{"title":"NiPd催化剂上环境CO2加氢生成甲酸酯","authors":"Jayashree Parthiban, Bhanu Priya, Rohit Kumar Rai, Satoshi Suganuma, Kiyotaka Nakajima, Sanjay Kumar Singh","doi":"10.1002/cctc.202500771","DOIUrl":null,"url":null,"abstract":"<p>The urgent need for sustainable CO<sub>2</sub> management has driven the development of efficient catalytic systems capable of converting CO<sub>2</sub> into value-added chemicals under mild conditions. Herein, we report a Ni<sub>9</sub>Pd<sub>1</sub> catalyst with a low Pd content (Ni/Pd = 9:1) for the selective CO<sub>2</sub> hydrogenation to formate at low temperatures. Remarkably, this catalyst exhibits exceptional versatility, efficiently hydrogenating both aqueous (bi)carbonate and CO<sub>2</sub> captured from air (as carbonate) to formate. Moreover, this catalyst shows appreciable robustness by achieving cumulative formate yields of 770.5 mmol g<sub>Pd</sub><sup>−1</sup> (TON of 82, STY of 32.18 mmol<sub>formate</sub> g<sub>Pd</sub><sup>−1 </sup>h<sup>−1</sup> at 28 °C) and 1371.9 mmol g<sub>Pd</sub><sup>−1</sup> (TON of 146, STY of 57.16 mmol<sub>formate</sub> g<sub>Pd</sub><sup>−1 </sup>h<sup>−1</sup> at 80 °C) over multiple cycles. The synergistic Ni-to-Pd interaction in this catalyst leads to the efficient CO<sub>2</sub> activation and H<sub>2</sub> dissociation, enabling operation under mild conditions. This study demonstrates an integrated and sustainable approach where CO<sub>2</sub> captured from air can be hydrogenated to formate at low temperature.</p>","PeriodicalId":141,"journal":{"name":"ChemCatChem","volume":"17 17","pages":""},"PeriodicalIF":3.9000,"publicationDate":"2025-08-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Ambient CO2 Hydrogenation to Formate Over NiPd Catalyst\",\"authors\":\"Jayashree Parthiban, Bhanu Priya, Rohit Kumar Rai, Satoshi Suganuma, Kiyotaka Nakajima, Sanjay Kumar Singh\",\"doi\":\"10.1002/cctc.202500771\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>The urgent need for sustainable CO<sub>2</sub> management has driven the development of efficient catalytic systems capable of converting CO<sub>2</sub> into value-added chemicals under mild conditions. Herein, we report a Ni<sub>9</sub>Pd<sub>1</sub> catalyst with a low Pd content (Ni/Pd = 9:1) for the selective CO<sub>2</sub> hydrogenation to formate at low temperatures. Remarkably, this catalyst exhibits exceptional versatility, efficiently hydrogenating both aqueous (bi)carbonate and CO<sub>2</sub> captured from air (as carbonate) to formate. Moreover, this catalyst shows appreciable robustness by achieving cumulative formate yields of 770.5 mmol g<sub>Pd</sub><sup>−1</sup> (TON of 82, STY of 32.18 mmol<sub>formate</sub> g<sub>Pd</sub><sup>−1 </sup>h<sup>−1</sup> at 28 °C) and 1371.9 mmol g<sub>Pd</sub><sup>−1</sup> (TON of 146, STY of 57.16 mmol<sub>formate</sub> g<sub>Pd</sub><sup>−1 </sup>h<sup>−1</sup> at 80 °C) over multiple cycles. The synergistic Ni-to-Pd interaction in this catalyst leads to the efficient CO<sub>2</sub> activation and H<sub>2</sub> dissociation, enabling operation under mild conditions. This study demonstrates an integrated and sustainable approach where CO<sub>2</sub> captured from air can be hydrogenated to formate at low temperature.</p>\",\"PeriodicalId\":141,\"journal\":{\"name\":\"ChemCatChem\",\"volume\":\"17 17\",\"pages\":\"\"},\"PeriodicalIF\":3.9000,\"publicationDate\":\"2025-08-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ChemCatChem\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/cctc.202500771\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemCatChem","FirstCategoryId":"92","ListUrlMain":"https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/cctc.202500771","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Ambient CO2 Hydrogenation to Formate Over NiPd Catalyst
The urgent need for sustainable CO2 management has driven the development of efficient catalytic systems capable of converting CO2 into value-added chemicals under mild conditions. Herein, we report a Ni9Pd1 catalyst with a low Pd content (Ni/Pd = 9:1) for the selective CO2 hydrogenation to formate at low temperatures. Remarkably, this catalyst exhibits exceptional versatility, efficiently hydrogenating both aqueous (bi)carbonate and CO2 captured from air (as carbonate) to formate. Moreover, this catalyst shows appreciable robustness by achieving cumulative formate yields of 770.5 mmol gPd−1 (TON of 82, STY of 32.18 mmolformate gPd−1 h−1 at 28 °C) and 1371.9 mmol gPd−1 (TON of 146, STY of 57.16 mmolformate gPd−1 h−1 at 80 °C) over multiple cycles. The synergistic Ni-to-Pd interaction in this catalyst leads to the efficient CO2 activation and H2 dissociation, enabling operation under mild conditions. This study demonstrates an integrated and sustainable approach where CO2 captured from air can be hydrogenated to formate at low temperature.
期刊介绍:
With an impact factor of 4.495 (2018), ChemCatChem is one of the premier journals in the field of catalysis. The journal provides primary research papers and critical secondary information on heterogeneous, homogeneous and bio- and nanocatalysis. The journal is well placed to strengthen cross-communication within between these communities. Its authors and readers come from academia, the chemical industry, and government laboratories across the world. It is published on behalf of Chemistry Europe, an association of 16 European chemical societies, and is supported by the German Catalysis Society.