Lei Jin, Hui Xu, Kun Wang, Yang Liu, Xingyue Qian, Guangyu He, Haiqun Chen
{"title":"Oxygen vacancy mediated and enhanced metal-P bonds for stabilizing reconstruction for alkaline freshwater and seawater electrolysis","authors":"Lei Jin, Hui Xu, Kun Wang, Yang Liu, Xingyue Qian, Guangyu He, Haiqun Chen","doi":"10.1039/d4ta06201a","DOIUrl":null,"url":null,"abstract":"The performance of electrochemical water splitting can be effectively enhanced by preventing irreversible structural distortion that leads to the leaching of active elements. In this study, a porous grass-shaped Fe<small><sub>2</sub></small>P/Ni<small><sub>5</sub></small>P<small><sub>4</sub></small>-Ov catalyst was synthesized using oxygen vacancies (Ov), exhibiting robust M–P bonds. Both experimental and theoretical investigations show that these strong M–P bonds play a crucial role in stabilizing electrochemical transformation of the precursor catalyst to active Ni, Fe-(oxy)hydroxide species, thereby reducing Fe loss. Additionally, the enhanced orbital coupling weakens the OH–H bonds in the H<small><sub>2</sub></small>O molecule. Remarkably, Fe<small><sub>2</sub></small>P/Ni<small><sub>5</sub></small>P<small><sub>4</sub></small>-Ov demonstrates exceptional OER and HER activity and stability in both alkaline freshwater and seawater solutions by preventing the leaching of Fe elements. This research underscores the transition from metal–organic frameworks to the evolution of metal oxides into metal phosphides and offers insights into inhibiting the leaching of active elements.","PeriodicalId":10,"journal":{"name":"ACS Central Science","volume":null,"pages":null},"PeriodicalIF":12.7000,"publicationDate":"2024-11-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Central Science","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1039/d4ta06201a","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
The performance of electrochemical water splitting can be effectively enhanced by preventing irreversible structural distortion that leads to the leaching of active elements. In this study, a porous grass-shaped Fe2P/Ni5P4-Ov catalyst was synthesized using oxygen vacancies (Ov), exhibiting robust M–P bonds. Both experimental and theoretical investigations show that these strong M–P bonds play a crucial role in stabilizing electrochemical transformation of the precursor catalyst to active Ni, Fe-(oxy)hydroxide species, thereby reducing Fe loss. Additionally, the enhanced orbital coupling weakens the OH–H bonds in the H2O molecule. Remarkably, Fe2P/Ni5P4-Ov demonstrates exceptional OER and HER activity and stability in both alkaline freshwater and seawater solutions by preventing the leaching of Fe elements. This research underscores the transition from metal–organic frameworks to the evolution of metal oxides into metal phosphides and offers insights into inhibiting the leaching of active elements.
期刊介绍:
ACS Central Science publishes significant primary reports on research in chemistry and allied fields where chemical approaches are pivotal. As the first fully open-access journal by the American Chemical Society, it covers compelling and important contributions to the broad chemistry and scientific community. "Central science," a term popularized nearly 40 years ago, emphasizes chemistry's central role in connecting physical and life sciences, and fundamental sciences with applied disciplines like medicine and engineering. The journal focuses on exceptional quality articles, addressing advances in fundamental chemistry and interdisciplinary research.