Electronegativity-induced charge balancing to boost stability and activity of amorphous electrocatalysts
Amorphization is an efficient strategy to activate intrinsically inert catalysts. However, the low crystallinity of amorphous catalysts often causes high solubility and poor electrochemical stability in aqueous solution. Here, a different mechanism is developed to simultaneously stabilize and activa...
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sg-ntu-dr.10356-1620502022-10-03T02:36:15Z Electronegativity-induced charge balancing to boost stability and activity of amorphous electrocatalysts Zhou, Yao Hao, Wei Zhao, Xiaoxu Zhou, Jiadong Yu, Huimei Lin, Bo Liu, Zheng Pennycook, Stephen J. Li, Shuzhou Fan, Hong Jin School of Physical and Mathematical Sciences School of Materials Science and Engineering School of Electrical and Electronic Engineering Engineering::Materials Amorphous Catalysts Aqueous Stability Amorphization is an efficient strategy to activate intrinsically inert catalysts. However, the low crystallinity of amorphous catalysts often causes high solubility and poor electrochemical stability in aqueous solution. Here, a different mechanism is developed to simultaneously stabilize and activate the water-soluble amorphous MoSx Oy via a charge-balancing strategy, which is induced by different electronegativity between the co-dopants Rh (2.28) and Sn (1.96). The electron-rich Sn prefers to stabilize the unstable apical O sites in MoSx Oy through charge transfer, which can prevent the H from attacking. Meanwhile, the Rh, as the charge regulator, shifts the main active sites on the basal plane from inert Sn to active apical Rh sites. As a result, the amorphous RhSn-MoSx Oy exhibits drastic enhancement in electrochemical stability (η10 increases only by 12 mV) after 1000 cycles and a distinct activity (η10 : 26 mV and Tafel: 30.8 mV dec-1 ) for the hydrogen evolution reaction in acidic solution. This work paves a route for turning impracticably water-soluble catalysts into treasure and inspires new ideas to design high-performance amorphous electrocatalysts. Agency for Science, Technology and Research (A*STAR) Ministry of Education (MOE) Nanyang Technological University H.J.F. and Y.Z. thank the financial support from Agency for Science, Technology and Research (A*STAR), Singapore by AME Individual Research Grants (A1983c0026), and from Singapore Ministry of Education by Tier 2 grant (MOE2017-T2-1-073). Y.Z. appreciates the support from Science and Technology Commission of Shanghai Municipality (19ZR1465100). S.Z.L. and H.W. appreciate the financial support from Singapore Ministry of Education by Tier 1 (RG8/20). X.X.Z. thanks the support from the Presidential Postdoctoral Fellowship, NTU, Singapore. Z.L., J.D.Z., and X.X.Z. thank the support from Singapore Ministry of Education via AcRF Tier 2 (MOE2019-T2-2-105 and MOE2016-T2-1-131) and AcRF Tier 1 (RG7/18). 2022-10-03T02:36:15Z 2022-10-03T02:36:15Z 2022 Journal Article Zhou, Y., Hao, W., Zhao, X., Zhou, J., Yu, H., Lin, B., Liu, Z., Pennycook, S. J., Li, S. & Fan, H. J. (2022). Electronegativity-induced charge balancing to boost stability and activity of amorphous electrocatalysts. Advanced Materials, 34(11), e2100537-. https://dx.doi.org/10.1002/adma.202100537 0935-9648 https://hdl.handle.net/10356/162050 10.1002/adma.202100537 34951727 2-s2.0-85124138336 11 34 e2100537 en A1983c0026 MOE2017-T2-1-073 RG8/20 MOE2019-T2-2-105 MOE2016-T2-1- 131 RG7/18 Advanced Materials © 2022 Wiley-VCH GmbH. All rights reserved. |
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Engineering::Materials Amorphous Catalysts Aqueous Stability Zhou, Yao Hao, Wei Zhao, Xiaoxu Zhou, Jiadong Yu, Huimei Lin, Bo Liu, Zheng Pennycook, Stephen J. Li, Shuzhou Fan, Hong Jin Electronegativity-induced charge balancing to boost stability and activity of amorphous electrocatalysts |
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Amorphization is an efficient strategy to activate intrinsically inert catalysts. However, the low crystallinity of amorphous catalysts often causes high solubility and poor electrochemical stability in aqueous solution. Here, a different mechanism is developed to simultaneously stabilize and activate the water-soluble amorphous MoSx Oy via a charge-balancing strategy, which is induced by different electronegativity between the co-dopants Rh (2.28) and Sn (1.96). The electron-rich Sn prefers to stabilize the unstable apical O sites in MoSx Oy through charge transfer, which can prevent the H from attacking. Meanwhile, the Rh, as the charge regulator, shifts the main active sites on the basal plane from inert Sn to active apical Rh sites. As a result, the amorphous RhSn-MoSx Oy exhibits drastic enhancement in electrochemical stability (η10 increases only by 12 mV) after 1000 cycles and a distinct activity (η10 : 26 mV and Tafel: 30.8 mV dec-1 ) for the hydrogen evolution reaction in acidic solution. This work paves a route for turning impracticably water-soluble catalysts into treasure and inspires new ideas to design high-performance amorphous electrocatalysts. |
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School of Physical and Mathematical Sciences |
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School of Physical and Mathematical Sciences Zhou, Yao Hao, Wei Zhao, Xiaoxu Zhou, Jiadong Yu, Huimei Lin, Bo Liu, Zheng Pennycook, Stephen J. Li, Shuzhou Fan, Hong Jin |
format |
Article |
author |
Zhou, Yao Hao, Wei Zhao, Xiaoxu Zhou, Jiadong Yu, Huimei Lin, Bo Liu, Zheng Pennycook, Stephen J. Li, Shuzhou Fan, Hong Jin |
author_sort |
Zhou, Yao |
title |
Electronegativity-induced charge balancing to boost stability and activity of amorphous electrocatalysts |
title_short |
Electronegativity-induced charge balancing to boost stability and activity of amorphous electrocatalysts |
title_full |
Electronegativity-induced charge balancing to boost stability and activity of amorphous electrocatalysts |
title_fullStr |
Electronegativity-induced charge balancing to boost stability and activity of amorphous electrocatalysts |
title_full_unstemmed |
Electronegativity-induced charge balancing to boost stability and activity of amorphous electrocatalysts |
title_sort |
electronegativity-induced charge balancing to boost stability and activity of amorphous electrocatalysts |
publishDate |
2022 |
url |
https://hdl.handle.net/10356/162050 |
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1746219657900064768 |