A detailed description of an isoperibol calorimeter for temperatures between 0.05 and 4 K is presented. The proposed setup can provide absolute values of the heat capacity of small samples (typically 1 mg). The extremely simple design of the sample platform, based on a sapphire substrate, and the experimental setup, which makes use only of a lock-in amplifier and a temperature controller, make the construction of such a calorimeter easy and inexpensive. The thermal-relaxation method is employed, which utilizes a permanent thermal link between the sample platform and the low-temperature bath. The temperature dependence of is shown for several platforms throughout the entire temperature range: is nearly constant down to 1 K, where it starts to decrease smoothly. The observed behavior is thoroughly explained by considering the thermal resistances of the platform constituents. A comparison between the values of for platforms based on sapphire and on silver is presented where no significant difference has been observed. Each platform can be assembled to have a particular value of at 1 K. Since the sample relaxation time , can be adjusted to to give a reasonably fast measuring time. Here, it is demonstrated how this calorimeter can be used in so-called single-shot refrigerators ( or demagnetization cryostats), where the time for a single measurement is limited. In addition, it can be used in moderate magnetic fields , because the platform constituents are weakly field dependent.
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September 2009
Research Article|
September 21 2009
Development of a relaxation calorimeter for temperatures between 0.05 and 4 K
a)
Present address: Max Planck Institute for Chemical Physics of Solids, Nöthnitzer Str. 40, 01187 Dresden, Germany. Electronic mail: manuel.brando@cpfs.mpg.de.
Rev. Sci. Instrum. 80, 095112 (2009)
Article history
Received:
February 11 2009
Accepted:
July 20 2009
Citation
M. Brando; Development of a relaxation calorimeter for temperatures between 0.05 and 4 K. Rev. Sci. Instrum. 1 September 2009; 80 (9): 095112. https://doi.org/10.1063/1.3202380
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