Hierarchically porous carbon wood sponge decorated with bimetallic sites: A highly efficient electrocatalyst for hydrogen evolution in universal-pH electrolytes and seawater
Jia Liu , Chenglin Liu , Xianglin Qiu , Tianshuo Zhang , Shanshan Gao , Xiaoming Song , Fushan Chen
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引用次数: 0
Abstract
Designing low-cost, non-noble metal electrocatalysts for complex seawater-splitting processes remains a significant challenge. In this study, we report a highly efficient electrocatalyst composed of Fe-Co alloy-embedded MXene nanosheets grown on a nitrogen and carbon-doped, low-tortuosity, hierarchically porous wood carbon sponge (FeCo@CN/MXene/CS). This FeCo@CN/MXene/CS catalyst, with its porous layered structure, demonstrates exceptional bifunctional electrocatalytic performance, including remarkable electrochemical activity and stability in seawater. Notably, in 0.5 M H2SO4 and 1.0 M KOH, the catalyst exhibits overpotentials of 70 mV and 64 mV, respectively, for the hydrogen evolution reaction (HER) at a current density of 10 mA cm−2. Furthermore, it shows excellent catalytic activity and durability in natural seawater, with only a slight decrease in HER activity after 5000 cyclic voltammetry (CV) cycles and negligible degradation after 20 h of continuous electrolysis. The outstanding performance of FeCo@CN/MXene/CS is attributed to its ability to lower the energy barrier for water dissociation, optimize the adsorption and desorption of H* intermediates, and facilitate rapid mass transfer through its porous structure, as supported by both density functional theory and experimental results. This research presents a novel approach for converting abundant biomass resources into highly efficient electrocatalysts, enhancing electrocatalytic hydrogen production in natural seawater.
为复杂的海水分解过程设计低成本、非贵金属电催化剂仍然是一个重大挑战。在这项研究中,我们报道了一种由Fe-Co合金嵌入的MXene纳米片组成的高效电催化剂,该纳米片生长在氮和碳掺杂、低扭曲、分层多孔的木质碳海绵上(FeCo@CN/MXene/CS)。该FeCo@CN/MXene/CS催化剂具有多孔层状结构,具有优异的双功能电催化性能,包括在海水中显着的电化学活性和稳定性。值得注意的是,在0.5 M H2SO4和1.0 M KOH中,在电流密度为10 mA cm−2时,催化剂的析氢反应(HER)的过电位分别为70 mV和64 mV。此外,它在天然海水中表现出优异的催化活性和耐久性,在5000个循环伏安(CV)循环后HER活性仅略有下降,在连续电解20 h后降解可以忽略不计。FeCo@CN/MXene/CS的优异性能归功于其降低水解离能垒,优化H*中间体的吸附和解吸,并通过其多孔结构促进快速传质的能力,这得到了密度功能理论和实验结果的支持。本研究提出了一种将丰富的生物质资源转化为高效电催化剂的新方法,提高了天然海水中电催化制氢的效率。
期刊介绍:
The exploration of energy sources remains a critical matter of study. For the past nine decades, fuel has consistently held the forefront in primary research efforts within the field of energy science. This area of investigation encompasses a wide range of subjects, with a particular emphasis on emerging concerns like environmental factors and pollution.