镍
催化作用
阳极
纳米颗粒
材料科学
吸附
化学工程
碳纤维
阴极
电催化剂
纳米技术
无机化学
化学
电化学
物理化学
电极
冶金
工程类
复合数
复合材料
生物化学
作者
Wenhao Ren,Xin Tan,Chen Jia,Anna Krammer,Qian Sun,Jiangtao Qu,Sean Campbell Smith,Andreas Schueler,Xile Hu,Chuan Zhao
标识
DOI:10.1002/ange.202203335
摘要
Abstract Electrocatalytic CO2 to CO conversion is approaching the industrial benchmark. Currently, Au electrodes show the best performance, whereas non-precious metal catalysts exhibit inferior activity. Here we show a densely populated Ni single-atom on nanoparticle catalyst (NiSA/NP) via direct solid-sate pyrolysis, where Ni nanoparticles donate electrons to Ni(i)-N-C sites via carbon nanotubes network, achieves a high CO current of 352 mA cm−2 at -0.55 V vs RHE in an alkaline flow cell. When coupled with a NiFe-based oxygen evolution anode into a zero-gap membrane electrolyser, it delivers an industrial-relevant CO current of 310 mA cm−2 at a low cell voltage of -2.3 V, corresponding to an overall energy efficiency of 57%. The superior CO2 electroreduction performance is attributed to the enhanced adsorption of key intermediate COOH* on electron-rich Ni single atom, together with the dense active sites.
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