Table 1.
Redox reaction | α, mV/K | YT = ΔТmax @300K, K | Qg/b @300K |
---|---|---|---|
2 H+ + 2e− → H2 (g) | 0.8 | 307 | 4.09,27 |
V3+ + e− → V2+ | 1.2–1.9* | 36 | 6.028 |
V5+ + e− → V4+ | −0.2* | 6 | 2.428 |
Br2(l) + e−→ 2Br− | 0.3* | 14 | 1.729 |
Fe(CN)63− + e− → Fe(CN)64− | −1.5* | 10.6 | 78.430 |
Fe3+ + e− → Fe2+ | 1.1* | 36 | 95.731 |
Cr3+ + e− → Cr2+ | 2.2 | 7 | 219.59,23,31 |
Ce5++e− → Ce4+ | 2.3 | 13 | 36.09,32 |
S22− + 2e− → 2S2− | −0.7 | 9.4 | 1.39,33 |
Qg/b and YT = ΔТmax are listed to illustrate the trade-off between overall cooling capacity, reversibility, and thermopower. Properties of reduction reactions denoted ‘*’ were measured expressly for this work, as described in the SI. Entropy of reduction varies with total concentration for some species. In these cases, ΔТmax and Qg/b were calculated based on the concentration yielding the highest ΔТmax. Activation energies Ea were estimated based on literature sources for exchange current density or reaction velocity, as described in the SI.