气凝胶
多孔性
催化作用
材料科学
碳纤维
纳米颗粒
化学工程
热解
退火(玻璃)
金属
贵金属
电容
化学
电极
纳米技术
复合材料
冶金
有机化学
物理化学
复合数
工程类
作者
Tao Wu,Shufei Zhu,Yiming Xie,Ma Qian,Can‐Zhong Lu
标识
DOI:10.1016/j.apcatb.2023.122685
摘要
In thrall to the low productivity and expensive price of the precious metal catalysts (PMC), it is imminent to develop high-efficient non-noble metal single-atom catalysts (SACs) to replace PMC. However, thermally induced aggregation into nanoparticles and micropores-dominated structures are commonly encountered issues in loading SACs on carbonaceous supports, leading to low exposure ratio of active sites and inadequate mass transference. Herein, we fabricated a series of gelatin-derived carbon-aerogels (GDCAx) to prevent the aggregation of Fe atom and form the hierarchically porous nanonetwork, and thus the Fe SACs (Fe-N-GDCAx) with abundant and hierarchical pores are obtained after pyrolysis. The Fe-N-GDCAx has plentiful accessible Fe-Nx active sites and mass transfer pathways, benefiting to ORR procedure. The optimal sample Fe-N-GDCA0.8 without other gas assisted during annealing (only in argon atmosphere) exhibits exceedingly excellent half-wave potential (E1/2) of 0.93 V (vs. RHE) in 0.1 M KOH. Aqueous zinc-air battery assembled with Fe-N-GDCA0.8 presents ultrahigh specific capacitance of 803.4 mAh gZn−1 (close to 824 mAh gZn−1 theoretical value) and long-term stability. Meanwhile, quasi-solid zinc-air battery has high peak density and specific capacitance of 82.6 mW cm−2 and 713.2 mAh gZn−1 respectively.
科研通智能强力驱动
Strongly Powered by AbleSci AI