Asymmetrically Coordinated Calcium Single Atom for High-Performance Oxygen Reduction Reaction

IF 4.3 2区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR Inorganic Chemistry Pub Date : 2024-06-27 DOI:10.1021/acs.inorgchem.4c02178
Yan Yang, Gang Wang, Changwei Liu, Yutao Lin, Chi Jiao, Qingqing Chen, Zhiwen Zhuo*, Junjie Mao* and Yan Liu*, 
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Abstract

S-block single atoms represent an ideal catalyst for the oxygen reduction reaction (ORR) as they can suppress the Fenton reaction. However, the symmetry of the s/p orbitals tends to generate either an excessively strong or weak interaction with intermediates. Herein, Ca single atoms coordinated with -S, -OP, and three N atoms (Ca/NPS-HC) were fabricated to modulate the adsorption of intermediates and promote the efficiency of s-block ORR catalysts. The experimental results from ORR demonstrated that the Ca/NPS-HC catalyst exhibited outstanding catalytic capability with a half-wave potential of 0.89 V, a kinetic current density of 56.6 mA cm–2 at 0.85 V, and a Tafel slope of 42 mV dec–1, outperforming commercial Pt/C. The detailed mechanistic studies revealed that the asymmetric coordination of Ca single atoms led to the symmetry-breaking of electron distribution in Ca single atoms, attenuating the s-p hybridization from the intermediate adsorption process, and thereby minimizing the energy barrier of the whole ORR.

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用于高性能氧还原反应的不对称配位钙单原子
S 块单原子是氧还原反应(ORR)的理想催化剂,因为它们可以抑制芬顿反应。然而,s/p 轨道的对称性往往会与中间产物产生过强或过弱的相互作用。在此,我们制作了与 -S、-OP 和三个 N 原子配位的 Ca 单原子(Ca/NPS-HC),以调节中间产物的吸附,提高 s-block ORR 催化剂的效率。ORR 实验结果表明,Ca/NPS-HC 催化剂的半波电位为 0.89 V,0.85 V 时的动力学电流密度为 56.6 mA cm-2,Tafel 斜率为 42 mV dec-1,催化能力优于商用 Pt/C。详细的机理研究表明,钙单质原子的不对称配位打破了钙单质原子电子分布的对称性,减弱了中间吸附过程的s-p杂化,从而最大限度地降低了整个ORR的能垒。
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来源期刊
Inorganic Chemistry
Inorganic Chemistry 化学-无机化学与核化学
CiteScore
7.60
自引率
13.00%
发文量
1960
审稿时长
1.9 months
期刊介绍: Inorganic Chemistry publishes fundamental studies in all phases of inorganic chemistry. Coverage includes experimental and theoretical reports on quantitative studies of structure and thermodynamics, kinetics, mechanisms of inorganic reactions, bioinorganic chemistry, and relevant aspects of organometallic chemistry, solid-state phenomena, and chemical bonding theory. Emphasis is placed on the synthesis, structure, thermodynamics, reactivity, spectroscopy, and bonding properties of significant new and known compounds.
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