{"title":"多金属合金纳米管库:从二进制到二进制","authors":"Cheng Yang, Jiasai Yao, Senyao Meng, Ping Wang, Miao He, Pangen Li, Peng Xiao, Jianyang Xiao, Yunpeng Liu* and Zhenxing Li*, ","doi":"10.1021/jacs.5c0059710.1021/jacs.5c00597","DOIUrl":null,"url":null,"abstract":"<p >The polymetallic alloy nanostructure has received widespread attention in electrocatalytic reactions due to the variability in composition and excellent performance. However, the controllable synthesis of one-dimensional (1D) polymetallic alloy nanomaterials remains a significant challenge. Herein, we propose a new and general low-temperature method to prepare a library of binary to septenary polymetallic alloy nanotubes, and this method can be used to synthesize 18 kinds of polymetallic alloy nanotube (NT), including eight kinds of high-entropy alloy (HEA) NT. A representative Cu<sub>30</sub>Ni<sub>26</sub>Co<sub>19</sub>Ru<sub>14</sub>Ir<sub>11</sub> HEA NT demonstrates efficient and stable catalytic performance for both oxygen evolution reaction (OER) and hydrogen evolution reaction (HER). The Cu<sub>30</sub>Ni<sub>26</sub>Co<sub>19</sub>Ru<sub>14</sub>Ir<sub>11</sub> HEA NT exhibits an overpotential of only 121 mV for the HER and 272 mV for the OER, respectively, when measured at a current density of 100 mA cm<sup>–2</sup>. In addition, the two-electrode system comprising the Cu<sub>30</sub>Ni<sub>26</sub>Co<sub>19</sub>Ru<sub>14</sub>Ir<sub>11</sub> HEA NT exhibits an impressive efficiency of 100 mA cm<sup>–2</sup> during overall water splitting, requiring only a potential of 1.67 V. The high catalytic activity of the Cu<sub>30</sub>Ni<sub>26</sub>Co<sub>19</sub>Ru<sub>14</sub>Ir<sub>11</sub> HEA NT is attributed to the downward shift of the <i>d</i>-band center. In the HER, the downward shift of the <i>d</i>-band center can reduce the binding energy with *H, which is beneficial for the desorption process of hydrogen. In the OER, the downward shift can also reduce the reaction energy barrier associated with the rate-determining step from *O to *OOH. This work seeks to offer a new and general method for synthesizing polymetallic alloy nanotubes with controllable structures and compositions under mild conditions.</p>","PeriodicalId":49,"journal":{"name":"Journal of the American Chemical Society","volume":"147 11","pages":"9865–9878 9865–9878"},"PeriodicalIF":15.6000,"publicationDate":"2025-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A Library of Polymetallic Alloy Nanotubes: From Binary to Septenary\",\"authors\":\"Cheng Yang, Jiasai Yao, Senyao Meng, Ping Wang, Miao He, Pangen Li, Peng Xiao, Jianyang Xiao, Yunpeng Liu* and Zhenxing Li*, \",\"doi\":\"10.1021/jacs.5c0059710.1021/jacs.5c00597\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The polymetallic alloy nanostructure has received widespread attention in electrocatalytic reactions due to the variability in composition and excellent performance. However, the controllable synthesis of one-dimensional (1D) polymetallic alloy nanomaterials remains a significant challenge. Herein, we propose a new and general low-temperature method to prepare a library of binary to septenary polymetallic alloy nanotubes, and this method can be used to synthesize 18 kinds of polymetallic alloy nanotube (NT), including eight kinds of high-entropy alloy (HEA) NT. A representative Cu<sub>30</sub>Ni<sub>26</sub>Co<sub>19</sub>Ru<sub>14</sub>Ir<sub>11</sub> HEA NT demonstrates efficient and stable catalytic performance for both oxygen evolution reaction (OER) and hydrogen evolution reaction (HER). The Cu<sub>30</sub>Ni<sub>26</sub>Co<sub>19</sub>Ru<sub>14</sub>Ir<sub>11</sub> HEA NT exhibits an overpotential of only 121 mV for the HER and 272 mV for the OER, respectively, when measured at a current density of 100 mA cm<sup>–2</sup>. In addition, the two-electrode system comprising the Cu<sub>30</sub>Ni<sub>26</sub>Co<sub>19</sub>Ru<sub>14</sub>Ir<sub>11</sub> HEA NT exhibits an impressive efficiency of 100 mA cm<sup>–2</sup> during overall water splitting, requiring only a potential of 1.67 V. The high catalytic activity of the Cu<sub>30</sub>Ni<sub>26</sub>Co<sub>19</sub>Ru<sub>14</sub>Ir<sub>11</sub> HEA NT is attributed to the downward shift of the <i>d</i>-band center. In the HER, the downward shift of the <i>d</i>-band center can reduce the binding energy with *H, which is beneficial for the desorption process of hydrogen. In the OER, the downward shift can also reduce the reaction energy barrier associated with the rate-determining step from *O to *OOH. 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引用次数: 0
摘要
多金属合金纳米结构由于其组成的多变性和优异的性能在电催化反应中受到了广泛的关注。然而,一维多金属合金纳米材料的可控合成仍然是一个重大挑战。本文提出了一种新的、通用的低温法制备二元至七元多金属合金纳米管库的方法,该方法可合成18种多金属合金纳米管(NT),包括8种高熵合金(HEA)纳米管,其中Cu30Ni26Co19Ru14Ir11 HEA纳米管在析氧反应(OER)和析氢反应(HER)中均表现出高效稳定的催化性能。当电流密度为100 mA cm-2时,Cu30Ni26Co19Ru14Ir11 HEA NT的HER过电位仅为121 mV, OER过电位为272 mV。此外,由Cu30Ni26Co19Ru14Ir11 HEA NT组成的双电极系统在整个水分解过程中表现出令人印象深刻的100 mA cm-2效率,只需要1.67 V的电位。Cu30Ni26Co19Ru14Ir11 HEA NT具有较高的催化活性是由于d波段中心的下移。在HER中,d带中心的下移降低了与*H的结合能,有利于氢的解吸过程。在OER中,向下移动还可以降低与从*O到*OOH的速率决定步骤相关的反应能垒。本工作旨在为在温和条件下合成具有可控结构和成分的多金属合金纳米管提供一种新的通用方法。
A Library of Polymetallic Alloy Nanotubes: From Binary to Septenary
The polymetallic alloy nanostructure has received widespread attention in electrocatalytic reactions due to the variability in composition and excellent performance. However, the controllable synthesis of one-dimensional (1D) polymetallic alloy nanomaterials remains a significant challenge. Herein, we propose a new and general low-temperature method to prepare a library of binary to septenary polymetallic alloy nanotubes, and this method can be used to synthesize 18 kinds of polymetallic alloy nanotube (NT), including eight kinds of high-entropy alloy (HEA) NT. A representative Cu30Ni26Co19Ru14Ir11 HEA NT demonstrates efficient and stable catalytic performance for both oxygen evolution reaction (OER) and hydrogen evolution reaction (HER). The Cu30Ni26Co19Ru14Ir11 HEA NT exhibits an overpotential of only 121 mV for the HER and 272 mV for the OER, respectively, when measured at a current density of 100 mA cm–2. In addition, the two-electrode system comprising the Cu30Ni26Co19Ru14Ir11 HEA NT exhibits an impressive efficiency of 100 mA cm–2 during overall water splitting, requiring only a potential of 1.67 V. The high catalytic activity of the Cu30Ni26Co19Ru14Ir11 HEA NT is attributed to the downward shift of the d-band center. In the HER, the downward shift of the d-band center can reduce the binding energy with *H, which is beneficial for the desorption process of hydrogen. In the OER, the downward shift can also reduce the reaction energy barrier associated with the rate-determining step from *O to *OOH. This work seeks to offer a new and general method for synthesizing polymetallic alloy nanotubes with controllable structures and compositions under mild conditions.
期刊介绍:
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