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铁、氮诱导生物质衍生碳上的镍钴尖晶石界面电子重新分布用于双功能氧转化

Fe, N-Inducing Interfacial Electron Redistribution in NiCo Spinel on Biomass-Derived Carbon for Bi-functional Oxygen Conversion.

作者信息

Liu Yanyan, Zhou Limin, Liu Shuling, Li Shuqi, Zhou Jingjing, Li Xin, Chen Xiangmeng, Sun Kang, Li Baojun, Jiang Jianchun, Pang Huan

机构信息

College of Science, Henan Agricultural University, Zhengzhou, 450002, P. R. China.

College of Chemistry, Zhengzhou University, Zhengzhou, 450001, P. R. China.

出版信息

Angew Chem Int Ed Engl. 2024 Apr 15;63(16):e202319983. doi: 10.1002/anie.202319983. Epub 2024 Mar 12.

Abstract

Herein, an interfacial electron redistribution is proposed to boost the activity of carbon-supported spinel NiCoO catalyst toward oxygen conversion via Fe, N-doping strategy. Fe-doping into octahedron induces a redistribution of electrons between Co and Ni atoms on NiCoFeO@N-carbon. The increased electron density of Co promotes the coordination of water to Co sites and further dissociation. The generation of proton from water improves the overall activity for the oxygen reduction reaction (ORR). The increased electron density of Ni facilitates the generation of oxygen vacancies. The Ni-V-Fe structure accelerates the deprotonation of *OOH to improve the activity toward oxygen evolution reaction (OER). N-doping modulates the electron density of carbon to form active sites for the adsorption and protonation of oxygen species. Fir wood-derived carbon endows catalyst with an integral structure to enable outstanding electrocatalytic performance. The NiCoFeO@N-carbon express high half-wave potential up to 0.86 V in ORR and low overpotential of 270 mV at 10 mA cm in OER. The zinc-air batteries (ZABs) assembled with the as-prepared catalyst achieve long-term cycle stability (over 2000 cycles) with peak power density (180 mWcm). Fe, N-doping strategy drives the catalysis of biomass-derived carbon-based catalysts to the highest level for the oxygen conversion in ZABs.

摘要

在此,我们提出通过铁、氮掺杂策略实现界面电子重新分布,以提高碳载尖晶石NiCoO催化剂对氧转化的活性。铁掺杂到八面体中会导致NiCoFeO@N-碳上Co和Ni原子之间的电子重新分布。Co电子密度的增加促进了水与Co位点的配位并进一步解离。水产生的质子提高了氧还原反应(ORR)的整体活性。Ni电子密度的增加促进了氧空位的产生。Ni-V-Fe结构加速了*OOH的去质子化,以提高对析氧反应(OER)的活性。氮掺杂调节了碳的电子密度,形成了氧物种吸附和质子化的活性位点。杉木衍生碳赋予催化剂整体结构,使其具有出色的电催化性能。NiCoFeO@N-碳在ORR中表现出高达0.86 V的高半波电位,在OER中在10 mA cm时过电位低至270 mV。用所制备的催化剂组装的锌空气电池(ZABs)实现了长期循环稳定性(超过2000次循环),峰值功率密度为180 mWcm。铁、氮掺杂策略将生物质衍生的碳基催化剂的催化性能提升到了ZABs中氧转化的最高水平。

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