reaction (HER) in 0.5 M H2SO4 aqueous solution, making it a promising candidate for metal-free carbonaceous catalysts in large-scale hydrogen production through electrochemical water splitting.