详细信息

Rational Manipulation of IrO2 Lattice Strain on α-MnO2 Nanorods as a Highly Efficient Water-Splitting Catalyst  ( SCI-EXPANDED收录 EI收录)  

文献类型:期刊文献

英文题名:Rational Manipulation of IrO2 Lattice Strain on α-MnO2 Nanorods as a Highly Efficient Water-Splitting Catalyst

作者:Sun, Wei[1];Zhou, Zhenhua[1];Zaman, Waqas Qamar[1];Cao, Li-mei[1];Yang, Ji[1]

机构:[1]East China Univ Sci & Technol, Sch Resources & Environm Engn, State Environm Protect Key Lab Environm Risk Asse, 130 Meilong Rd, Shanghai 200237, Peoples R China

年份:2017

卷号:9

期号:48

起止页码:41855

外文期刊名:ACS APPLIED MATERIALS & INTERFACES

收录:;EI(收录号:20175004539545);WOS:【SCI-EXPANDED(收录号:WOS:000417669300023)】;

基金:This work is financially support by the National Natural Science Fundation of China (51778229). We thank beamline BL14W1 (Shanghai Synchrotron Radiation Facility) for providing the beam time.

语种:英文

外文关键词:IrO2; alpha-MnO2; lattice strain; interface mismatch; OER

摘要:Developing more efficient and stable oxygen evolution reaction (OER) catalysts is critical for future energy conversion and storage technologies. We demonstrate that inducing a lattice strain in IrO2 crystal structure due to interface lattice mismatch enables an enhancement of the OER catalytic activity. The lattice strain is obtained by the direct growth of IrO2 nanoparticles on a specially exposed surface of alpha-MnO2 nanorods via a simple two-step hydrothermal synthesis. Interestingly, the prepared hydride OER activity increases with a lower IrO2 grown mass, which offers an opportunity to reduce the usage of precious iridium and ultimately obtains a specific mass activity of 3.7 times than that of IrO2 prepared under the same conditions and exhibits equivalent stability. The lattice mismatch in the underlying interface induces the formation of lattice strain in IrO2 rather than the charge transfer between the materials. The lattice strain changes are in good agreement with the order of the OER activity. Our experimental results indicate that using the special exposed surface substrates or tuning the supporting morphology structure can manipulate the catalyst materials lattice strain for the design of more efficient OER catalysts.

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