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镍铁共掺杂调控的具有丰富氧空位的非晶态/晶态异质结构钴基氢氧化物/钨酸盐用于高效水氧化催化

NiFe codoping-regulated amorphous/crystalline heterostructured Co-based hydroxides/tungstate with rich oxygen vacancies for efficient water oxidation catalysis.

作者信息

Feng Jiejie, Chu Changshun, Liu Jianting, Wei Liling, Li Huayi, Shen Jianquan

机构信息

Beijing National Laboratory for Molecular Sciences (BNLMS), Key Laboratory of Green Printing, Institute of Chemistry, Chinese Academy of Sciences, Zhongguancun North First Street 2, Beijing 100190, China; University of Chinese Academy of Sciences, Beijing 100049, China.

Beijing National Laboratory for Molecular Sciences (BNLMS), Key Laboratory of Green Printing, Institute of Chemistry, Chinese Academy of Sciences, Zhongguancun North First Street 2, Beijing 100190, China.

出版信息

J Colloid Interface Sci. 2024 Apr;659:330-338. doi: 10.1016/j.jcis.2023.12.133. Epub 2023 Dec 24.

Abstract

Oxygen evolution reaction (OER) is a crucial half-reaction in water splitting, generating hydrogen for sustainable development, but it is often subject to sluggish kinetics. Abundant transition metal-based OER electrocatalysts have been utilized to expedite the process. However, traditional amorphous catalysts suffer from low conductivity, while the activity of crystalline catalysts is also unsatisfactory. Herein, an amorphous/crystalline heterostructured Co-based hydroxide/tungstate was meticulously constructed and further tailored using a NiFe codoping method (NiFeCoW). Following NiFe codoping, the electronic structure had been modulated, subsequently altering the adsorption toward intermediates. From the electrochemical measurements, the NiFeCoW catalyst demonstrated superior electrocatalytic activity for OER in alkaline media, with a minimal overpotential of 297 mV at 10 mA cm and a cell voltage of 1.57 V for water splitting. This study provides valuable guidance for regulating the amorphous/crystalline heterophase in catalysts through bimetallic modulating engineering.

摘要

析氧反应(OER)是水分解中的一个关键半反应,为可持续发展产生氢气,但它的动力学往往较为迟缓。大量基于过渡金属的OER电催化剂已被用于加速这一过程。然而,传统的非晶态催化剂导电性低,而晶态催化剂的活性也不尽人意。在此,精心构建了一种非晶态/晶态异质结构的钴基氢氧化物/钨酸盐,并采用镍铁共掺杂方法(NiFeCoW)进行进一步优化。镍铁共掺杂后,电子结构得到调制,进而改变了对中间体的吸附。通过电化学测量,NiFeCoW催化剂在碱性介质中对OER表现出优异的电催化活性,在10 mA cm时的过电位低至297 mV,水分解的电池电压为1.57 V。本研究为通过双金属调制工程调节催化剂中的非晶态/晶态异相提供了有价值的指导。

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