Journal
JOURNAL OF MATERIALS CHEMISTRY A
Volume 10, Issue 34, Pages 17544-17551Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d2ta05327f
Keywords
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Funding
- National Natural Science Foundation of China [52002139, 51872101]
- National Program for Support of Topnotch Young Professionals [52025027]
- Program for HUST Academic Frontier Youth Team [2017QYTD11]
- Fundamental Research Funds for the Central Universities [HUST: 2020JYCXJJ074]
- Director Fund of WNLO
- Center for Nanoscale Characterization & Devices, WNLO-HUST
- Analysis and Testing Center of Huazhong University of Science and Technology
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A multi-level three-dimensional carbon electrode was designed to improve the output current and Carnot-relative efficiency of thermoelectrochemical cells (TECs). By loading nitrogen-doped carbon nanowires on carbon cloth fibers, the composite electrode enhances ion transmission and reaction kinetics. When combined with an optimized thermosensitive crystallization-boosting electrolyte, the electrode achieves the highest reported efficiency for TECs.
Thermoelectrochemical cells (TECs) are promising and cost-effective for harvesting low-grade heat. However, the low efficiency hinders their practical application. Here, a multi-level three-dimensional carbon electrode was designed for high-efficiency TECs. The composite electrode is prepared by loading nitrogen-doped carbon nanowires on carbon cloth fibers (N-CNW@CC); it improves the transition kinetics of Fe(CN)(6)(3-)/Fe(CN)(6)(4-) and accelerates the ion transmission simultaneously. As a result, the output current of the N-CNW@CC based TEC is 26.3% higher than that of the initial CC. Upon combining it with an optimized thermosensitive crystallization-boosting electrolyte, the Carnot-relative efficiency of the N-CNW@CC based TEC reaches up to 13.02%, which is the highest efficiency ever reported. In addition, a simple pack of a series of TECs can drive a commercial timer to work for an hour continuously. This N-CNW@CC electrode holds great potential to realize the commercial application of TECs.
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