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Modulating the interfacial microenvironment via zwitterionic additive for long-cycling aqueous Zn-ion batteries

Science China Materials 2024年第9期67卷 2898-2907页

作者： Yawen Xie Shuang Feng Jiechang Gao Tao Cheng Liang Zhang Institute of Functional Nano&Soft Materials(FUNSOM) Soochow UniversitySuzhou215123China Jiangsu Key Laboratory of Advanced Negative Carbon Technologies Soochow UniversitySuzhou215123China

Aqueous zinc-ion batteries(AZIBs)have garnered extensive attention as promising energy storage systems because of the advantages of low cost and high ***,severe parasitic reactions at the Zn anode surface pose a huge challenge for the practical application of AZIBs,especially the intricate hydrogen evolution reaction(HER)and Zn dendrite ***,zwitterionic taurine with isoelectric point property is introduced as an electrolyte additive to construct a passivation layer by adapting its net charge to the microenvironment variation for stabilizing the Zn *** experimental and theoretical results reveal that taurine can not only in-situ form a hydrophobic and zincophilic layer on the Zn anode surface via the chelation with Zn^(2+)in the alkaline interfacial microenvironment,but also buffer the pH change dynamically,thus effectively suppressing the HER and Zn dendrite *** a consequence,the taurine-containing electrolyte enables a stable cycling of Zn anodes in symmetric Zn∥Zn cells for more than 1800 h under a deep plating/stripping condition(5 mA cm^(-2)and 5 mAh cm^(-2)).More encouragingly,the full cells coupled with the NH_(4)V_(4)O_(10)cathode can also exhibit an excellent capacity retention of 89.8%after 1200 *** efficient strategy with an environmental adaptive additive offers valuable insights for mitigating the side reactions to achieve practical AZIBs and beyond.

关键词： aqueous zinc-ion batteries passivation layer pH buffer interfacial microenvironment zwitterionic additive

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Molecular surface functionalization of In_(2)O_(3) to tune interfacial microenvironment for enhanced catalytic performance of CO_(2) electroreduction

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Nano Research 2024年第3期17卷 1242-1250页

作者： Suwen WangQiang GaoCui Xu Shuai Jiang Mengyang Zhang Xianjun Yin Hui-Qing Peng Bin Liu Yu-Fei Song State Key Laboratory of Chemical Resource Engineering Beijing Advanced Innovation Center for Soft Matter Science and EngineeringCollege of ChemistryBeijing University of Chemical TechnologyBeijing 100029China

Indium-based materials(e.g.,In_(2)O_(3))are a class of promising non-noble metal-based catalysts for electroreduction of carbon dioxide(CO_(2)).However,competitive hydrogen reduction reaction(HER)on indium-based catalysts hampers CO_(2) reduction reaction(CO_(2)RR)*** herein tune the interfacial microenvironment of In_(2)O_(3) through chemical graft of alkyl phosphoric acid molecules using a facile solution-processed strategy for the first time,which is distinguished from other researches that tailor intrinsic activity of In_(2)O_(3) *** surface functionalization of alkyl phosphoric acids over In_(2)O_(3) is demonstrated to remarkably boost CO_(2) *** example,octadecylphosphonic acid modified In_(2)O_(3) exhibits Faraday efficiency for H_(2) H_(2) H_(2)(FE)of as low as 6.6%and FEHCOOH of 86.5%at-0.67 V ***,which are far superior to parent In_(2)O_(3) counterparts(FE of 24.0%and FEHCOOH of 63.1%).Moreover,the enhancing effect of alkyl phosphoric acid functionalization is found to be closely related to the length of alkyl *** virtue of comprehensive experimental characterizations and molecular dynamics simulations,it is revealed that the modification of alkyl phosphoric acids significantly alters the interface microenvironment of the electrocatalyst,which changes the electrocatalyst surface from hydrophilic and aerophobic to hydrophobic and *** this case,the water molecules are pushed away and more CO_(2) molecules are trapped,increasing local CO_(2) concentration at In_(2)O_(3) active sites,thus leading to the significantly enhanced CO_(2)RR and suppressed *** work highlights the importance of regulating the interfacial microenvironment of inorganic catalysts by molecular surface functionalization as a means for promoting the electrochemical performance in electrosynthesis and beyond.

关键词： carbon dioxide(CO_(2))electroreduction interfacial microenvironment molecular surface functionalization In_(2)O_(3)catalyst water and CO_(2)diffusion

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