详细信息

Ultrathin and dense Ag nanosheets synthesis under suppressed face (111) growth and surface diffusion  ( SCI-EXPANDED收录 EI收录)  

文献类型:期刊文献

英文题名:Ultrathin and dense Ag nanosheets synthesis under suppressed face (111) growth and surface diffusion

作者:Yan, Shenglin[1];Mahyoub, Samah A.[1];Zhong, Juhua[2];Chen, Chengzhen[1];Zhang, Fanghua[1];Cheng, Zhenmin[1]

机构:[1]East China Univ Sci & Technol, Sch Chem Engn, State Key Lab Chem Engn, Shanghai 200237, Peoples R China;[2]East China Univ Sci & Technol, Sch Sci, Dept Phys, Shanghai 200237, Peoples R China

年份:2021

卷号:488

外文期刊名:JOURNAL OF POWER SOURCES

收录:;EI(收录号:20210309787874);WOS:【SCI-EXPANDED(收录号:WOS:000615923600001)】;

基金:The authors acknowledge the support of the National Nature Science Foundation of China (No. 21676085).

语种:英文

外文关键词:Ag nanosheets; H3BO3 concentration; Deposition temperature; CO2 electroreduction; CO

摘要:Ultrathin and dense Ag nanosheets (ANS) with large electrochemically active surface area and rich edge active sites over Ag foils are synthesized via a facile electrodeposition approach in a double electrode system. By adjusting the concentration of H3BO3 and changing deposition temperature, ANS with varying thickness are fabricated. Interestingly, ANS gradually become thinner with H3BO3 concentration increasing, as BO33- ions preferentially adsorb on the Ag (111) faces, thereby inhibit the growth of Ag on the (111) faces. Furthermore, the morphologies and dimensions of ANS are also found to strongly depend on the deposition temperature. Thinner and denser ANS are more easily obtained at low deposition temperature as it can suppress the surface diffusion of Ag atoms, while when the deposition temperature is high, thinner and denser ANS can only be obtained at high H3BO3 concentration. Especially, ANS fabricated with 0.5 M H3BO3 at 0 degrees C (ANS-0.5M-0 degrees C) with an ultrathin thickness of about 11 nm exhibits a remarkable CO Faradaic efficiency of 97.11% and the total current density of 11.50 mA cm(-2) at -0.9 V vs. the reversible hydrogen electrode towards CO2 electroreduction.

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