I am doing the SKPFM of some sample. The scale bar ( nap potentail image) is giving the maximum and minimum value of Vcpd. I want to know whether the average value of Vcpd is equal to work function or we need to multiply the cpd value by charge.
Considering the tip-sample system as a capacitor, the contact potential difference (CPD) is the difference in work function Φ between sample and tip:
VCPD = (Φsample-Φtip)/e (eq. 1), where e is the elementary charge.
While the KPFM measurement results in the determination of the CPD, which
is the work function of the sample relative to that of the tip,the above equation can be used to deduce the sample’s work function on an absolute scale. Using a calibrated tip with a known work function, the work function of the sample can be calculated from
the CPD measurement according to (eq. 1). However, for absolute work function measurements, operation under ultrahigh vacuum (UHV) conditions is mandatory, as it is well known that the work function is highly sensitive to the surface
I think, you could measure CPD for any well known material, for example, for a thick gold film, like a referee. An amorphous film would be better to avoid crystal orientation dependence.
Standard reference samples for calibration of the AFM tip in air is HOPG. The hydrophobic and inert surface of freshly cleaved HOPG is not covered by the adsorbed layer.
Robin, probably you have done something wrong, or it is error signal against bias voltage, you need a bias voltage of this map, and if you're measured it right, it will be equal to difference of work functions between sample and tip. If you know one of them, you can calculate other one. Polarity of voltage depends on what kind of AFM setup is used, bias can be applied either as voltage on sample, or voltage on tip with second electrode grounded and taken as reference.
KPFM require conductive tip, metal coatings can work up to 1V of bias, more strong coatings like TiN, W2C or DLC can work up to 10 V, it require some sort of reference electrode on sample, connected to right place of the setup, it require right height of second pass in two-pass methods and so on.
I had used Ti/Pt tip with a tip biased of 1V and I am attaching potential image and corresponding height image, please look into this. I tell me if I had done something wrong
First of all, you have a bias value subtracted from both images (both has a mean-centered Z-scale). You need to disable all this postprocessing for Kelvin probe images.
You need a raw Z scale (disable all background subtraction and line processing) like at image below, and you need a bias voltage during the scan (see metadata image, Bias Voltage is what you need). Sum of voltage at image and bias voltage is contact potential difference between tip and sample point. At this example it is -0.43 V for background (gold surface), about -0.3 V on dark graphene flakes (single layer) and about -0.22 V for more charged (light) graphene flakes (two or three layers).
-0.43 V is than contact potential difference (or difference of two work functions) between gold surface on sample and tip material.
Example file taken from NTMDT scan gallery (link below) and processed with Gwyddion software.
It should not, the voltage distribution on smaller scan should be the same as in chunk of larger scan. However, you can measure the Kelvin probe with something like 35 nm resolution at its best (it defined by tip sharpness, its form and distance between tip and sample while measuring), so 1 mkm scan will have to much sample points to be measured properly, and 20 mkm scan will have gaps between points if you use 512 data points per scan dimension. Also measurement noise should be affected by scan sampling.
i am also using the ambient kelvin proble to measure the work function of VO2 thin films. The CPD goes from positive to negative values with respect to the points. is this normal to have varying CPD (negative)?
When we use KPFM signal to calculate the work function of tip through HOPG, it is a map (distribution of surface potential). So, how can we calculate the workfunction of Tip? Is it calculated through the average value of surface potential?
When we use KPFM to scan HOPG, we usually peel a new layer of HOPG for the calibration of the tip work function. This is because the HOPG layer might be contaminated, thus it will show a distribution of surface potential. However, if the surface potential measurement is not done under ultrahigh vacuum (UHV) condition, the quantitative measurement of the surface potential will be inaccurate, thus we will normally analyze the contact potential difference (CPD) of the measurement.
Concerning the use of HOPG as 'calibration' sample: it is true, as Nadim wrote, thatHOPG is hydrophobic but I wouldn't be sure that no water layer is in between the tip and the sample, in ambient air (RH as high as 50 or 60%), also dut to the tip side (durface) of the interface (ie water squeezed in between anyway, at the meniscus).
Marco Salerno Nadim Davletkildeev Freshly cleaved HOPG is actually hydrophilic. Check : Effect of airborne contaminants on the wettability of supported graphene and graphite Article Effect of airborne contaminants on the wettability of suppor...
While calculating W.F. of the sample, should we take W.F. of the tip as -ve value? For e.g. if the work function of tip is 4.7 eV and CPD is 0.1 V, then W.F. of sample will be 4.7-0.1= 4.6 eV or -4.7-0.1=-4.8 eV?
Urvashi Bothra It depends on how the UDC is connected. If DC voltage is applied to the sample, then W.F.sample=W.F.sample-CPD*e;if DC voltage is applied to the probe, then W.F.sample=W.F.sample+CPD*e,where e is the electronic charge.
Urvashi Bothra sorry, I made an editing mistake. If DC voltage is applied to the probe, then W.F.sample=W.F.tip-CPD*e;if DC voltage is applied to the sample, then W.F.sample=W.F.tip+CPD*e. I hope you can refer to the following ref:
1) Two-dimensional surface band structure of operating light emitting devices (
J. Appl. Phys. 86, 107 (1999); doi: 10.1063/1.370706)
2) High-resolution work function imaging of single grains of semiconductor surfaces (Appl. Phys. Lett. 80, 2979 (2002); doi: 10.1063/1.1471375)
3) Kelvin probe force microscopy in ultra high vacuum using amplitude modulation detection of the electrostatic forces ( Applied Surface Science 157 2000 263–268)
4) High-sensitivity quantitative Kelvin probe microscopy by noncontact ultrahigh-vacuum atomic force microscopy (Appl. Phys. Lett. 75, 286 (1999); doi: 10.1063/1.124357)
Yes, I got that also, BUT the negative sign on the right of the CPD can result in two numbers, a lower or higher. How do we know which is the correct to report as It is making me a question do I have lower CPD meaning n-type doping or if I calculate higher CPD because of the sign, is it because of MoO3, in MoS2, I see both in my data, but they are opposite to each other. How we interpret WF in such a scenario.
Sanju Gupta To solve your problem, we must know the relationship between Udc and Ucpd. Udc is obtained in the experiment, not Ucpd. We only know that |Udc|=|Ucpd|, then Udc=Ucpd or Udc=-Ucpd? This is a key. It depends on the following two questions:
1) The definition of Ucpd: -eV_CPD = WF_tip - WF_s or eV_CPD = WF_tip - WF_s ?
2) The DC voltage is applied to the sample or the tip?
① If -eV_CPD = WF_tip - WF_s and the DC voltage is applied to the sample, Udc=Ucpd. So, W.F.sample=W.F.tip+Udc*e.
② If -eV_CPD = WF_tip - WF_s and the DC voltage is applied to the tip, Udc=-Ucpd. So, W.F.sample=W.F.tip-Udc*e.
Is it possible to calculate the work functions of nanoparticles such as HgTe, HgSe QDs, or nanolayers of Bi2Te3 film with respect to references like HOPG or Au?
I started to scan them at room temperature and got foe them some different values of CPD, now the question is will it be a more sensitive measurement to scan them in dry air like purging by Ar or N2 gas flow. Is it necessary to do the experiment in the UHV condition to calculate the WF of nanoparticles as QD & 2D layers?