{"title":"Synergistic lactic acid dehydrogenation and hydrogen evolution catalyzed by an electrodeposited Ni–Co alloy on rGO-SWCNTs","authors":"Xiaojun Su, Qing Wan, Congming Tang and Xinli Li","doi":"10.1039/D5NJ02635K","DOIUrl":null,"url":null,"abstract":"<p >We investigated the synergistic coupling of lactic acid direct dehydrogenation (LAOR) and the hydrogen evolution reaction (HER) in acidic media using a Ni–Co alloy catalyst supported on reduced graphene oxide-single-walled carbon nanotubes (rGO-SWCNTs). Compared with pristine Ni or Co, the Ni–Co alloy exhibited superior activity for both the HER and LAOR. Specifically, the CoNi11 alloy (Co/Ni = 1) demonstrated exceptional HER performance, achieving a low overpotential of 162.2 mV (<em>vs.</em> RHE) at 10 mA cm<small><sup>−2</sup></small>, a Tafel slope of 69.2 mV dec<small><sup>−1</sup></small>, and a high electrochemically active surface area (ECSA) of 200.3 mF cm<small><sup>−2</sup></small>. At the anode, the LAOR selectively produced pyruvic acid (PA) and hydrogen <em>via</em> direct dehydrogenation, dominating over the oxygen evolution reaction (OER). The PA selectivity was significantly enhanced to 90% with the addition of Br<small><sup>−</sup></small>. Crucially, the CoNi11 catalyst displayed excellent stability during three consecutive electrochemical cycles and a 12-hour chronopotentiometric operation. This work provides an efficient strategy for the co-production of renewable hydrogen and value-added pyruvic acid using Ni–Co alloy catalysts.</p>","PeriodicalId":95,"journal":{"name":"New Journal of Chemistry","volume":" 38","pages":" 16559-16569"},"PeriodicalIF":2.5000,"publicationDate":"2025-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"New Journal of Chemistry","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/nj/d5nj02635k","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
We investigated the synergistic coupling of lactic acid direct dehydrogenation (LAOR) and the hydrogen evolution reaction (HER) in acidic media using a Ni–Co alloy catalyst supported on reduced graphene oxide-single-walled carbon nanotubes (rGO-SWCNTs). Compared with pristine Ni or Co, the Ni–Co alloy exhibited superior activity for both the HER and LAOR. Specifically, the CoNi11 alloy (Co/Ni = 1) demonstrated exceptional HER performance, achieving a low overpotential of 162.2 mV (vs. RHE) at 10 mA cm−2, a Tafel slope of 69.2 mV dec−1, and a high electrochemically active surface area (ECSA) of 200.3 mF cm−2. At the anode, the LAOR selectively produced pyruvic acid (PA) and hydrogen via direct dehydrogenation, dominating over the oxygen evolution reaction (OER). The PA selectivity was significantly enhanced to 90% with the addition of Br−. Crucially, the CoNi11 catalyst displayed excellent stability during three consecutive electrochemical cycles and a 12-hour chronopotentiometric operation. This work provides an efficient strategy for the co-production of renewable hydrogen and value-added pyruvic acid using Ni–Co alloy catalysts.
我们利用还原氧化石墨烯-单壁碳纳米管(rGO-SWCNTs)负载的镍钴合金催化剂,研究了酸性介质中乳酸直接脱氢(LAOR)和析氢反应(HER)的协同耦合。与原始Ni或Co合金相比,Ni - Co合金在HER和LAOR中表现出更强的活性。具体来说,CoNi11合金(Co/Ni = 1)表现出优异的HER性能,在10 mA cm - 2时的过电位为162.2 mV(相对于RHE), Tafel斜率为69.2 mV dec - 1,电化学活性表面积(ECSA)为200.3 mF cm - 2。在阳极,LAOR通过直接脱氢选择性地生成丙酮酸(PA)和氢气,主导析氧反应(OER)。添加Br−后,PA的选择性显著提高到90%。关键是,CoNi11催化剂在连续三个电化学循环和12小时的计时电位操作中表现出优异的稳定性。本研究为镍钴合金催化剂协同生产可再生氢和增值丙酮酸提供了一种有效的策略。