材料科学
化学工程
催化作用
制氢
氢
电化学
可逆氢电极
电催化剂
电极
吸附
碳纤维
联氨(抗抑郁剂)
碳纳米管
氢燃料
分解水
纳米技术
离解(化学)
电解水
蒸汽重整
电流密度
无机化学
电解
电池电压
功率密度
多孔性
氢气储存
作者
Zhuohui Niu,Zhikai Shi,Jianlin Huang,GaiXiu YANG,Yan Chen
标识
DOI:10.1021/acssuschemeng.5c13256
摘要
It is highly attractive but challenging for simultaneously achieving hydrazine degradation and hydrogen production via renewable-energy-driven electrocatalysis. Here, we report an innovative catalyst composed of MoC-incorporated MoS 2 nanosheets grown on hierarchically porous delignified wood carbon (MoC/MoS 2 @DWC). In situ Raman characterization and density functional theory (DFT) calculations reveal that the MoC/MoS 2 heterointerface induces lattice strain and phase transformation, which collectively lower the hydrogen adsorption free energy (Δ G H* ) and accelerate the water dissociation kinetics. Consequently, the optimized MoC/MoS 2 @DWC catalyst exhibits competitive overpotentials of 345 mV (1.0 M KOH) and 425 mV (0.5 M H 2 SO 4 ) at 1000 mA cm –2 for the hydrogen evolution reaction (HER). Moreover, it demonstrates exceptional long-term durability, maintaining pH-universal HER activity over 1000 h at 500 mA cm –2 and 300 h at 1000 mA cm –2, respectively. Further, a two-electrode overall hydrazine splitting (OHzS) electrolyzer based on MoC/MoS 2 @DWC achieves an ultralow cell voltage of 102 mV at 10 mA cm –2 and sustains a stable operation over 100 h with negligible voltage attenuation. This synergistic design of interfacial engineering coupled with a self-supporting electrode architecture provides an effective strategy to enhance electrocatalytic activity and stability, enabling simultaneous energy-saving hydrogen production and pollutants removal.
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