镍氮共掺杂生物质碳基催化剂用于电化学还原CO2制备合成气

    Nickel and Nitrogen Co-doped Biomass Carbon-based Catalysts Used for the Electrochemical Reduction of CO2 to Prepare Syngas

    • 摘要: 针对化石燃料过度消耗引发的二氧化碳排放问题,本文以农业废弃物玉米秸秆为原料,通过开发新型镍氮共掺杂生物质碳基催化剂(Ni-NBC-800),旨在实现电化学二氧化碳还原(CO2 Reduction Reaction, CO2RR)制备可调比例合成气(CO/H2),推动CO2资源化利用。本文采用氯化铵辅助造孔工艺,结合镍浸渍与高温热解策略,构建了兼具分级多孔结构与金属–氮活性位点的复合催化剂。实验结果表明,优化负载Ni的质量分数(2%)与煅烧温度(800 ℃)后,催化剂在–0.8 V电位下CO法拉第效率达72.8%,CO与H2的物质的量比可通过电位调控在0.75~3.15范围内,满足合成气下游工艺需求。对比商业活性炭基催化剂(Ni-NAC-800),Ni-NBC-800展现出更高的CO分电流密度(–4.75 mA/cm2)及稳定性(24小时电流保持率为90.3%)。结合表征分析揭示氯化铵热解产生的NH3/HCl气体协同刻蚀形成的分级多孔结构能促进反应物传质,提高催化反应活性。该研究不仅验证了农业废弃物衍生碳材料替代商业碳载体的可行性,更通过金属−载体协同设计为低成本、可调控合成气电合成提供了新策略。

       

      Abstract: To address CO2 emissions caused by excessive fossil fuel consumption, a novel Ni-N co-doped biomass-derived carbon catalyst (Ni-NBC-800) is developed using agricultural waste corn stalks, aiming to achieve electrochemical CO2 reduction (CO2 Reduction Reaction, CO2RR) for synthesizing syngas (CO/H2) with tunable ratios and promote CO2 resource utilization. A NH4Cl-assisted pore-forming strategy combined with nickel impregnation and high-temperature pyrolysis is employed to construct a composite catalyst featuring hierarchical porous structures and metal-nitrogen active sites. Experimental results demonstrate that with the optimized mass fraction of the load Ni (2%) and calcination temperature (800 ℃), the catalyst achieved a CO Faradaic efficiency of 72.8% at –0.8 V, while the molar ratio of CO to H2 can be continuously adjusted within the range of 0.75 to 3.15 through potential regulation, meeting downstream syngas process requirements. Compared with commercial activated carbon-based catalyst (Ni-NAC-800), Ni-NBC-800 exhibited superior CO partial current density (–4.75 mA/cm2) and stability (the 24-hour current retention rate of 90.3%). Characterization analyses revealed that the hierarchical porous structure formed by NH3/HCl gas synergistic etching during NH4Cl pyrolysis significantly enhanced reactant mass transfer and catalytic activity. This work not only validates the feasibility of agricultural waste-derived carbon materials as alternatives to commercial carbon supports, but also provides a new strategy for low-cost and tunable syngas electrosynthesis through metal-support synergistic design.

       

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