跨尺度强化锭状氧化铜支撑钨单原子催化剂以提高电化学制氢能力

IF 24.4 1区 材料科学 Q1 CHEMISTRY, PHYSICAL Advanced Energy Materials Pub Date : 2024-10-15 DOI:10.1002/aenm.202402825
Chaoqun Chang, Xiaodong Li, Shizhong Wei, Yang Zhao, Lihua Gong, Yonghui Zhang, Jian Liu, Feilong Gong
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引用次数: 0

摘要

电催化剂的过程强化工程对于促进电催化反应至关重要,而其跨尺度调控则是一项巨大挑战。本文报告了具有可调中尺度电场和原子尺度配位结构的锭状氧化铜支撑钨单原子催化剂(W SACs),旨在增强电化学氢气进化过程。有限元分析表明,通过将主轴配置的尖端角度从 74° 调整到 27°,可以增强中尺度电场,从而将产氢率提高 5 倍。根据密度泛函理论计算,构型调节还能增加 W-O 的配位数,从而增加电荷转移并使 d 带中心下移,稳定 W 位点并优化氢气解吸过程。与制备的 WSA/CuO-56 和 WSA/CuO-74 类似物相比,优化后的 WSA/CuO-27 表现出更好的氢进化活性(η100 = 94 mV)和稳定性(200 mA cm-2 持续 120 小时)。令人印象深刻的是,使用 WSA/CuO-27 制备的阴离子交换膜电解槽具有与商用电催化剂相当的优异活性,并且在连续电催化 120 小时后,在 300 mA cm-2 下具有 0.085 mA cm-2 h-1 的超低衰减。
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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Cross-Scale Process Intensification of Spindle CuO Supported Tungsten Single-Atom Catalysts toward Enhanced Electrochemical Hydrogen Production
Process intensification engineering of electrocatalysts is crucial to facilitate electrocatalytic reaction, while its cross-scale modulation is of great challenge. Herein, the spindle CuO supported tungsten single-atom catalysts (W SACs) with tunable mesoscale electric field and atomic-scale coordination structure are reported toward enhanced electrochemical hydrogen evolution process. Finite element analysis indicates the mesoscale electric field can be enhanced by tailoring the tip angle of spindle configuration from 74° to 27°, enhancing hydrogen production rate by 5 times. Based on the density functional theory calculations, the configuration regulation also triggers the increase of coordination number of W–O, which increases charge transfer and downshifts d-band center, stabilizing W sites and optimizing hydrogen desorption process. The optimized WSA/CuO-27 exhibits much better hydrogen evolution activity (η100 = 94 mV) and stability (200 mA cm−2 for 120 h) than as-prepared WSA/CuO-56 and WSA/CuO-74 analogues. Impressively, the anion exchange membrane electrolyzer fabricated with the WSA/CuO-27 presents excellent activity comparable to that of commercial electrocatalysts, and also delivers an ultra-low attenuation of 0.085 mA cm−2 h−1 at 300 mA cm−2 after continuous electrocatalysis for 120 h. This work inspires the design of high-efficiency supported metal catalysts for electrochemical synthesis via the cross-scale process intensification engineering.
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来源期刊
Advanced Energy Materials
Advanced Energy Materials CHEMISTRY, PHYSICAL-ENERGY & FUELS
CiteScore
41.90
自引率
4.00%
发文量
889
审稿时长
1.4 months
期刊介绍: Established in 2011, Advanced Energy Materials is an international, interdisciplinary, English-language journal that focuses on materials used in energy harvesting, conversion, and storage. It is regarded as a top-quality journal alongside Advanced Materials, Advanced Functional Materials, and Small. With a 2022 Impact Factor of 27.8, Advanced Energy Materials is considered a prime source for the best energy-related research. The journal covers a wide range of topics in energy-related research, including organic and inorganic photovoltaics, batteries and supercapacitors, fuel cells, hydrogen generation and storage, thermoelectrics, water splitting and photocatalysis, solar fuels and thermosolar power, magnetocalorics, and piezoelectronics. The readership of Advanced Energy Materials includes materials scientists, chemists, physicists, and engineers in both academia and industry. The journal is indexed in various databases and collections, such as Advanced Technologies & Aerospace Database, FIZ Karlsruhe, INSPEC (IET), Science Citation Index Expanded, Technology Collection, and Web of Science, among others.
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