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微流控辅助合成分级结构的CuO纳米晶体作为C选择性CO还原电催化剂

Microfluidics-Assisted Synthesis of Hierarchical Cu O Nanocrystal as C -Selective CO Reduction Electrocatalyst.

作者信息

Jun Minki, Kwak Changmo, Lee Si Young, Joo Jinwhan, Kim Ji Min, Im Do Jin, Cho Min Kyung, Baik Hionsuck, Hwang Yun Jeong, Kim Heejin, Lee Kwangyeol

机构信息

Department of Chemistry and Research Institute for Natural Science, Korea University, Seoul, 02841, Republic of Korea.

Department of Chemistry, Seoul National University, Seoul, 08826, Republic of Korea.

出版信息

Small Methods. 2022 May;6(5):e2200074. doi: 10.1002/smtd.202200074. Epub 2022 Feb 25.

DOI:10.1002/smtd.202200074
PMID:35212468
Abstract

Copper-based catalysts have attracted enormous attention due to their high selectivity for C products during the electrochemical reduction of CO (CO RR). In particular, grain boundaries on the catalysts contribute to the generation of various Cu coordination environments, which have been found essential for C-C coupling. However, smooth-surfaced Cu O nanocrystals generally lack the ability for the surface reorganization to form multiple grain boundaries and desired Cu undercoordination sites. Flow chemistry armed with the unparalleled ability to mix reaction mixture can achieve a very high concentration of unstable reaction intermediates, which in turn are used up rapidly to lead to kinetics-driven nanocrystal growth. Herein, the synthesis of a unique hierarchical structure of Cu O with numerous steps (h-Cu O ONS) via flow chemistry-assisted modulation of nanocrystal growth kinetics is reported. The surface of h-Cu O ONS underwent rapid surface reconstruction under CO RR conditions to exhibit multiple heterointerfaces between Cu O and Cu phases, setting the preferable condition to facilitate C-C bond formation. Notably, the h-Cu O ONS obtained the increased C H Faradaic efficiency from 31.9% to 43.5% during electrocatalysis concurrent with the morphological reorganization, showing the role of the stepped surface. Also, the h-Cu O ONS demonstrated a 3.8-fold higher ethylene production rate as compared to the Cu O nanocube.

摘要

铜基催化剂因其在电化学还原CO(CO RR)过程中对C产物具有高选择性而备受关注。特别是,催化剂上的晶界有助于形成各种铜配位环境,已发现这些环境对于C-C偶联至关重要。然而,表面光滑的CuO纳米晶体通常缺乏表面重组以形成多个晶界和所需的铜低配位位点的能力。具有无与伦比的混合反应混合物能力的流动化学可以实现非常高浓度的不稳定反应中间体,这些中间体又会迅速消耗,从而导致动力学驱动的纳米晶体生长。在此,报道了通过流动化学辅助调节纳米晶体生长动力学合成具有众多台阶的独特分级结构的CuO(h-CuO ONS)。在CO RR条件下,h-CuO ONS的表面经历了快速的表面重构,以在CuO和Cu相之间呈现多个异质界面,为促进C-C键形成设定了有利条件。值得注意的是,在电催化过程中,随着形态重组,h-CuO ONS的C2H4法拉第效率从31.9%提高到43.5%,显示了台阶表面的作用。此外,与CuO纳米立方体相比,h-CuO ONS的乙烯生成速率高出3.8倍。

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