{"title":"Electrochemical hydrogen pump using SnO2-stabilized CsH2PO4 proton transport membrane: A performance evaluation at 250°C","authors":"Minal Gupta , Kangkang Zhang , Kevin Huang","doi":"10.1016/j.ceja.2025.100884","DOIUrl":null,"url":null,"abstract":"<div><div>Proton transport membrane (PTM) based electrochemical cells are a more efficient way to separate hydrogen than conventional porous membrane-based technologies. Herein, we report an investigation on the performance (e.g., hydrogen yield, Faradaic efficiency and stability) of an electrochemical hydrogen pump (EHP) based on super-protonic CsH<sub>2</sub>PO<sub>4</sub> (CDP) and 18wt%SnO<sub>2</sub>-stabilized CDP (CS-18) PTM under different current densities, voltages, water contents, electrode compositions and H<sub>2</sub> concentrations. The results show that both CDP and CS-18 cells perform well under 10 mA/cm<sup>2</sup> and 0.38 atm of partial pressure of water vapor (p(H<sub>2</sub>O), while under lower p(H<sub>2</sub>O)=0.20 atm, only CS-18 cells can stably operate. Under higher 25 mA/cm<sup>2</sup> and p(H<sub>2</sub>O)=0.20 atm, CS-18 cell also fails to retain its original performance, exhibiting degradation. The reason for the instability under either high current density or low p(H<sub>2</sub>O) is fundamentally rooted in dehydration of the membrane induced by either low p(H<sub>2</sub>O) or electrochemical splitting of H<sub>2</sub>O inside the membrane at potentials higher than 1.23 V. We show that operation at a constant 1 V is a safe way to avoid CDP’s internal water splitting and ensure stable operation. Overall, this work has demonstrated technical feasibility and favorable operating conditions for using CDP, particularly the SnO<sub>2</sub>-stabilzied CDP, to electrochemically separate H<sub>2</sub> from different H<sub>2</sub>-containing sources.</div></div>","PeriodicalId":9749,"journal":{"name":"Chemical Engineering Journal Advances","volume":"24 ","pages":"Article 100884"},"PeriodicalIF":7.1000,"publicationDate":"2025-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Engineering Journal Advances","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666821125001814","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Proton transport membrane (PTM) based electrochemical cells are a more efficient way to separate hydrogen than conventional porous membrane-based technologies. Herein, we report an investigation on the performance (e.g., hydrogen yield, Faradaic efficiency and stability) of an electrochemical hydrogen pump (EHP) based on super-protonic CsH2PO4 (CDP) and 18wt%SnO2-stabilized CDP (CS-18) PTM under different current densities, voltages, water contents, electrode compositions and H2 concentrations. The results show that both CDP and CS-18 cells perform well under 10 mA/cm2 and 0.38 atm of partial pressure of water vapor (p(H2O), while under lower p(H2O)=0.20 atm, only CS-18 cells can stably operate. Under higher 25 mA/cm2 and p(H2O)=0.20 atm, CS-18 cell also fails to retain its original performance, exhibiting degradation. The reason for the instability under either high current density or low p(H2O) is fundamentally rooted in dehydration of the membrane induced by either low p(H2O) or electrochemical splitting of H2O inside the membrane at potentials higher than 1.23 V. We show that operation at a constant 1 V is a safe way to avoid CDP’s internal water splitting and ensure stable operation. Overall, this work has demonstrated technical feasibility and favorable operating conditions for using CDP, particularly the SnO2-stabilzied CDP, to electrochemically separate H2 from different H2-containing sources.