hg hgo Search Results


hg/hgo reference electrode filled with 1 m naoh  (CH Instruments)
90
CH Instruments hg/hgo reference electrode filled with 1 m naoh
Hg/Hgo Reference Electrode Filled With 1 M Naoh, supplied by CH Instruments, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/hg+hgo/1+m+koh+hg+hgo+reference+electrode/pmc11267498-55-7-11
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hg/hgo reference electrode filled with 1 m naoh - by Bioz Stars, 2026-09
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koh  (CH Instruments)
90
CH Instruments koh
Koh, supplied by CH Instruments, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/hg+hgo/hg+hgo++1+m+koh+/pm33937224-49-23-34
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koh - by Bioz Stars, 2026-09
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hg/hgo/1 m koh  (Bioanalytical Systems Inc)
90
Bioanalytical Systems Inc hg/hgo/1 m koh
(A) Potentiostatic electrolysis at +1.03 V RHE recorded for the Pt/C catalyst layers of varying ionomer content. (B) Typical cell voltage in a CO 2 electrolyzer when OER is performed at the Ir anode catalyst, compared to an electrolyzer in which the OER is replaced with GOR. Conditions in the OER case were: j = 200 mA cm –2 , 1 M <t>KOH,</t> 1 cm 3 cm –2 min –1 electrolyte flow rate. Conditions in the GOR case are identical to the measurement presented in panel A: the electrolyte was 1 M KOH + 0.5 M glycerol flowed through the cell in a single pass mode. The electrolyte flow rate was set to 5 cm 3 cm –2 min –1 , while the CO 2 flow rate was maintained at 12 cm 3 cm –2 min –1 . (C) Glycerol oxidation product distribution as a function of the CST ionomer content in the Pt/C catalyst layer. Samples were taken during the potentiostatic holds presented in panel A. Error bars were calculated for three measurements, each performed using fresh cathode and anode catalyst layers. All measurements were performed in a membraneless microfluidic flow electrolyzer cell.
Hg/Hgo/1 M Koh, supplied by Bioanalytical Systems Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/hg+hgo/hg+hgo+1+m+koh/pmc11075010-77-12-13
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hg/hgo/1 m koh - by Bioz Stars, 2026-09
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hg|hgo reference electrode l120-s7  (Origalys Inc)
90
Origalys Inc hg|hgo reference electrode l120-s7
(A) Potentiostatic electrolysis at +1.03 V RHE recorded for the Pt/C catalyst layers of varying ionomer content. (B) Typical cell voltage in a CO 2 electrolyzer when OER is performed at the Ir anode catalyst, compared to an electrolyzer in which the OER is replaced with GOR. Conditions in the OER case were: j = 200 mA cm –2 , 1 M <t>KOH,</t> 1 cm 3 cm –2 min –1 electrolyte flow rate. Conditions in the GOR case are identical to the measurement presented in panel A: the electrolyte was 1 M KOH + 0.5 M glycerol flowed through the cell in a single pass mode. The electrolyte flow rate was set to 5 cm 3 cm –2 min –1 , while the CO 2 flow rate was maintained at 12 cm 3 cm –2 min –1 . (C) Glycerol oxidation product distribution as a function of the CST ionomer content in the Pt/C catalyst layer. Samples were taken during the potentiostatic holds presented in panel A. Error bars were calculated for three measurements, each performed using fresh cathode and anode catalyst layers. All measurements were performed in a membraneless microfluidic flow electrolyzer cell.
Hg|Hgo Reference Electrode L120 S7, supplied by Origalys Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/hg+hgo/hg+hgo+reference+electrode+l120+s7/pm35501344-316-5-9
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hg|hgo reference electrode l120-s7 - by Bioz Stars, 2026-09
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hg/hgo reference electrode chi152  (CH Instruments)
90
CH Instruments hg/hgo reference electrode chi152
(A) Potentiostatic electrolysis at +1.03 V RHE recorded for the Pt/C catalyst layers of varying ionomer content. (B) Typical cell voltage in a CO 2 electrolyzer when OER is performed at the Ir anode catalyst, compared to an electrolyzer in which the OER is replaced with GOR. Conditions in the OER case were: j = 200 mA cm –2 , 1 M <t>KOH,</t> 1 cm 3 cm –2 min –1 electrolyte flow rate. Conditions in the GOR case are identical to the measurement presented in panel A: the electrolyte was 1 M KOH + 0.5 M glycerol flowed through the cell in a single pass mode. The electrolyte flow rate was set to 5 cm 3 cm –2 min –1 , while the CO 2 flow rate was maintained at 12 cm 3 cm –2 min –1 . (C) Glycerol oxidation product distribution as a function of the CST ionomer content in the Pt/C catalyst layer. Samples were taken during the potentiostatic holds presented in panel A. Error bars were calculated for three measurements, each performed using fresh cathode and anode catalyst layers. All measurements were performed in a membraneless microfluidic flow electrolyzer cell.
Hg/Hgo Reference Electrode Chi152, supplied by CH Instruments, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/hg+hgo/hg+hgo+chi152/10__1021_slash_acs__jpcc__9b03589-49-26-32
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hg/hgo reference electrode chi152 - by Bioz Stars, 2026-09
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screwable ag/agcl electrode re-3vt  (C3 Prozess)
90
C3 Prozess screwable ag/agcl electrode re-3vt
(A) Potentiostatic electrolysis at +1.03 V RHE recorded for the Pt/C catalyst layers of varying ionomer content. (B) Typical cell voltage in a CO 2 electrolyzer when OER is performed at the Ir anode catalyst, compared to an electrolyzer in which the OER is replaced with GOR. Conditions in the OER case were: j = 200 mA cm –2 , 1 M <t>KOH,</t> 1 cm 3 cm –2 min –1 electrolyte flow rate. Conditions in the GOR case are identical to the measurement presented in panel A: the electrolyte was 1 M KOH + 0.5 M glycerol flowed through the cell in a single pass mode. The electrolyte flow rate was set to 5 cm 3 cm –2 min –1 , while the CO 2 flow rate was maintained at 12 cm 3 cm –2 min –1 . (C) Glycerol oxidation product distribution as a function of the CST ionomer content in the Pt/C catalyst layer. Samples were taken during the potentiostatic holds presented in panel A. Error bars were calculated for three measurements, each performed using fresh cathode and anode catalyst layers. All measurements were performed in a membraneless microfluidic flow electrolyzer cell.
Screwable Ag/Agcl Electrode Re 3vt, supplied by C3 Prozess, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/hg+hgo/hg+hgo+reference+electrode/10__3390_slash_app10031133-63-6-9
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screwable ag/agcl electrode re-3vt - by Bioz Stars, 2026-09
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hg/hg 2 so 4 reference electrode hge 11-s  (SensorTechnik Meinsberg)
90
SensorTechnik Meinsberg hg/hg 2 so 4 reference electrode hge 11-s
(A) Potentiostatic electrolysis at +1.03 V RHE recorded for the Pt/C catalyst layers of varying ionomer content. (B) Typical cell voltage in a CO 2 electrolyzer when OER is performed at the Ir anode catalyst, compared to an electrolyzer in which the OER is replaced with GOR. Conditions in the OER case were: j = 200 mA cm –2 , 1 M <t>KOH,</t> 1 cm 3 cm –2 min –1 electrolyte flow rate. Conditions in the GOR case are identical to the measurement presented in panel A: the electrolyte was 1 M KOH + 0.5 M glycerol flowed through the cell in a single pass mode. The electrolyte flow rate was set to 5 cm 3 cm –2 min –1 , while the CO 2 flow rate was maintained at 12 cm 3 cm –2 min –1 . (C) Glycerol oxidation product distribution as a function of the CST ionomer content in the Pt/C catalyst layer. Samples were taken during the potentiostatic holds presented in panel A. Error bars were calculated for three measurements, each performed using fresh cathode and anode catalyst layers. All measurements were performed in a membraneless microfluidic flow electrolyzer cell.
Hg/Hg 2 So 4 Reference Electrode Hge 11 S, supplied by SensorTechnik Meinsberg, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/hg+hgo/commercial+hg+hgo+reference+electrode/pmc08064305-76-11-15
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hg/hg 2 so 4 reference electrode hge 11-s - by Bioz Stars, 2026-09
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hg/hgo reference electrode ch152  (CH Instruments)
90
CH Instruments hg/hgo reference electrode ch152
(A) Potentiostatic electrolysis at +1.03 V RHE recorded for the Pt/C catalyst layers of varying ionomer content. (B) Typical cell voltage in a CO 2 electrolyzer when OER is performed at the Ir anode catalyst, compared to an electrolyzer in which the OER is replaced with GOR. Conditions in the OER case were: j = 200 mA cm –2 , 1 M <t>KOH,</t> 1 cm 3 cm –2 min –1 electrolyte flow rate. Conditions in the GOR case are identical to the measurement presented in panel A: the electrolyte was 1 M KOH + 0.5 M glycerol flowed through the cell in a single pass mode. The electrolyte flow rate was set to 5 cm 3 cm –2 min –1 , while the CO 2 flow rate was maintained at 12 cm 3 cm –2 min –1 . (C) Glycerol oxidation product distribution as a function of the CST ionomer content in the Pt/C catalyst layer. Samples were taken during the potentiostatic holds presented in panel A. Error bars were calculated for three measurements, each performed using fresh cathode and anode catalyst layers. All measurements were performed in a membraneless microfluidic flow electrolyzer cell.
Hg/Hgo Reference Electrode Ch152, supplied by CH Instruments, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/hg+hgo/reference+electrode+hg+hgo+ch152/10__1016_slash_j__nanoen__2018__12__098-55-10-13
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hg/hgo reference electrode ch152 - by Bioz Stars, 2026-09
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hg/hgo reference electrode #152  (CH Instruments)
90
CH Instruments hg/hgo reference electrode #152
(A) Potentiostatic electrolysis at +1.03 V RHE recorded for the Pt/C catalyst layers of varying ionomer content. (B) Typical cell voltage in a CO 2 electrolyzer when OER is performed at the Ir anode catalyst, compared to an electrolyzer in which the OER is replaced with GOR. Conditions in the OER case were: j = 200 mA cm –2 , 1 M <t>KOH,</t> 1 cm 3 cm –2 min –1 electrolyte flow rate. Conditions in the GOR case are identical to the measurement presented in panel A: the electrolyte was 1 M KOH + 0.5 M glycerol flowed through the cell in a single pass mode. The electrolyte flow rate was set to 5 cm 3 cm –2 min –1 , while the CO 2 flow rate was maintained at 12 cm 3 cm –2 min –1 . (C) Glycerol oxidation product distribution as a function of the CST ionomer content in the Pt/C catalyst layer. Samples were taken during the potentiostatic holds presented in panel A. Error bars were calculated for three measurements, each performed using fresh cathode and anode catalyst layers. All measurements were performed in a membraneless microfluidic flow electrolyzer cell.
Hg/Hgo Reference Electrode #152, supplied by CH Instruments, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/hg+hgo/hg+hgo+reference+electrode++152/10__1039_slash_c7se00086c-50-6-9
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hg/hgo reference electrode #152 - by Bioz Stars, 2026-09
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mercury-mercury oxide electrode hg|hgo|naoh, moe  (Origalys Inc)
90
Origalys Inc mercury-mercury oxide electrode hg|hgo|naoh, moe
(A) Potentiostatic electrolysis at +1.03 V RHE recorded for the Pt/C catalyst layers of varying ionomer content. (B) Typical cell voltage in a CO 2 electrolyzer when OER is performed at the Ir anode catalyst, compared to an electrolyzer in which the OER is replaced with GOR. Conditions in the OER case were: j = 200 mA cm –2 , 1 M <t>KOH,</t> 1 cm 3 cm –2 min –1 electrolyte flow rate. Conditions in the GOR case are identical to the measurement presented in panel A: the electrolyte was 1 M KOH + 0.5 M glycerol flowed through the cell in a single pass mode. The electrolyte flow rate was set to 5 cm 3 cm –2 min –1 , while the CO 2 flow rate was maintained at 12 cm 3 cm –2 min –1 . (C) Glycerol oxidation product distribution as a function of the CST ionomer content in the Pt/C catalyst layer. Samples were taken during the potentiostatic holds presented in panel A. Error bars were calculated for three measurements, each performed using fresh cathode and anode catalyst layers. All measurements were performed in a membraneless microfluidic flow electrolyzer cell.
Mercury Mercury Oxide Electrode Hg|Hgo|Naoh, Moe, supplied by Origalys Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/hg+hgo/mercury+mercury+oxide+electrode+hg+hgo+naoh++moe/10__1021_slash_acsaem__0c01008-242-16-21
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mercury-mercury oxide electrode hg|hgo|naoh, moe - by Bioz Stars, 2026-09
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hg/hgo storage condition electrode manufacturer hughes eaglepicher whittaker/ yardney gates hprt26  (EaglePicher)
90
EaglePicher hg/hgo storage condition electrode manufacturer hughes eaglepicher whittaker/ yardney gates hprt26
(A) Potentiostatic electrolysis at +1.03 V RHE recorded for the Pt/C catalyst layers of varying ionomer content. (B) Typical cell voltage in a CO 2 electrolyzer when OER is performed at the Ir anode catalyst, compared to an electrolyzer in which the OER is replaced with GOR. Conditions in the OER case were: j = 200 mA cm –2 , 1 M <t>KOH,</t> 1 cm 3 cm –2 min –1 electrolyte flow rate. Conditions in the GOR case are identical to the measurement presented in panel A: the electrolyte was 1 M KOH + 0.5 M glycerol flowed through the cell in a single pass mode. The electrolyte flow rate was set to 5 cm 3 cm –2 min –1 , while the CO 2 flow rate was maintained at 12 cm 3 cm –2 min –1 . (C) Glycerol oxidation product distribution as a function of the CST ionomer content in the Pt/C catalyst layer. Samples were taken during the potentiostatic holds presented in panel A. Error bars were calculated for three measurements, each performed using fresh cathode and anode catalyst layers. All measurements were performed in a membraneless microfluidic flow electrolyzer cell.
Hg/Hgo Storage Condition Electrode Manufacturer Hughes Eaglepicher Whittaker/ Yardney Gates Hprt26, supplied by EaglePicher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/hg+hgo/hg+hgo+storage+condition+electrode+manufacturer+hughes+eaglepicher+whittaker++yardney+gates+hprt26/10__1016_slash_0378___7753_ascii40_90_ascii41_85024___7-155-0-6
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hg/hgo storage condition electrode manufacturer hughes eaglepicher whittaker/ yardney gates hprt26 - by Bioz Stars, 2026-09
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enriched stable isotopes of hg (as 199 hgo, 200 hgo, and 201 hgo)  (Cambridge Isotope Laboratories)
90
Cambridge Isotope Laboratories enriched stable isotopes of hg (as 199 hgo, 200 hgo, and 201 hgo)
(A) Potentiostatic electrolysis at +1.03 V RHE recorded for the Pt/C catalyst layers of varying ionomer content. (B) Typical cell voltage in a CO 2 electrolyzer when OER is performed at the Ir anode catalyst, compared to an electrolyzer in which the OER is replaced with GOR. Conditions in the OER case were: j = 200 mA cm –2 , 1 M <t>KOH,</t> 1 cm 3 cm –2 min –1 electrolyte flow rate. Conditions in the GOR case are identical to the measurement presented in panel A: the electrolyte was 1 M KOH + 0.5 M glycerol flowed through the cell in a single pass mode. The electrolyte flow rate was set to 5 cm 3 cm –2 min –1 , while the CO 2 flow rate was maintained at 12 cm 3 cm –2 min –1 . (C) Glycerol oxidation product distribution as a function of the CST ionomer content in the Pt/C catalyst layer. Samples were taken during the potentiostatic holds presented in panel A. Error bars were calculated for three measurements, each performed using fresh cathode and anode catalyst layers. All measurements were performed in a membraneless microfluidic flow electrolyzer cell.
Enriched Stable Isotopes Of Hg (As 199 Hgo, 200 Hgo, And 201 Hgo), supplied by Cambridge Isotope Laboratories, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/hg+hgo/enriched+stable+isotopes+of+hg++as+199+hgo++200+hgo++and+201+hgo+/pmc04014141-46-11-16
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Image Search Results


(A) Potentiostatic electrolysis at +1.03 V RHE recorded for the Pt/C catalyst layers of varying ionomer content. (B) Typical cell voltage in a CO 2 electrolyzer when OER is performed at the Ir anode catalyst, compared to an electrolyzer in which the OER is replaced with GOR. Conditions in the OER case were: j = 200 mA cm –2 , 1 M KOH, 1 cm 3 cm –2 min –1 electrolyte flow rate. Conditions in the GOR case are identical to the measurement presented in panel A: the electrolyte was 1 M KOH + 0.5 M glycerol flowed through the cell in a single pass mode. The electrolyte flow rate was set to 5 cm 3 cm –2 min –1 , while the CO 2 flow rate was maintained at 12 cm 3 cm –2 min –1 . (C) Glycerol oxidation product distribution as a function of the CST ionomer content in the Pt/C catalyst layer. Samples were taken during the potentiostatic holds presented in panel A. Error bars were calculated for three measurements, each performed using fresh cathode and anode catalyst layers. All measurements were performed in a membraneless microfluidic flow electrolyzer cell.

Journal: ACS Catalysis

Article Title: Stable Operation of Paired CO 2 Reduction/Glycerol Oxidation at High Current Density

doi: 10.1021/acscatal.3c05952

Figure Lengend Snippet: (A) Potentiostatic electrolysis at +1.03 V RHE recorded for the Pt/C catalyst layers of varying ionomer content. (B) Typical cell voltage in a CO 2 electrolyzer when OER is performed at the Ir anode catalyst, compared to an electrolyzer in which the OER is replaced with GOR. Conditions in the OER case were: j = 200 mA cm –2 , 1 M KOH, 1 cm 3 cm –2 min –1 electrolyte flow rate. Conditions in the GOR case are identical to the measurement presented in panel A: the electrolyte was 1 M KOH + 0.5 M glycerol flowed through the cell in a single pass mode. The electrolyte flow rate was set to 5 cm 3 cm –2 min –1 , while the CO 2 flow rate was maintained at 12 cm 3 cm –2 min –1 . (C) Glycerol oxidation product distribution as a function of the CST ionomer content in the Pt/C catalyst layer. Samples were taken during the potentiostatic holds presented in panel A. Error bars were calculated for three measurements, each performed using fresh cathode and anode catalyst layers. All measurements were performed in a membraneless microfluidic flow electrolyzer cell.

Article Snippet: All data were collected in a three-electrode configuration, where a Hg/HgO/1 M KOH (Bioanalytical Systems Inc.) was employed as a reference electrode.

Techniques: Electrolysis

(A) Anode potential and (B) cell voltage during the measurement at j = 150 mA cm –2 . The CO 2 flow rate was maintained at 12 cm 3 cm –2 min –1 , while the 1 M KOH + 0.5 M glycerol electrolyte flow rate was set to 5 cm 3 cm –2 min –1 . All measurements were performed in a membraneless microfluidic flow electrolyzer cell. (C) GOR product distribution during the measurement shown in (A)–(B).

Journal: ACS Catalysis

Article Title: Stable Operation of Paired CO 2 Reduction/Glycerol Oxidation at High Current Density

doi: 10.1021/acscatal.3c05952

Figure Lengend Snippet: (A) Anode potential and (B) cell voltage during the measurement at j = 150 mA cm –2 . The CO 2 flow rate was maintained at 12 cm 3 cm –2 min –1 , while the 1 M KOH + 0.5 M glycerol electrolyte flow rate was set to 5 cm 3 cm –2 min –1 . All measurements were performed in a membraneless microfluidic flow electrolyzer cell. (C) GOR product distribution during the measurement shown in (A)–(B).

Article Snippet: All data were collected in a three-electrode configuration, where a Hg/HgO/1 M KOH (Bioanalytical Systems Inc.) was employed as a reference electrode.

Techniques: