Selective Electrochemical CO2-to-Syngas Conversion Enabled by Electronic-Structure-Modulated Copper-Zinc Alloy Nanosheets

IF 13 2区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Small Pub Date : 2025-05-30 DOI:10.1002/smll.202501030
Ruyu Zou, Rui Luo, Fanghuang Liu, Yan Wang, Muhammad Sohail Riaz, Shuling Shen, Guangzhi Yang, Zhihong Tang, Hengbo Huang, Guisheng Li, Qingyuan Bi
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Abstract

Developing cost-effective materials for efficient selective electrochemical CO2-to-syngas under actionable conditions is a practical and promising way to sustain low-carbon energy supplies, which remains a significant challenge. Herein, the efficient CuZn alloy nanosheets with prominent electronic structure modulation and alloy effect and the active CuZn5 phase are successfully fabricated by the facile electrodeposition strategy are reported. The electronic synergy via electron transferring from Zn to Cu can influence the catalyst's surface electron density and thus regulate the chemical adsorption properties of both small molecules and the key step of C═O bond cleavage. Significantly, the engineered Cu0.07 Zn alloy catalyst achieves an outstanding electrochemical CO2-to-syngas conversion, accompanying Faraday efficiency of near 100% and a high production rate of syngas with tunable CO/H2 ratio of 1.1 to 4.3 over a wide potential range of −0.65 to −1.25 V as well as excellent stability in CO2-saturated 0.1 m KHCO3 system. Moreover, the comprehensive understanding of the alloy phase evolution, electronic structure modulation, structure-activity relationship, and possible CO2-to-syngas conversion mechanism involving the rate-determining step of C═O bond breakage to *CO species over the versatile CuZn alloy catalyst via theoretical calculations and in situ spectroscopy is demonstrated.

Abstract Image

电子结构调制铜锌合金纳米片实现co2到合成气的选择性电化学转换
在可行的条件下,开发具有成本效益的材料,用于高效的选择性电化学二氧化碳制合成气,是维持低碳能源供应的一种实用而有希望的方法,但这仍然是一项重大挑战。本文报道了采用简易电沉积策略成功制备出具有显著电子结构调制和合金效应的高效CuZn合金纳米片和活性CuZn5相。通过电子从Zn转移到Cu的电子协同作用可以影响催化剂的表面电子密度,从而调节小分子的化学吸附性能和C = O键裂解的关键步骤。值得注意的是,设计的Cu0.07 Zn合金催化剂实现了出色的电化学co2 -合成气转化,法拉第效率接近100%,合成气产量高,CO/H2比为1.1至4.3,在−0.65至−1.25 V的宽电位范围内可调,并且在co2饱和的0.1 m KHCO3体系中具有优异的稳定性。此外,通过理论计算和原位光谱分析,全面了解了合金的相演化、电子结构调制、构效关系以及可能的二氧化碳到合成气的转化机制,包括在通用CuZn合金催化剂上C = O键断裂到*CO物种的速率决定步骤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Small
Small 工程技术-材料科学:综合
CiteScore
17.70
自引率
3.80%
发文量
1830
审稿时长
2.1 months
期刊介绍: Small serves as an exceptional platform for both experimental and theoretical studies in fundamental and applied interdisciplinary research at the nano- and microscale. The journal offers a compelling mix of peer-reviewed Research Articles, Reviews, Perspectives, and Comments. With a remarkable 2022 Journal Impact Factor of 13.3 (Journal Citation Reports from Clarivate Analytics, 2023), Small remains among the top multidisciplinary journals, covering a wide range of topics at the interface of materials science, chemistry, physics, engineering, medicine, and biology. Small's readership includes biochemists, biologists, biomedical scientists, chemists, engineers, information technologists, materials scientists, physicists, and theoreticians alike.
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