Electrochemical alcohols oxidation offers a promising approach to produce valuable chemicals and facilitate coupled H(2) production. However, the corresponding current density is very low at moderate cell potential that substantially limits the overall productivity. Here we report the electrooxidation of benzyl alcohol coupled with H(2) production at high current density (540âmAâcm(-2) at 1.5âV vs. RHE) over a cooperative catalyst of Au nanoparticles supported on cobalt oxyhydroxide nanosheets (Au/CoOOH). The absolute current can further reach 4.8âA at 2.0âV in a more realistic two-electrode membrane-free flow electrolyzer. Experimental combined with theoretical results indicate that the benzyl alcohol can be enriched at Au/CoOOH interface and oxidized by the electrophilic oxygen species (OH*) generated on CoOOH, leading to higher activity than pure Au. Based on the finding that the catalyst can be reversibly oxidized/reduced at anodic potential/open circuit, we design an intermittent potential (IP) strategy for long-term alcohol electrooxidation that achieves high current density (>250âmAâcm(-2)) over 24âh with promoted productivity and decreased energy consumption.
Alcohols electrooxidation coupled with H(2) production at high current densities promoted by a cooperative catalyst.
在协同催化剂的促进下,醇类电氧化与高电流密度下的 H(2) 生成耦合
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作者:Li Zhenhua, Yan Yifan, Xu Si-Min, Zhou Hua, Xu Ming, Ma Lina, Shao Mingfei, Kong Xianggui, Wang Bin, Zheng Lirong, Duan Haohong
| 期刊: | Nature Communications | 影响因子: | 15.700 |
| 时间: | 2022 | 起止号: | 2022 Jan 10; 13(1):147 |
| doi: | 10.1038/s41467-021-27806-3 | ||
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