在工业电流密度下,硫调节的金属-支撑相互作用提高了海水中 Ru 簇的氢进化性能

EES catalysis Pub Date : 2024-05-24 DOI:10.1039/D4EY00076E
Ranran Tang, Ping Yan, Yitong Zhou and Xin-Yao Yu
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引用次数: 0

摘要

调节金属-支撑相互作用(MSI)是提高电催化剂催化活性的有效策略。在此,我们以 Ru 簇为示范,报告了一种在硫和氮共掺杂碳(Ru/SNC)空心球上锚定超细 Ru 纳米簇的混合电催化剂,用于在碱性电解质和实际海水中进行高效氢进化反应(HER)。玻璃碳电极上的最佳 Ru/SNC 空心球表现出卓越的氢进化活性,在碱性介质和碱性海水中的过电位分别仅为 18 和 23 mV,达到 10 mA cm-2。将 Ru/SNC 空心球装载到碳纸上时,只需要 171 毫伏(在碱性溶液中)和 205 毫伏(在碱性海水中)的小过电位,就能提供 1000 毫安厘米-2 的工业电流密度。此外,组装好的 Ru/SNC||RuO2 电解池在 2.3 V 的电池电压下显示出 1000 mA cm-2 的高电流密度,并且在 80 oC 的高温条件下,在碱性真实海水中以 1000 mA cm-2 的电流密度工作长达 100 小时,其稳定性令人印象深刻。密度泛函理论(DFT)计算表明,S掺杂能诱导Ru团簇和碳支撑之间产生强MSI,从而提高HER的活性和稳定性。S 掺杂会引发 d 波段中心下移,削弱 H* 在 Ru 簇上的吸附,从而增强氢外溢。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Sulfur-regulated metal–support interaction boosting the hydrogen evolution performance of Ru clusters in seawater at industrial current densities†

Sulfur-regulated metal–support interaction boosting the hydrogen evolution performance of Ru clusters in seawater at industrial current densities†

Regulating the metal–support interaction (MSI) is an effective strategy to enhance the catalytic activity of electrocatalysts. Herein, taking Ru clusters as an example, we report a hybrid electrocatalyst with ultrafine Ru nanoclusters anchored on sulfur and nitrogen co-doped carbon (Ru/SNC) hollow spheres for efficient hydrogen evolution reaction (HER) in an alkaline electrolyte and real seawater. The optimal Ru/SNC hollow spheres on a glassy carbon electrode exhibit superior HER activity, with small overpotentials of only 12 and 30 mV to reach 10 mA cm−2 in alkaline media and alkaline real seawater, respectively. When loaded on carbon paper, the Ru/SNC hollow spheres only need small overpotentials of 171 (in alkaline solution) and 205 mV (in alkaline real seawater) to deliver an industrial current density of 1000 mA cm−2. Furthermore, the assembled Ru/SNC||RuO2 electrolysis cell displays a high current density of 1000 mA cm−2 at a cell voltage of 2.3 V and impressive stability up to 100 h at a current density of 1000 mA cm−2 in alkaline real seawater at an elevated temperature of 80 °C. Density functional theory (DFT) calculations suggest that S-doping can induce a strong MSI between Ru clusters and the carbon support to boost the HER activity and stability. S-doping triggers the downshift of the d-band center, weakening the adsorption of H* on Ru clusters and thereby enhancing the hydrogen spillover.

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