| Literature DB >> 33839383 |
Lin-Lin Ma1, Xiao Hu2, Wu-Jun Liu3, Hong-Chao Li2, Paul K S Lam4, Raymond Jianxiong Zeng5, Han-Qing Yu6.
Abstract
The large scale lignocellulosic biomass wastes could also be regarded as abundantly-available renewable resources, and how to convert them into value-added products via sustainable approaches is still a big challenge. In this work, we demonstrated a facile pyrolysis method to construct N, P-dually doped biochar materials from the lignocellulosic biomass wastes. The as-synthesized N, P-dually doped biochar samples could act as electrocatalysts for oxygen reduction and evolution reactions (ORR/OER), showing excellent catalytic performance and long-term durability, as well as robust tolerance to CO and methanol. The unique hierarchical porous structure, favorable electronic structure modified by the N and P doping, as well as a variety of defect sites induced by the N and P doping into the carbon framework were identified as the main contributions to the prominent catalytic activity of the as-synthesized N, P-dually doped biochar materials. We expect this work would spur more efforts into developing advanced materials from the large scale lignocellulosic biomass wastes.Entities:
Keywords: Biochar; Biomass wastes; Oxygen evolution reaction; Oxygen reduction reaction; Pyrolysis
Year: 2021 PMID: 33839383 DOI: 10.1016/j.chemosphere.2021.130508
Source DB: PubMed Journal: Chemosphere ISSN: 0045-6535 Impact factor: 7.086