Journal
MATERIALS TODAY ENERGY
Volume 27, Issue -, Pages -Publisher
ELSEVIER SCI LTD
DOI: 10.1016/j.mtener.2022.101042
Keywords
Three-dimensional titanium; Atomic layer deposition; HER; Charge transfer; Self-supporting electrode
Funding
- Beijing Municipal Great Wall Scholar Training Plan Project [KZ202210005003]
- Beijing Municipal Commission of Education [22JB0019, CIT TCD20190307]
- National Natural Science Foundation of China [U1607110, 51621003]
- Beijing Natural Science Foundation [Z210016]
- Beijing Hundred, Thousand and Ten Thousand Talent Project [2020016]
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In this study, the performance of Pt catalyst for hydrogen evolution was improved by fabricating TiO2 nanotube arrays on titanium substrate and subsequently loading Pt nanoclusters through chemical bonding. The stability and capability for hydrogen evolution of Pt catalyst were enhanced by the Ti-O-Pt bond. Furthermore, the 3D porous titanium substrate with open structure further improved the performance of hydrogen evolution reaction.
Electrode design plays an important role in improving hydrogen evolution reaction (HER), and the self-supporting electrode with three-dimensional (3D) porous structure is widely adopted in the electrocatalytic hydrogen evolution. To better the performance of Pt catalyst for hydrogen evolution, a layer of TiO2 nanotube arrays (TiO2 NTs) fabricated on titanium mesh (3D-Ti) or plate Ti (P-Ti) substrate, respectively, has been selected as support materials to load Pt nanocluster (Pt-x/TiO2 NTs@3D-Ti and Pt-x/TiO2 NTs@P-Ti) via an atomic layer deposition method. It has been revealed that one chemical bond of Ti-O-Pt had been formed between Pt nanocluster and TiO2 nanotube. The theoretical calculations confirm that Ti-O-Pt bond can not only improve the stability of Pt nanocluster but also improve its capability for hydrogen evolution. In addition, the 3D-Ti substrate with open structure can further better Pt nanoclusters' performance on hydrogen evolution. The obtained Pt-x/TiO2 NTs@3D-Ti electrode exhibits an overpotential of 53 mV in 0.5 M H2SO4 at -10 mA cm(-2), and its mass activity has been improved by a factor of 18 compared with Pt-x/TiO2 NTs@P-Ti. (c) 2022 Elsevier Ltd. All rights reserved.
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