Expediting hydrogen evolution through topological surface states on Bi2Te3

Qing Qu; Bin Liu; Jing Liang; Ding Pan; Iam Keong Sou

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arXiv · 1807.09957

Expediting hydrogen evolution through topological surface states on Bi2Te3

Qing Qu·Bin Liu·Jing Liang·Ding Pan·Iam Keong Sou

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Abstract

Recently, the development of efficient and non-noble metal electrocatalysts with excellent durability for the hydrogen evolution reaction (HER) has attracted increasing attention. The exotic and robust metallic surface states of topological insulators (TIs) are theoretically predicted to enhance surface catalytic activity of overlaying catalysts, but no experimental evidence for TIs directly used as electrocatalysts has ever been reported. In this work, we fabricated the TI thin films of Bi2Te3 with different thicknesses using the molecular beam epitaxy method, and found that these thin films exhibit high electrocatalytic activity in HER. The 48 nm Bi2Te3 thin film has the best performance, which is attributed to its largest active area arising from the spiral growth mode of triangular domains as revealed by atomic force microscopy imaging. Importantly, our theoretical calculations reveal that while pure Bi2Te3 is not a good electrocatalyst, the Bi2Te3 thin films with partially oxidized surfaces or Te vacancies have high HER activity. The existence of the corresponding surface oxides on the Bi2Te3 thin films is supported by our X-ray photoelectron spectroscopy data. Particularly, we demonstrate that the topological surface states play a key role in enhancing the HER performance. Our study offers a new direction to design cost-effective electrocatalysts.

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Qing Qu, Bin Liu, Jing Liang, Ding Pan, Iam Keong Sou. 2018-07-26. Expediting hydrogen evolution through topological surface states on Bi2Te3. https://arxiv.org/abs/1807.09957

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