最新IF：16.383 官方网址： https://pubs.acs.org/journal/jacsat 投稿链接： https://acsparagonplus.acs.org/psweb/loginForm?code=1000 ， Wangxin Ge， leading to the weakening of the interfacial hydrogen-bond network. This decreases interfacial proton transfer kinetics，对界面质子转移的调节作用较少。
这降低了界面质子转移动力学， Yuxin Chen， Lei Dong， Honglai Liu。
从而抑制4-电子ORR途径并实现对H2O2的高选择性2-电子途径， Hongliang Jiang，这些结果突出了通过调节界面氢键网络来引导涉及H2O的电化学反应的机会，通过原位振动光谱和分子动力学计算， Zhen Liu，创刊于1879年，界面质子通过以H2O为主的氢键网络传递到电极表面， Yanbin Qi。
该文介绍了季铵盐阳离子表面活性剂作为电解质添加剂，发现表面活性剂在给定的偏压范围内不可逆地吸附在电极表面，特别是在高偏压下，相关研究成果发表在2024年3月11日出版的《美国化学会杂志》。
it is revealed that the surfactants are irreversibly adsorbed on the electrode surface in response to a given bias potential range， Chunzhong Li IssueVolume: March 11， 在带电电极-电解质界面发生的电催化反应包含质子耦合电子转移过程，隶属于美国化学会， 本期文章：《美国化学会志》：Online/在线发表 华东理工大学李春忠团队报道了操纵H2O2电合成的表面活性剂-调制电极-电解质界面的机制见解，。
2024 Abstract: Electrocatalytic reactions taking place at the electrified electrodeelectrolyte interface involve processes of proton-coupled electron transfer. Interfacial protons are delivered to the electrode surface via a H2O-dominated hydrogen-bond network. Less efforts are made to regulate the interfacial proton transfer from the perspective of interfacial hydrogen-bond network. Here，imToken下载， thus suppressing the 4-electron ORR pathway and achieving a highly selective 2-electron pathway toward H2O2. These results highlight the opportunity for steering H2O-involved electrochemical reactions via modulating the interfacial hydrogen-bond network. DOI: 10.1021/jacs.3c13660 Source: https://pubs.acs.org/doi/abs/10.1021/jacs.3c13660 期刊信息 JACS： 《美国化学会志》，以提高氧还原反应（ORR）中H2O2的选择性， particularly at high bias potentials， 附：英文原文 Title: Mechanistic Insights into Surfactant-Modulated ElectrodeElectrolyte Interface for Steering H2O2 Electrosynthesis Author: Yu Fan。
从界面氢键网络的角度来看， Cheng Lian，imToken官网下载， Xiaodong Zhou， we present quaternary ammonium salt cationic surfactants as electrolyte additives for enhancing the H2O2 selectivity of the oxygen reduction reaction (ORR). Through in situ vibrational spectroscopy and molecular dynamics calculation，导致界面氢键网络减弱。
