Electrochemical energy conversion and storage are playing an increasingly important role in shaping the sustainable future. Differential electrochemical mass spectrometry (DEMS) offers an and cost-effective tool to monitor the evolution of gaseous/volatile intermediates and products during these processes. It can deliver potential-, time-, mass- and space-resolved signals which facilitate the understanding of reaction kinetics. In this review, we show the latest developments and applications of DEMS in various energy-related electrochemical reactions from three distinct perspectives. (I) What is DEMS addresses the working principles and key components of DEMS, highlighting the new and distinct instrumental configurations for different applications. (II) How to use DEMS tackles practical matters including the electrochemical test protocols, quantification of both potential and mass signals, and error analysis. (III) Where to apply DEMS is the focus of this review, dealing with concrete examples and unique values of DEMS studies in both energy conversion applications (CO reduction, water electrolysis, carbon corrosion, N-related catalysis, electrosynthesis, fuel cells, photo-electrocatalysis and beyond) and energy storage applications (Li-ion batteries and beyond, metal-air batteries, supercapacitors and flow batteries). The recent development of DEMS-hyphenated techniques and the outlook of the DEMS technique are discussed at the end. As DEMS celebrates its 40th anniversary in 2024, we hope this review can offer electrochemistry researchers a comprehensive understanding of the latest developments of DEMS and will inspire them to tackle emerging scientific questions using DEMS.
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http://dx.doi.org/10.1039/d3cs00840a | DOI Listing |
ACS Appl Mater Interfaces
January 2025
University of Michigan - Shanghai Jiao Tong University Joint Institute, Shanghai Jiao Tong University, Shanghai 200240, China.
Proton conducting electrochemical cells (PCECs) are efficient and clean intermediate-temperature energy conversion devices. The proton concentration across the PCECs is often nonuniform, and characterizing the distribution of proton concentration can help to locate the position of rate-limiting reactions. However, the determination of the local proton concentration under operating conditions remains challenging.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Shanghai Advanced Research Institute Chinese Academy of Sciences: Chinese Academy of Sciences Shanghai Advanced Research Institute, Low-Carbon Conversion Science and Engineering Cente, 100 Haike Road, 201203, Shanghai, CHINA.
Renewable energy-driven electrochemical CO2 reduction has emerged as a promising technology for a sustainable future. However, achieving efficient production of storable liquid fuels at ampere-level current densities remains a significant hurdle in the large-scale implementation of CO2 electroreduction. Here we report a novel catalytic electrode comprising chlorine-doped SnO2 nanoflowers arrayed on the exterior of three-dimensional nickel hollow fibers.
View Article and Find Full Text PDFJ Mol Model
January 2025
School of Chemistry & Chemical Engineering, Linyi University, Linyi, 276000, China.
Context: In this work, a comparative study on the catalytic conversion of 5-hydroxymethyl furfural (HMF) to 2,5-bis(hydroxymethyl)furan (BHMF) on precious Pd(111) and nonprecious Cu(111) was systematically performed. On the basis of the calculated activation energy (E) and reaction energy (E), the optimal energy path for the hydrogenation of HMF (F-CHO) into BHMF (F-CHOH) on Pd(111) is as follows: F-CHO + 2H → F-CHOH + H → F-CHOH; the minimum reaction path on Cu(111) is F-CHO + 2H → F-CHO + H → F-CHOH. On Cu(111), the formation of F-CHOH from F-CHO hydrogenation is the rate-determining step because it has the highest reaction energy barrier and the smallest rate constant.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
Department of Hydrogen and Electrochemistry, Idaho National Laboratory, Idaho Falls, ID 83415, United States.
Reducing the energy and carbon intensity of the conventional chemical processing industry can be achieved by electrochemically transforming natural gases into higher-value chemicals with higher efficiency and near-zero emissions. In this work, the direct conversion of methane to aromatics and electricity has been achieved in a protonic ceramic electrocatalytic membrane reactor through the integration of a proton-conducting membrane assembly and a trimetallic Pt-Cu/Mo/ZSM-5 catalyst for the nonoxidative methane dehydro-aromatization reaction. In this integrated system, a remarkable 15.
View Article and Find Full Text PDFChem Commun (Camb)
January 2025
Institute for Carbon Neutralization Technology, College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou, Zhejiang 325035, China.
Single-atom catalysts (SACs) have become the forefront and hotspot in energy storage and conversion research, inheriting the advantages of both homogeneous and heterogeneous catalysts. In particular, carbon-supported SACs (CS-SACs) are excellent candidates for many energy storage and conversion applications, due to their maximum atomic efficiency, unique electronic and coordination structures, and beneficial synergistic effects between active catalytic sites and carbon substrates. In this review, we briefly review the atomic-level regulation strategies for optimizing CS-SACs for energy storage and conversion, including coordination structure control, nonmetallic elemental doping, axial coordination design, and polymetallic active site construction.
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