{"title":"晶格氢参与的钯氢化物茂金属气凝胶用于高效氢进化反应","authors":"Hengjia Wang, Ying Qin, Yu Wu, Yiwei Qiu, Ling Ling, Qie Fang, Canglong Wang, Liuyong Hu, Wenling Gu, Chengzhou Zhu","doi":"10.1038/s41467-024-54601-7","DOIUrl":null,"url":null,"abstract":"<p>Hydrogen adsorption and desorption in single-phase catalysts often occur at a single catalytic site based on the traditional hydrogen evolution reaction (HER) pathway, which makes it difficult to break the limitation entailed by the Sabatier principle. Herein, β-Pd hydride metallene (β-PdHene) aerogels are synthesized as advanced HER catalysts. A lattice hydrogen-involved mechanism is reported to separate adsorption and desorption sites, which is thermodynamically favorable compared to the traditional reaction pathway. In situ differential electrochemical mass spectrometry and theoretical calculations reveal that lattice hydrogen as additional active sites directly participate in the HER process. Consequently, β-PdHene aerogels exhibit a low overpotential of only 20 mV at 10 mA cm<sup>−2</sup> and remarkable HER stability, which are even comparable to commercial Pt/C. Our work opens an avenue to rationally develop highly active HER catalysts, bypassing the design limitations of catalysts under traditional mechanisms.</p>","PeriodicalId":19066,"journal":{"name":"Nature Communications","volume":"22 1","pages":""},"PeriodicalIF":14.7000,"publicationDate":"2024-11-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Pd hydride metallene aerogels with lattice hydrogen participation for efficient hydrogen evolution reaction\",\"authors\":\"Hengjia Wang, Ying Qin, Yu Wu, Yiwei Qiu, Ling Ling, Qie Fang, Canglong Wang, Liuyong Hu, Wenling Gu, Chengzhou Zhu\",\"doi\":\"10.1038/s41467-024-54601-7\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Hydrogen adsorption and desorption in single-phase catalysts often occur at a single catalytic site based on the traditional hydrogen evolution reaction (HER) pathway, which makes it difficult to break the limitation entailed by the Sabatier principle. Herein, β-Pd hydride metallene (β-PdHene) aerogels are synthesized as advanced HER catalysts. A lattice hydrogen-involved mechanism is reported to separate adsorption and desorption sites, which is thermodynamically favorable compared to the traditional reaction pathway. In situ differential electrochemical mass spectrometry and theoretical calculations reveal that lattice hydrogen as additional active sites directly participate in the HER process. Consequently, β-PdHene aerogels exhibit a low overpotential of only 20 mV at 10 mA cm<sup>−2</sup> and remarkable HER stability, which are even comparable to commercial Pt/C. Our work opens an avenue to rationally develop highly active HER catalysts, bypassing the design limitations of catalysts under traditional mechanisms.</p>\",\"PeriodicalId\":19066,\"journal\":{\"name\":\"Nature Communications\",\"volume\":\"22 1\",\"pages\":\"\"},\"PeriodicalIF\":14.7000,\"publicationDate\":\"2024-11-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nature Communications\",\"FirstCategoryId\":\"103\",\"ListUrlMain\":\"https://doi.org/10.1038/s41467-024-54601-7\",\"RegionNum\":1,\"RegionCategory\":\"综合性期刊\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MULTIDISCIPLINARY SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature Communications","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.1038/s41467-024-54601-7","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
引用次数: 0
摘要
根据传统的氢进化反应(HER)途径,单相催化剂中的氢吸附和解吸通常发生在单一催化位点上,因此很难打破萨巴蒂尔原理的限制。在此,我们合成了β-钯氢化物茂金属(β-PdHene)气凝胶作为先进的氢进化反应催化剂。据报道,一种晶格氢参与机制分离了吸附和解吸位点,与传统反应途径相比,这种机制在热力学上是有利的。原位差分电化学质谱法和理论计算显示,晶格氢作为额外的活性位点直接参与了 HER 过程。因此,β-钯烯气凝胶在 10 mA cm-2 条件下的过电位很低,仅为 20 mV,而且具有显著的 HER 稳定性,甚至可与商用 Pt/C 相媲美。我们的工作为合理开发高活性 HER 催化剂开辟了一条途径,绕过了传统机制下催化剂的设计限制。
Pd hydride metallene aerogels with lattice hydrogen participation for efficient hydrogen evolution reaction
Hydrogen adsorption and desorption in single-phase catalysts often occur at a single catalytic site based on the traditional hydrogen evolution reaction (HER) pathway, which makes it difficult to break the limitation entailed by the Sabatier principle. Herein, β-Pd hydride metallene (β-PdHene) aerogels are synthesized as advanced HER catalysts. A lattice hydrogen-involved mechanism is reported to separate adsorption and desorption sites, which is thermodynamically favorable compared to the traditional reaction pathway. In situ differential electrochemical mass spectrometry and theoretical calculations reveal that lattice hydrogen as additional active sites directly participate in the HER process. Consequently, β-PdHene aerogels exhibit a low overpotential of only 20 mV at 10 mA cm−2 and remarkable HER stability, which are even comparable to commercial Pt/C. Our work opens an avenue to rationally develop highly active HER catalysts, bypassing the design limitations of catalysts under traditional mechanisms.
期刊介绍:
Nature Communications, an open-access journal, publishes high-quality research spanning all areas of the natural sciences. Papers featured in the journal showcase significant advances relevant to specialists in each respective field. With a 2-year impact factor of 16.6 (2022) and a median time of 8 days from submission to the first editorial decision, Nature Communications is committed to rapid dissemination of research findings. As a multidisciplinary journal, it welcomes contributions from biological, health, physical, chemical, Earth, social, mathematical, applied, and engineering sciences, aiming to highlight important breakthroughs within each domain.