过电位
材料科学
格式化
法拉第效率
可逆氢电极
化学工程
催化作用
堆积
纳米材料
电极
电催化剂
电化学
纳米技术
物理化学
工作电极
有机化学
工程类
化学
作者
Thành Trần‐Phú,Rahman Daiyan,Zelio Fusco,Zhipeng Ma,Rose Amal,Antonio Tricoli
标识
DOI:10.1002/adfm.201906478
摘要
Abstract 3D Bi 2 O 3 fractal nanostructures (f‐Bi 2 O 3 ) are directly self‐assembled on carbon fiber papers (CFP) using a scalable hot‐aerosol synthesis strategy. This approach provides high versatility in modulating the physiochemical properties of the Bi 2 O 3 catalyst by a tailorable control of its crystalline size, loading, electron density as well as providing exposed stacking of the nanomaterials on the porous CFP substrate. As a result, when tested for electrochemical CO 2 reduction reactions (CO 2 RR), these f‐Bi 2 O 3 electrodes demonstrate superior conversion of CO 2 to formate (HCOO − ) with low onset overpotential and a high mass‐specific formate partial current density of −52.2 mA mg −1 , which is ≈3 times higher than that of the drop‐casted control Bi 2 O 3 catalyst (−15.5 mA mg −1 ), and a high Faradaic efficiency (FE HCOO − ) of 87% at an applied potential of −1.2 V versus reversible hydrogen electrode. The findings reveal that the high exposure of roughened β‐phase Bi 2 O 3 /Bi edges and the improved electron density of these fractal structures are key contributors in attainment of high CO 2 RR activity.
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