Abstract:Passive fuel cells, using diffusion and natural convection for fuel delivery, are regarded as promising candidates for powering portable devices including mobile phones and laptops. However, the performance of passive fuel cells which employ typical liquid alcohol fuels are still limited, which thereby greatly hampered their commercialization progress. Recently, a novel concept named the electrically rechargeable liquid fuel (e-fuel), with its rechargeability, cost-effectiveness, and superior reactivity, has a… Show more
“…It also indicated that palladium catalyst had high activity for formic acid oxidation at very low anode potential. The cell voltage was recorded to be well above 0.8 V. R.I Masel et al, also reported that the current density of the cell increased to 0.63 A, on using Palladium Black Anode as the catalyst, which was 200 times higher, when using a Platinum Catalyst at 0.4 V. The CV [313] (Reproduced with permission from reference 315, American Chemical Society, 2021) measurements carried out for palladium Black indicated a big anodic oxidation peak at 0.3 V. It was also reported that, on operating the DFAFC at 50°C, a maximum power density of 375 mW/cm 2 was achieved. [311] Kenis et al reported the performance output of a Si-Based DFAFC, where the fuel and oxidants are fed to the electrodes in a passive way, that is the liquid formic acid is in contact with the anodic part (Pd or Pt Catalyst) of MEA and on the other side, quiescent air is fed to the cathode (Pt Catalyst) which is more of an air breather setup.…”
Section: Unsupported Pt and Pd Based Catalystsmentioning
confidence: 82%
“…Figure 13. (a) Working principle (b) Hardware components (c) Fabrication of a of a passive fuel cell[313] (Reproduced with permission from reference 315, American Chemical Society, 2021)…”
Direct formic acid fuel cells (DFAFCs) have gained immense importance as a source of clean energy for portable electronic devices. It outperforms other fuel cells in several key operational and safety parameters. However, slow kinetics of the formic acid oxidation at the anode remains the main obstacle in achieving a high power output in DFAFCs. Noble metal‐based electrocatalysts are effective, but are expensive and prone to CO poisoning. Recently, a substantial volume of research work have been dedicated to develop inexpensive, high activity and long lasting electrocatalysts. Herein, recent advances in the development of anode electrocatalysts for DFAFCs are presented focusing on understanding the relationship between activity and structure. This review covers the literature related to the electrocatalysts based on noble metals, non‐noble metals, metal‐oxides, synthesis route, support material, and fuel cell performance. The future prospects and bottlenecks in the field are also discussed at the end.
“…It also indicated that palladium catalyst had high activity for formic acid oxidation at very low anode potential. The cell voltage was recorded to be well above 0.8 V. R.I Masel et al, also reported that the current density of the cell increased to 0.63 A, on using Palladium Black Anode as the catalyst, which was 200 times higher, when using a Platinum Catalyst at 0.4 V. The CV [313] (Reproduced with permission from reference 315, American Chemical Society, 2021) measurements carried out for palladium Black indicated a big anodic oxidation peak at 0.3 V. It was also reported that, on operating the DFAFC at 50°C, a maximum power density of 375 mW/cm 2 was achieved. [311] Kenis et al reported the performance output of a Si-Based DFAFC, where the fuel and oxidants are fed to the electrodes in a passive way, that is the liquid formic acid is in contact with the anodic part (Pd or Pt Catalyst) of MEA and on the other side, quiescent air is fed to the cathode (Pt Catalyst) which is more of an air breather setup.…”
Section: Unsupported Pt and Pd Based Catalystsmentioning
confidence: 82%
“…Figure 13. (a) Working principle (b) Hardware components (c) Fabrication of a of a passive fuel cell[313] (Reproduced with permission from reference 315, American Chemical Society, 2021)…”
Direct formic acid fuel cells (DFAFCs) have gained immense importance as a source of clean energy for portable electronic devices. It outperforms other fuel cells in several key operational and safety parameters. However, slow kinetics of the formic acid oxidation at the anode remains the main obstacle in achieving a high power output in DFAFCs. Noble metal‐based electrocatalysts are effective, but are expensive and prone to CO poisoning. Recently, a substantial volume of research work have been dedicated to develop inexpensive, high activity and long lasting electrocatalysts. Herein, recent advances in the development of anode electrocatalysts for DFAFCs are presented focusing on understanding the relationship between activity and structure. This review covers the literature related to the electrocatalysts based on noble metals, non‐noble metals, metal‐oxides, synthesis route, support material, and fuel cell performance. The future prospects and bottlenecks in the field are also discussed at the end.
“…During the test, the e-fuel was delivered to the anode by a peristaltic pump at a flow rate of 60 mL min –1 from a tank of 120 mL e-fuel, while pure oxygen was fed to the cathode at a flow rate of 10 sccm. The polarization curve tests were conducted using other homemade active − and passive fuel cells, as reported before, both of which have an active area of 2.0*2.0 cm 2 . For the active fuel cell, the e-fuel and the oxygen were fed into the cell at 60 mL min –1 and 10 sccm, respectively.…”
Section: Methodsmentioning
confidence: 99%
“…For the active fuel cell, the e-fuel and the oxygen were fed into the cell at 60 mL min –1 and 10 sccm, respectively. While for the passive fuel cell, a current collector with an open ratio of 70% was adopted . Both cells used 20 mL of e-fuel during the tests.…”
Section: Methodsmentioning
confidence: 99%
“…Recently, a novel fuel cell using the electrically rechargeable fuel (e-fuel) for power generation has been demonstrated. , The e-fuel can be made of a wide range of electroactive materials. In our previous studies, we developed a liquid e-fuel cell employing vanadium-based e-fuel and oxygen as reactants − and demonstrated its power generation capability under different operating conditions. While the cell is proved to exhibit a substantially improved performance that exceeds other conventional direct alcohol fuel cells, it is found that the water generated at the cathode during the cell operation due to the oxygen reduction reaction could lead to a water flooding problem .…”
The
liquid fuel cell, with its high energy density and ease of
fuel handling, has attracted great attention worldwide. However, its
real application is still being greatly hindered by its limited power
density. Hence, the recently proposed and demonstrated fuel cell,
using an electrically rechargeable liquid fuel (e-fuel), is believed
to be a candidate with great potential due to its significant performance
advancement. Unlike the conventional alcoholic liquid fuels, the e-fuel
possesses excellent reactivity, even on carbon-based materials, which
therefore allows the e-fuel cell to achieve superior performance without
any noble metal catalysts. However, it is found that, during the cell
operation, the water generated at the cathode following the oxygen
reduction reaction could lead to a water flooding problem and further
limit the cell performance. To address this issue, in this work, by
manipulating the cathode composition, a blended binder cathode using
both Nafion and polytetrafluoroethylene as binding agents is fabricated
and demonstrated its superiority in the fuel cell to achieve an enhanced
water management and cell performance. Furthermore, using the developed
cathode, a fuel cell stack is designed and fabricated to power a 3D-printed
toy car, presenting this system as a promising device feasible for
future study and real applications.
The direct liquid fuel cell (DLFC) constitutes a promising energy conversion system that directly conveys the chemical energy of liquid fuels into electrical energy. In certain DLFCs, gas is produced as a product of electrochemical reactions during operation. However, the accumulation of gas inside the porous electrode can significantly hinder the transport of reactants, leading to the failure of active sites and severe concentration loss. To address this issue, a gradient‐ordered membrane electrode assembly (MEA) is designed and fabricated, consisting of a dual‐gradient diffusion layer that comprises a pore‐size gradient and a wettability gradient as well as a catalyst layer constructed by nanoneedle catalyst. This MEA promptly removes the produced gas and delivers the fresh solution, thereby enhancing the cell power output and stability. The fuel cell with the gradient‐ordered MEA achieves a remarkable peak power density of 177 mW cm−2 and a discharging time of 19 h, which are more than four times and 30 times, respectively, higher than those of the conventional MEA.
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