Wood-derived continuously oriented channels coupled with tunable built-in electric fields for efficient oxygen evolution

Luosong Zheng, Heping Luo, Yuxin Zhong, Wanqian Li, Han Xu, Fuquan Xiong, Jiahao Pi, Yan Qing, Yiqiang Wu
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Abstract

Interface engineering has emerged as a promising strategy for efficiently enhancing catalytic performance. Herein, we present a built-in electric field (BEF) strategy to assemble CoS/NiS heterojunctions confined in S-doped carbon matrix (SC) and anchored S-doped carbide wood framework (SCW). Leveraging BEF, Co-S-Ni charge transfer channels and the superior mass transfer properties inherent in wood’s unique structure, (CoS/NiS)@SC/SCW exhibits a low overpotential of 220 mV at 50 mA cm, and remarkable stability. The experimental characterizations and theoretical simulation indicate that the constructed BEF can induce the directional transfer of electrons from CoS to NiS, which is beneficial for the adsorption of OH owing to the electrostatic interaction, thereby promotes the formation of the highly active amorphous metal hydroxide oxides at lower OER potentials. This work provides a new perspective for exploring the design of energy storage and conversion catalysts based on renewable wood substrates.
木质连续定向通道与可调内置电场相结合,实现高效氧气进化
界面工程已成为有效提高催化性能的一种有前途的策略。在此,我们提出了一种内置电场(BEF)策略,用于在掺杂 S 的碳基质(SC)和锚定掺杂 S 的碳化木框架(SCW)中组装 CoS/NiS 异质结。利用 BEF、Co-S-Ni 电荷转移通道和木材独特结构中固有的优异传质特性,(CoS/NiS)@SC/SCW 在 50 mA cm 时具有 220 mV 的低过电位和出色的稳定性。实验表征和理论模拟表明,所构建的 BEF 能诱导电子从 CoS 定向转移到 NiS,由于静电作用,这有利于 OH 的吸附,从而在较低的 OER 电位下促进高活性非晶态金属氢氧化物氧化物的形成。这项工作为探索基于可再生木材基质的能量存储和转换催化剂的设计提供了一个新的视角。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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