材料科学
阴极
碳纤维
化学工程
热解
生物量(生态学)
氧气
氮气
磷
反键分子轨道
析氧
工作(物理)
氧化物
密度泛函理论
功率密度
电化学
电极
阳极
动力学
纳米技术
作者
Luyao Zhang,Hongjiao Chen,Xiangyu Wang,Jiaqi Cong,Zhixin Xue,Yan Wu,Bin Hui
出处
期刊:Small
[Wiley]
日期:2026-10-19
卷期号:: e76341-e76341
摘要
ABSTRACT The sluggish kinetics of the oxygen reduction reaction (ORR) at the cathode hinder the development of zinc‐air batteries (ZABs). Herein, a nitrogen and phosphorus dual‐doped honeycomb‐like carbon (K‐NPCW‐900) derived from waste wood is fabricated to boost oxygen activation efficiency and enhance ZABs performance. Potassium hydroxide‐assisted high‐temperature pyrolysis converted poplar wood into a three‐dimensional honeycomb‐like carbon architecture with high microporosity and large specific surface area, exposing active sites and facilitating mass transport. Density functional theory reveals that asymmetric N─C─P sites inject more electrons than N─C into the O 2 antibonding orbitals, elongating O─O bond to 1.53 Å, facilitating O 2 activation. These sites optimize oxygen‐intermediate adsorption, shifting the rate‐determining step from * OOH on N─C to * O reduction. K‐NPCW‐900 exhibits a high half‐wave potential of 0.835 V, indicating favorable electrocatalytic performance. The K‐NPCW‐900‐assembled ZABs deliver a high specific capacity of 797.12 mAh g −1 and stable cycling for 550 h at room temperature. Impressively, the ZABs retain robust cycling at elevated temperatures of 40°C and 60°C, achieving peak power densities of 180.62 and 265.93 mW cm −2 . This work demonstrates a compositional and structural engineering strategy to convert waste woody biomass into value‐added carbon electrodes, facilitating sustainable ZABs development.
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