Journal
ACS APPLIED MATERIALS & INTERFACES
Volume 13, Issue 23, Pages 26989-26997Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c04508
Keywords
evaporation-induced electricity generation; 3D printed rGO film; salt solution; microchannel; electric double layer (EDL)
Funding
- National Natural Science Foundation of China [21822202, 22072104]
- National Key R&D Program of China (International Collaboration program) - Chinese Ministry of Science and Technology [2018YFE0200700]
- Guangdong Basic and Applied Basic Research Foundation [2019A1515110019]
- CIC
- 111 project
- Joint International Research Laboratory of Carbon-Based Functional Materials and Devices
- Collaborative Innovation Center of Suzhou Nano Science and Technology
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This study demonstrates an enhanced evaporation-induced output power in salt solution by utilizing a honeycomb-structured rGO film, leading to a 2-fold increase in open-circuit voltage and a 3.3-fold increase in power density compared to DI water. The generator can work continuously in natural seawater for over 240 hours, showing stable performance and advancing practical applications in water-evaporation-induced electricity generation.
Water-evaporation-induced electricity generation provides an ideal strategy to solve growing energy demand and supply power for self-powered systems because of its advantages of a highly spontaneous process, continuous power generation, and low cost. However, the reported evaporation-induced generators are limited to working only in deionized (DI) water, leading to a low output power. Herein, we utilize a modified multiple ion mode to demonstrate that the streaming potential can be optimized in microchannels filled with salt solution and achieve an enhanced evaporation-induced output power in salt solution by a generator based on honeycomb-structured reduced graphene oxide (rGO) film with abundant interconnected microchannels. This generator enables an around 2-fold open-circuit voltage (V-oc) and a 3.3-fold power density of 0.91 mu W cm(-2) in 0.6 M NaCl solution compared to that in DI water. Experiments evidence that the honeycomb structure with abundant interconnected microchannels plays a key role in achieving high and stable output power in salt solution because of its large specific surface area and excellent ion-exchange capacity. Notably, it can work at all times of day and night for more than 240 h in natural seawater, delivering a stable V-oc of similar to 0.83 V with a power density of 0.79 mu W cm(-2). This study expands a working solution for water-evaporation-induced electricity generation from DI water to natural seawater, advancing a great step toward practical applications.
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