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

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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Abstract

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.

Abstract Image

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
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。
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