材料科学
生物量(生态学)
生物炭
热解
碳纤维
催化作用
背景(考古学)
制氢
可再生能源
氢
纳米材料基催化剂
化学工程
纳米技术
废物管理
合金
纳米颗粒
环境科学
绿色废弃物
焦耳(编程语言)
木屑
闪光灯(摄影)
气凝胶
木质纤维素生物量
金属
甲烷化
作者
Jianguo Lin,Quan Yao,Xin Lin,Dechao Wang,Kaiyue Wu,Haihan Huang,Cheng Zhang,Jianchun Jiang,Yuanbo Huang,Jianming Zheng,Zhifeng Zheng
标识
DOI:10.1021/acssuschemeng.5c07805
摘要
In the context of global energy transition and carbon neutrality goals, developing sustainable technologies for converting biomass waste into high-value green hydrogen (H2) is critical for advancing cleaner production and a circular economy. This study presents a novel approach to synthesizing carbon-supported ultrasmall FeCoNiCuZn high-entropy alloy (HEA) nanoparticles via flash Joule heating (FJH) carbothermal shock, enabling efficient catalytic valorization of poplar sawdust waste into H2. The FJH process at 1000 °C suppresses volatile metal (e.g., Zn) loss and promotes rapid reduction, yielding high-density active sites with enhanced metallic states. Structural characterizations confirm the formation of a single-phase face-centered cubic HEA structure, uniformly dispersed on nitric acid-modified biochar with strong metal-support interactions, stabilized by oxygen-containing functional groups. The synergistic effects of ultrasmall particle size (<5 nm), high specific surface area (1636 m2/g), and graphitized carbon framework significantly boost catalytic efficiency in ex situ biomass pyrolysis. The optimized catalyst (FeCoNiCuZn/C-8-HNO3) achieves a H2 yield of 23.56 mmol/gbiomass-daf (48.66 vol %), which is 37-fold higher than noncatalytic pyrolysis and 1.3-fold higher than conventional tube furnace-synthesized catalysts. This work establishes a sustainable pathway for converting low-value biomass waste into green H2 using cost-effective, high-performance HEA catalysts, addressing key challenges in cleaner production, resource utilization, and carbon-neutral energy systems.
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