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生长在多通道碳基质上的BiO纳米片用于催化高效的CO电还原为HCOOH。

Bi O Nanosheets Grown on Multi-Channel Carbon Matrix to Catalyze Efficient CO Electroreduction to HCOOH.

作者信息

Liu Subiao, Lu Xue Feng, Xiao Jing, Wang Xin, Lou Xiong Wen David

机构信息

School of Chemical and Biomedical Engineering, Nanyang Technological University, 62 Nanyang Drive, Singapore, 637459, Singapore.

Department of Chemical and Materials Engineering, University of Alberta, Edmonton, Alberta, T6G 1H7, Canada.

出版信息

Angew Chem Int Ed Engl. 2019 Sep 23;58(39):13828-13833. doi: 10.1002/anie.201907674. Epub 2019 Aug 16.

Abstract

Bi O nanosheets were grown on a conductive multiple channel carbon matrix (MCCM) for CO RR. The obtained electrocatalyst shows a desirable partial current density of ca. 17.7 mA cm at a moderate overpotential, and it is highly selective towards HCOOH formation with Faradaic efficiency approaching 90 % in a wide potential window and its maximum value of 93.8 % at -1.256 V. It also exhibits a maximum energy efficiency of 55.3 % at an overpotential of 0.846 V and long-term stability of 12 h with negligible degradation. The superior performance is attributed to the synergistic contribution of the interwoven MCCM and the hierarchical Bi O nanosheets, where the MCCM provides an accelerated electron transfer, increased CO adsorption, and a high ratio of pyrrolic-N and pyridinic-N, while ultrathin Bi O nanosheets offer abundant active sites, lowered contact resistance and work function as well as a shortened diffusion pathway for electrolyte.

摘要

在用于CO RR的导电多通道碳基质(MCCM)上生长了BiO纳米片。所获得的电催化剂在适度的过电位下显示出约17.7 mA cm的理想分电流密度,并且在宽电位窗口中对HCOOH形成具有高度选择性,法拉第效率接近90%,在-1.256 V时其最大值为93.8%。在0.846 V的过电位下,它还表现出55.3%的最大能量效率以及12小时的长期稳定性,降解可忽略不计。优异的性能归因于交织的MCCM和分级BiO纳米片的协同作用,其中MCCM提供加速的电子转移、增加的CO吸附以及高比例的吡咯氮和吡啶氮,而超薄BiO纳米片提供丰富的活性位点、降低的接触电阻和功函数以及缩短的电解质扩散路径。

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