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多金属氧酸盐簇诱导的高熵氧化物亚1纳米纳米片作为锌空气电池的光电催化剂

Polyoxometallate Cluster Induced High-Entropy Oxide Sub-1 nm Nanosheets as Photoelectrocatalysts for Zn-Air Batteries.

作者信息

Ge Huaiyun, Zheng Lirong, Yuan Guobao, Shi Wenxiong, Liu Junli, Zhang Yu, Wang Xun

机构信息

School of Chemistry, Key Laboratory of Bio-inspired Smart Interfacial Science and Technology of Ministry of Education, Beihang University, Beijing 100191, China.

Beijing Synchrotron Radiation Facility, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049, China.

出版信息

J Am Chem Soc. 2024 Apr 17;146(15):10735-10744. doi: 10.1021/jacs.4c00652. Epub 2024 Apr 4.

Abstract

The lack of highly efficient and inexpensive catalysts severely hinders the large-scale application of Zn-air batteries (ZABs). High-entropy oxides (HEOs) exhibit unique structures and attractive properties; thus, they are promising to be used in ZABs. However, conventional high-temperature synthesis methods tend to obtain microscale HEOs with a lower exposure rate of active sites. Here, we report a facile solvothermal strategy for preparing two-dimensional (2D) HEO sub-1 nm nanosheets (SNSs) induced by polyoxometalate (POM) clusters. Taking advantage of the special 2D sub-1 nm structure and precise element regulation, these 2D HEOs-POM SNSs exhibit enhanced bifunctional oxygen evolution and oxygen reduction reaction activity under light irradiation. Further applying these 2D HEOs-POM SNSs to ZABs as cathode catalysts, the CoFeNiMnCuZnO-phosphomolybdic acid SNSs-based ZABs deliver a low charge/discharge voltage gap of 0.25 V at 2 mA cm under light irradiation. Meanwhile, it could maintain an ultralong-term stability for 1600 h at 2 mA cm and 930 h at 10 mA cm. The 2D sub-1 nm structure and fine element control in HEOs provide opportunities to solve the problems of low intrinsic activity, limited active sites, and instability of air cathodes in ZABs.

摘要

高效且廉价的催化剂的缺乏严重阻碍了锌空气电池(ZABs)的大规模应用。高熵氧化物(HEOs)具有独特的结构和吸引人的性能;因此,它们有望用于ZABs。然而,传统的高温合成方法往往会得到活性位点暴露率较低的微米级HEOs。在此,我们报道了一种简便的溶剂热策略,用于制备由多金属氧酸盐(POM)簇诱导的二维(2D)亚1纳米高熵氧化物纳米片(SNSs)。利用特殊的二维亚1纳米结构和精确的元素调控,这些二维HEOs-POM SNSs在光照下表现出增强的双功能析氧和氧还原反应活性。进一步将这些二维HEOs-POM SNSs作为阴极催化剂应用于ZABs,基于CoFeNiMnCuZnO-磷钼酸SNSs的ZABs在光照下2 mA cm时具有0.25 V的低充/放电电压间隙。同时,它在2 mA cm时可保持1600 h的超长稳定性,在10 mA cm时可保持930 h的超长稳定性。HEOs中的二维亚1纳米结构和精细的元素控制为解决ZABs中空气阴极的固有活性低、活性位点有限和稳定性差等问题提供了机会。

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