策略性掺杂镍改善了 Bi3O4Br 在碱性水中的电催化 H2 产率

IF 3.2 Q2 CHEMISTRY, PHYSICAL Energy advances Pub Date : 2024-05-24 DOI:10.1039/D4YA00228H
Manodip Pal, Rathindranath Biswas, Sanmitra Barman and Arnab Dutta
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引用次数: 0

摘要

为氢进化反应(HER)建立一种经济高效的电催化途径是我们实现碳中和能源格局的关键。我们报告了一种简单直接的方法来合成高效、稳定和低成本的无贵金属 Bi3O4Br 电催化剂。在 Bi3O4Br 中战术性地掺入镍离子可有效提高电导率,加速电荷转移过程,并提供更多的催化活性位点,从而显著提高 Bi3O4Br 的碱性电化学 HER 性能。 这种掺镍的 Bi3O4Br 在更高的电流密度(100 mA/cm2)下工作时,能量效率提高了 17%。此外,与原始 Bi3O4Br 相比,这种掺杂材料的 HER 动力学在塔菲尔斜率方面也提高了 35%,这与质量活性的显著提高(从 52 A/g 提高到 98 A/g)相吻合。值得注意的是,掺杂镍的 Bi3O4Br 在光电化学 HER 性能中的过电位进一步降低了 23%,法拉第效率提高了 10%。最后,掺杂镍后,Bi3O4Br 材料的耐久性得到了提高。因此,这一策略强调了通过合理掺杂来揭示丰富材料的升级催化行为的重要性。
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Strategic Ni-doping improved electrocatalytic H2 production by Bi3O4Br in alkaline water†

Establishing a cost-effective and efficient electrocatalytic pathway for the hydrogen evolution reaction (HER) is the key to our quest for a carbon-neutral energy landscape. We report a simple and straightforward approach to synthesize an efficient, stable, and low-cost noble metal-free Bi3O4Br electrocatalyst. Tactical doping of Ni ions into Bi3O4Br effectively enhanced the conductivity, accelerated the charge transfer process, and provided more catalytic active sites to significantly boost the alkaline electrochemical HER performance of Bi3O4Br. This Ni-doped Bi3O4Br exhibited a lower overpotential of 662 mV compared to that of Bi3O4Br (736 mV) at a higher current density (50 mA cm−2). Additionally, the HER kinetics were also enhanced in terms of Tafel slope for this doped material (159 mV dec−1) compared to the pristine Bi3O4Br (245 mV dec−1), which coincides with a significant improvement in the mass activity (52 A g−1 to 98 A g−1). Notably, the overpotential of Ni-doped Bi3O4Br was further reduced to 614 mV at the same current density of 50 mA cm−2 during photoelectrochemical HER performance testing, and the faradaic efficiency was improved from 79% to 87%. Finally, an enhanced durability of the material was observed for Bi3O4Br following the Ni-doping. Hence, this strategy highlights the importance of unravelling upgraded catalytic behaviour for abundant materials with rational doping.

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