Qi Kun, Zhang Yang, Li Ji, Charmette Christophe, Ramonda Michel, Cui Xiaoqiang, Wang Ying, Zhang Yupeng, Wu Huali, Wang Wensen, Zhang Xiaolin, Voiry Damien
Institut Européen des Membranes, IEM, UMR 5635, Université Montpellier, ENSCM, CNRS, Montpellier 34000, France.
Institute of Microscale Optoelectronics, Shenzhen University, Shenzhen, Guangdong 518060, China.
ACS Nano. 2021 Apr 27;15(4):7682-7693. doi: 10.1021/acsnano.1c01281. Epub 2021 Apr 16.
The electrochemical reduction of CO in a highly selective and efficient manner is a crucial step toward its reuse for the production of chemicals and fuels. Nanostructured Ag catalysts have been found to be effective candidates for the conversion of CO-to-CO. However, the ambiguous determination of the intrinsic CO activity and the maximization of the density of exposed active sites have greatly limited the use of Ag toward the realization of practical electrocatalytic devices. Here, we report a superstructure design strategy prepared by the self-assembly of two-dimensional Ag nanoprisms for maximizing the exposure of active edge ribs. The vertically stacked Ag nanoprisms allow the exposure of >95% of the edge sites, resulting in an enhanced selectivity and activity toward the production of CO from CO with an overpotential of 152 mV. The Ag superstructures also demonstrate a selectivity of over 90% for 100 h together with a current retention of ≈94% at -600 mV versus the reversible hydrogen electrode and a partial energy efficiency for CO production of 70.5%. Our electrochemical measurements on individual Ag nanoprisms with various edge-to-basal plane ratios and the Ag superstructures led to the identification of the edge ribs as the active sites thanks to the ≈400 mV decrease in the onset potential compared to that of the Ag (111) basal planes and a turnover frequency of 9.2 × 10 ± 1.9 × 10 s at 0 V overpotential.
以高度选择性和高效的方式对CO进行电化学还原是其再用于化学品和燃料生产的关键一步。已发现纳米结构的Ag催化剂是将CO转化为CO的有效候选物。然而,本征CO活性的不确定测定以及暴露活性位点密度的最大化极大地限制了Ag在实际电催化装置实现中的应用。在此,我们报道了一种通过二维Ag纳米棱镜自组装制备的超结构设计策略,以最大化活性边缘肋的暴露。垂直堆叠的Ag纳米棱镜可使>95%的边缘位点暴露,从而提高了从CO生产CO的选择性和活性,过电位为152 mV。Ag超结构在100 h内还表现出超过90%的选择性,在相对于可逆氢电极-600 mV时电流保持率约为94%,CO生产的部分能量效率为70.5%。我们对具有不同边缘与基面比率的单个Ag纳米棱镜和Ag超结构进行的电化学测量表明,由于与Ag(111)基面相比起始电位降低了约400 mV,且在0 V过电位下周转频率为9.2×10±1.9×10 s⁻¹,边缘肋是活性位点。