Min Hong , Yiyuan Yang , Jianhang Nie , Xiaohua Zhang , Wenjing Zhang , Cuicui Du , Jinhua Chen
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Herein, Co<sub>9</sub>S<sub>8</sub> nanoparticles incorporated into atomic Fe dispersed N-enriched porous graphene carbon aerogels (Co<sub>9</sub>S<sub>8</sub>/Fe-N-C) were fabricated via two rounds of hydrothermal treatment followed by high-temperature pyrolysis. DFT calculations and experimental investigation revealed that, in virtue of the strong interactions effect between Co<sub>9</sub>S<sub>8</sub> nanoparticles and Fe-N-C, the regulated electronic structure of Co<sub>9</sub>S<sub>8</sub>/Fe-N-C and the introduced abundant sulfur vacancies induced the d-band center modulation of FeN<sub>x</sub> sites closer to the Fermi level, which can optimize the binding energy for oxygen-containing intermediates, thereby endowing the catalyst with enhanced bifunctional catalytic performance. Therefrom, the Co<sub>9</sub>S<sub>8</sub>/Fe-N-C catalyst presented efficient bifunctional ORR/OER activity with a narrower ΔE (0.68V), outstripping the Pt/C + RuO<sub>2</sub> catalysts. Additionally, the Zn-air battery assembled with Co<sub>9</sub>S<sub>8</sub>/Fe-N-C delivered a large specific capacity (798 mAh g<sub>Zn</sub><sup>−1</sup>) with a power density of 103 mW cm<sup>−2</sup> and a long-term stability over 140 h. This research presents an innovative perspective on theoretical design of highly efficient atomically dispersed Fe based catalysts for reversible Zn-air battery.</div></div>","PeriodicalId":18253,"journal":{"name":"Materials Today Physics","volume":"54 ","pages":"Article 101728"},"PeriodicalIF":10.0000,"publicationDate":"2025-04-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"D-band center modulation of atomic dispersed FeNx sites by incorporating Co9S8 nanoparticles towards augmented ORR/OER electrocatalysis in Zn-air batteries\",\"authors\":\"Min Hong , Yiyuan Yang , Jianhang Nie , Xiaohua Zhang , Wenjing Zhang , Cuicui Du , Jinhua Chen\",\"doi\":\"10.1016/j.mtphys.2025.101728\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Atomically dispersed Fe-N-C catalysts have currently received extremely widespread attention as one of encouraging candidates for Pt-based oxygen reduction reaction (ORR) catalysts owing to their high intrinsic activity and atomic utilization efficiency as well as the affluent reserve, but further optimizing the adsorption behaviors of the primitive FeN<sub>x</sub> sites in Fe-N-C for oxygen-related intermediates is significant for bifunctional oxygen catalytic performances to propel their applications for reversible Zn-air battery. Herein, Co<sub>9</sub>S<sub>8</sub> nanoparticles incorporated into atomic Fe dispersed N-enriched porous graphene carbon aerogels (Co<sub>9</sub>S<sub>8</sub>/Fe-N-C) were fabricated via two rounds of hydrothermal treatment followed by high-temperature pyrolysis. DFT calculations and experimental investigation revealed that, in virtue of the strong interactions effect between Co<sub>9</sub>S<sub>8</sub> nanoparticles and Fe-N-C, the regulated electronic structure of Co<sub>9</sub>S<sub>8</sub>/Fe-N-C and the introduced abundant sulfur vacancies induced the d-band center modulation of FeN<sub>x</sub> sites closer to the Fermi level, which can optimize the binding energy for oxygen-containing intermediates, thereby endowing the catalyst with enhanced bifunctional catalytic performance. Therefrom, the Co<sub>9</sub>S<sub>8</sub>/Fe-N-C catalyst presented efficient bifunctional ORR/OER activity with a narrower ΔE (0.68V), outstripping the Pt/C + RuO<sub>2</sub> catalysts. 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引用次数: 0
摘要
原子分散的Fe-N-C催化剂由于具有较高的内在活性和原子利用效率以及丰富的储量,目前作为pt基氧还原反应(ORR)催化剂的令人鼓舞的候选物之一受到了广泛的关注。但进一步优化Fe-N-C中原始FeNx位点对氧相关中间体的吸附行为对于促进双官能团氧催化性能,推动其在可逆锌空气电池中的应用具有重要意义。本研究通过两轮水热处理和高温热解制备了Co9S8纳米颗粒,并将其掺入Fe分散的富n多孔石墨烯碳气凝胶(Co9S8/Fe- n - c)中。DFT计算和实验研究表明,由于Co9S8纳米粒子与Fe-N-C之间的强相互作用,Co9S8/Fe-N-C的电子结构调控以及引入的丰富的硫空位诱导了FeNx位靠近费米能级的d波段中心调制,从而优化了含氧中间体的结合能,从而增强了催化剂的双功能催化性能。因此,Co9S8/Fe-N-C催化剂表现出高效的双功能ORR/OER活性,其ΔE (0.68V)较窄,优于Pt/C + RuO2催化剂。此外,Co9S8/Fe- n- c组装的锌-空气电池具有798 mAh gZn - 1的大比容量,功率密度为103 mW cm-2,长期稳定性超过140 h。本研究为可逆锌-空气电池高效原子分散铁基催化剂的理论设计提供了创新的视角。
D-band center modulation of atomic dispersed FeNx sites by incorporating Co9S8 nanoparticles towards augmented ORR/OER electrocatalysis in Zn-air batteries
Atomically dispersed Fe-N-C catalysts have currently received extremely widespread attention as one of encouraging candidates for Pt-based oxygen reduction reaction (ORR) catalysts owing to their high intrinsic activity and atomic utilization efficiency as well as the affluent reserve, but further optimizing the adsorption behaviors of the primitive FeNx sites in Fe-N-C for oxygen-related intermediates is significant for bifunctional oxygen catalytic performances to propel their applications for reversible Zn-air battery. Herein, Co9S8 nanoparticles incorporated into atomic Fe dispersed N-enriched porous graphene carbon aerogels (Co9S8/Fe-N-C) were fabricated via two rounds of hydrothermal treatment followed by high-temperature pyrolysis. DFT calculations and experimental investigation revealed that, in virtue of the strong interactions effect between Co9S8 nanoparticles and Fe-N-C, the regulated electronic structure of Co9S8/Fe-N-C and the introduced abundant sulfur vacancies induced the d-band center modulation of FeNx sites closer to the Fermi level, which can optimize the binding energy for oxygen-containing intermediates, thereby endowing the catalyst with enhanced bifunctional catalytic performance. Therefrom, the Co9S8/Fe-N-C catalyst presented efficient bifunctional ORR/OER activity with a narrower ΔE (0.68V), outstripping the Pt/C + RuO2 catalysts. Additionally, the Zn-air battery assembled with Co9S8/Fe-N-C delivered a large specific capacity (798 mAh gZn−1) with a power density of 103 mW cm−2 and a long-term stability over 140 h. This research presents an innovative perspective on theoretical design of highly efficient atomically dispersed Fe based catalysts for reversible Zn-air battery.
期刊介绍:
Materials Today Physics is a multi-disciplinary journal focused on the physics of materials, encompassing both the physical properties and materials synthesis. Operating at the interface of physics and materials science, this journal covers one of the largest and most dynamic fields within physical science. The forefront research in materials physics is driving advancements in new materials, uncovering new physics, and fostering novel applications at an unprecedented pace.