调节电子分布加速CO2光催化还原为C2H4

IF 16 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Chao An, Yu Nie, Jian-Hua Mei, Xin Tan, Zhuofeng Hu*, Jinhua Ye and Tao Yu*, 
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引用次数: 0

摘要

如何提高C-C耦合效率是光催化还原CO2制C2H4过程中的瓶颈问题。本文通过在CoS2中植入Ga原子,合成了一种将CO2转化为C2H4的高效光催化剂(产率为~ 12.45 μmol h-1,选择性为~ 94.5%)。Ga促进原始CoS2上相邻硫空位的形成,由于硫空位周围的电子离域,导致Co原子周围的电子分布高度不对称。理论计算证明,不对称的电子分布增强了相邻原子之间的吸引力,使得相邻Coδ+ (δ = 2,3)原子之间的距离从3.91缩短到2.49 Å。相邻Coδ+的共存使得d带中心更接近费米能级,有利于*CO的强吸附和随后的*COCO二聚化。Ga-CoS2上相邻Coδ+原子之间的不对称电子结构为C-C偶联提供了较低的激活势垒,从而显著促进了C2H4的形成。本研究提出了一种调节CO2光催化还原为C2H4的选择性的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Regulating the Electron Distribution to Accelerate the Photocatalytic Reduction of CO2 to C2H4

Regulating the Electron Distribution to Accelerate the Photocatalytic Reduction of CO2 to C2H4

How to promote the efficiency of C–C coupling is a bottleneck problem in the process of the photocatalytic reduction of CO2 to C2H4. Herein, a highly efficient photocatalyst for converting CO2 into C2H4 (with a yield of ∼12.45 μmol h–1 and a selectivity of ∼94.5%) was synthesized by implanting Ga atoms in CoS2. Ga promotes the formation of neighboring sulfur vacancies on pristine CoS2, which induces a highly asymmetric distribution of electrons around Co atoms due to the delocalization of electrons around sulfur vacancies. Theoretical calculations prove that the asymmetric electron distribution enhances the attraction between adjacent atoms, leading to a shortened distance between adjacent Coδ+ (δ = 2, 3) atoms from 3.91 to 2.49 Å. The coexistence of adjacent Coδ+ makes the d-band center closer to the Fermi level, which is conducive to the strong adsorption of *CO and subsequent *COCO dimerization. The asymmetric electronic structure between adjacent Coδ+ atoms on Ga-CoS2 provides a lower activation barrier for C–C coupling, thereby significantly promoting C2H4 formation. This study proposes a strategy to modulate the selectivity of the photocatalytic reduction of CO2 to C2H4.

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来源期刊
ACS Nano
ACS Nano 工程技术-材料科学:综合
CiteScore
26.00
自引率
4.10%
发文量
1627
审稿时长
1.7 months
期刊介绍: ACS Nano, published monthly, serves as an international forum for comprehensive articles on nanoscience and nanotechnology research at the intersections of chemistry, biology, materials science, physics, and engineering. The journal fosters communication among scientists in these communities, facilitating collaboration, new research opportunities, and advancements through discoveries. ACS Nano covers synthesis, assembly, characterization, theory, and simulation of nanostructures, nanobiotechnology, nanofabrication, methods and tools for nanoscience and nanotechnology, and self- and directed-assembly. Alongside original research articles, it offers thorough reviews, perspectives on cutting-edge research, and discussions envisioning the future of nanoscience and nanotechnology.
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