Chaotropic nanoelectrocatalysis: chemically disrupting water intermolecular network at the point-of-catalysis to boost green hydrogen electrosynthesis

Efficient green hydrogen production through electrocatalytic water splitting serves as a powerful catalyst for realizing a carbon-free hydrogen economy. However, current electrocatalytic designs face challenges such as poor hydrogen evolution reaction (HER) performance (Tafel slope, 100-140 mV dec-1...

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Main Authors: Ng, Li Shiuan, Chah, Chloe Eu Li, Ngieng, Min Hui, Boong, Siew Kheng, Chong, Carice, Raja Mogan, Tharishinny, Lee, Jinn-Kye, Li, Haitao, Lee, Ken Chi-Lik, Lee, Hiang Kwee
Other Authors: School of Chemistry, Chemical Engineering and Biotechnology
Format: Article
Language:English
Published: 2024
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Online Access:https://hdl.handle.net/10356/174654
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Institution: Nanyang Technological University
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spelling sg-ntu-dr.10356-1746542024-04-12T15:32:06Z Chaotropic nanoelectrocatalysis: chemically disrupting water intermolecular network at the point-of-catalysis to boost green hydrogen electrosynthesis Ng, Li Shiuan Chah, Chloe Eu Li Ngieng, Min Hui Boong, Siew Kheng Chong, Carice Raja Mogan, Tharishinny Lee, Jinn-Kye Li, Haitao Lee, Ken Chi-Lik Lee, Hiang Kwee School of Chemistry, Chemical Engineering and Biotechnology Institute of Materials Research and Engineering, A*STAR Chemistry Chaotropic Electrocatalysis Efficient green hydrogen production through electrocatalytic water splitting serves as a powerful catalyst for realizing a carbon-free hydrogen economy. However, current electrocatalytic designs face challenges such as poor hydrogen evolution reaction (HER) performance (Tafel slope, 100-140 mV dec-1 ) because water molecules are thermodynamically trapped within their extensive hydrogen bonding network. Herein, we drive efficient HER by manipulating the local water microenvironment near the electrocatalyst. This is achieved by functionalizing the nanoelectrocatalyst's surface with a monolayer of chaotropic molecules to chemically weaken water-water interactions directly at the point-of-catalysis. Notably, our chaotropic design demonstrates a superior Tafel slope (77 mV dec-1 ) and the lowest overpotential (0.3 V at 10 mA cm-2 ECSA ), surpassing its kosmotropic counterparts (which reinforces the water molecular network) and previously reported electrocatalytic designs by up to ≈2-fold and ≈3-fold, respectively. Comprehensive mechanistic investigations highlight the critical role of chaotropic surface chemistry in disrupting the water intermolecular network, thereby releasing free/weakly bound water molecules that strongly interact with the electrocatalyst to boost HER. Our study provides a unique molecular approach that can be readily integrated with emerging electrocatalytic materials to rapidly advance the electrosynthesis of green hydrogen, holding immense promise for sustainable chemical and energy applications. Agency for Science, Technology and Research (A*STAR) Ministry of Education (MOE) Nanyang Technological University Submitted/Accepted version H. K. L. thanks the funding supports from the Singapore Ministry of Education (AcRF Tier1 RS13/20 and RG4/21), A*STAR Singapore (AME YIRG A2084c0158), the National University of Singapore Center of Hydrogen Innovation (CHI-P2022-05), and the Nanyang Technological University start-up grants. The research was conducted as a part of NICES (NTU-IMRE Chemistry Lab for Eco Sustainability; REQ0275931), a joint research initiative between Nanyang Technological University (NTU) and Institute of Materials Research and Engineering (IMRE) from Agency for Science, Technology, and Research (A*STAR). 2024-04-07T02:28:24Z 2024-04-07T02:28:24Z 2024 Journal Article Ng, L. S., Chah, C. E. L., Ngieng, M. H., Boong, S. K., Chong, C., Raja Mogan, T., Lee, J., Li, H., Lee, K. C. & Lee, H. K. (2024). Chaotropic nanoelectrocatalysis: chemically disrupting water intermolecular network at the point-of-catalysis to boost green hydrogen electrosynthesis. Angewandte Chemie International Edition, 63(8), e202317751-. https://dx.doi.org/10.1002/anie.202317751 1433-7851 https://hdl.handle.net/10356/174654 10.1002/anie.202317751 38179729 2-s2.0-85182432648 8 63 e202317751 en RS13/20 RG4/21 AME-YIRG-A2084c0158 CHI-P2022-05 REQ0275931 Angewandte Chemie International Edition © 2024 Wiley-VCH GmbH. All rights reserved. This article may be downloaded for personal use only. Any other use requires prior permission of the copyright holder. The Version of Record is available online at http://doi.org/10.1002/anie.202317751. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Chemistry
Chaotropic
Electrocatalysis
spellingShingle Chemistry
Chaotropic
Electrocatalysis
Ng, Li Shiuan
Chah, Chloe Eu Li
Ngieng, Min Hui
Boong, Siew Kheng
Chong, Carice
Raja Mogan, Tharishinny
Lee, Jinn-Kye
Li, Haitao
Lee, Ken Chi-Lik
Lee, Hiang Kwee
Chaotropic nanoelectrocatalysis: chemically disrupting water intermolecular network at the point-of-catalysis to boost green hydrogen electrosynthesis
description Efficient green hydrogen production through electrocatalytic water splitting serves as a powerful catalyst for realizing a carbon-free hydrogen economy. However, current electrocatalytic designs face challenges such as poor hydrogen evolution reaction (HER) performance (Tafel slope, 100-140 mV dec-1 ) because water molecules are thermodynamically trapped within their extensive hydrogen bonding network. Herein, we drive efficient HER by manipulating the local water microenvironment near the electrocatalyst. This is achieved by functionalizing the nanoelectrocatalyst's surface with a monolayer of chaotropic molecules to chemically weaken water-water interactions directly at the point-of-catalysis. Notably, our chaotropic design demonstrates a superior Tafel slope (77 mV dec-1 ) and the lowest overpotential (0.3 V at 10 mA cm-2 ECSA ), surpassing its kosmotropic counterparts (which reinforces the water molecular network) and previously reported electrocatalytic designs by up to ≈2-fold and ≈3-fold, respectively. Comprehensive mechanistic investigations highlight the critical role of chaotropic surface chemistry in disrupting the water intermolecular network, thereby releasing free/weakly bound water molecules that strongly interact with the electrocatalyst to boost HER. Our study provides a unique molecular approach that can be readily integrated with emerging electrocatalytic materials to rapidly advance the electrosynthesis of green hydrogen, holding immense promise for sustainable chemical and energy applications.
author2 School of Chemistry, Chemical Engineering and Biotechnology
author_facet School of Chemistry, Chemical Engineering and Biotechnology
Ng, Li Shiuan
Chah, Chloe Eu Li
Ngieng, Min Hui
Boong, Siew Kheng
Chong, Carice
Raja Mogan, Tharishinny
Lee, Jinn-Kye
Li, Haitao
Lee, Ken Chi-Lik
Lee, Hiang Kwee
format Article
author Ng, Li Shiuan
Chah, Chloe Eu Li
Ngieng, Min Hui
Boong, Siew Kheng
Chong, Carice
Raja Mogan, Tharishinny
Lee, Jinn-Kye
Li, Haitao
Lee, Ken Chi-Lik
Lee, Hiang Kwee
author_sort Ng, Li Shiuan
title Chaotropic nanoelectrocatalysis: chemically disrupting water intermolecular network at the point-of-catalysis to boost green hydrogen electrosynthesis
title_short Chaotropic nanoelectrocatalysis: chemically disrupting water intermolecular network at the point-of-catalysis to boost green hydrogen electrosynthesis
title_full Chaotropic nanoelectrocatalysis: chemically disrupting water intermolecular network at the point-of-catalysis to boost green hydrogen electrosynthesis
title_fullStr Chaotropic nanoelectrocatalysis: chemically disrupting water intermolecular network at the point-of-catalysis to boost green hydrogen electrosynthesis
title_full_unstemmed Chaotropic nanoelectrocatalysis: chemically disrupting water intermolecular network at the point-of-catalysis to boost green hydrogen electrosynthesis
title_sort chaotropic nanoelectrocatalysis: chemically disrupting water intermolecular network at the point-of-catalysis to boost green hydrogen electrosynthesis
publishDate 2024
url https://hdl.handle.net/10356/174654
_version_ 1800916375728816128