High-efficiency electrochemical H2O2 synthesis by heteroatom-doped NiX/Ni nanocomposites with honeycomb-like porous carbon

IF 15.7 1区 化学 Q1 CHEMISTRY, APPLIED Chinese Journal of Catalysis Pub Date : 2024-11-01 DOI:10.1016/S1872-2067(24)60121-X
Mengran Liu , Canyu Liu , Tianfang Yang , Shixiang Hu , Siyun Li , Shizhe Liu , Yang Liu , Ye Chen , Bingcheng Ge , Shuyan Gao
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Abstract

Transition metal Ni anchored in carbon material represents outstanding 2e oxygen reduction reaction (ORR) catalytic selectivity, but enhancing the adsorption strength of intermediate *OOH to promote its selectivity remains a major challenge. Herein, the NiX/Ni@NCHS composite catalyst with heteroatom doping (O,S) is modulated by controlling partial pyrolysis strategies on honeycomb-like porous carbon to manipulate the electronic structure of the metal Ni. With the synergistic effect of honeycomb structure and O atom, NiO/Ni@NCHS-700 exhibits an exceptional H2O2 selectivity of above 89.1% across a wide potential range from 0.1 to 0.6 V in an alkaline electrolyte, and an unexpected H2O2 production rate up to 1.47 mol gcat‒1 h‒1@0.2 V, which outperforms most of the state-of-the-art catalyst. Meanwhile, NiS/Ni@NCHS exhibits excellent electrocatalytic performance, with 2e ORR selectivity of 91.3%, H2O2 yield of 1.85 @0.3 V. Density functional theory simulations and experiments results reveal that the heteroatom doping (O,S) method has been employed to regulate the adsorption strength of Ni atoms with *OOH, and combined with the self-sacrificing template-assisted pyrolysis approach to improve the microstructure of catalysts and optimize the active site. The heteroatom doping method in this work provides significant guidance for promoting 2e ORR electrocatalysis to produce H2O2.
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杂原子掺杂的 NiX/Ni 纳米复合材料与蜂窝状多孔碳高效电化学合成 H2O2
锚定在碳材料中的过渡金属镍具有出色的2e-氧还原反应(ORR)催化选择性,但增强中间体*OOH的吸附强度以提高其选择性仍是一大挑战。在此,通过控制蜂窝状多孔碳的部分热解策略,调控金属镍的电子结构,从而制备出具有杂原子掺杂(O,S)的NiX/Ni@NCHS复合催化剂。在蜂窝状结构和 O 原子的协同作用下,NiO/Ni@NCHS-700 在碱性电解质中 0.1 至 0.6 V 的宽电位范围内表现出超过 89.1% 的优异 H2O2 选择性,H2O2 生成率也出乎意料地高达 1.47 mol gcat-1 h-1@0.2 V,优于大多数最先进的催化剂。密度泛函理论模拟和实验结果表明,采用杂原子掺杂(O,S)方法调节了镍原子与*OOH的吸附强度,并结合自牺牲模板辅助热解方法改善了催化剂的微观结构,优化了活性位点。这项工作中的杂原子掺杂方法为促进 2e- ORR 电催化产生 H2O2 提供了重要指导。
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来源期刊
Chinese Journal of Catalysis
Chinese Journal of Catalysis 工程技术-工程:化工
CiteScore
25.80
自引率
10.30%
发文量
235
审稿时长
1.2 months
期刊介绍: The journal covers a broad scope, encompassing new trends in catalysis for applications in energy production, environmental protection, and the preparation of materials, petroleum chemicals, and fine chemicals. It explores the scientific foundation for preparing and activating catalysts of commercial interest, emphasizing representative models.The focus includes spectroscopic methods for structural characterization, especially in situ techniques, as well as new theoretical methods with practical impact in catalysis and catalytic reactions.The journal delves into the relationship between homogeneous and heterogeneous catalysis and includes theoretical studies on the structure and reactivity of catalysts.Additionally, contributions on photocatalysis, biocatalysis, surface science, and catalysis-related chemical kinetics are welcomed.
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