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Fuel Cell Topics: Activation Process of Proton Electrode Membrane Fuel Cell

Views: 0     Author: IHFCA     Publish Time: 2021-06-17      Origin: IHFCA

Original Author: IHFCA

Translate & Edit: Andy, Kewell


#currentcontrol #test #testsystem #Kewell


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ABSTRACT

Fuel cell stack needs to be activated after assembly to reach the best performance state. Traditionally, there are two ways to complete the activation process, constant current and varying current. But, traditional ways are no longer compatible with the current development of fuel cell industry as they are too time-taking and hydrogen consuming. Therefore, the call for a fast and low-damaging activation process has emerged.

Activation process usually includes the following:

a) Humidification of PEM;

b) Channeling of materials (electrons, protons, gas, water);

c) Optimization of electrode structure;

d) Increase the activity and using rate of catalyst layer.




Traditional Online Activation: Current Control

Current control can be divided into three types: 

a) Constant current natural activation;

b) Constant current forcing activation;

c) Varying current forcing activation. 

Amongst the traditional methods, c) is the most widely adopted approach as it takes less time while providing the best result to stack performance. Some lab reports suggest that cycling constant voltage activation is even more effective than current control methods due to the fact that current control methods are more prone to silver nanoparticle clusters at the MEA therefore decreasing the ECSA of catalyst.


Traditional Online Activation: Potential Control

Electrode short-circuit is a rather special way to activate a stack by constant voltage control. It is commonly adopted in pre-activation and independent activation process. By bridging the positive and negative electrodes, voltage level can be kept at 0V. Then input water and gas at certain levels into the system, switching the gas flow at two levels (high and low) while ensuring the reverse polarity time of single cell is within safe range. Proven by experiment, the activation time of such method can be shortened to 1/10 of traditional methods while reducing hydrogen consumption significantly.

On top of that, the activation effect can be greatly enhanced by increasing the gas temperature and pressure as the using rate of catalyst is greatly improved as well.


Fast Online Activation: Hydrogen Pump Activation

Hydrogen pump activation is an activation method that improves the performance of a fuel cell by transferring hydrogen from one side of the membrane to the other. The chemical equation is as follows:

. Anode: H2 = 2H+ + 2e-

. Cathode: 2H+ + 2e- = H2

. Overall: H2 (Anode) = H2 (Cathode)

The principle of such activation is to reduce the overpotential of REDOX. In this process, the porosity and tortuosity of the catalyst layer are changed due to the hydrogen precipitation process, and the number of three phases of the reactant, catalyst and electrolyte in the catalyst layer is increased.

The activation process can be summarized as follows:

. Use pure hydrogen on the anode side. Replace the air on the cathode side with nitrogen;

. Use external power supply with current density at 200mA cm-2;

. Hydrogen is oxidized at the anode. Protons are reduced at the cathode by travelling through the membrane.

In addition, a Ballard test showed that the average cell voltage can be increased by 20-32mV by passing dry and unheated hydrogen through the anode and cathode sides of the cell for five minutes. Another test showed that a brief exposure to the heated and moist hydrogen (80°C, 100%RH, for 5 minutes) allows the cell to reach to nominal operating voltage (within 95% of the normal voltage).


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Fast Online Activation: Air Starvation

The cathodic air starvation method is a brief loading process that works under non-oxidant condition to activate a stack. In the absence of oxidant, reduction can be realized at the cathode. The process can be summarized as follows:

. Load the system without air supply, allowing the voltage level to drop down to 0V or so.

. Restore air supply allowing the voltage level to rise.

. The method can be used to activate a stack right after production, or applied to recovery-activation.


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Fast Online Activation: CO Oxidative Stripping

Carbon monoxide can easily be absorbed on the catalyst causing serious pollution to the PEMFC. However, the phenomenon can also be used as an activation method. The diagram below shows the comparison between the performance of regular activation and CO oxidative stripping condition. As manifested in the diagram, cell density rises after each stripping. 


SUMMARY

Online activation mechanism comes in many ways, each bringing effective results to fuel cell activation. By combining these methods in specific orders, activation process can be accelerated while optimizing cell performance.

The diagram below shows the comparison between the activation time of different methods.

Inappropriate working conditions such as temperature, RH, potential, and duty cycle, can cause serious impact on the microstructure of MEA, therefore affecting the performance and durability of MEA in the long run. 

However, it is also critical to keep the activation process time-efficient and cost-effective. To satisfy both goals, many leading companies have developed their own patented activation processes. Fuel Cell China, for instance, has adopted the cathodic air starvation method to activate a 160-layered fuel cell stack. Hydrogen consumption is reduced to 1/6 of the traditional way, saving 60% of time. Hyundai has applied for a patent on hydrogen pump activation. Activation time is reduced to 35 minutes, with performance state reaching nearly 100%.


Recovery-activation

The performance of fuel cell stack needs to be recovered after a while of storage. Similar to activation process, recovery process exposes the cathode to hydrogen gas, revitalizing the fuel cell after a long period of storage.

To avoid repeated activation, there are a few ways to prevent from momentary performance loss for fuel cell. The main mechanism is to prevent the formation of oxides and/or hydroxides on the cathode catalyst. This method also includes applying an electric potential to the fuel cell during storage (e.g., from 0 to 0.6V/layer), storing it at temperatures below the ambient temperature (e.g., under -20 ° C) or injecting an inert gas to the fuel cell cathode.


Kewell Solutions: Fuel Cell Stack Activation Test Equipment

Listed in the STAR Market of Shanghai Stock Exchange (code 688551), Hefei Kewell Power System is a high-tech enterprise focusing on the development of fuel cell test systems, stack test bench (500W-150kW), and EoL test equipment, satisfying the versatile requirements of activation processes. The product features of stack test bench are as follows:

a) Precise gas flow/mixing control over multi-channel at both anode and cathode. Quick purging. Foreign gas mixing test. CO poisoning/activation tests;

b) Load works under 0V, satisfying the requirement of cathode air starvation test;

c) Gas humidification reaches up to 100%RH. Fast response to gas pressure/flow regulation. Available with two modes: constant voltage/constant current load modes;

d) Bypass pipe design at both inlet and outlet for anode and cathode gas. Match for H2 Soak Activation and satisfy the requirements of EoL testing;

e) Flexible alarm handling procedures that trigger certain recovering process at special working conditions. For instance, air supply can be restored automatically when single cell voltage reaches below preset value after air starvation at the cathode side;

f) Closed hydrogen circulation. Fuel-efficient;

g) Low heat capacity for the thermal management system. Swift adjustment over temperature based on activation processes. Coolant Recycle.

h) Complete safety monitoring procedures: Hydrogen leakage at the stack, insulation failure, exhaust gas flow, upper limits and lower limits of pressure/temperature/CVM, three-stage alarm system etc.


We are dedicated to becoming a world leading brand for test power supplies & systems.

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