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用于锌-银-氧催化剂的“瓶中双船”设计实现选择性和持久的CO电还原

"Two Ships in a Bottle" Design for Zn-Ag-O Catalyst Enabling Selective and Long-Lasting CO Electroreduction.

作者信息

Zhang Zhen, Wen Guobin, Luo Dan, Ren Bohua, Zhu Yanfei, Gao Rui, Dou Haozhen, Sun Guiru, Feng Ming, Bai Zhengyu, Yu Aiping, Chen Zhongwei

机构信息

Department of Chemical Engineering, Waterloo Institute for Nanotechnology, Waterloo Institute for Sustainable Energy, University of Waterloo, Waterloo, Ontario N2L 3G1, Canada.

Key Laboratory of Functional Materials Physics and Chemistry of the Ministry of Education, Jilin Normal University, Changchun 130103, China.

出版信息

J Am Chem Soc. 2021 May 12;143(18):6855-6864. doi: 10.1021/jacs.0c12418. Epub 2021 Apr 14.

DOI:10.1021/jacs.0c12418
PMID:33852301
Abstract

Electrochemical CO reduction (CORR) using renewable energy sources represents a sustainable means of producing carbon-neutral fuels. Unfortunately, low energy efficiency, poor product selectivity, and rapid deactivation are among the most intractable challenges of CORR electrocatalysts. Here, we strategically propose a "two ships in a bottle" design for ternary Zn-Ag-O catalysts, where ZnO and Ag phases are twinned to constitute an individual ultrafine nanoparticle impregnated inside nanopores of an ultrahigh-surface-area carbon matrix. Bimetallic electron configurations are modulated by constructing a Zn-Ag-O interface, where the electron density reconfiguration arising from electron delocalization enhances the stabilization of the COOH intermediate favorable for CO production, while promoting CO selectivity and suppressing HCOOH generation by altering the rate-limiting step toward a high thermodynamic barrier for forming HCOO. Moreover, the pore-constriction mechanism restricts the bimetallic particles to nanosized dimensions with abundant Zn-Ag-O heterointerfaces and exposed active sites, meanwhile prohibiting detachment and agglomeration of nanoparticles during CORR for enhanced stability. The designed catalysts realize 60.9% energy efficiency and 94.1 ± 4.0% Faradaic efficiency toward CO, together with a remarkable stability over 6 days. Beyond providing a high-performance CORR electrocatalyst, this work presents a promising catalyst-design strategy for efficient energy conversion.

摘要

利用可再生能源进行电化学一氧化碳还原(CORR)是生产碳中和燃料的一种可持续方式。不幸的是,低能量效率、差的产物选择性和快速失活是CORR电催化剂最棘手的挑战。在此,我们战略性地提出了一种用于三元Zn-Ag-O催化剂的“瓶中双船”设计,其中ZnO和Ag相孪晶形成单个超细纳米颗粒,浸渍在超高表面积碳基质的纳米孔内。通过构建Zn-Ag-O界面来调节双金属电子构型,其中由电子离域引起的电子密度重新配置增强了有利于CO生成的COOH中间体的稳定性,同时通过将限速步骤改变为形成HCOO的高热力学势垒来提高CO选择性并抑制HCOOH生成。此外,孔收缩机制将双金属颗粒限制在具有丰富Zn-Ag-O异质界面和暴露活性位点的纳米尺寸,同时在CORR期间禁止纳米颗粒的脱离和团聚以提高稳定性。所设计的催化剂实现了60.9%的能量效率和94.1±4.0%的CO法拉第效率,以及超过6天的显著稳定性。除了提供一种高性能的CORR电催化剂外,这项工作还提出了一种用于高效能量转换的有前景的催化剂设计策略。

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